S. Gong

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..

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.

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.

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.

[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.

De novo frameshift variant in MT-ND1 causes a mitochondrial complex I deficiency associated with MELAS syndrome.

Luying Zhang, Hezhi Fang, Fang Fang, 2023, Gene.