Found: 16
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Baseline characteristics from TANGO: Phase 2 study to evaluate gosuranemab (BIIB092) in patients with early Alzheimer's disease: Human: Improving clinical trial methodology.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.044910
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- Publication type:
- Article
Allele-Specific Amplification for the Diagnosis of Autosomal Recessive Spinal Muscular Atrophy.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 1999, v. 37, n. 2, p. 133
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- Publication type:
- Article
Correction: Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry.
- Published in:
- 2015
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- Publication type:
- Correction Notice
Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry.
- Published in:
- PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0127045
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- Publication type:
- Article
Resistance strength training exercise in children with spinal muscular atrophy.
- Published in:
- 2015
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- Publication type:
- journal article
Riluzole pharmacokinetics in young patients with spinal muscular atrophy.
- Published in:
- British Journal of Clinical Pharmacology, 2011, v. 71, n. 3, p. 403, doi. 10.1111/j.1365-2125.2010.03843.x
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- Publication type:
- Article
A sensitive assay for measuring SMN mRNA levels in peripheral blood and in muscle samples of patients affected with spinal muscular atrophy.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 10, p. 1054, doi. 10.1038/sj.ejhg.5201885
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- Publication type:
- Article
Refined genetic mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.3 and evidence of linkage disequilibrium in European families.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 6, p. 483, doi. 10.1038/sj.ejhg.5201177
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- Publication type:
- Article
Dominant and recessive central core disease associated with RYR1 mutations and fetal akinesia.
- Published in:
- Brain: A Journal of Neurology, 2003, v. 126, n. 11, p. 2341, doi. 10.1093/brain/awg244
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- Publication type:
- Article
Operation and decline of the Barbegal mill complex, the largest industrial complex of antiquity.
- Published in:
- Geoarchaeology, 2024, v. 39, n. 6, p. 594, doi. 10.1002/gea.22016
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- Publication type:
- Article
A rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation.
- Published in:
- Annals of Neurology, 2012, v. 71, n. 4, p. 509, doi. 10.1002/ana.22684
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- Publication type:
- Article
Mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.
- Published in:
- Annals of Neurology, 2002, v. 51, n. 5, p. 585, doi. 10.1002/ana.10182
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- Publication type:
- Article
Study of LPIN1, LPIN2 and LPIN3 in rhabdomyolysis and exercise-induced myalgia.
- Published in:
- Journal of Inherited Metabolic Disease, 2012, v. 35, n. 6, p. 1119, doi. 10.1007/s10545-012-9461-6
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- Publication type:
- Article
Evoked Potentials in Spinal Muscular Atrophy.
- Published in:
- Journal of Child Neurology, 2003, v. 18, n. 6, p. 383, doi. 10.1177/08830738030180061101
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- Publication type:
- Article
The loss of the snoRNP chaperone Nopp140 from Cajal bodies of patient fibroblasts correlates with the severity of spinal muscular atrophy.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 7, p. 1181, doi. 10.1093/hmg/ddp009
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- Publication type:
- Article
A novel association of the SMN protein with two major non-ribosomal nucleolar proteins and its implication in spinal muscular atrophy.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 9, p. 1017, doi. 10.1093/hmg/11.9.1017
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- Publication type:
- Article