HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA) | Heart Rhythm | 2011 | 737 |
An absolute requirement for Pax7-positive satellite cells in acute injury-induced skeletal muscle regeneration | Development (Cambridge) | 2011 | 696 |
HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA) | Europace | 2011 | 557 |
Breastfeeding and reduced risk of sudden infant death syndrome: a meta-analysis | Pediatrics | 2011 | 266 |
A social-ecological model of readiness for transition to adult-oriented care for adolescents and young adults with chronic health conditions | Child: Care, Health and Development | 2011 | 208 |
Adeno-associated virus antibody profiles in newborns, children, and adolescents | Vaccine Journal | 2011 | 197 |
SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy | Neurology | 2011 | 150 |
Diagnosis, classification, and genetics of phenylketonuria and tetrahydrobiopterin (BH4) deficiencies | Molecular Genetics and Metabolism | 2011 | 145 |
Phase I trial of MK-0752 in children with refractory CNS malignancies: a pediatric brain tumor consortium study | Journal of Clinical Oncology | 2011 | 129 |
Health care transition for youth living with HIV/AIDS | Pediatrics | 2011 | 123 |
Cardiomyopathy of Duchenne muscular dystrophy: current understanding and future directions | Muscle and Nerve | 2011 | 119 |
Pediatric insomnia | Pediatric Clinics of North America | 2011 | 114 |
Screening for sudden cardiac death in the young: report from a national heart, lung, and blood institute working group | Circulation | 2011 | 111 |
Secretome signature of invasive glioblastoma multiforme | Journal of Proteome Research | 2011 | 96 |
The status of exon skipping as a therapeutic approach to duchenne muscular dystrophy | Molecular Therapy | 2011 | 89 |
Losartan decreases cardiac muscle fibrosis and improves cardiac function in dystrophin-deficient mdx mice | Journal of Cardiovascular Pharmacology and Therapeutics | 2011 | 84 |
The effect of observation on cranial computed tomography utilization for children after blunt head trauma | Pediatrics | 2011 | 82 |
Restoring dystrophin expression in duchenne muscular dystrophy muscle progress in exon skipping and stop codon read through | American Journal of Pathology | 2011 | 79 |
Spectrum of neurodevelopmental disabilities in children with cerebellar malformations | Developmental Medicine and Child Neurology | 2011 | 78 |
Lovastatin as treatment for neurocognitive deficits in neurofibromatosis type 1: phase I study | Pediatric Neurology | 2011 | 75 |
SRY-box containing gene 17 regulates the Wnt/β-catenin signaling pathway in oligodendrocyte progenitor cells | Journal of Neuroscience | 2011 | 73 |
Children with generalized anxiety disorder do not have peer problems, just fewer friends | Child Psychiatry and Human Development | 2011 | 62 |
Asthmatic airway epithelium is intrinsically inflammatory and mitotically dyssynchronous | American Journal of Respiratory Cell and Molecular Biology | 2011 | 60 |
Population pharmacokinetics of meropenem in plasma and cerebrospinal fluid of infants with suspected or complicated intra-abdominal infections | Pediatric Infectious Disease Journal | 2011 | 59 |
One-year treatment of morpholino antisense oligomer improves skeletal and cardiac muscle functions in dystrophic mdx mice | Molecular Therapy | 2011 | 59 |