Pavanello RC - Search Results

1

Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a Brazilian study.

Vainzof M, Pavanello RC, Pavanello Filho I, Passos-Bueno MR, Rapaport D, Hsi CT, Zatz M. Vainzof M, et al. Among authors: pavanello rc, pavanello filho i. J Neurol Sci. 1990 Sep;98(2-3):221-33. doi: 10.1016/0022-510x(90)90263-m. J Neurol Sci. 1990. PMID: 1700808

2

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

3

A model to estimate the expression of the dystrophin gene in muscle from female Becker muscular dystrophy carriers.

Vainzof M, Passos-Bueno MR, Pavanello RC, Schreiber R, Zatz M. Vainzof M, et al. Among authors: pavanello rc. J Med Genet. 1992 Jul;29(7):476-9. J Med Genet. 1992. PMID: 1640426 Free PMC article.

4

Immunofluorescence dystrophin study in Duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and the amino-terminal region of the protein.

Vainzof M, Zubrzycka-Gaarn EE, Rapaport D, Passos-Bueno MR, Pavanello RC, Pavanello-Filho I, Zatz M. Vainzof M, et al. Among authors: pavanello rc, pavanello filho i. J Neurol Sci. 1991 Feb;101(2):141-7. doi: 10.1016/0022-510x(91)90038-9. J Neurol Sci. 1991. PMID: 1709683

5

Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of Duchenne's and Becker muscular dystrophies of different ages.

Vainzof M, Pavanello RC, Pavanello I, Tsanaclis AM, Levy JA, Passos-Bueno MR, Rapaport D, Zatz M. Vainzof M, et al. Among authors: pavanello rc, pavanello i. Neuromuscul Disord. 1991;1(3):177-83. doi: 10.1016/0960-8966(91)90022-k. Neuromuscul Disord. 1991. PMID: 1822792

6

Screening of male patients with autosomal recessive Duchenne dystrophy through dystrophin and DNA studies.

Vainzof M, Pavanello RC, Pavanello-Filho I, Rapaport D, Passos-Bueno MR, Zubrzycka-Gaarn EE, Bulman DE, Zatz M. Vainzof M, et al. Among authors: pavanello rc, pavanello filho i. Am J Med Genet. 1991 Apr 1;39(1):38-41. doi: 10.1002/ajmg.1320390110. Am J Med Genet. 1991. PMID: 1867262

7

Hypothesis: the existence of embryonic and adult isoforms of mRNA dystrophin provides an explanation for unusual clinical findings.

Zatz M, Passos-Bueno MR, Vainzof M, Pavanello RC. Zatz M, et al. Among authors: pavanello rc. Am J Med Genet. 1989 Mar;32(3):438-41. doi: 10.1002/ajmg.1320320336. Am J Med Genet. 1989. PMID: 2658593 No abstract available.

8

Is dystrophin always altered in Becker muscular dystrophy patients?

Vainzof M, Passos-Bueno MR, Pavanello RC, Zatz M. Vainzof M, et al. Among authors: pavanello rc. J Neurol Sci. 1995 Jul;131(1):99-104. doi: 10.1016/0022-510x(95)00104-a. J Neurol Sci. 1995. PMID: 7561956

9

Sarcolemmal distribution of abnormal dystrophin in Xp21 carriers.

Vainzof M, Nicholson LV, Bulman DE, Tsanaclis AM, Passos-Bueno MR, Pavanello RC, Zatz M. Vainzof M, et al. Among authors: pavanello rc. Neuromuscul Disord. 1993 Mar;3(2):135-40. doi: 10.1016/0960-8966(93)90005-5. Neuromuscul Disord. 1993. PMID: 7689380

10

Assessment of the 50-kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophy.

Zatz M, Matsumura K, Vainzof M, Passos-Bueno MR, Pavanello RC, Marie SK, Campbell KP. Zatz M, et al. Among authors: pavanello rc. J Neurol Sci. 1994 May;123(1-2):122-8. doi: 10.1016/0022-510x(94)90213-5. J Neurol Sci. 1994. PMID: 8064304

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