Mingshi S. Gao

No.12 Middle Wulumuqi Road
Shanghai, China

Last Updated: 09/26/2026

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Found 26 publications

Clinical characteristics of IgG4-related hypertrophic pachymeningitis with and without serum ANCA positivity.

Clinical characteristics of IgG4-related hypertrophic pachymeningitis with and without serum ANCA positivity.

Journal: Journal of neuroimmunology

Published: May 08, 2026

Case Report: Anti-cavin-4-positive immune-mediated rippling muscle disease co-occurring with isolated ocular myasthenia gravis.

Case Report: Anti-cavin-4-positive immune-mediated rippling muscle disease co-occurring with isolated ocular myasthenia gravis.

Journal: Frontiers in immunology

Published: December 08, 2025

Phospho-MLKL Upregulation in Immune-Mediated Necrotizing Myopathy: Implications for Disease Pathophysiology and Diagnosis.

Phospho-MLKL Upregulation in Immune-Mediated Necrotizing Myopathy: Implications for Disease Pathophysiology and Diagnosis.

Journal: Neuropathology : official journal of the Japanese Society of Neuropathology

Published: December 01, 2025

An Alu mediated intergenic inversion in RBCK1 causing Polyglucosan body myopathy type 1.

An Alu mediated intergenic inversion in RBCK1 causing Polyglucosan body myopathy type 1.

Journal: Human molecular genetics

Published: November 17, 2025

Vacuolar myopathy caused by CASQ1 p.Asp244His: pathogenic evidence from two unrelated Chinese families.

Vacuolar myopathy caused by CASQ1 p.Asp244His: pathogenic evidence from two unrelated Chinese families.

Journal: Journal of human genetics

Published: September 16, 2025

Clinical features and prognosis of patients with peripheral neuropathy with systemic light chain amyloidosis

Clinical features and prognosis of patients with peripheral neuropathy with systemic light chain amyloidosis

Journal: Zhonghua yi xue za zhi

Published: July 07, 2025

Expanded spectrum of MEGF10 related myopathies: late-onset myofibrillar myopathy-like phenotype with novel variants.

Expanded spectrum of MEGF10 related myopathies: late-onset myofibrillar myopathy-like phenotype with novel variants.

Journal: Neuromuscular disorders : NMD

Published: May 26, 2025

Pseudoexon activating by a deep intronic variant and phenotype variation in a Chinese family with dystrophinopathy.

Pseudoexon activating by a deep intronic variant and phenotype variation in a Chinese family with dystrophinopathy.

Journal: Journal of human genetics

Published: February 21, 2025

Translation of GGC repeats into a toxic polyglycine protein in oculopharyngodistal myopathy type 2.

Translation of GGC repeats into a toxic polyglycine protein in oculopharyngodistal myopathy type 2.

Journal: Brain : a journal of neurology

Published: February 20, 2025

Diverse electrophysiological demyelinating features in a late-onset glycogen storage disease type IIIa case.

Diverse electrophysiological demyelinating features in a late-onset glycogen storage disease type IIIa case.

Journal: Open medicine (Warsaw, Poland)

Published: November 08, 2024

Human induced pluripotent stem cell line (FDHSi005-A) derived from a patient with a deep intronic variant in the GNE gene.

Human induced pluripotent stem cell line (FDHSi005-A) derived from a patient with a deep intronic variant in the GNE gene.

Journal: Stem cell research

Published: July 05, 2024

4qA D4Z4 Methylation Test as a Valuable Complement for Differential Diagnosis in Patients with a Facioscapulohumeral Muscular Dystrophy-Like Phenotype.

4qA D4Z4 Methylation Test as a Valuable Complement for Differential Diagnosis in Patients with a Facioscapulohumeral Muscular Dystrophy-Like Phenotype.

Journal: The Journal of molecular diagnostics : JMD

Published: July 04, 2024

Showing 1-12 of 26

Last Updated: 09/26/2026