Found: 18
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Diagnostic utility of different dysphagia screening tools to detect dysphagia in individuals with amyotrophic lateral sclerosis.
- Published in:
- Neurological Sciences, 2023, v. 44, n. 11, p. 3919, doi. 10.1007/s10072-023-06918-2
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- Publication type:
- Article
Correction to: Genetic analysis in Chinese patients with familial or young‑onset amyotrophic lateral sclerosis.
- Published in:
- 2022
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- Publication type:
- Correction Notice
Genetic analysis in Chinese patients with familial or young-onset amyotrophic lateral sclerosis.
- Published in:
- Neurological Sciences, 2022, v. 43, n. 4, p. 2579, doi. 10.1007/s10072-021-05634-z
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- Publication type:
- Article
Biallelic loss-of-function variants in NEMF cause central nervous system impairment and axonal polyneuropathy.
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- Human Genetics, 2021, v. 140, n. 4, p. 579, doi. 10.1007/s00439-020-02226-3
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- Publication type:
- Article
Diaphragmatic ultrasonography as a predictor of respiratory muscle fatigue in myasthenia gravis.
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- Muscle & Nerve, 2024, v. 69, n. 2, p. 199, doi. 10.1002/mus.28020
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- Article
Hyperhomocysteinemia in patients with riboflavin‐responsive multiple acyl‐CoA dehydrogenase deficiency.
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- Muscle & Nerve, 2023, v. 68, n. 5, p. 750, doi. 10.1002/mus.27960
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- Article
Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.
- Published in:
- Scientific Reports, 2017, p. 44155, doi. 10.1038/srep44155
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- Publication type:
- Article
Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12435-8
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- Publication type:
- Article
Magnetic and Electrical Properties of (Mn, La)-Codoped SrTiO<sub>3</sub> Thin Films.
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- Journal of the American Ceramic Society, 2008, v. 91, n. 10, p. 3263, doi. 10.1111/j.1551-2916.2008.02602.x
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- Publication type:
- Article
Polarization of High-Permittivity Dielectric NiO-Based Ceramics.
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- Journal of the American Ceramic Society, 2005, v. 88, n. 7, p. 1808, doi. 10.1111/j.1551-2916.2005.00361.x
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- Publication type:
- Article
The male-to-female ratio in late-onset multiple acyl-CoA dehydrogenase deficiency: a systematic review and meta-analysis.
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- Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03072-6
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- Article
SLC39A5 dysfunction impairs extracellular matrix synthesis in high myopia pathogenesis.
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- Journal of Cellular & Molecular Medicine, 2021, v. 25, n. 17, p. 8432, doi. 10.1111/jcmm.16803
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- Publication type:
- Article
Relative frequencies and clinical features of Guillain-Barré Syndrome before and during the COVID-19 pandemic in North China.
- Published in:
- BMC Infectious Diseases, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12879-024-09401-1
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- Publication type:
- Article
A novel autosomal dominant ERLIN2 variant activates endoplasmic reticulum stress in a Chinese HSP family.
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- Annals of Clinical & Translational Neurology, 2023, v. 10, n. 11, p. 2139, doi. 10.1002/acn3.51902
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- Article
Efgartigimod in the treatment of Guillain–Barré syndrome.
- Published in:
- 2024
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- Publication type:
- Case Study
GGC repeat expansions in NOTCH2NLC causing a phenotype of lower motor neuron syndrome.
- Published in:
- Journal of Neurology, 2022, v. 269, n. 8, p. 4469, doi. 10.1007/s00415-022-11092-0
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- Publication type:
- Article
autism risk gene CNTN4 modulates dendritic spine formation.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 2, p. 207, doi. 10.1093/hmg/ddab233
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- Publication type:
- Article
Novel mutation of EDA causes new asymmetrical X‐linked hypohidrotic ectodermal dysplasia phenotypes in a female.
- Published in:
- Journal of Dermatology, 2019, v. 46, n. 8, p. 731, doi. 10.1111/1346-8138.14978
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- Publication type:
- Article