Zatz M - Search Results

1

Analysis of the disease risk locus DXS1047 polymorphism in Brazilian Alzheimer patients.

Nishimura AL, Oliveira JR, Matioli SR, Brito-Marques PR, Bahia VS, Nitrini R, Zatz M. Nishimura AL, et al. Among authors: zatz m. Mol Psychiatry. 2000 Sep;5(5):563-6. doi: 10.1038/sj.mp.4000767. Mol Psychiatry. 2000. PMID: 11032393

2

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

3

Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive Duchenne-like muscular dystrophy in Brazilian families.

Passos-Bueno MR, Bakker E, Marie SK, Pavanello RC, Vainzof M, Carvalho AA, Cohen D, Beckmann J, Zatz M. Passos-Bueno MR, et al. Among authors: zatz m. Hum Mol Genet. 1993 Feb;2(2):201-2. doi: 10.1093/hmg/2.2.201. Hum Mol Genet. 1993. PMID: 8499908 No abstract available.

4

A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy.

Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SK, Pereira L, Akiyama J, Roberds SL, Campbell KP, Zatz M. Bueno MR, et al. Among authors: zatz m. Hum Mol Genet. 1995 Jul;4(7):1163-7. doi: 10.1093/hmg/4.7.1163. Hum Mol Genet. 1995. PMID: 8528203

5

Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD.

Passos-Bueno MR, Moreira ES, Vainzof M, Marie SK, Zatz M. Passos-Bueno MR, et al. Among authors: zatz m. Hum Mol Genet. 1996 Jun;5(6):815-20. doi: 10.1093/hmg/5.6.815. Hum Mol Genet. 1996. PMID: 8776597

6

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.

7

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.

8

Familial spongiform encephalopathy associated with a novel prion protein gene mutation.

Nitrini R, Rosemberg S, Passos-Bueno MR, da Silva LS, Iughetti P, Papadopoulos M, Carrilho PM, Caramelli P, Albrecht S, Zatz M, LeBlanc A. Nitrini R, et al. Among authors: zatz m. Ann Neurol. 1997 Aug;42(2):138-46. doi: 10.1002/ana.410420203. Ann Neurol. 1997. PMID: 9266722

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: zatz m. 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

The short variant of the polymorphism within the promoter region of the serotonin transporter gene is a risk factor for late onset Alzheimer's disease.

Oliveira JR, Gallindo RM, Maia LG, Brito-Marques PR, Otto PA, Passos-Bueno MR, Morais MA Jr, Zatz M. Oliveira JR, et al. Among authors: zatz m. Mol Psychiatry. 1998 Sep;3(5):438-41. doi: 10.1038/sj.mp.4000417. Mol Psychiatry. 1998. PMID: 9774779

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