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Year | Number of Results |
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2005 | 2 |
2023 | 1 |
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A case of mitochondrial DNA depletion syndrome type 11 - expanding the genotype and phenotype.
Neuromuscul Disord. 2023 Aug;33(8):692-696. doi: 10.1016/j.nmd.2023.06.004. Epub 2023 Jun 21.
Neuromuscul Disord. 2023.
PMID: 37429773
[Analysis of the expression of collagen VI in congenital muscular dystrophy].
Freitas RT, Zanoteli E, Morita Mda P, Oliveira AS.
Freitas RT, et al. Among authors: morita mda p.
Arq Neuropsiquiatr. 2005 Jun;63(2B):514-8. doi: 10.1590/s0004-282x2005000300027. Epub 2005 Jul 25.
Arq Neuropsiquiatr. 2005.
PMID: 16059608
Free article.
Portuguese.
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X-linked spinal and bulbar muscular atrophy (Kennedy's disease) with long-term electrophysiological evaluation: case report.
Kouyoumdjian JA, Morita Mda P, Araújo RG.
Kouyoumdjian JA, et al. Among authors: morita mda p.
Arq Neuropsiquiatr. 2005 Mar;63(1):154-9. doi: 10.1590/s0004-282x2005000100028. Epub 2005 Apr 13.
Arq Neuropsiquiatr. 2005.
PMID: 15830083
Free article.
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