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285 peer-reviewed articles • 9,778 peer-reviewed citations • Sorted by year • Download PDF (PDF by citations)
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1Can we predict the risk of venous thromboembolism in patients with Cushing’s syndrome: a nationwide cohort analysis
Pituitary, 2025, 28,
2.68Citations (PDF)
2Cushing’s syndrome related to higher rates and earlier onset of cataract: A nationwide retrospective cohort study1.81Citations (PDF)
3Osilodrostat improves blood pressure and glycemic control in patients with Cushing’s disease: a pooled analysis of LINC 3 and LINC 4 studies
Pituitary, 2025, 28,
2.619Citations (PDF)
4Leukocytosis in Cushing’s syndrome persists post-surgical remission and could predict a lower remission prognosis in patients with Cushing’s disease2.84Citations (PDF)
5Delphi panel consensus on recommendations for thromboprophylaxis of venous thromboembolism in endogenous Cushing's syndrome: a position statement4.017Citations (PDF)
6Osilodrostat Treatment for Adrenal and Ectopic Cushing Syndrome: Integration of Clinical Studies With Case Presentations0.315Citations (PDF)
7Impact of remission status in endogenous Cushing's syndrome on cancer incidence4.06Citations (PDF)
8Cancer screening in patients with acromegaly: a plea for a personalized approach and international registries6.713Citations (PDF)
9Osilodrostat Treatment of Cushing Syndrome in Real-World Clinical Practice: Findings From the ILLUSTRATE study0.314Citations (PDF)
10Mortality in Cushing's syndrome: declining over 2 decades but remaining higher than the general population4.012Citations (PDF)
11PANOMEN-3 grading score is reliable in predicting pituitary adenoma behavior and prognosis: a single center cohort study
Endocrine, 2025, 89, 834-845
2.57Citations (PDF)
12Predictors of cancer in patients with endogenous Cushing’s syndrome3.51Citations (PDF)
13Weight gain reversibility and BMI following treatment for Cushing’s syndrome: long-term outcomes and potential predictors
Pituitary, 2025, 28,
2.610Citations (PDF)
14Prolactin-secreting adenomas: pathogenesis, diagnosis, and management21.728Citations (PDF)
15Reply to ‘The shift of therapeutic strategy for prolactinomas: surgery as the first-line option’
Nature Reviews Endocrinology, 2024, 20, 311-311
31.81Citations (PDF)
16Reply to ‘Tumour fibrosis in dopamine agonist-exposed prolactinomas is a diminishing concern’
Nature Reviews Endocrinology, 2024, 20, 315-315
31.81Citations (PDF)
17Improvement in clinical features of hypercortisolism during osilodrostat treatment: findings from the Phase III LINC 3 trial in Cushing's disease2.812Citations (PDF)
18Hypopituitarism and bone disease: pathophysiology, diagnosis and treatment outcomes
Pituitary, 2024, 27, 778-788
2.610Citations (PDF)
19Hypopituitarism
Lancet, The, 2024, 403, 2632-2648
62.1100Citations (PDF)
20Impact of etiology, sex, diabetes mellitus and remission status on erythrocytic profile in patients with cushing’s syndrome: a large population database study
Pituitary, 2024, 27, 389-402
2.65Citations (PDF)
21Medical treatment of functional pituitary adenomas, trials and tribulations
Journal of Neuro-Oncology, 2024, 168, 197-213
2.59Citations (PDF)
22Oral octreotide capsules for acromegaly treatment: application of clinical trial insights to real-world use2.99Citations (PDF)
23Diabetes mellitus in patients with acromegaly: pathophysiology, clinical challenges and management
Nature Reviews Endocrinology, 2024, 20, 541-552
31.849Citations (PDF)
24The conundrum of differentiating Cushing’s syndrome from non-neoplastic hypercortisolism: a systematic review and meta-analysis
Pituitary, 2024, 27, 345-359
2.612Citations (PDF)
25Acromegaly and COVID-19, lessons, and new opportunities
Pituitary, 2024, 27, 935-944
2.62Citations (PDF)
26Conundrums of Diagnosis and Management of Cushing’s Syndrome in Pregnancy3.59Citations (PDF)
27Endogenous Cushing's syndrome and cancer risk4.016Citations (PDF)
28Improved Clinical Outcomes During Long-term Osilodrostat Treatment of Cushing Disease With Normalization of Late-night Salivary Cortisol and Urinary Free Cortisol0.320Citations (PDF)
29Delayed cerebral ischemia associated with surgery for pituitary macroadenomas that express elevated levels of PACAP
Brain Hemorrhages, 2023, 4, 1-5
0.81Citations (PDF)
30Dynamic Testing for Differential Diagnosis of ACTH-Dependent Cushing Syndrome: A Systematic Review and Meta-analysis4.044Citations (PDF)
31Pituitary and SARS CoV-2: An unremitting conundrum5.127Citations (PDF)
32Symptoms at presentation in conservatively managed patients with non-functioning pituitary adenomas
Hormones, 2023, 22, 305-309
1.85Citations (PDF)
33Sellar Metastatic Neuroendocrine Carcinoma of Unknown Origin: A Case Report and Review of the Literature0.61Citations (PDF)
34Treatment Patterns in Acromegaly: Analysis of Real-World US Insurance Claims from the MarketScan® Database0.00Citations (PDF)
35MPOWERED Trial Open-Label Extension: Long-term Efficacy and Safety Data for Oral Octreotide Capsules in Acromegaly4.021Citations (PDF)
36Cushing Syndrome16.5235Citations (PDF)
37An individualized approach to the management of Cushing disease
Nature Reviews Endocrinology, 2023, 19, 581-599
31.870Citations (PDF)
38Diagnosis and management of prolactin-secreting pituitary adenomas: a Pituitary Society international Consensus Statement
Nature Reviews Endocrinology, 2023, 19, 722-740
31.8362Citations (PDF)
39Treatment Patterns, Adherence, Persistence, and Health Care Resource Utilization in Acromegaly: A Real-World Analysis0.315Citations (PDF)
40THU061 Treatment Patterns In Acromegaly: Analysis Of Real-World US Insurance Claims From The MarketScan® Database0.30Citations (PDF)
41Long-term efficacy and safety of subcutaneous pasireotide alone or in combination with cabergoline in Cushing’s disease3.821Citations (PDF)
42Cushing's syndrome
Lancet, The, 2023, 402, 2237-2252
62.1160Citations (PDF)
43Hypophysitis, the Growing Spectrum of a Rare Pituitary Disease4.0139Citations (PDF)
44Nonfunctioning Pituitary Microadenomas: Should Imaging Interval be Extended? A Large Single-center Cohort Study4.024Citations (PDF)
45Prevalence of comorbidities and concomitant medication use in acromegaly: analysis of real-world data from the United States
Pituitary, 2022, 25, 296-307
2.635Citations (PDF)
46Personalized Medical Treatment of Patients With Acromegaly: A Review
Endocrine Practice, 2022, 28, 321-332
3.329Citations (PDF)
47Patient-reported outcomes in patients with acromegaly treated with pegvisomant in the ACROSTUDY extension: A real-world experience
Pituitary, 2022, 25, 420-432
2.619Citations (PDF)
48Response to Letter to the Editor From Asa and Mete: “Hypophysitis, the Growing Spectrum of a Rare Pituitary Disease”4.00Citations (PDF)
49Perioperative Management of a Patient With Cushing Disease0.333Citations (PDF)
50Maintenance of response to oral octreotide compared with injectable somatostatin receptor ligands in patients with acromegaly: a phase 3, multicentre, randomised controlled trial21.750Citations (PDF)
51Clinical Study and Systematic Review of Pituitary Microadenomas vs. Macroadenomas in Cushing’s Disease: Does Size Matter?2.512Citations (PDF)
52Clinical Biology of the Pituitary Adenoma
Endocrine Reviews, 2022, 43, 1003-1037
24.6302Citations (PDF)
53A systematic literature review to evaluate extended dosing intervals in the pharmacological management of acromegaly0.00Citations (PDF)
54Adult Growth Hormone Deficiency: Diagnostic and Treatment Journeys From the Patients’ Perspective0.311Citations (PDF)
55Change in androgens and adrenal hormones during long-term osilodrostat treatment in patients with Cushing's disease: Results from the Phase III, prospective LINC 3 study0.00Citations (PDF)
56Impact of urinary and late-night salivary cortisol levels on clinical signs of hypercortisolism and quality of life in patients with Cushing's disease treated with osilodrostat0.00Citations (PDF)
57Osilodrostat therapy improves physical manifestations of hypercortisolism in patients with cushing's disease: findings from the phase III LINC 3 study0.00Citations (PDF)
58The MPOWERED Trial Comparing the Effectiveness, Safety, and Patient Experiences’ of Monthly Injections and Oral Medication Used to Treat Acromegaly0.90Citations (PDF)
59Treatment of Cushing’s syndrome with osilodrostat: practical applications of recent studies with case examples
Pituitary, 2022, 25, 795-809
2.647Citations (PDF)
60Levoketoconazole in the treatment of patients with endogenous Cushing’s syndrome: a double-blind, placebo-controlled, randomized withdrawal study (LOGICS)
Pituitary, 2022, 25, 911-926
2.643Citations (PDF)
61Acromegaly: pathogenesis, diagnosis, and management21.7266Citations (PDF)
62Novel approaches for cushing’s medical management: Guidelines to clinical practice0.00Citations (PDF)
63Long-term efficacy and safety of osilodrostat in Cushing’s disease: final results from a Phase II study with an optional extension phase (LINC 2)
Pituitary, 2022, 25, 959-970
2.637Citations (PDF)
64OR27-4 Placebo-Controlled and Open-Label Extension Study of a Novel Hepatic-Targeted Antisense Cimdelirsen (IONIS-GHR-LRx) Under Investigation in Acromegaly Patients0.36Citations (PDF)
65PMON163 Effect of Osilodrostat on Androgens and Adrenal Hormones in Patients With Cushing's Disease: Long-Term Findings From the Phase III, Prospective LINC 3 Study0.30Citations (PDF)
66PMON160 Improvements in Clinical Signs of Hypercortisolism and Quality of Life According to Urinary and Late-Night Salivary Cortisol Levels in Patients with Cushing's Disease Treated with Osilodrostat0.30Citations (PDF)
67PMON66 A Systematic Literature Review to Evaluate Extended Dosing Intervals in the Pharmacological Management of Acromegaly0.30Citations (PDF)
68A systematic literature review to evaluate extended dosing intervals in the pharmacological management of acromegaly
Pituitary, 2022, 26, 9-41
2.611Citations (PDF)
69Cushing’s syndrome in women: age-related differences in etiology and clinical picture
Pituitary, 2022, 26, 144-151
2.67Citations (PDF)
70EGFR/ErbB2-Targeting Lapatinib Therapy for Aggressive Prolactinomas4.066Citations (PDF)
71Results from ACROCOVID: an international survey on the care of acromegaly during the COVID-19 era
Endocrine, 2021, 71, 273-280
2.526Citations (PDF)
72Glucocorticoid Receptor Antagonism as a New “Remedy” for Insulin Resistance—Not There Yet!4.03Citations (PDF)
73Pituitary Neoplasm Nomenclature Workshop: Does Adenoma Stand the Test of Time?0.354Citations (PDF)
74Thromboembolic disease in hypercortisolism2.210Citations (PDF)
75Disease and Treatment-Related Burden in Patients With Acromegaly Who Are Biochemically Controlled on Injectable Somatostatin Receptor Ligands3.837Citations (PDF)
76Cushing’s syndrome Part 2: Advances in Treatment and in Understanding Complications’ Impact5.11Citations (PDF)
77Pituitary Disorders and COVID-19, Reimagining Care: The Pandemic A Year and Counting3.814Citations (PDF)
78Levoketoconazole in the Treatment of Patients With Cushing’s Syndrome and Diabetes Mellitus: Results From the SONICS Phase 3 Study3.824Citations (PDF)
79Glucose metabolism outcomes in acromegaly patients on treatment with pasireotide-LAR or pasireotide-LAR plus Pegvisomant
Endocrine, 2021, 73, 658-666
2.532Citations (PDF)
80Echocardiographic findings in acromegaly: prevalence of concentric left ventricular remodeling in a large single-center cohort2.813Citations (PDF)
81A Phase 3 Large International Noninferiority Trial (MPOWERED): Assessing Maintenance of Response to Oral Octreotide Capsules in Comparison to Injectable Somatostatin Receptor Ligands0.00Citations (PDF)
82Addition of cabergoline to oral octreotide capsules may improve biochemical control in patients with acromegaly who are inadequately controlled with monotherapy0.00Citations (PDF)
83A Phase 3 Large International Noninferiority Trial (MPOWERED): Assessing Maintenance of Response to Oral Octreotide Capsules in Comparison to Injectable Somatostatin Receptor Ligands0.35Citations (PDF)
84Osilodrostat is an effective and well-tolerated treatment option for patients with Cushing’s disease (CD): Final results from the LINC3 study0.01Citations (PDF)
85Oral octreotide capsules lowered incidence and improved severity of acromegaly symptoms compared to injectable somatostatin receptor ligands—results from the MPOWERED trial0.01Citations (PDF)
86Safety and Efficacy of Levoketoconazole in the Treatment of Endogenous Cushing’s Syndrome (LOGICS): Results From a Double-Blind, Placebo-Controlled, Randomized Withdrawal Study0.34Citations (PDF)
87Safety results from MPOWERED, a phase 3 trial of oral octreotide capsules in adults with acromegaly0.00Citations (PDF)
88Safety Results From MPOWERED, a Phase 3 Trial of Oral Octreotide Capsules in Adults With Acromegaly0.32Citations (PDF)
89A double-blind, randomized, placebo-controlled trial of SPI-62 safety and efficacy for the treatment of Cushing’s syndrome0.02Citations (PDF)
90Osilodrostat provides sustained control of urinary free cortisol in patients with Cushing’s disease: final results from a prospective, open-label study (LINC 2)0.00Citations (PDF)
91Improved acromegaly patient satisfaction with oral octreotide capsules compared with injectable somatostatin receptor ligands in the MPOWERED trial0.01Citations (PDF)
92Can the follow-up imaging interval for non-functioning pituitary microadenomas be extended?0.00Citations (PDF)
93Oral octreotide capsules for the treatment of acromegaly: comparison of 2 phase 3 trial results
Pituitary, 2021, 24, 943-953
2.619Citations (PDF)
94Levoketoconazole: a novel treatment for endogenous Cushing's syndrome2.914Citations (PDF)
95Pituitary Society Delphi Survey: An international perspective on endocrine management of patients undergoing transsphenoidal surgery for pituitary adenomas
Pituitary, 2021, 25, 64-73
2.618Citations (PDF)
96Pituitary society expert Delphi consensus: operative workflow in endoscopic transsphenoidal pituitary adenoma resection
Pituitary, 2021, 24, 839-853
2.670Citations (PDF)
97COVID-19 and hypopituitarism6.734Citations (PDF)
98What to Do with Incidentally Discovered Pituitary Abnormalities?
Medical Clinics of North America, 2021, 105, 1081-1098
3.112Citations (PDF)
99Updates in adrenal steroidogenesis inhibitors for Cushing’s syndrome – A practical guide5.149Citations (PDF)
100Cushing’s syndrome Part 1: Journey to Improving Diagnosis and Outcomes5.10Citations (PDF)
101Consensus on diagnosis and management of Cushing's disease: a guideline update21.7865Citations (PDF)
102Effects of Pegvisomant and Pasireotide LAR on Vertebral Fractures in Acromegaly Resistant to First-generation SRLs4.057Citations (PDF)
103A Consensus on the Diagnosis and Treatment of Acromegaly Comorbidities: An Update4.0332Citations (PDF)
104Fertility and Pregnancy in Women With Hypopituitarism: A Systematic Literature Review4.045Citations (PDF)
105The tale in evolution: clarity, consistency and consultation, not contradiction and confusion
Pituitary, 2020, 23, 476-477
2.622Citations (PDF)
106Updates in the Medical Treatment of Pituitary Adenomas1.831Citations (PDF)
107Hypercoagulability in Cushing Syndrome, Prevalence of Thrombotic Events: A Large, Single-Center, Retrospective Study0.360Citations (PDF)
108Salivary Cortisol in the Diagnosis of Cushing Syndrome, Always More Than One!0.34Citations (PDF)
109Efficacy and safety of osilodrostat in patients with Cushing's disease (LINC 3): a multicentre phase III study with a double-blind, randomised withdrawal phase21.7208Citations (PDF)
110A Novel Etiology of Hypophysitis3.521Citations (PDF)
111Management of patients with persistent or recurrent Cushing’s disease after initial pituitary surgery2.924Citations (PDF)
112Depression and Impulsivity Self-Assessment Tools to Identify Dopamine Agonist Side Effects in Patients With Pituitary Adenomas3.833Citations (PDF)
113Cystic appearance on magnetic resonance imaging in bihormonal growth hormone and prolactin tumors in acromegaly
Pituitary, 2020, 23, 672-680
2.619Citations (PDF)
114MON-311 Glucose Metabolism in Acromegaly Patients Resistant to First Generation Somatostatin Receptor Ligands Treated with Pegvisomant And/Or Pasireotide Lar0.30Citations (PDF)
115Multidisciplinary management of acromegaly: A consensus6.7325Citations (PDF)
116Maintenance of Acromegaly Control in Patients Switching From Injectable Somatostatin Receptor Ligands to Oral Octreotide4.090Citations (PDF)
117MON-332 Safety and Efficacy of Levoketoconazole in the Treatment of Endogenous Cushing’s Syndrome (LOGICS): A Double-Blind, Placebo-Controlled, Withdrawal Study0.33Citations (PDF)
118The journey in diagnosis and treatment, from pituitary adenoma to aggressive pituitary tumors6.78Citations (PDF)
119Pituitary society guidance: pituitary disease management and patient care recommendations during the COVID-19 pandemic—an international perspective
Pituitary, 2020, 23, 327-337
2.656Citations (PDF)
120MON-297 Withdrawal from Long-Acting Somatostatin Receptor Ligand Injections in Adult Patients with Acromegaly: Results from the Phase 3, Randomized, Double-Blind, Placebo-Controlled CHIASMA OPTIMAL Study0.30Citations (PDF)
121Off-Label Use and Misuse of Testosterone, Growth Hormone, Thyroid Hormone, and Adrenal Supplements: Risks and Costs of a Growing Problem
Endocrine Practice, 2020, 26, 340-353
3.329Citations (PDF)
122OR23-07 Results From the Phase 3, Randomized, Double-Blind, Placebo-Controlled CHIASMA OPTIMAL Study of Oral Octreotide Capsules in Adult Patients with Acromegaly0.31Citations (PDF)
123Acromegaly in the elderly patients
Endocrine, 2020, 68, 16-31
2.538Citations (PDF)
124An evaluation of the Acromegaly Treatment Satisfaction Questionnaire (Acro-TSQ) in adult patients with acromegaly, including correlations with other patient-reported outcome measures: data from two large multicenter international studies
Pituitary, 2020, 23, 347-358
2.628Citations (PDF)
125A Pituitary Society update to acromegaly management guidelines
Pituitary, 2020, 24, 1-13
2.6299Citations (PDF)
126Levoketoconazole improves clinical signs and symptoms and patient-reported outcomes in patients with Cushing’s syndrome
Pituitary, 2020, 24, 104-115
2.624Citations (PDF)
127MON-323 IGF-I Variability and Its Association with Demographic and Clinical Characteristics in Patients with Acromegaly Treated with Injectable Somatostatin Receptor Ligands (SRLS); Results from an International Prospective Phase III Study0.31Citations (PDF)
128Updates in rare and not-so-rare complications of acromegaly: focus on respiratory function and quality of life in acromegaly
F1000Research, 2020, 9, 791
0.512Citations (PDF)
129AcroCOVID: An international survey on care for acromegaly during the COVID-19 era0.03Citations (PDF)
130Results from the phase 3, randomized, double-blind, placebo-controlled OPTIMAL study of oral octreotide capsules in adult patients with acromegaly0.02Citations (PDF)
131MON-308 Pituitary Magnetic Resonance Imaging in the Postoperative Follow-Up of Patients with Acromegaly, Less Is More!0.31Citations (PDF)
132MON-LB55 Biochemical Control of Most Patients Reverting to Injectable Long-Acting Somatostatin Receptor Ligands Is Achieved After One Dose: Results From the Phase 3, Randomized, Double Blind, Placebo-Controlled Optimal Study0.30Citations (PDF)
133MON-314 Analysis of Adverse Events in Adult Patients with Acromegaly Receiving Oral Octreotide Capsules: Results from the Phase 3, Randomized, Double-Blind, Placebo-Controlled CHIASMA OPTIMAL Study0.30Citations (PDF)
134MON-LB53 Prior Injectable Somatostatin Receptor Ligand Dose Does Not Predict Oral Octreotide Response In The Treatment Of Acromegaly: Results From The Phase 3 OPTIMAL Study0.30Citations (PDF)
135Biochemical control of most patients reverting to injectable long-acting somatostatin receptor ligands is achieved after one dose: Results from the phase 3, randomized, double blind, placebo-controlled optimal study0.00Citations (PDF)
136Predictors of response to medical therapy with pegvisomant and pasireotide lar in SRLs-resistant acromegaly0.00Citations (PDF)
137Impact of imputation method on efficacy results from the phase 3 optimal study of oral octreotide capsules in adult patients with acromegaly0.00Citations (PDF)
138Analysis of adverse events in adult patients with acromegaly receiving oral octreotide capsules: Results from the phase 3, randomized, double-blind, placebo-controlled optimal study0.00Citations (PDF)
139Levoketoconazole in the treatment of endogenous Cushing’s syndrome: Extended evaluation phase results of the SONICS study0.02Citations (PDF)
140Sustained response to treatment with oral octreotide capsules: Results from the phase 3, randomized, double blind, placebo-controlled optimal study0.00Citations (PDF)
141IGF-I variability and its association with demographic and clinical characteristics in patients with acromegaly treated with injectable somatostatin receptor ligands (SRLs); results from OPTIMAL, an international prospective phase 3 study0.00Citations (PDF)
142Patients receiving a range of doses of prior injectable somatostatin receptor ligands respond to oral octreotide in the treatment of acromegaly: Results from the phase 3 optimal study0.00Citations (PDF)
143Durability of response and gender-based analysis from the LINC3 trial of osilodrostat in the treatment in cushing’s disease0.00Citations (PDF)
144Withdrawal from long-acting somatostatin receptor ligand injections in adult patients with acromegaly: Results from the phase 3, randomized, double-blind, placebo-controlled optimal study0.00Citations (PDF)
145MON-320 Inter-Rater Reliability of T2 MRI Intensity of Somatotroph Adenomas; Endocrinologists vs. Neuroradiologist Pilot Study0.30Citations (PDF)
146MON-LB57 Impact of Imputation Method and Response Cutoffs on Results From the Phase 3 OPTIMAL Study of Oral Octreotide Capsules in Adult Patients With Acromegaly0.30Citations (PDF)
147Safety and Efficacy of Subcutaneous Pasireotide in Patients With Cushing's Disease: Results From an Open-Label, Multicenter, Single-Arm, Multinational, Expanded-Access Study3.818Citations (PDF)
148Ipilimumab-induced hypophysitis, a single academic center experience
Pituitary, 2019, 22, 488-496
2.637Citations (PDF)
149Functioning Pituitary Adenomas – Current Treatment Options and Emerging Medical Therapies2.557Citations (PDF)
150Long‐term efficacy and safety of once‐monthly pasireotide in Cushing's disease: A Phase III extension study
Clinical Endocrinology, 2019, 91, 776-785
2.341Citations (PDF)
151Mifepristone Increases Thyroid Hormone Requirements in Patients With Central Hypothyroidism: A Multicenter Study0.312Citations (PDF)
152Development of a novel patient-reported measure for acromegaly: the Acro-TSQ
Pituitary, 2019, 22, 581-593
2.620Citations (PDF)
153A tale of pituitary adenomas: to NET or not to NET
Pituitary, 2019, 22, 569-573
2.675Citations (PDF)
154Efficacy and safety of levoketoconazole in the treatment of endogenous Cushing's syndrome (SONICS): a phase 3, multicentre, open-label, single-arm trial21.794Citations (PDF)
155Diagnostic utility of Gallium-68-somatostatin receptor PET/CT in ectopic ACTH-secreting tumors: a systematic literature review and single-center clinical experience
Pituitary, 2019, 22, 445-455
2.647Citations (PDF)
156Medical Management of Cushing’s Syndrome: Current and Emerging Treatments
Drugs, 2019, 79, 935-956
11.450Citations (PDF)
157The Evaluation of Incidentally Discovered Adrenal Masses
Endocrine Practice, 2019, 25, 178-192
3.374Citations (PDF)
158Hypercoagulability and Risk of Venous Thromboembolic Events in Endogenous Cushing's Syndrome: A Systematic Meta-Analysis3.8100Citations (PDF)
159Response to letter to the editor from Professor Jean-François Bonneville
Pituitary, 2019, 22, 103-103
2.60Citations (PDF)
160Hypercortisolemia Recurrence in Cushing's Disease; a Diagnostic Challenge3.840Citations (PDF)
161Systemic Complications of Acromegaly and the Impact of the Current Treatment Landscape: An Update
Endocrine Reviews, 2019, 40, 268-332
24.6343Citations (PDF)
162Magnetic resonance imaging in the management of prolactinomas; a review of the evidence
Pituitary, 2019, 23, 16-26
2.639Citations (PDF)
163OR16-2 Osilodrostat Treatment in Cushing's Disease (CD): Results from a Phase III, Multicenter, Double-Blind, Randomized Withdrawal Study (LINC 3)0.33Citations (PDF)
164SUN-LB080 ACROSTUDY - Safety and Efficacy of a Cohort of 110 Naïve Patients with Acromegaly Treated with Pegvisomant0.33Citations (PDF)
165Silent somatotroph pituitary adenomas: an update
Pituitary, 2018, 21, 194-202
2.639Citations (PDF)
166Efficacy and safety of once-monthly pasireotide in Cushing's disease: a 12 month clinical trial21.7156Citations (PDF)
167Updates in Diagnosis and Treatment of Acromegaly2.561Citations (PDF)
168Growth hormone deficiency and replacement effect on adult bone mass: A clinical update1.07Citations (PDF)
169Clinical outcomes in male patients with lactotroph adenomas who required pituitary surgery: a retrospective single center study
Pituitary, 2018, 21, 454-462
2.634Citations (PDF)
170Pituitary-Directed Therapies for Cushing’s Disease3.825Citations (PDF)
171Physicians’ awareness of gadolinium retention and MRI timing practices in the longitudinal management of pituitary tumors: a “Pituitary Society” survey
Pituitary, 2018, 22, 37-45
2.631Citations (PDF)
172High prevalence of adrenal insufficiency at diagnosis and headache recovery in surgically resected Rathke’s cleft cysts—a large retrospective single center study
Endocrine, 2018, 63, 463-469
2.522Citations (PDF)
173Late-night salivary cortisol (LNSC) levels in a Phase III study of long-acting pasireotide in patients with Cushing's disease (CD)0.02Citations (PDF)
174An open-label, multicentre, single-arm, expanded-access study of subcutaneous (s.c.) pasireotide in patients with Cushing's disease (CD)0.00Citations (PDF)
175Update on adrenal insufficiency: diagnosis and management in pregnancy2.238Citations (PDF)
176Evaluation and Management of Adrenal Insufficiency in Critically ill Patients: Disease State Review
Endocrine Practice, 2017, 23, 716-725
3.340Citations (PDF)
177Clinical profile of silent growth hormone pituitary adenomas; higher recurrence rate compared to silent gonadotroph pituitary tumors, a large single center experience
Endocrine, 2017, 58, 528-534
2.540Citations (PDF)
178Candida Meningitis After Transsphenoidal Surgery: A Single-Institution Case Series and Literature Review
World Neurosurgery, 2017, 108, 41-49
1.514Citations (PDF)
179Stereotactic Radiation Therapy in Pituitary Adenomas, is it Better than Conventional Radiation Therapy
Acta Endocrinologica, 2017, 13, 476-490
0.324Citations (PDF)
180Medical Therapy with Pasireotide in Recurrent Cushing’s Disease: Experience of Patients Treated for At Least 1 Year at a Single Center3.89Citations (PDF)
181Recent Progress in the Medical Therapy of Pituitary Tumors3.531Citations (PDF)
182Predictors of silent corticotroph adenoma recurrence; a large retrospective single center study and systematic literature review
Pituitary, 2017, 21, 32-40
2.669Citations (PDF)
183Pasireotide alone or in combination with cabergoline effectively controls urinary free cortisol levels: results from a prospective study in patients with Cushing's disease (CAPACITY)0.06Citations (PDF)
184Pasireotide: a novel treatment for patients with acromegaly6.936Citations (PDF)
185American Association of Clinical Endocrinologists and American College of Endocrinology Disease State Clinical Review: Diagnosis of Recurrence in Cushing Disease
Endocrine Practice, 2016, 22, 1436-1448
3.363Citations (PDF)
186Congress of Neurological Surgeons Systematic Review and Evidence-Based Guidelines on the Management of Patients With Nonfunctioning Pituitary Adenomas
Neurosurgery, 2016, 79, 521-523
2.050Citations (PDF)
187Congress of Neurological Surgeons Systematic Review and Evidence-Based Guideline for Pretreatment Endocrine Evaluation of Patients With Nonfunctioning Pituitary Adenomas
Neurosurgery, 2016, 79, E527-E529
2.053Citations (PDF)
188Congress of Neurological Surgeons Systematic Review and Evidence-Based Guideline on Posttreatment Follow-up Evaluation of Patients With Nonfunctioning Pituitary Adenomas
Neurosurgery, 2016, 79, E541-E543
2.043Citations (PDF)
189Late-night salivary cortisol may be valuable for assessing treatment response in patients with Cushing’s disease: 12-month, Phase III pasireotide study
Endocrine, 2016, 54, 516-523
2.530Citations (PDF)
190Updates on the role of adrenal steroidogenesis inhibitors in Cushing’s syndrome: a focus on novel therapies
Pituitary, 2016, 19, 643-653
2.684Citations (PDF)
191Dopamine agonist therapy induces significant recovery of HPA axis function in prolactinomas independent of tumor size: a large single center experience
Endocrine, 2016, 54, 191-197
2.54Citations (PDF)
192Update on medical treatment for Cushing’s disease1.436Citations (PDF)
193Hormonal Replacement in Hypopituitarism in Adults: An Endocrine Society Clinical Practice Guideline4.0892Citations (PDF)
194Switching patients with acromegaly from octreotide to pasireotide improves biochemical control: crossover extension to a randomized, double-blind, Phase III study2.974Citations (PDF)
195Effect of pasireotide on glucose- and growth hormone-related biomarkers in patients with inadequately controlled acromegaly
Endocrine, 2016, 53, 210-219
2.575Citations (PDF)
196Safety and tolerability of pasireotide long-acting release in acromegaly—results from the acromegaly, open-label, multicenter, safety monitoring program for treating patients who have a need to receive medical therapy (ACCESS) study
Endocrine, 2016, 55, 247-255
2.550Citations (PDF)
197The role of combination medical therapy in the treatment of acromegaly
Pituitary, 2016, 20, 136-148
2.631Citations (PDF)
198Longitudinal assessment of response to treatment with oral octreotide capsules in patients with acromegaly: post-hoc analysis of a phase 3 trial0.04Citations (PDF)
199American Association of Clinical Endocrinologists and American College of Endocrinology Disease State Clinical Review: Management of Acromegaly Patients: What is the Role of Pre-Operative Medical Therapy?
Endocrine Practice, 2015, 21, 668-673
3.349Citations (PDF)
200Medical Treatment of Cushing Disease3.526Citations (PDF)
201Pituitary-directed medical therapy in Cushing’s disease
Pituitary, 2015, 18, 238-244
2.68Citations (PDF)
202Medical therapy for Cushing’s disease: adrenal steroidogenesis inhibitors and glucocorticoid receptor blockers
Pituitary, 2015, 18, 245-252
2.629Citations (PDF)
203Recovery rate of adrenal function after surgery in patients with acromegaly is higher than in those with non-functioning pituitary tumors: a large single center study
Pituitary, 2015, 18, 701-709
2.627Citations (PDF)
204Preoperative Lateralization Modalities for Cushing Disease: Is Dynamic Magnetic Resonance Imaging or Cavernous Sinus Sampling More Predictive of Intraoperative Findings?0.69Citations (PDF)
205Fracture risk in adult patients treated with growth hormone replacement therapy for growth hormone deficiency: a prospective observational cohort study21.760Citations (PDF)
206Discovery of Cushing’s Syndrome After Bariatric Surgery: Multicenter Series of 16 Patients
Obesity Surgery, 2015, 25, 2306-2313
2.120Citations (PDF)
207Landscape of Familial Isolated and Young-Onset Pituitary Adenomas: Prospective Diagnosis inAIPMutation Carriers4.0168Citations (PDF)
208Osilodrostat, a potent oral 11β-hydroxylase inhibitor: 22-week, prospective, Phase II study in Cushing’s disease
Pituitary, 2015, 19, 138-148
2.6153Citations (PDF)
209Metformin-based oral antidiabetic therapy proved effective in hyperglycaemia associated with pasireotide in patients with acromegaly0.05Citations (PDF)
210Phase III, multicentre, double-blind, randomised withdrawal study of osilodrostat (LCI699) in patients with Cushing's disease: a study design0.00Citations (PDF)
211Pasireotide long-acting release maintains biochemical control in patients with acromegaly: results from the extension of randomised, Phase III, PAOLA study0.00Citations (PDF)
212Management of pasireotide-induced hyperglycaemia with proactive monitoring and early intervention: key learnings from the phase III, 24-week PAOLA study0.01Citations (PDF)
213Challenges and pitfalls in the diagnosis of hyperprolactinemia1.472Citations (PDF)
214Changes in Plasma ACTH Levels and Corticotroph Tumor Size in Patients With Cushing's Disease During Long-term Treatment With the Glucocorticoid Receptor Antagonist Mifepristone4.087Citations (PDF)
215Factors Associated with Biochemical Remission after Microscopic Transsphenoidal Surgery for Acromegaly0.660Citations (PDF)
216LCI699, a Potent 11β-hydroxylase Inhibitor, Normalizes Urinary Cortisol in Patients With Cushing's Disease: Results From a Multicenter, Proof-of-Concept Study4.0186Citations (PDF)
217FRAX score in acromegaly: does it tell the whole story?
Clinical Endocrinology, 2014, 80, 614-616
2.333Citations (PDF)
218Pasireotide versus continued treatment with octreotide or lanreotide in patients with inadequately controlled acromegaly (PAOLA): a randomised, phase 3 trial21.7381Citations (PDF)
219Pasireotide Versus Octreotide in Acromegaly: A Head-to-Head Superiority Study4.0384Citations (PDF)
220Polycystic ovarian syndrome and Cushing's syndrome: a persistent diagnostic quandary0.929Citations (PDF)
221Acromegaly: Assessing the Disorder and Navigating the Therapeutic Options for Treatment
Endocrine Practice, 2014, 20, 7-17
3.322Citations (PDF)
222Case Report: Reversible cabergoline-associated cardiac valvulopathy post drug discontinuation
F1000Research, 2014, 3, 171
0.53Citations (PDF)
223Recent advances in the medical treatment of Cushing’s disease4.110Citations (PDF)
224Effect of pasireotide on GH, IGF1, IGFBP2, IGFBP3, HbA1C and glucose in patients with inadequately controlled acromegaly: exploratory results from a multicentre, randomized, 24-week study (PAOLA)0.02Citations (PDF)
225Study Design of a Phase II trial of pasireotide s.c. alone or in combination with cabergoline in patients with Cushing's disease0.00Citations (PDF)
226New avenues in the medical treatment of Cushing’s disease: corticotroph tumor targeted therapy
Journal of Neuro-Oncology, 2013, 114, 1-11
2.528Citations (PDF)
227Monitoring Patient Improvement Parameters following Pasireotide Treatment in Cushing’s Disease0.57Citations (PDF)
228A New Era of Cushing Disease Therapeutics
Acta Endocrinologica, 2013, 9, 89-96
0.30Citations (PDF)
229The role of combination medical therapy in acromegaly2.216Citations (PDF)
230A New Therapeutic Approach in the Medical Treatment of Cushing’S SYNDROME: GLUCOCORTICOID RECEPTOR BLOCKADE WITH MIFEPRISTONE
Endocrine Practice, 2013, 19, 313-326
3.364Citations (PDF)
231Absence of immunostaining for growth hormone in a subset of patients with acromegaly
Pituitary, 2013, 17, 103-108
2.68Citations (PDF)
232Self-perception of cognitive function among patients with active acromegaly, controlled acromegaly, and non-functional pituitary adenoma: a pilot study
Endocrine, 2013, 46, 585-593
2.550Citations (PDF)
233Can we predict long-term remission after somatostatin analog withdrawal in patients with acromegaly? Results from a multicenter prospective trial
Endocrine, 2013, 46, 577-584
2.524Citations (PDF)
234Extended treatment of Cushing’s disease with pasireotide: results from a 2-year, Phase II study
Pituitary, 2013, 17, 320-326
2.647Citations (PDF)
235Switching patients with acromegaly from octreotide LAR to pasireotide LAR improves biochemical control: crossover extension to a randomized, double-blind, multicenter, Phase III study0.05Citations (PDF)
236Factors Associated with Biochemical Remission after Open Transsphenoidal Surgery for Acromegaly0.60Citations (PDF)
237Evaluation of late-night salivary cortisol during a Phase III study with pasireotide in patients with Cushing's disease0.01Citations (PDF)
238Short-Term Risk of Recurrence of Surgically Treated, Radiotherapy-Naive Pituitary Adenomas0.60Citations (PDF)
239Medical Management of Persistent and Recurrent Cushing Disease1.331Citations (PDF)
240Mifepristone, a Glucocorticoid Receptor Antagonist, Produces Clinical and Metabolic Benefits in Patients with Cushing's Syndrome4.0474Citations (PDF)
241Medical management of Cushing’s disease: what is the future?
Pituitary, 2012, 15, 330-341
2.685Citations (PDF)
242Serum IGF-1 In the Diagnosis of Acromegaly and the Profile of Patients with Elevated IGF-1 but Normal Glucose-Suppressed Growth Hormone
Endocrine Practice, 2012, 18, 817-825
3.332Citations (PDF)
243Remission rate after transsphenoidal surgery in patients with pathologically confirmed Cushing’s disease, the role of cortisol, ACTH assessment and immediate reoperation: a large single center experience
Pituitary, 2012, 16, 452-458
2.698Citations (PDF)
244Growth hormone granulation pattern and somatostatin receptor subtype 2A correlate with postoperative somatostatin receptor ligand response in acromegaly: a large single center experience
Pituitary, 2012, 16, 490-498
2.6145Citations (PDF)
245Mifepristone: is there a place in the treatment of Cushing’s disease?
Endocrine, 2012, 44, 20-32
2.531Citations (PDF)
246Discordant growth hormone and IGF-1 levels post pituitary surgery in patients with acromegaly naïve to medical therapy and radiation: what to follow, GH or IGF-1 values?
Pituitary, 2011, 15, 562-570
2.641Citations (PDF)
247Normal Hypothalamic-Pituitary-Adrenal Axis by High-Dose Cosyntropin Testing in Patients with Abnormal Response to Low-Dose Cosyntropin Stimulation: A Retrospective Review
Endocrine Practice, 2010, 16, 64-70
3.323Citations (PDF)
248Cabergoline-Induced Cerebral Spinal Fluid Leak in a Patient With a Large Prolactinoma and MEN1
2010, 20, 198-202
6Citations (PDF)
249Temozolomide for corticotroph pituitary adenomas refractory to standard therapy
Pituitary, 2010, 14, 80-91
2.663Citations (PDF)
250Clinical efficacy and safety results for dose escalation of somatostatin receptor ligands in patients with acromegaly: a literature review
Pituitary, 2010, 14, 184-193
2.679Citations (PDF)
251Diabetes Insipidus, Panhypopituitarism, and Severe Mental Status Deterioration in a Patient with Chordoid Glioma: Case Report and Literature Review
Endocrine Practice, 2009, 15, 240-245
3.320Citations (PDF)
252“Relative” adRenal insufficiency in cRitical illness
Endocrine Practice, 2009, 15, 632-640
3.314Citations (PDF)
253Cushing's syndrome might be underappreciated in patients seeking bariatric surgery: a plea for screening2.521Citations (PDF)
254Anti-CTLA-4 antibody therapy associated autoimmune hypophysitis: serious immune related adverse events across a spectrum of cancer subtypes
Pituitary, 2009, 13, 29-38
2.6282Citations (PDF)
255Second-line treatment for Cushing's disease when initial pituitary surgery is unsuccessful2.222Citations (PDF)
256Successful Treatment of Sulfonylurea-Induced Prolonged Hypoglycemia with Use of Octreotide
Endocrine Practice, 2006, 12, 635-640
3.313Citations (PDF)
257Giant invasive pituitary prolactinoma with falsely low serum prolactin: the significance of ‘hook effect’
Journal of Neuro-Oncology, 2006, 79, 41-43
2.559Citations (PDF)
258Failure of successful renal transplant to produce appropriate levels of 1,25-dihydroxyvitamin D
Osteoporosis International, 2006, 18, 363-368
4.132Citations (PDF)
259CAm<sup>2</sup>029 octreotide subcutaneous depot provides stable control of IGF-I and improves key symptoms throughout a 4-week post-dose interval: analysis from the ACROINNOVA 1 trial0.00Citations (PDF)
260Impact of pasireotide LAR on lipid and glucose metabolism in patients with acromegaly: a systematic review and meta-analysis0.00Citations (PDF)
261Pituitary incidentaloma: a Pituitary Society international consensus guideline statement31.844Citations (PDF)
262Impact of pasireotide on lipid and glucose metabolism in patients with acromegaly: a systematic review and meta-analysis2.89Citations (PDF)
263Development of a Minimum Dataset for the Global Monitoring of the Safety and Efficacy of Growth Hormone Replacement in Adults With Growth Hormone Deficiency (AGHD)
Clinical Endocrinology, 0, 103, 841-851
2.31Citations (PDF)
264Natural history of nonfunctioning pituitary microadenomas: a systematic review and individual participant data meta-analysis4.02Citations (PDF)
265Osilodrostat dose impact on efficacy/safety in Cushing's disease: large, pooled analysis of LINC 2, 3, and 44.06Citations (PDF)
266Osilodrostat-associated Adrenal Gland Shrinkage: A Case Series of Patients With ACTH-dependent Cushing's Syndrome4.010Citations (PDF)
267Rapid and Sustained Response of Biochemically Uncontrolled Acromegaly to Once-daily Oral Paltusotine Treatment4.012Citations (PDF)
268Mortality in patients with dopamine agonist-treated hyperprolactinemia: a large matched-cohort study
Pituitary, 0, 28,
2.62Citations (PDF)
269Clomiphene Citrate in Men With Hypogonadism—Do we Need to Monitor IGF-1 in All Patients?0.30Citations (PDF)
270A Novel Evaluation of 24-hour Energy Metabolism in Cushing's Syndrome: The Metabolic Cost of Hypercortisolism0.30Citations (PDF)
271Patient perceptions of pituitary incidentaloma diagnosis and follow-up: a Pituitary Society international patient survey
Pituitary, 0, 29,
2.60Citations (PDF)
272Approach to the Patient with Cushing’s Syndrome: Use of Anticoagulation Therapy4.01Citations (PDF)
273Efficacy and Safety of Once-Weekly Lonapegsomatropin in Adults With Growth Hormone Deficiency: foresiGHt Trial Results4.03Citations (PDF)
274Cavernous Sinus Medial Wall Resection: A Retrospective Single-Institution Study on Outcomes in Functional Pituitary Adenomas0.60Citations (PDF)
275Impact of sex on mortality in patients with pituitary adenomas
Pituitary, 0, 29,
2.60Citations (PDF)
276CAM2029 octreotide subcutaneous depot maintains control of IGF-I and symptoms of acromegaly across a 4-week dosing interval and for intervals greater than 28 days: data from the ACROINNOVA 1 trial0.00Citations (PDF)
277Acromegaly complications: an update4.01Citations (PDF)
278Age and hematologic parameters can predict prolonged glucocorticoid replacement after remission of cushing disease and adrenal Cushing’s syndrome: A nationwide cohort study
Pituitary, 0, 29,
2.60Citations (PDF)
279Increased risk of atrial fibrillation and flutter in patients with Cushing's syndrome: a population-based matched cohort study4.00Citations (PDF)
280Impact of Osilodrostat on Health‐Related Quality of Life in Cushing's Disease: Analysis of Patient‐Reported Outcomes From the Phase III LINC 3 and LINC 4 Clinical Trials2.30Citations (PDF)
281Glucagon-like peptide-1 receptor agonist exposure and malignancy risk in patients with endogenous Cushing’s syndrome4.01Citations (PDF)
282Cancer risk in acromegaly: reassessing the evidence and impact of biochemical control4.00Citations (PDF)
283Risk of infection-related hospitalization is more than doubled in Cushing’s syndrome vs matched controls2.00Citations (PDF)
284Consensus on Biomarker Utility for ACTH-Dependent Cushing’s Syndrome: A Pituitary Society Modified Delphi Panel4.00Citations (PDF)
285Functioning pituitary adenomas in pregnancy: updates and controversies2.20Citations (PDF)