Pathogenesis of Lethal Cardiac Arrhythmias in Mecp2 Mutant Mice: Implication for Therapy in Rett Syndrome

Nav1.5-dependent persistent Na+ influx activates CaMKII in rat ventricular myocytes and N1325S mice

(2011) Lina Yao et al.   AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY

Complexities of Rett Syndrome and MeCP2

(2011) R. C. Samaco et al.   JOURNAL OF NEUROSCIENCE

Rett syndrome: Revised diagnostic criteria and nomenclature

(2010) Jeffrey L. Neul et al.   ANNALS OF NEUROLOGY

Autonomic modulation and antiarrhythmic therapy in a model of long QT syndrome type 3

(2010) Larissa Fabritz et al.   CARDIOVASCULAR RESEARCH

Ryanodine Receptor Phosphorylation by Calcium/Calmodulin-Dependent Protein Kinase II Promotes Life-Threatening Ventricular Arrhythmias in Mice With Heart Failure

(2010) Ralph J. van Oort et al.   CIRCULATION

Autonomic and cellular mechanisms mediating detrimental cardiac effects of status epilepticus

(2010) Steven L. Bealer et al.   EPILEPSY RESEARCH

Epilepsy and the natural history of Rett syndrome

(2010) D. G. Glaze et al.   NEUROLOGY

Sudden Infant Death Syndrome in Mice With an Inherited Mutation in RyR2

(2009) Nitin Mathur et al.   Circulation-Arrhythmia and Electrophysiology

Severe congenital encephalopathy caused by MECP2 null mutations in males: central hypoxia and reduced neuronal dendritic structure

(2009) B Schüle et al.   CLINICAL GENETICS

Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities

(2009) R. C. Samaco et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Autonomy of Autonomic Dysfunction in Major Depression

(2009) Mandy Koschke et al.   PSYCHOSOMATIC MEDICINE

Arrhythmia in Heart and Brain: KCNQ1 Mutations Link Epilepsy and Sudden Unexplained Death

(2009) A. M. Goldman et al.   Science Translational Medicine

EFFECTS OF ATROPINE ON THE TIME AND FREQUENCY DOMAIN ESTIMATES OF BLOOD PRESSURE AND HEART RATE VARIABILITY IN MICE

(2008) Dominique Laude et al.   CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY

A partial loss of function allele of Methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome

(2008) R. C. Samaco et al.   HUMAN MOLECULAR GENETICS

The QT syndromes: long and short

(2008) Hiroshi Morita et al.   LANCET

Specific mutations in Methyl-CpG-Binding Protein 2 confer different severity in Rett syndrome

(2008) J. L. Neul et al.   NEUROLOGY

Autonomic dysregulation in young girls with Rett Syndrome during nighttime in-home recordings

(2008) Debra E. Weese-Mayer et al.   PEDIATRIC PULMONOLOGY

MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription

(2008) M. Chahrour et al.   SCIENCE