Mei Hou

Long-Term Outcomes in Tyrosine Hydroxylase Deficiency: A Case Series of Four Paediatric Patients.

Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience

Published: August 05, 2025

Sotos Syndrome With NSD1 Mutations in a Chinese Cohort: Identification of Two Novel Mutations and Literature Review.

Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience

Published: March 26, 2025

Clinical characteristics and genetic analysis of four pediatric patients with Kleefstra syndrome.

Journal: BMC medical genomics

Published: May 12, 2024

Heterozygous inversion on chromosome 17 involving PAFAH1B1 detected by whole genome sequencing in a patient suffering from pachygyria.

Journal: European journal of medical genetics

Published: April 11, 2024

Microcephaly, disproportionate pontine, and cerebellar hypoplasia syndrome: Two novel mutations in the CASK gene were discovered in Chinese females.

Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience

Published: November 01, 2020

Four novel compound heterozygous mutations in C5orf42 gene in patients with pure and mild Joubert syndrome.

Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience

Published: February 03, 2020

Novel variants in TBC1D24 associated with epilepsy and deafness: Report of two cases.

Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience

Published: December 10, 2019

Chinese Cases of Metachromatic Leukodystrophy with the Novel Missense Mutations in ARSA Gene.

Journal: Journal of molecular neuroscience : MN

Published: October 31, 2019

Effects of acupuncture treatment on motor function in patients with subacute hemorrhagic stroke: A randomized controlled study.

Journal: Complementary therapies in medicine

Published: April 28, 2019

Chinese cases of early infantile epileptic encephalopathy: a novel mutation in the PCDH19 gene was proved in a mosaic male- case report.

Journal: BMC medical genetics

Published: February 16, 2018

Long-Term Outcomes in Tyrosine Hydroxylase Deficiency: A Case Series of Four Paediatric Patients.

Long-Term Outcomes in Tyrosine Hydroxylase Deficiency: A Case Series of Four Paediatric Patients.

Sotos Syndrome With NSD1 Mutations in a Chinese Cohort: Identification of Two Novel Mutations and Literature Review.

Sotos Syndrome With NSD1 Mutations in a Chinese Cohort: Identification of Two Novel Mutations and Literature Review.

Clinical characteristics and genetic analysis of four pediatric patients with Kleefstra syndrome.

Clinical characteristics and genetic analysis of four pediatric patients with Kleefstra syndrome.

Heterozygous inversion on chromosome 17 involving PAFAH1B1 detected by whole genome sequencing in a patient suffering from pachygyria.

Heterozygous inversion on chromosome 17 involving PAFAH1B1 detected by whole genome sequencing in a patient suffering from pachygyria.

Microcephaly, disproportionate pontine, and cerebellar hypoplasia syndrome: Two novel mutations in the CASK gene were discovered in Chinese females.

Microcephaly, disproportionate pontine, and cerebellar hypoplasia syndrome: Two novel mutations in the CASK gene were discovered in Chinese females.

Four novel compound heterozygous mutations in C5orf42 gene in patients with pure and mild Joubert syndrome.

Four novel compound heterozygous mutations in C5orf42 gene in patients with pure and mild Joubert syndrome.

Novel variants in TBC1D24 associated with epilepsy and deafness: Report of two cases.

Novel variants in TBC1D24 associated with epilepsy and deafness: Report of two cases.

Chinese Cases of Metachromatic Leukodystrophy with the Novel Missense Mutations in ARSA Gene.

Chinese Cases of Metachromatic Leukodystrophy with the Novel Missense Mutations in ARSA Gene.

Effects of acupuncture treatment on motor function in patients with subacute hemorrhagic stroke: A randomized controlled study.

Effects of acupuncture treatment on motor function in patients with subacute hemorrhagic stroke: A randomized controlled study.

Effects of Acupuncture Treatment on Lower Limb Spasticity in Patients Following Hemorrhagic Stroke: A Pilot Study.

Effects of Acupuncture Treatment on Lower Limb Spasticity in Patients Following Hemorrhagic Stroke: A Pilot Study.

Clinical characteristics and functional status of children with different subtypes of dyskinetic cerebral palsy.

Clinical characteristics and functional status of children with different subtypes of dyskinetic cerebral palsy.

Chinese cases of early infantile epileptic encephalopathy: a novel mutation in the PCDH19 gene was proved in a mosaic male- case report.

Chinese cases of early infantile epileptic encephalopathy: a novel mutation in the PCDH19 gene was proved in a mosaic male- case report.