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Publications by Ruolin Hou
Novel CDKL5 Mutations Were Found in Patients in China: Retrospective Investigation in Cases of CDKL5-related Disorders
Italian Journal of Pediatrics
Child Health
Pediatrics
Perinatology
Related publications
Pathogenicity of C-Terminal Mutations in CDKL5
Journal of Pediatric Epilepsy
Heterozygous CDKL5 Knockout Female Mice Are a Valuable Animal Model for CDKL5 Disorder
Neural Plasticity
Neurology
Neurodevelopmental and Neurobehavioral Characteristics in Males and Females With CDKL5 Duplications
European Journal of Human Genetics
Genetics
Characterization of the Relationship of CDKL5 With MeCP2 and Dnmt1 in PrimaryRat Cortical Neurons
Brazilian Archives of Biology and Technology
Multidisciplinary
CDKL5/STK9 Is Mutated in Rett Syndrome Variant With Infantile Spasms
Journal of Medical Genetics
Genetics
Pathogenic Mutations in ARX, CDKL5 and STXBP1 Genes Are Not Associated With the Early-Onset Epileptic Encephalopathy in Malaysian Pediatric Patients: A Pilot Study
Neuroscience Research Notes
SMAD4 Mutations Found in Unselected HHT Patients
Journal of Medical Genetics
Genetics
Open-Label Use of Highly* Purified CBD (Epidiolex®) in Patients With CDKL5 Deficiency Disorder and Aicardi, Dup15q, and Doose Syndromes
Epilepsy and Behavior
Neurology
Behavioral Neuroscience
Detection of BRAF Mutations in Patients With Hairy Cell Leukemia and Related Lymphoproliferative Disorders
Haematologica
Hematology
