Otto PA - Search Results

1

Serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) in female relatives and patients with X-linked muscular dystrophies (Duchenne and Becker).

Zatz M, Shapiro LJ, Campion DS, Kaback MM, Otto PA. Zatz M, et al. Among authors: otto pa. J Neurol Sci. 1980 Jun;46(3):267-79. doi: 10.1016/0022-510x(80)90051-9. J Neurol Sci. 1980. PMID: 7381516

2

Evaluation of carrier detection rates for Duchenne and Becker muscular dystrophies using serum creatine-kinase (CK) and pyruvate-kinase (PK) through discriminant analysis.

Zatz M, Otto PA. Zatz M, et al. Among authors: otto pa. Am J Med Genet. 1986 Oct;25(2):219-30. doi: 10.1002/ajmg.1320250204. Am J Med Genet. 1986. PMID: 3777019

3

Effect of age on the detection rate in Duchenne muscular dystrophy.

Zatz M, Otto PA. Zatz M, et al. Among authors: otto pa. J Neurol Sci. 1980 Sep;47(3):407-10. doi: 10.1016/0022-510x(80)90093-3. J Neurol Sci. 1980. PMID: 7420114

4

The use of concomitant serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) for carrier detection in Duchenne's muscular dystrophy through discriminant analysis.

Zatz M, Otto PA. Zatz M, et al. Among authors: otto pa. J Neurol Sci. 1980 Sep;47(3):411-7. doi: 10.1016/0022-510x(80)90094-5. J Neurol Sci. 1980. PMID: 7420115

5

Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers.

Sumita DR, Vainzof M, Campiotto S, Cerqueira AM, Cánovas M, Otto PA, Passos-Bueno MR, Zatz M. Sumita DR, et al. Among authors: otto pa. Am J Med Genet. 1998 Dec 4;80(4):356-61. Am J Med Genet. 1998. PMID: 9856563

6

Serum CK-MB activity in progressive muscular dystrophy: is it of nosologic value?

Vainzof M, Zatz M, Otto PA. Vainzof M, et al. Among authors: otto pa. Am J Med Genet. 1985 Sep;22(1):81-7. doi: 10.1002/ajmg.1320220109. Am J Med Genet. 1985. PMID: 4050853

7

Effect of mazindol on growth hormone levels in patients with Duchenne muscular dystrophy.

Zatz M, Rapaport D, Vainzof M, Pavanello Rde C, Rocha JM, Betti RT, Otto PA. Zatz M, et al. Among authors: otto pa. Am J Med Genet. 1988 Dec;31(4):821-33. doi: 10.1002/ajmg.1320310415. Am J Med Genet. 1988. PMID: 3239574

8

X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg.

Zatz M, Penha-Serrano C, Otto PA. Zatz M, et al. Among authors: otto pa. J Med Genet. 1976 Jun;13(3):217-22. doi: 10.1136/jmg.13.3.217. J Med Genet. 1976. PMID: 1084423 Free PMC article.

9

Analysis of a novel functional polymorphism within the promoter region of the serotonin transporter gene (5-HTT) in Brazilian patients affected by bipolar disorder and schizophrenia.

Mendes de Oliveira JR, Otto PA, Vallada H, Lauriano V, Elkis H, Lafer B, Vasquez L, Gentil V, Passos-Bueno MR, Zatz M. Mendes de Oliveira JR, et al. Among authors: otto pa. Am J Med Genet. 1998 May 8;81(3):225-7. doi: 10.1002/(sici)1096-8628(19980508)81:3<225::aid-ajmg4>3.0.co;2-v. Am J Med Genet. 1998. PMID: 9603609

10

Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) families.

Iughetti P, Otto PA, Zatz M, Passos Bueno MR, Marie SK. Iughetti P, et al. Among authors: otto pa. Am J Med Genet. 1998 May 18;77(3):246-8. Am J Med Genet. 1998. PMID: 9605593 No abstract available.

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