Integrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors | Cancer Cell | 2016 | 135 |
What Is Trophoblast? A Combination of Criteria Define Human First-Trimester Trophoblast | Stem Cell Reports | 2016 | 120 |
PINK1 Is a Negative Regulator of Growth and the Warburg Effect in Glioblastoma | Cancer Research | 2016 | 80 |
Targeted detection of genetic alterations reveal the prognostic impact of H3K27M and MAPK pathway aberrations in paediatric thalamic glioma | Acta Neuropathologica Communications | 2016 | 77 |
Mitochondrial dysfunction is an important cause of neurological deficits in an inflammatory model of multiple sclerosis | Scientific Reports | 2016 | 62 |
Biodistribution of cisplatin revealed by imaging mass cytometry identifies extensive collagen binding in tumor and normal tissues | Scientific Reports | 2016 | 58 |
Hepatocellular Carcinoma in Children: Does Modified Platinum- and Doxorubicin-Based Chemotherapy Increase Tumor Resectability and Change Outcome? Lessons Learned From the SIOPEL 2 and 3 Studies | Journal of Clinical Oncology | 2016 | 53 |
Diagnosis of neuronal ceroid lipofuscinosis type 2 (CLN2 disease): Expert recommendations for early detection and laboratory diagnosis | Molecular Genetics and Metabolism | 2016 | 50 |
Response of 33 UK patients with infantile-onset Pompe disease to enzyme replacement therapy | Journal of Inherited Metabolic Disease | 2016 | 40 |
Secondary neurotransmitter deficiencies in epilepsy caused by voltage-gated sodium channelopathies: A potential treatment target? | Molecular Genetics and Metabolism | 2016 | 34 |
Body weight lower limits of fetal postmortem MRI at 1.5 T | Ultrasound in Obstetrics and Gynecology | 2016 | 28 |
TFE3-positive renal cell carcinomas are not always Xp11 translocation carcinomas: Report of a case with a TPM3-ALK translocation | Pathology Research and Practice | 2016 | 27 |
Large B-Cell Lymphoma in an Adolescent Patient With Interleukin-10 Receptor Deficiency and History of Infantile Inflammatory Bowel Disease | Journal of Pediatric Gastroenterology and Nutrition | 2016 | 26 |
Defining the Newborn Blood Spot Screening Reference Interval for TSH: Impact of Ethnicity | Journal of Clinical Endocrinology and Metabolism | 2016 | 25 |
Hepatocyte Nuclear Factor-4 Alfa Mutation Associated with Hyperinsulinaemic Hypoglycaemia and Atypical Renal Fanconi Syndrome: Expanding the Clinical Phenotype | Hormone Research in Paediatrics | 2016 | 21 |
Primary Cutaneous Lymphomas in Children and Adolescents | Pediatric Blood and Cancer | 2016 | 18 |
Visualizing the Propagation of Acute Lung Injury | Anesthesiology | 2016 | 16 |
Identification of quantitative trait loci influencing inflammation-mediated alveolar bone loss: insights into polygenic inheritance of host-biofilm disequilibria in periodontitis | Journal of Periodontal Research | 2016 | 14 |
Contribution of domain 30 of tropoelastin to elastic fiber formation and material elasticity | Biopolymers | 2016 | 14 |
Assessment of body composition in Wistar rat offspring by DXA in relation to prenatal and postnatal nutritional manipulation | Pediatric Research | 2016 | 12 |
Hemorrhagic presentations of cerebellar pilocytic astrocytomas in children resulting in death: report of 2 cases | Journal of Neurosurgery: Pediatrics | 2016 | 11 |
Maternal Floor Infarction/Massive Perivillous Fibrin Deposition Associated with Hypercoiling of a Single-Artery Umbilical Cord: A Case Report | Pediatric and Developmental Pathology | 2016 | 10 |
Coenzyme Q and Pyridoxal Phosphate Deficiency Is a Common Feature in Mucopolysaccharidosis Type III | JIMD Reports | 2016 | 4 |
Social and behavioural factors in Non-suspicious unexpected death in infancy; experience from metropolitan police project indigo investigation | BMC Pediatrics | 2016 | 2 |
The Incidence and Clinical Features of Dual Thyroid Ectopia in Congenital Hypothyroidism | Journal of Clinical Endocrinology and Metabolism | 2016 | 2 |