Found: 15
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A meta-analysis of randomized double-blind clinical trials in CMT1A to assess the change from baseline in CMTNS and ONLS scales after one year of treatment.
- Published in:
- Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13023-015-0293-y
- By:
- Publication type:
- Article
A meta-analysis of randomized double-blind clinical trials in CMT1A to assess the change from baseline in CMTNS and ONLS scales after one year of treatment.
- Published in:
- 2015
- By:
- Publication type:
- Letter
Polytherapy with a combination of three repurposed drugs (PXT3003) down-regulates Pmp22 overexpression and improves myelination, axonal and functional parameters in models of CMT1A neuropathy.
- Published in:
- Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 282, doi. 10.1186/s13023-014-0201-x
- By:
- Publication type:
- Article
Polytherapy with a combination of three repurposed drugs (PXT3003) down-regulates Pmp22 over-expression and improves myelination, axonal and functional parameters in models of CMT1A neuropathy.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Molecular Biological Studies of the Cardiac Sodium-Calcium Exchanger<sup>a</sup>.
- Published in:
- Annals of the New York Academy of Sciences, 1996, v. 779, n. 1, p. 103, doi. 10.1111/j.1749-6632.1996.tb44774.x
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- Publication type:
- Article
Continuum of overlapping clones spanning the entire human chromosome 21q.
- Published in:
- Nature, 1992, v. 359, n. 6394, p. 380, doi. 10.1038/359380a0
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- Publication type:
- Article
Combination of acamprosate and baclofen as a promising therapeutic approach for Parkinson's disease.
- Published in:
- Scientific Reports, 2015, p. 16084, doi. 10.1038/srep16084
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- Publication type:
- Article
A Multi-Marker Genetic Association Test Based on the Rasch Model Applied to Alzheimer’s Disease.
- Published in:
- PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0138223
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- Publication type:
- Article
Complete Mitochondrial Genome and Phylogeny of Pleistocene Mammoth Mammuthus primigenius.
- Published in:
- PLoS Biology, 2006, v. 4, n. 3, p. 403, doi. 10.1371/journal.pbio.0040073
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- Publication type:
- Article
Characterization of a YAC contig containing the NBCCS locus and a novel Kruppel-type zinc finger sequence on chromosome segment 9q22.3.
- Published in:
- Genes, Chromosomes & Cancer, 1997, v. 18, n. 3, p. 212, doi. 10.1002/(SICI)1098-2264(199703)18:3<212::AID-GCC7>3.0.CO;2-4
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- Publication type:
- Article
Integrated YAC contig containing the 3pl4.2 hereditary renal carcinoma 3;8 translocation breakpoint and the fragile site FRA3B.
- Published in:
- Genes, Chromosomes & Cancer, 1994, v. 11, n. 4, p. 216, doi. 10.1002/gcc.2870110403
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- Publication type:
- Article
A YAC contig map of the human genome.
- Published in:
- Nature, 1995, v. 377, n. 6547, p. 175
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- Publication type:
- Article
Survey of CAG/CTG Repeats in Human cDNAs Representing New Genes: Candidates for Inherited Neurological Disorders.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 7, p. 1001, doi. 10.1093/hmg/5.7.1001
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- Publication type:
- Article
Linkage of Polymorphic Congenital Cataract to the γ-Crystallin Gene Locus on Human Chromosome 2q33–35.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 5, p. 699, doi. 10.1093/hmg/5.5.699
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- Publication type:
- Article
Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy.
- Published in:
- Human Molecular Genetics, 1994, v. 3, n. 2, p. 285
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- Publication type:
- Article