Jianying Duo
Changchun Street
Beijing, 100053, China
Beijing, 100053, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 12 publications
Clinical and laboratory features of juvenile-onset anti-NF155 autoimmune nodopathy.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: September 26, 2025
Association of Demographic, Clinical, and Environmental Factors With Disease Severity in Adult Myasthenia Gravis: A Multicenter Cross-Sectional Study.
Journal: CNS neuroscience & therapeutics
Published: July 25, 2025
Dynamic Changes in Peripheral Immune Cells During Efgartigimod Treatment in Naive Generalized Myasthenia Gravis.
Journal: CNS neuroscience & therapeutics
Published: April 14, 2025
Peripheral immune profiling highlights a dynamic role of low-density granulocytes in myasthenia gravis.
Journal: Journal of autoimmunity
Published: February 24, 2025
Platelet activation plays a pro-inflammatory role in myasthenia gravis.
Journal: Nature communications
Published: June 13, 2024
A rare complex structural variant of novel intragenic inversion combined with reciprocal translocation t(X;1)(p21.2;p13.3) in Duchenne muscular dystrophy.
Journal: Neuromuscular disorders : NMD
Published: January 18, 2024
Environmental factors affecting the risk of generalization for ocular-onset myasthenia gravis: a nationwide cohort study.
Journal: QJM : monthly journal of the Association of Physicians
Published: August 23, 2023
A synonymous codon variant altering splicing of RBCK1 expands the phenotype and genotype spectra of polyglucosan body myopathy 1.
Journal: Clinical genetics
Published: February 02, 2023
Delayed Respiratory Insufficiency and Extramuscular Abnormalities in Selenoprotein N-Related Myopathies.
Journal: Frontiers in neurology
Published: August 30, 2021
VNTR2/VNTR3 genotype in the FCGRT gene is associated with reduced effectiveness of intravenous immunoglobulin in patients with myasthenia gravis.
Journal: Therapeutic advances in neurological disorders
Published: June 03, 2020
Limb girdle muscular dystrophy D3 HNRNPDL related in a Chinese family with distal muscle weakness caused by a mutation in the prion-like domain.
Journal: Journal of neurology
Published: September 05, 2018
Showing 1-12 of 12
Last Updated: 09/26/2026