Zatz M - Search Results

1

African ancestry protects against Alzheimer's disease-related neuropathology.

Schlesinger D, Grinberg LT, Alba JG, Naslavsky MS, Licinio L, Farfel JM, Suemoto CK, de Lucena Ferretti RE, Leite RE, de Andrade MP, dos Santos AC, Brentani H, Pasqualucci CA, Nitrini R, Jacob-Filho W, Zatz M; Brazilian Aging Brain Study Group. Schlesinger D, et al. Among authors: zatz m. Mol Psychiatry. 2013 Jan;18(1):79-85. doi: 10.1038/mp.2011.136. Epub 2011 Nov 8. Mol Psychiatry. 2013. PMID: 22064377 Free PMC article.

2

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

3

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

4

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

5

No evidence of association between the D10S1423 locus and Alzheimer disease in Brazilian patients.

Nishimura AL, Oliveira JR, Otto PA, Matioli SR, Brito-Marques PR, Bahia VS, Nitrini R, Zatz M. Nishimura AL, et al. Among authors: zatz m. J Neural Transm (Vienna). 2001;108(3):305-10. doi: 10.1007/s007020170076. J Neural Transm (Vienna). 2001. PMID: 11341482

6

Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17.

Nitrini R, Teixeira da Silva LS, Rosemberg S, Caramelli P, Carrilho PE, Iughetti P, Passos-Bueno MR, Zatz M, Albrecht S, LeBlanc A. Nitrini R, et al. Among authors: zatz m. Arq Neuropsiquiatr. 2001 Jun;59(2-A):161-4. doi: 10.1590/s0004-282x2001000200001. Arq Neuropsiquiatr. 2001. PMID: 11400017 Free article.

7

Lack of association between the brain-derived neurotrophin factor (C-270T) polymorphism and late-onset Alzheimer's disease (LOAD) in Brazilian patients.

Nishimura AL, Oliveira JR, Mitne-Neto M, Guindalini C, Nitrini R, Bahia VS, de Brito-Marques PR, Otto PA, Zatz M. Nishimura AL, et al. Among authors: zatz m. J Mol Neurosci. 2004;22(3):257-60. doi: 10.1385/JMN:22:3:257. J Mol Neurosci. 2004. PMID: 14997020

8

Association of genetic variants in alcohol dehydrogenase 4 with alcohol dependence in Brazilian patients.

Guindalini C, Scivoletto S, Ferreira RG, Breen G, Zilberman M, Peluso MA, Zatz M. Guindalini C, et al. Among authors: zatz m. Am J Psychiatry. 2005 May;162(5):1005-7. doi: 10.1176/appi.ajp.162.5.1005. Am J Psychiatry. 2005. PMID: 15863808

9

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

10

A family with McLeod syndrome and calpainopathy with clinically overlapping diseases.

Starling A, Schlesinger D, Kok F, Passos-Bueno MR, Vainzof M, Zatz M. Starling A, et al. Among authors: zatz m. Neurology. 2005 Dec 13;65(11):1832-3. doi: 10.1212/01.wnl.0000187073.58307.41. Neurology. 2005. PMID: 16344536

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