Found: 29
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A Randomized Open-Labeled Trial of Methotrexate as a Steroid-Sparing Agent for Patients With Generalized Myasthenia Gravis.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.839075
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- Article
Successful treatment of periodic paralysis with coenzyme Q10: two case reports.
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- Acta Myologica, 2016, v. 35, p. 107
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- Article
Favorable Effects of Tacrolimus Monotherapy on Myasthenia Gravis Patients.
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- Frontiers in Neurology, 2020, v. 11, p. N.PAG, doi. 10.3389/fneur.2020.594152
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- Article
Myasthenia Gravis Coexisting With Primary Sjögren's Syndrome: Report of Three Cases and Literature Review.
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- Frontiers in Neurology, 2020, v. 11, p. N.PAG, doi. 10.3389/fneur.2020.00939
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- Article
Differentiation of Glial Cells From hiPSCs: Potential Applications in Neurological Diseases and Cell Replacement Therapy.
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- Frontiers in Cellular Neuroscience, 2018, p. N.PAG, doi. 10.3389/fncel.2018.00239
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- Article
Integrative multi-omics analysis identifies genetically supported druggable targets and immune cell specificity for myasthenia gravis.
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- Journal of Translational Medicine, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s12967-024-04994-2
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- Article
A synonymous codon variant altering splicing of RBCK1 expands the phenotype and genotype spectra of polyglucosan body myopathy 1.
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- Clinical Genetics, 2023, v. 104, n. 3, p. 387, doi. 10.1111/cge.14350
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- Article
Unusual electrophysiological findings in a Chinese ALS 4 family with SETX-L389S mutation: a three-year follow-up.
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- Journal of Neurology, 2021, v. 268, n. 3, p. 1050, doi. 10.1007/s00415-020-10246-2
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- Article
Limb girdle muscular dystrophy D3 HNRNPDL related in a Chinese family with distal muscle weakness caused by a mutation in the prion-like domain.
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- Journal of Neurology, 2019, v. 266, n. 2, p. 498, doi. 10.1007/s00415-018-9165-4
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- Article
Atypical familial amyotrophic lateral sclerosis with initial symptoms of pain or tremor in a Chinese family harboring VAPB-P56S mutation.
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- Journal of Neurology, 2016, v. 263, n. 2, p. 263, doi. 10.1007/s00415-015-7965-3
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- Article
Mortality of myasthenia gravis: a national population‐based study in China.
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- Annals of Clinical & Translational Neurology, 2023, v. 10, n. 7, p. 1095, doi. 10.1002/acn3.51792
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- Article
Comparison between mono‐tacrolimus and mono‐glucocorticoid in the treatment of myasthenia gravis.
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- Annals of Clinical & Translational Neurology, 2023, v. 10, n. 4, p. 589, doi. 10.1002/acn3.51746
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- Article
A Novel Autosomal Dominant Inclusion Body Myopathy Linked to 7q22.1-31.1.
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- PLoS ONE, 2012, v. 7, n. 6, p. 1, doi. 10.1371/journal.pone.0039288
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- Article
Short-term outcome prediction for myasthenia gravis: an explainable machine learning model.
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- Therapeutic Advances in Neurological Disorders, 2023, p. 1, doi. 10.1177/17562864231154976
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- Publication type:
- Article
Short-term outcome prediction for myasthenia gravis: an explainable machine learning model.
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- Therapeutic Advances in Neurological Disorders, 2023, v. 16, p. 1, doi. 10.1177/17562864231154976
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- Article
Missense Mutations of Codon 116 in the SOD1 Gene Cause Rapid Progressive Familial ALS and Predict Short Viability With PMA Phenotype.
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- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.776831
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- Article
A Case Study and Literature Review of the Diagnosis of Danon Disease in Patients Presenting Only with Severe Cardiac Symptoms.
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- Pharmacogenomics & Personalized Medicine, 2023, v. 16, p. 767, doi. 10.2147/PGPM.S392800
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- Article
VNTR2/VNTR3 genotype in the FCGRT gene is associated with reduced effectiveness of intravenous immunoglobulin in patients with myasthenia gravis.
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- Therapeutic Advances in Neurological Disorders, 2021, p. 1, doi. 10.1177/1756286420986747
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- Publication type:
- Article
VNTR2/VNTR3 genotype in the FCGRT gene is associated with reduced effectiveness of intravenous immunoglobulin in patients with myasthenia gravis.
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- Therapeutic Advances in Neurological Disorders, 2021, p. 1, doi. 10.1177/1756286420986747
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- Publication type:
- Article
Neurological manifestations, laboratory and neuroimaging features in HIV-infected patients.
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- Neurosciences, 2017, v. 22, n. 4, p. 311, doi. 10.17712/nsj.2017.4.20160606
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- Article
Different sensorimotor mechanism in fast and slow progression amyotrophic lateral sclerosis.
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- Human Brain Mapping, 2022, v. 43, n. 5, p. 1710, doi. 10.1002/hbm.25752
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- Article
Hashimoto's encephalopathy mimicking spinocerebellar ataxia.
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- 2011
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- Letter
Telbivudine myopathy in a patient with chronic hepatitis B.
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- 2012
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- Publication type:
- Report
Characterization of genotype-phenotype correlation with MORC2 mutated Axonal Charcot-Marie-Tooth disease in a cohort of Chinese patients.
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- 2021
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- Publication type:
- journal article
Broadening the spectrum of controls for skin biopsy in painful neuropathies.
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- Muscle & Nerve, 2010, v. 42, n. 3, p. 435, doi. 10.1002/mus.21747
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- Article
Nomogram for short-term outcome assessment in AChR subtype generalized myasthenia gravis.
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- 2021
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- Publication type:
- journal article
Beyond the Motor Cortex: Thalamic Iron Deposition Accounts for Disease Severity in Amyotrophic Lateral Sclerosis.
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- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.791300
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- Publication type:
- Article
Clinical Predictors of Relapse in a Cohort of Steroid-Treated Patients With Well-Controlled Myasthenia Gravis.
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- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.816243
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- Publication type:
- Article
Delayed Respiratory Insufficiency and Extramuscular Abnormalities in Selenoprotein N-Related Myopathies.
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- Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.766942
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- Article