Related references
Note: Only part of the references are listed.Genetic and environmental influences on structural brain measures in twins with autism spectrum disorder
John P. Hegarty et al.
MOLECULAR PSYCHIATRY (2020)
CDKL5 Deficiency Disorder-A Complex Epileptic Encephalopathy
Martyna Jakimiec et al.
BRAIN SCIENCES (2020)
Molecular and Synaptic Bases of CDKL5 Disorder
Yong-Chuan Zhu et al.
DEVELOPMENTAL NEUROBIOLOGY (2019)
Cyclin-Dependent Kinase-Like 5 Deficiency Disorder: Clinical Review
Heather E. Olson et al.
PEDIATRIC NEUROLOGY (2019)
Morphometric MRI findings challenge the concept of the unaffected hemisphere in Rasmussen encephalitis
Bastian David et al.
EPILEPSIA (2019)
Surface- and voxel-based brain morphologic study in Rett and Rett-like syndrome with MECP2 mutation
Tadashi Shiohama et al.
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE (2019)
CDKL5 deficiency disorder: Relationship between genotype, epilepsy, cortical visual impairment, and development
Scott T. Demarest et al.
EPILEPSIA (2019)
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study
Christopher D. Whelan et al.
BRAIN (2018)
Imaging structural and functional brain development in early childhood
John H. Gilmore et al.
NATURE REVIEWS NEUROSCIENCE (2018)
Clinical and genetic Rett syndrome variants are defined by stable electrophysiological profiles
Conor Keogh et al.
BMC PEDIATRICS (2018)
Loss of CDKL5 in Glutamatergic Neurons Disrupts Hippocampal Microcircuitry and Leads to Memory Impairment in Mice
Sheng Tang et al.
JOURNAL OF NEUROSCIENCE (2017)
&ITCDKL5&IT variants Improving our understanding of a rare neurologic disorder
Ralph D. Hector et al.
NEUROLOGY-GENETICS (2017)
Pontine and cerebral atrophy in Lennox-Gastaut syndrome
Benjamin J. C. Newham et al.
EPILEPSY RESEARCH (2016)
CDKL5 knockout leads to altered inhibitory transmission in the cerebellum of adult mice
S. Sivilia et al.
GENES BRAIN AND BEHAVIOR (2016)
Trajectories of cortical thickness maturation in normal brain development - The importance of quality control procedures
Simon Ducharme et al.
NEUROIMAGE (2016)
The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository
Terry L. Jernigan et al.
NEUROIMAGE (2016)
Seizure variables and their relationship to genotype and functional abilities in the CDKL5 disorder
Stephanie Fehr et al.
NEUROLOGY (2016)
Quantitative magnetic resonance imaging evidence for altered structural remodeling of the temporal lobe in West syndrome
Tangunu Fosi et al.
EPILEPSIA (2015)
Loss of CDKL5 impairs survival and dendritic growth of newborn neurons by altering AKT/GSK-3β signaling
Claudia Fuchs et al.
NEUROBIOLOGY OF DISEASE (2014)
Genetic topography of brain morphology
Chi-Hua Chen et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)
The neuropathological consequences of CDKL5 mutation
S. M. L. Paine et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2012)
Historic, Clinical, and Prognostic Features of Epileptic Encephalopathies Caused by CDKL5 Mutations
Brian D. Moseley et al.
PEDIATRIC NEUROLOGY (2012)
CDKL5 gene-related epileptic encephalopathy: electroclinical findings in the first year of life
Federico Melani et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2011)
CDKL5 alterations lead to early epileptic encephalopathy in both genders
Jao-Shwann Liang et al.
EPILEPSIA (2011)
Distinct Genetic Influences on Cortical Surface Area and Cortical Thickness
Matthew S. Panizzon et al.
CEREBRAL CORTEX (2009)
Key clinical features to identify girls with CDKL5 mutations
Nadia Bahi-Buisson et al.
BRAIN (2008)
The three stages of epilepsy in patients with CDKL5 mutations
Nadia Bahi-Buisson et al.
EPILEPSIA (2008)
Attention-deficit/hyperactivity disorder is characterized by a delay in cortical maturation
P. Shaw et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients
H. L. Archer et al.
JOURNAL OF MEDICAL GENETICS (2006)
An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest
Rahul S. Desikan et al.
NEUROIMAGE (2006)
Cortical thinning in cingulate and occipital cortices in first episode schizophrenia
KL Narr et al.
BIOLOGICAL PSYCHIATRY (2005)
Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation
LS Weaving et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Disruption of the Serine/Threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation
VM Kalscheuer et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)