Found: 14
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Effect of High-Caloric Nutrition on Survival in Amyotrophic Lateral Sclerosis.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Potential implications of a ciliary neurotrophic factor gene mutation in a German population of patients with motor neuron disease.
- Published in:
- 1998
- By:
- Publication type:
- journal article
Mutation in TACO1, encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome.
- Published in:
- Nature Genetics, 2009, v. 41, n. 7, p. 833, doi. 10.1038/ng.390
- By:
- Publication type:
- Article
Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: a prospective observational study.
- Published in:
- Journal of Neurology, 2015, v. 262, n. 4, p. 849, doi. 10.1007/s00415-015-7646-2
- By:
- Publication type:
- Article
A Randomized, Double Blind, Placebo-Controlled Trial of Pioglitazone in Combination with Riluzole in Amyotrophic Lateral Sclerosis.
- Published in:
- PLoS ONE, 2012, v. 7, n. 6, p. 1, doi. 10.1371/journal.pone.0037885
- By:
- Publication type:
- Article
Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial.
- Published in:
- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-26
- By:
- Publication type:
- Article
Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Oculopharyngeal muscular dystrophy as a rare cause of dysphagia.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Health-related quality of life in ALS, myasthenia gravis and facioscapulohumeral muscular dystrophy.
- Published in:
- Journal of Neurology, 2010, v. 257, n. 9, p. 1473, doi. 10.1007/s00415-010-5549-9
- By:
- Publication type:
- Article
Socioeconomic burden of amyotrophic lateral sclerosis, myasthenia gravis and facioscapulohumeral muscular dystrophy.
- Published in:
- Journal of Neurology, 2010, v. 257, n. 1, p. 15, doi. 10.1007/s00415-009-5256-6
- By:
- Publication type:
- Article
Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease.
- Published in:
- Human Mutation, 2021, v. 42, n. 4, p. 460, doi. 10.1002/humu.24181
- By:
- Publication type:
- Article
ANO5 Gene Analysis in a Large Cohort of Patients with Anoctaminopathy: Confirmation of Male Prevalence and High Occurrence of the Common Exon 5 Gene Mutation.
- Published in:
- Human Mutation, 2013, v. 34, n. 8, p. 1111, doi. 10.1002/humu.22342
- By:
- Publication type:
- Article
A Genetic Mapping System in Caenorhabditis elegans Based on Polymorphic Sequence-Tagged Sites.
- Published in:
- Genetics, 1992, v. 131, n. 3, p. 609
- By:
- Publication type:
- Article
Novel variants broaden the phenotypic spectrum of PLEKHG5‐associated neuropathies.
- Published in:
- European Journal of Neurology, 2021, v. 28, n. 4, p. 1344, doi. 10.1111/ene.14649
- By:
- Publication type:
- Article