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Protein Expression and Purification|June 2, 2007
A mutation in human VAP-B--MSP domain, present in ALS patients, affects the interaction with other cellular proteinsM Mitne-Neto, C R R Ramos, D C Pimenta, et al.
Molecular Psychiatry|October 17, 1998
The short variant of the polymorphism within the promoter region of the serotonin transporter gene is a risk factor for late onset Alzheimer's diseaseJ R Oliveira, R M Gallindo, L G Maia, et al.
Molecular and Cellular Probes|October 1, 1995
Molecular characterization of further dystrophin gene microsatellitesS C King, A L Roche, M R Passos-Bueno, et al.
American Journal of Medical Genetics|May 29, 1998
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 schizophreniaJ R Mendes de Oliveira, P A Otto, H Vallada, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1994
A Caucasian family with the 3271 mutation in mitochondrial DNAS K Marie, Y Goto, M R Passos-Bueno, et al.
Arquivos De Neuro-Psiquiatria|June 16, 2001
Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17R Nitrini, L S Teixeira da Silva, S Rosemberg, et al.
Annals of Neurology|August 1, 1997
Familial spongiform encephalopathy associated with a novel prion protein gene mutationR Nitrini, S Rosemberg, M R Passos-Bueno, et al.
Revista Do Hospital Das Clinicas|January 10, 2002
Friedreich's ataxia: clinical and molecular study of 25 Brazilian casesL M Albano, M Zatz, C A Kim, et al.
Molecular Psychiatry|September 30, 2015
A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disabilityT Figueiredo, U S Melo, A L S Pessoa, et al.
Psychiatric Genetics|November 4, 1998
Linkage analysis between bipolar affective disorder and markers on chromosome XH P Vallada, L Vasques, D Curtis, et al.
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