Jiu-wei Li

发表

Chinese patients with p.Arg756 mutations of ATP1A3: Clinical manifestations, treatment, and follow‐up

Fang Fang, C. Ding, Weihua Zhang, 2022, Pediatric investigation.

Compound Heterozygous CHAT Gene Mutations of a Large Deletion and a Missense Variant in a Chinese Patient With Severe Congenital Myasthenic Syndrome With Episodic Apnea

S. Qian, F. Fang, C. Ding, 2019, Front. Pharmacol..

Arterial ischemic stroke: experience in Chinese children.

L. Zou, E. Mix, F. Fang, 2008, Pediatric neurology.

Long-term efficacy of mycophenolate mofetil in myelin oligodendrocyte glycoprotein antibody-associated disorders

L. Cui, Yicheng Zhu, Tao Xu, 2020, Neurology: Neuroimmunology & Neuroinflammation.

HPDL deficiency causes a neuromuscular disease by impairing the mitochondrial respiration.

J. Lyu, Yongguo Yu, Wei Yang, 2021, Journal of genetics and genomics = Yi chuan xue bao.

A 5‐year‐old child presenting with tumor‐like primary angiitis of the central nervous system

Weihua Zhang, Jiu-wei Li, Ji Zhou, 2022, Pediatric investigation.

Mycophenolate mofetil: An alternative disease-modifying agent for MOG-IgG-associated disorders in childhood: A single-center bidirectional cohort study.

C. Ren, C. Ding, Weihua Zhang, 2022, Multiple sclerosis and related disorders.

Long-term e ﬃ cacy of mycophenolate mofetil in myelin oligodendrocyte glycoprotein antibody-associated disorders A prospective study

L. Cui, Yicheng Zhu, B. Peng, 2022 .

Clinical and genetic spectrum of hereditary spastic paraplegia in Chinese children

X. Bao, Jiaping Wang, Yun Wu, 2022, Developmental medicine and child neurology.

Phenotypes and genotypes of mitochondrial diseases with mtDNA variations in Chinese children: a multi-center study.

Yi Wang, Dan Sun, C. Ding, 2021, Mitochondrion.

Novel truncating mutations in ASXL1 identified in two Chinese boys with Bohring-Opitz syndrome.

F. Fang, C. Ding, Jiu-wei Li, 2021, European journal of medical genetics.

Risk factors for arterial ischemic and hemorrhagic stroke in childhood.

L. Zou, F. Fang, O. Caspi, 2009, Pediatric neurology.

Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes

Yun Wu, F. Fang, Weihua Zhang, 2021, Frontiers in Genetics.

NAD(P)HX dehydratase (NAXD) deficiency: a novel neurodegenerative disorder exacerbated by febrile illnesses.

H. Prokisch, F. Fang, S. L. Stenton, 2019, Brain : a journal of neurology.

Clinical Characteristics and Outcome Analysis of 94 Children With Brain Abscess in Beijing: A Single-center Retrospective Study.

M. Ge, M. Hei, Huyong Zheng, 2020, The Pediatric infectious disease journal.

A Centralized Report on Pediatric Japanese Encephalitis Cases from Beijing Children's Hospital, 2013.

Xiao-juan Tan, Wei Zhang, Z. Yin, 2016, Biomedical and environmental sciences : BES.

Next-Generation Sequencing Analysis Reveals Novel Pathogenic Variants in Four Chinese Siblings With Late-Infantile Neuronal Ceroid Lipofuscinosis

F. Fang, C. Ren, C. Ding, 2019, Front. Genet..

Expanding the mutational spectrum of Rahman syndrome: A rare disorder with severe intellectual disability and particular facial features in two Chinese patients

V. Zhang, C. Ding, Weihua Zhang, 2022, Molecular genetics & genomic medicine.

Neurologic Manifestations as Initial Clinical Presentation of Familial Hemophagocytic Lymphohistiocytosis Type2 Due to PRF1 Mutation in Chinese Pediatric Patients

Yun Wu, F. Fang, C. Ding, 2020, Frontiers in Genetics.

Epileptic seizure, as the first symptom of hypoparathyroidism in children, does not require antiepileptic drugs

L. Zou, Xiu-yu Shi, Jiu-wei Li, 2016, Child's Nervous System.

Neurological Abnormality Could be the First and Only Symptom of Familial Hemophagocytic Lymphohistiocytosis: Report of Two Families

Tianyou Wang, Zhigang Li, C. Ding, 2018, Chinese medical journal.

Report of a case with ferredoxin reductase (FDXR) gene variants in a Chinese boy exhibiting hearing loss, visual impairment, and motor retardation

Zhenfeng Song, Z. Yi, Wei Zhang, 2021, International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience.

Lack of association between valproic acid response and polymorphisms of its metabolism, transport, and receptor genes in children with focal seizures

S. Mei, Leting Zhu, Zhigang Zhao, 2018, Neurological Sciences.

Molecular spectrum of excision repair cross-complementation group 8 gene defects in Chinese patients with Cockayne syndrome type A

Ming Yan, F. Fang, Yanling Yang, 2017, Scientific Reports.

[Clinical effect of tacrolimus in the treatment of myasthenia gravis in children].

F. Fang, Hu-sheng Wu, C. Ren, 2020, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

WITHDRAWN: Clinical and molecular analysis of six novel GALC mutations identified in 7 Chinese children with Krabbe disease.

F. Fang, Jiu-wei Li, X. Ren, 2017, Brain & development.

Case Report: Autoimmune Encephalitis Associated With Anti-glutamic Acid Decarboxylase Antibodies: A Pediatric Case Series

H. Ren, H. Guan, F. Fang, 2021, Frontiers in Neurology.

Clinical Features and Outcomes of Anti-N-Methyl-d-Aspartate Receptor Encephalitis in Infants and Toddlers.

H. Ren, F. Fang, C. Ren, 2021, Pediatric neurology.

Molecular spectrum of excision repair cross-complementation group 8 gene defects in Chinese patients with Cockayne syndrome type A

Ming Yan, F. Fang, Yanling Yang, 2017, Scientific Reports.

Predictors of survival in children with methymalonic acidemia with homocystinuria in Beijing, China: A prospective cohort study

Qiang Sun, Xiaoxia Peng, Wenqi Song, 2015, Indian Pediatrics.