4.2 Article

Brain morphological abnormalities in children with cyclin-dependent kinase-like 5 deficiency disorder

Related references

Note: Only part of the references are listed.
Article Biochemistry & Molecular Biology

Genetic and environmental influences on structural brain measures in twins with autism spectrum disorder

John P. Hegarty et al.

MOLECULAR PSYCHIATRY (2020)

Article Neurosciences

CDKL5 Deficiency Disorder-A Complex Epileptic Encephalopathy

Martyna Jakimiec et al.

BRAIN SCIENCES (2020)

Article Developmental Biology

Molecular and Synaptic Bases of CDKL5 Disorder

Yong-Chuan Zhu et al.

DEVELOPMENTAL NEUROBIOLOGY (2019)

Review Clinical Neurology

Cyclin-Dependent Kinase-Like 5 Deficiency Disorder: Clinical Review

Heather E. Olson et al.

PEDIATRIC NEUROLOGY (2019)

Article Developmental Biology

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)

Review Neurosciences

Imaging structural and functional brain development in early childhood

John H. Gilmore et al.

NATURE REVIEWS NEUROSCIENCE (2018)

Article Genetics & Heredity

&ITCDKL5&IT variants Improving our understanding of a rare neurologic disorder

Ralph D. Hector et al.

NEUROLOGY-GENETICS (2017)

Article Clinical Neurology

Pontine and cerebral atrophy in Lennox-Gastaut syndrome

Benjamin J. C. Newham et al.

EPILEPSY RESEARCH (2016)

Article Behavioral Sciences

CDKL5 knockout leads to altered inhibitory transmission in the cerebellum of adult mice

S. Sivilia et al.

GENES BRAIN AND BEHAVIOR (2016)

Article Neurosciences

The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository

Terry L. Jernigan et al.

NEUROIMAGE (2016)

Article Multidisciplinary Sciences

Genetic topography of brain morphology

Chi-Hua Chen et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)

Letter Clinical Neurology

The neuropathological consequences of CDKL5 mutation

S. M. L. Paine et al.

NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2012)

Article Clinical Neurology

Historic, Clinical, and Prognostic Features of Epileptic Encephalopathies Caused by CDKL5 Mutations

Brian D. Moseley et al.

PEDIATRIC NEUROLOGY (2012)

Article Clinical Neurology

CDKL5 gene-related epileptic encephalopathy: electroclinical findings in the first year of life

Federico Melani et al.

DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2011)

Article Clinical Neurology

CDKL5 alterations lead to early epileptic encephalopathy in both genders

Jao-Shwann Liang et al.

EPILEPSIA (2011)

Article Neurosciences

Distinct Genetic Influences on Cortical Surface Area and Cortical Thickness

Matthew S. Panizzon et al.

CEREBRAL CORTEX (2009)

Article Clinical Neurology

Key clinical features to identify girls with CDKL5 mutations

Nadia Bahi-Buisson et al.

BRAIN (2008)

Article Clinical Neurology

The three stages of epilepsy in patients with CDKL5 mutations

Nadia Bahi-Buisson et al.

EPILEPSIA (2008)

Article Multidisciplinary Sciences

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)

Article Genetics & Heredity

Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation

LS Weaving et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2004)

Article Genetics & Heredity

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)