Pavanello RC - Search Results

1

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.

2

Additional dystrophin fragment in Becker muscular dystrophy patients: correlation with the pattern of DNA deletion.

Vainzof M, Passos-Bueno MR, Rapaport D, Pavanello RC, Zatz M, Bulman DE. Vainzof M, et al. Among authors: pavanello rc. Am J Med Genet. 1992 Oct 1;44(3):382-4. doi: 10.1002/ajmg.1320440323. Am J Med Genet. 1992. PMID: 1488991 No abstract available.

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

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

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

Nocturnal rhythm of growth hormone in Duchenne patients: effect of different doses of mazindol and/or cyproheptadine.

Zatz M, Rapaport D, Pavanello RC, Rocha JM, Vainzof M, Nicolau W. Zatz M, et al. Among authors: pavanello rc. Am J Med Genet. 1989 Aug;33(4):457-67. doi: 10.1002/ajmg.1320330408. Am J Med Genet. 1989. PMID: 2596504

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

Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?

Passos-Bueno MR, Byth BC, Rosenberg S, Takata RI, Bakker E, Beggs AH, Pavanello RC, Vainzof M, Davies KE, Zatz M. Passos-Bueno MR, et al. Among authors: pavanello rc. Am J Med Genet. 1993 Apr 15;46(2):172-5. doi: 10.1002/ajmg.1320460214. Am J Med Genet. 1993. PMID: 8484404

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