Moreira ES - Search Results

1

Telethonin protein expression in neuromuscular disorders.

Vainzof M, Moreira ES, Suzuki OT, Faulkner G, Valle G, Beggs AH, Carpen O, Ribeiro AF, Zanoteli E, Gurgel-Gianneti J, Tsanaclis AM, Silva HC, Passos-Bueno MR, Zatz M. Vainzof M, et al. Among authors: moreira es. Biochim Biophys Acta. 2002 Oct 9;1588(1):33-40. doi: 10.1016/s0925-4439(02)00113-8. Biochim Biophys Acta. 2002. PMID: 12379311 Free article.

2

Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin.

Moreira ES, Wiltshire TJ, Faulkner G, Nilforoushan A, Vainzof M, Suzuki OT, Valle G, Reeves R, Zatz M, Passos-Bueno MR, Jenne DE. Moreira ES, et al. Nat Genet. 2000 Feb;24(2):163-6. doi: 10.1038/72822. Nat Genet. 2000. PMID: 10655062

3

The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies.

Vainzof M, Passos-Bueno MR, Canovas M, Moreira ES, Pavanello RC, Marie SK, Anderson LV, Bonnemann CG, McNally EM, Nigro V, Kunkel LM, Zatz M. Vainzof M, et al. Among authors: moreira es. Hum Mol Genet. 1996 Dec;5(12):1963-9. doi: 10.1093/hmg/5.12.1963. Hum Mol Genet. 1996. PMID: 8968750

4

Deficiency of alpha-actinin-3 (ACTN3) occurs in different forms of muscular dystrophy.

Vainzof M, Costa CS, Marie SK, Moreira ES, Reed U, Passos-Bueno MR, Beggs AH, Zatz M. Vainzof M, et al. Among authors: moreira es. Neuropediatrics. 1997 Aug;28(4):223-8. doi: 10.1055/s-2007-973704. Neuropediatrics. 1997. PMID: 9309713

5

A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies.

Moreira ES, Vainzof M, Marie SK, Nigro V, Zatz M, Passos-Bueno MR. Moreira ES, et al. J Med Genet. 1998 Nov;35(11):951-3. doi: 10.1136/jmg.35.11.951. J Med Genet. 1998. PMID: 9832045 Free PMC article.

6

Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G.

Passos-Bueno MR, Vainzof M, Moreira ES, Zatz M. Passos-Bueno MR, et al. Among authors: moreira es. Am J Med Genet. 1999 Feb 19;82(5):392-8. doi: 10.1002/(sici)1096-8628(19990219)82:5<392::aid-ajmg7>3.0.co;2-0. Am J Med Genet. 1999. PMID: 10069710

7

Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complex.

Vainzof M, Moreira ES, Ferraz G, Passos-Bueno MR, Marie SK, Zatz M. Vainzof M, et al. Among authors: moreira es. Eur J Hum Genet. 1999 Feb-Mar;7(2):251-4. doi: 10.1038/sj.ejhg.5200263. Eur J Hum Genet. 1999. PMID: 10196712

8

Partial alpha-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family.

Vainzof M, Moreira ES, Canovas M, Anderson LV, Pavanello RC, Passos-Bueno MR, Zatz M. Vainzof M, et al. Among authors: moreira es. Muscle Nerve. 2000 Jun;23(6):984-8. doi: 10.1002/(sici)1097-4598(200006)23:6<984::aid-mus24>3.0.co;2-#. Muscle Nerve. 2000. PMID: 10842281

9

Dysferlin protein analysis in limb-girdle muscular dystrophies.

Vainzof M, Anderson LV, McNally EM, Davis DB, Faulkner G, Valle G, Moreira ES, Pavanello RC, Passos-Bueno MR, Zatz M. Vainzof M, et al. Among authors: moreira es. J Mol Neurosci. 2001 Aug;17(1):71-80. doi: 10.1385/JMN:17:1:71. J Mol Neurosci. 2001. PMID: 11665864

10

A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy.

Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SK, Pereira L, Akiyama J, Roberds SL, Campbell KP, Zatz M. Bueno MR, et al. Among authors: moreira es. Hum Mol Genet. 1995 Jul;4(7):1163-7. doi: 10.1093/hmg/4.7.1163. Hum Mol Genet. 1995. PMID: 8528203

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