Xiongying Yu

Nanchang, China

Last Updated: 09/26/2026

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Found 12 publications

LAMA2 variants associated with muscular dystrophy, brain structural abnormalities, and epilepsy: a genotype-phenotype study.

LAMA2 variants associated with muscular dystrophy, brain structural abnormalities, and epilepsy: a genotype-phenotype study.

Journal: Frontiers in neurology

Published: October 20, 2025

Identification of novel BCL11A variant in a patient with developmental delay and behavioural differences.

Identification of novel BCL11A variant in a patient with developmental delay and behavioural differences.

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

Published: July 10, 2024

A potential therapeutic agent for the treatment of hyperuricemia and gout: 3,4-Dihydroxy-5-nitrobenzaldehyde phenylthiosemicarbazide.

A potential therapeutic agent for the treatment of hyperuricemia and gout: 3,4-Dihydroxy-5-nitrobenzaldehyde phenylthiosemicarbazide.

Journal: European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences

Published: January 08, 2024

Reversible splenial lesion syndrome in children: a retrospective study of 130 cases.

Reversible splenial lesion syndrome in children: a retrospective study of 130 cases.

Journal: Frontiers in neurology

Published: June 16, 2023

Efficacy and safety of phenobarbital for benign convulsions with mild gastroenteritis: A prospective randomized controlled study.

Efficacy and safety of phenobarbital for benign convulsions with mild gastroenteritis: A prospective randomized controlled study.

Journal: Medicine

Published: December 23, 2022

De novo variants in PHF21A cause intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures: A case report and literature review.

De novo variants in PHF21A cause intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures: A case report and literature review.

Journal: Seizure

Published: November 17, 2022

Novel variants of SYNGAP1 associated epileptic encephalopathy: two cases report and literature review.

Novel variants of SYNGAP1 associated epileptic encephalopathy: two cases report and literature review.

Journal: Acta epileptologica

Published: July 26, 2022

Case report: A novel de novo variant of SCN8A in a child with benign convulsions with mild gastroenteritis.

Case report: A novel de novo variant of SCN8A in a child with benign convulsions with mild gastroenteritis.

Journal: Frontiers in neurology

Published: July 16, 2022

Case report of two affected siblings in a family with thiamine metabolism dysfunction syndrome 5: a rare, but treatable neurodegenerative disease.

Case report of two affected siblings in a family with thiamine metabolism dysfunction syndrome 5: a rare, but treatable neurodegenerative disease.

Journal: BMC neurology

Published: April 20, 2022

A case report of atypical hemiplegic migraine with nonheadache onset in a Chinese child.

A case report of atypical hemiplegic migraine with nonheadache onset in a Chinese child.

Journal: BMC neurology

Published: March 30, 2021

Balamuthia mandrillaris encephalitis in a child: case report and literature review.

Balamuthia mandrillaris encephalitis in a child: case report and literature review.

Journal: Diagnostic microbiology and infectious disease

Published: April 29, 2020

Clinical and molecular genetic characterization of familial MECP2 duplication syndrome in a Chinese family.

Clinical and molecular genetic characterization of familial MECP2 duplication syndrome in a Chinese family.

Journal: BMC medical genetics

Published: July 17, 2016

Showing 1-12 of 12

Last Updated: 09/26/2026