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Year | Number of Results |
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2002 | 1 |
2004 | 2 |
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Page 1
Increased serum miR-193a-5p during non-alcoholic fatty liver disease progression: Diagnostic and mechanistic relevance.
JHEP Rep. 2021 Nov 25;4(2):100409. doi: 10.1016/j.jhepr.2021.100409. eCollection 2022 Feb.
JHEP Rep. 2021.
PMID: 35072021
Free PMC article.
Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD).
Tonini MM, Passos-Bueno MR, Cerqueira A, Matioli SR, Pavanello R, Zatz M.
Tonini MM, et al.
Neuromuscul Disord. 2004 Jan;14(1):33-8. doi: 10.1016/j.nmd.2003.07.001.
Neuromuscul Disord. 2004.
PMID: 14659410
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New mutations, hotspots, and founder effects in Brazilian patients with steroid 5alpha-reductase deficiency type 2.
Hackel C, Oliveira LE, Ferraz LF, Tonini MM, Silva DN, Toralles MB, Stuchi-Perez EG, Guerra-Junior G.
Hackel C, et al. Among authors: tonini mm.
J Mol Med (Berl). 2005 Jul;83(7):569-76. doi: 10.1007/s00109-005-0651-7. Epub 2005 Mar 16.
J Mol Med (Berl). 2005.
PMID: 15770495
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Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye?
Tonini MM, Passos-Bueno MR, Cerqueira A, Pavanello R, Vainzof M, Dubowitz V, Zatz M.
Tonini MM, et al.
Neuromuscul Disord. 2002 Aug;12(6):554-7. doi: 10.1016/s0960-8966(02)00014-7.
Neuromuscul Disord. 2002.
PMID: 12117479
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Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype.
Tonini MM, Pavanello RC, Gurgel-Giannetti J, Lemmers RJ, van der Maarel SM, Frants RR, Zatz M.
Tonini MM, et al.
J Med Genet. 2004 Feb;41(2):e17. doi: 10.1136/jmg.2003.010637.
J Med Genet. 2004.
PMID: 14757867
Free PMC article.
No abstract available.
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Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy.
Tonini MM, Lemmers RJ, Pavanello RC, Cerqueira AM, Frants RR, van der Maarel SM, Zatz M.
Tonini MM, et al.
Hum Genet. 2006 Mar;119(1-2):23-8. doi: 10.1007/s00439-005-0100-2. Epub 2005 Dec 8.
Hum Genet. 2006.
PMID: 16341710
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[5alpha-reductase type 2 deficiency: experiences from Campinas (SP) and Salvador (BA)].
Hackel C, Oliveira LE, Toralles MB, Nunes-Silva D, Tonini MM, Ferraz LF, Steinmetz L, Damiani D, Oliveira LC, Maciel-Guerra AT, Stuchi-Perez EG, Guerra-Júnior G.
Hackel C, et al. Among authors: tonini mm.
Arq Bras Endocrinol Metabol. 2005 Feb;49(1):103-11. doi: 10.1590/s0004-27302005000100014. Epub 2006 Mar 16.
Arq Bras Endocrinol Metabol. 2005.
PMID: 16544041
Portuguese.
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