Tsanaclis AM - 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: tsanaclis am. Neuromuscul Disord. 1991;1(3):177-83. doi: 10.1016/0960-8966(91)90022-k. Neuromuscul Disord. 1991. PMID: 1822792

2

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: tsanaclis am. Neuromuscul Disord. 1993 Mar;3(2):135-40. doi: 10.1016/0960-8966(93)90005-5. Neuromuscul Disord. 1993. PMID: 7689380

3

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: tsanaclis am. Brain Dev. 1999 Jun;21(4):274-8. doi: 10.1016/s0387-7604(98)00100-4. Brain Dev. 1999. PMID: 10392752

4

The effect of calpain 3 deficiency on the pattern of muscle degeneration in the earliest stages of LGMD2A.

Vainzof M, de Paula F, Tsanaclis AM, Zatz M. Vainzof M, et al. Among authors: tsanaclis am. J Clin Pathol. 2003 Aug;56(8):624-6. doi: 10.1136/jcp.56.8.624. J Clin Pathol. 2003. PMID: 12890817 Free PMC article.

5

[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: tsanaclis am. Arq Neuropsiquiatr. 1987 Jun;45(2):153-8. doi: 10.1590/s0004-282x1987000200008. Arq Neuropsiquiatr. 1987. PMID: 3426422 Portuguese.

6

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

Reed UC, Tsanaclis AM, Ferreira LM, Carvalho MS, Diament A, Levy JA. Reed UC, et al. Among authors: tsanaclis am. 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.

7

[Minicore disease: report of a case].

Tsanaclis AM, Levy JA. Tsanaclis AM, et al. 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

Does the A3333G mutation in the CACNL1A3 gene, detected in malignant hyperthermia, also occur in central core disease?

Vainzof M, Muniz VP, Tsanaclis AM, Silva HC, Rusticci MS. Vainzof M, et al. Among authors: tsanaclis am. Genet Test. 2000;4(4):383-6. doi: 10.1089/109065700750065135. Genet Test. 2000. PMID: 11216663

9

Screening for mutations in the RYR1 gene in families with malignant hyperthermia.

Muniz VP, Silva HC, Tsanaclis AM, Vainzof M. Muniz VP, et al. Among authors: tsanaclis am. J Mol Neurosci. 2003;21(1):35-42. doi: 10.1385/JMN:21:1:35. J Mol Neurosci. 2003. PMID: 14500992

10

Mitochondrial dysfunction in myasthenia gravis. Report of a case.

Marchiori PE, Levy JA, Carvalho-Alegro MS, Lusvarghi ES, Tsanaclis AM, De Assis JL, Scaff M. Marchiori PE, et al. Among authors: tsanaclis am. Arq Neuropsiquiatr. 1989 Sep;47(3):355-8. doi: 10.1590/s0004-282x1989000300018. Arq Neuropsiquiatr. 1989. PMID: 2619615

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