Levy JA - Search Results

1

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: levy ja. Neuromuscul Disord. 1991;1(3):177-83. doi: 10.1016/0960-8966(91)90022-k. Neuromuscul Disord. 1991. PMID: 1822792

2

[Congenital fiber disproportion: atrophy of type I fibers. Report of 11 cases].

Levy JA, Alegro MS, Lusvarghi ES, Salum PN, Tsanaclis AM, Levy A. Levy JA, et al. Among authors: levy a. Arq Neuropsiquiatr. 1987 Jun;45(2):153-8. doi: 10.1590/s0004-282x1987000200008. Arq Neuropsiquiatr. 1987. PMID: 3426422 Portuguese.

3

Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiency.

Reed UC, Marie SK, Vainzof M, Salum PB, Levy JA, Zatz M, Diament A. Reed UC, et al. Among authors: levy ja. Brain Dev. 1996 Jan-Feb;18(1):53-8. doi: 10.1016/0387-7604(95)00095-x. Brain Dev. 1996. PMID: 8907344

4

Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardation.

Reed UC, Tsanaclis AM, Vainzof M, Marie SK, Carvalho MS, Roizenblatt J, Pedreira CC, Diament A, Levy JA. Reed UC, et al. Among authors: levy ja. Brain Dev. 1999 Jun;21(4):274-8. doi: 10.1016/s0387-7604(98)00100-4. Brain Dev. 1999. PMID: 10392752

5

[Centronuclear (myotubular) myopathy: a case report].

Reed UC, Tsanaclis AM, Ferreira LM, Carvalho MS, Diament A, Levy JA. Reed UC, et al. Among authors: levy ja. Rev Hosp Clin Fac Med Sao Paulo. 1992 Sep-Oct;47(5):237-9. Rev Hosp Clin Fac Med Sao Paulo. 1992. PMID: 1340609 Review. Portuguese.

6

Creatine-phosphokinase (CPK) activity in relatives of patients with X-linked muscular dystrophies: a Brazilian study.

Zatz M, Frota-Pessoa O, Levy JA, Peres CA. Zatz M, et al. Among authors: levy ja. J Genet Hum. 1976 Jun;24(2):153-68. J Genet Hum. 1976. PMID: 965952

7

[Minicore disease: report of a case].

Tsanaclis AM, Levy JA. Tsanaclis AM, et al. Among authors: levy ja. Rev Hosp Clin Fac Med Sao Paulo. 1982 Oct;37(5):241-3. Rev Hosp Clin Fac Med Sao Paulo. 1982. PMID: 7170579 Portuguese. No abstract available.

8

[Myotonic dystrophy: study of clinico-genetic correlation in a pair of relatives (father-son)].

Reed UC, Passos-Bueno MR, Nagahashi-Marie SK, Cerqueira A, Mendonça LI, Levy JA, Diament A, Zatz M. Reed UC, et al. Among authors: levy ja. Arq Neuropsiquiatr. 1994 Dec;52(4):545-8. doi: 10.1590/s0004-282x1994000400015. Arq Neuropsiquiatr. 1994. PMID: 7611950 Portuguese.

9

Benign Duchenne muscular dystrophy in a patient with growth hormone deficiency.

Zatz M, Betti RT, Levy JA. Zatz M, et al. Among authors: levy ja. Am J Med Genet. 1981;10(3):301-4. doi: 10.1002/ajmg.1320100313. Am J Med Genet. 1981. PMID: 7304674 No abstract available.

10

A Caucasian family with the 3271 mutation in mitochondrial DNA.

Marie SK, Goto Y, Passos-Bueno MR, Zatz M, Carvalho AA, Carvalho M, Levy JA, Palou VB, Campiotto S, Horai S, et al. Marie SK, et al. Among authors: levy ja. Biochem Med Metab Biol. 1994 Aug;52(2):136-9. doi: 10.1006/bmmb.1994.1045. Biochem Med Metab Biol. 1994. PMID: 7993661

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