Found: 14
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Clinical, pathological, and molecular genetic analysis of 7 Chinese patients with hereditary myopathy with early respiratory failure.
- Published in:
- Neurological Sciences, 2022, v. 43, n. 5, p. 3371, doi. 10.1007/s10072-021-05783-1
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- Publication type:
- Article
DNM2 mutations in Chinese Han patients with centronuclear myopathy.
- Published in:
- 2016
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- Publication type:
- journal article
Clinico‐sero‐pathological profiles and risk prediction model of idiopathic inflammatory myopathy (IIM) patients with different perifascicular changes.
- Published in:
- CNS Neuroscience & Therapeutics, 2024, v. 30, n. 8, p. 1, doi. 10.1111/cns.14882
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- Publication type:
- Article
Myofascial edema of gastrocnemius: A prominent MRI characteristic in dermatomyositis patients with anti‐transcriptional intermediate factor 1‐γ antibody.
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- CNS Neuroscience & Therapeutics, 2024, v. 30, n. 2, p. 1, doi. 10.1111/cns.14647
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- Publication type:
- Article
Juvenile idiopathic inflammatory myopathies with anti‐3‐hydroxy‐3‐methylglutaryl‐coenzyme A reductase antibodies in a Chinese cohort.
- Published in:
- CNS Neuroscience & Therapeutics, 2021, v. 27, n. 9, p. 1041, doi. 10.1111/cns.13658
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- Publication type:
- Article
Glymphatic dysfunction in patients with early-stage amyotrophic lateral sclerosis.
- Published in:
- Brain: A Journal of Neurology, 2024, v. 147, n. 1, p. 100, doi. 10.1093/brain/awad274
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- Publication type:
- Article
Clinical and molecular genetic analysis in Chinese patients with distal myopathy with rimmed vacuoles.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 4, p. 335, doi. 10.1038/jhg.2011.15
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- Publication type:
- Article
Amygdala abnormalities across disease stages in patients with sporadic amyotrophic lateral sclerosis.
- Published in:
- Human Brain Mapping, 2022, v. 43, n. 18, p. 5421, doi. 10.1002/hbm.26016
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- Publication type:
- Article
Skeletal muscle involvement in systemic amyloidosis is often overlooked.
- Published in:
- Neuropathology & Applied Neurobiology, 2024, v. 50, n. 4, p. 1, doi. 10.1111/nan.12996
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- Publication type:
- Article
Genetic variations and clinical spectrum of dystroglycanopathy in a large cohort of Chinese patients.
- Published in:
- Clinical Genetics, 2021, v. 99, n. 3, p. 384, doi. 10.1111/cge.13886
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- Publication type:
- Article
Hypothalamic subregion abnormalities are related to body mass index in patients with sporadic amyotrophic lateral sclerosis.
- Published in:
- Journal of Neurology, 2022, v. 269, n. 6, p. 2980, doi. 10.1007/s00415-021-10900-3
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- Publication type:
- Article
Anti-HMGCR myopathy overlaps with dermatomyositis-like rash: a distinct subtype of idiopathic inflammatory myopathy.
- Published in:
- Journal of Neurology, 2022, v. 269, n. 1, p. 280, doi. 10.1007/s00415-021-10621-7
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- Publication type:
- Article
Choroid plexus enlargement in amyotrophic lateral sclerosis patients and its correlation with clinical disability and blood-CSF barrier permeability.
- Published in:
- Fluids & Barriers of the CNS, 2024, v. 21, n. 1, p. 1, doi. 10.1186/s12987-024-00536-6
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- Publication type:
- Article
Distal myopathy due to TCAP variants in four unrelated Chinese patients.
- Published in:
- Neurogenetics, 2021, v. 22, n. 1, p. 1, doi. 10.1007/s10048-020-00623-4
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- Publication type:
- Article