Rapaport D - Search Results

1

Relation between height and clinical course in Duchenne muscular dystrophy.

Zatz M, Rapaport D, Vainzof M, Rocha JM, Pavanello Rde C, Colletto GM, Peres CA. Zatz M, et al. Among authors: rapaport d. Am J Med Genet. 1988 Feb;29(2):405-10. doi: 10.1002/ajmg.1320290223. Am J Med Genet. 1988. PMID: 3354613

2

Different mosaicism frequencies for proximal and distal Duchenne muscular dystrophy (DMD) mutations indicate difference in etiology and recurrence risk.

Passos-Bueno MR, Bakker E, Kneppers AL, Takata RI, Rapaport D, den Dunnen JT, Zatz M, van Ommen GJ. Passos-Bueno MR, et al. Among authors: rapaport d. Am J Hum Genet. 1992 Nov;51(5):1150-5. Am J Hum Genet. 1992. PMID: 1415256 Free PMC article.

3

A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardation.

Rapaport D, Passos-Bueno MR, Takata RI, Campiotto S, Eggers S, Vainzof M, Makover A, Nudel U, Yaffe D, Zatz M. Rapaport D, et al. Neuromuscul Disord. 1992;2(2):117-20. doi: 10.1016/0960-8966(92)90043-6. Neuromuscul Disord. 1992. PMID: 1422198

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: rapaport d. 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

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: rapaport d. J Neurol Sci. 1991 Feb;101(2):141-7. doi: 10.1016/0022-510x(91)90038-9. J Neurol Sci. 1991. PMID: 1709683

6

Estimate of the intrafamilial correlation for serum creatine kinase and pyruvate kinase in females at risk for Duchenne and Becker muscular dystrophies.

Rabbi-Bortolini E, Dal Colletto GM, Passos-Bueno MR, Vainzof M, Rapaport D, Zatz M. Rabbi-Bortolini E, et al. Among authors: rapaport d. Hum Hered. 1991;41(6):370-8. doi: 10.1159/000154029. Hum Hered. 1991. PMID: 1797630

7

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

8

Short stature in Duchenne muscular dystrophy.

Rapaport D, Colletto GM, Vainzof M, Duaik MC, Zatz M. Rapaport D, et al. Growth Regul. 1991 Mar;1(1):11-5. Growth Regul. 1991. PMID: 1842555

9

Familial occurrence of Duchenne dystrophy through paternal lines in four families.

Zatz M, Passos-Bueno MR, Rapaport D, Vainzof M. Zatz M, et al. Among authors: rapaport d. Am J Med Genet. 1991 Jan;38(1):80-4. doi: 10.1002/ajmg.1320380118. Am J Med Genet. 1991. PMID: 1849353

10

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: rapaport d. Am J Med Genet. 1991 Apr 1;39(1):38-41. doi: 10.1002/ajmg.1320390110. Am J Med Genet. 1991. PMID: 1867262

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