Zatz M - Search Results

1

Monoamine oxidase a polymorphism in Brazilian patients: risk factor for late-onset Alzheimer's disease?

Nishimura AL, Guindalini C, Oliveira JR, Nitrini R, Bahia VS, de Brito-Marques PR, Otto PA, Zatz M. Nishimura AL, et al. Among authors: zatz m. J Mol Neurosci. 2005;27(2):213-7. doi: 10.1385/JMN:27:2:213. J Mol Neurosci. 2005. PMID: 16186632

2

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. 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.

3

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. Am J Med Genet. 1988 Dec;31(4):821-33. doi: 10.1002/ajmg.1320310415. Am J Med Genet. 1988. PMID: 3239574

4

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. Am J Med Genet. 1986 Oct;25(2):219-30. doi: 10.1002/ajmg.1320250204. Am J Med Genet. 1986. PMID: 3777019

5

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: zatz m. Am J Med Genet. 1985 Sep;22(1):81-7. doi: 10.1002/ajmg.1320220109. Am J Med Genet. 1985. PMID: 4050853

6

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

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

7

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. J Neurol Sci. 1980 Sep;47(3):411-7. doi: 10.1016/0022-510x(80)90094-5. J Neurol Sci. 1980. PMID: 7420115

8

Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysis.

Passos-Bueno MR, Oliveira JR, Bakker E, Anderson RD, Marie SK, Vainzof M, Roberds S, Campbell KP, Zatz M. Passos-Bueno MR, et al. Among authors: zatz m. Hum Mol Genet. 1993 Nov;2(11):1945-7. doi: 10.1093/hmg/2.11.1945. Hum Mol Genet. 1993. PMID: 8281158

9

Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families.

Passos-Bueno MR, Moreira ES, Marie SK, Bashir R, Vasquez L, Love DR, Vainzof M, Iughetti P, Oliveira JR, Bakker E, Strachan T, Bushby K, Zatz M. Passos-Bueno MR, et al. Among authors: zatz m. J Med Genet. 1996 Feb;33(2):97-102. doi: 10.1136/jmg.33.2.97. J Med Genet. 1996. PMID: 8929943 Free PMC article.

10

The use of apolipoprotein E genotype for preclinical detection of risk's group for Alzheimer's disease.

Oliveira JR, Lima Filho JL, Shimokomaki CM, Okuma M, Passos-Bueno MR, Zatz M, Brito-Marques PR. Oliveira JR, et al. Among authors: zatz m. Am J Med Genet. 1997 Apr 18;74(2):216-7. doi: 10.1002/(sici)1096-8628(19970418)74:2<216::aid-ajmg22>3.0.co;2-k. Am J Med Genet. 1997. PMID: 9129729 No abstract available.

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