Maria Paula Mourao do Amaral Coutinho
AuthID: R-000-CFK
31
TITLE: Mitochondrial DNA Analysis in Ocular Myopathy
AUTHORS: Laura Vilarinho; Filippo M Santorelli; Maria Luís Cardoso; Teresa Coelho; António Guimarães; Paula Coutinho;
PUBLISHED: 1998, SOURCE: European Neurology - Eur Neurol, VOLUME: 39, ISSUE: 3
AUTHORS: Laura Vilarinho; Filippo M Santorelli; Maria Luís Cardoso; Teresa Coelho; António Guimarães; Paula Coutinho;
PUBLISHED: 1998, SOURCE: European Neurology - Eur Neurol, VOLUME: 39, ISSUE: 3
32
TITLE: Frequency of the CAG repeat mutations causing spinocerebellar ataxia in a large group of Portuguese ataxia families.
AUTHORS: Silveira, I; Coutinho, P; Maciel, P; Gaspar, C; Hayes, S; Dias, A; Guimaraes, J; Loureiro, L; Sequeiros, J ; Rouleau, GA;
PUBLISHED: 1997, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 61, ISSUE: 4
AUTHORS: Silveira, I; Coutinho, P; Maciel, P; Gaspar, C; Hayes, S; Dias, A; Guimaraes, J; Loureiro, L; Sequeiros, J ; Rouleau, GA;
PUBLISHED: 1997, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 61, ISSUE: 4
INDEXED IN: 
WOS
WOS33
TITLE: Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2 Full Text
AUTHORS: Dürr, A; C.-S Davoine; Paternotte, C; von Fellenberg, J; Cogilnicean, S; Coutinho, P; Lamy, C; Bourgeois, S; J.-F Prud'homme; Penet, C; J.-L Mas; J.-M Burgunder; Hazan, J; Weissenbach, J; Brice, A; Fontaine, B;
PUBLISHED: 1996, SOURCE: Brain, VOLUME: 119, ISSUE: 5
AUTHORS: Dürr, A; C.-S Davoine; Paternotte, C; von Fellenberg, J; Cogilnicean, S; Coutinho, P; Lamy, C; Bourgeois, S; J.-F Prud'homme; Penet, C; J.-L Mas; J.-M Burgunder; Hazan, J; Weissenbach, J; Brice, A; Fontaine, B;
PUBLISHED: 1996, SOURCE: Brain, VOLUME: 119, ISSUE: 5
34
TITLE: Genetic Linkage Studies of Machado-Joseph Disease with Chromosome 14q STRPs in 16 Portuguese-Azorean Kindreds Full Text
AUTHORS: Jorge Sequeiros; Isabel Silveira; Patrı́cia Maciel; Paula Coutinho; Alexandra Manaia; Claudia Gaspar; Philippe Burlet; Leal Loureiro; João Guimarães; Hajime Tanaka; Yoshihisa Takiyama; Hirosuke Sakamoto; Masatoyo Nishizawa; Yoshiko Nomura; Masaya Segawa; Shoji Tsuji; Judith Melki; Arnold Munnich;
PUBLISHED: 1994, SOURCE: Genomics, VOLUME: 21, ISSUE: 3
AUTHORS: Jorge Sequeiros; Isabel Silveira; Patrı́cia Maciel; Paula Coutinho; Alexandra Manaia; Claudia Gaspar; Philippe Burlet; Leal Loureiro; João Guimarães; Hajime Tanaka; Yoshihisa Takiyama; Hirosuke Sakamoto; Masatoyo Nishizawa; Yoshiko Nomura; Masaya Segawa; Shoji Tsuji; Judith Melki; Arnold Munnich;
PUBLISHED: 1994, SOURCE: Genomics, VOLUME: 21, ISSUE: 3
35
TITLE: Machado-Joseph Disease Is Genetically Different from Holguin Dominant Ataxia (SCA2) Full Text
AUTHORS: Isabel Silveira; Alexandra Manaia; Judith Melki; Carlos Magariño; Astrid Lunkes; Ana Hernandez; Suzana Gispert; Philippe Burlet; Jean-Michel Rozet; Paula Coutinho; J.E.Leal Loureiro; João Guimarães; Georg Auburger; Arnold Munnich; Jorge Sequeiros;
PUBLISHED: 1993, SOURCE: Genomics, VOLUME: 17, ISSUE: 3
AUTHORS: Isabel Silveira; Alexandra Manaia; Judith Melki; Carlos Magariño; Astrid Lunkes; Ana Hernandez; Suzana Gispert; Philippe Burlet; Jean-Michel Rozet; Paula Coutinho; J.E.Leal Loureiro; João Guimarães; Georg Auburger; Arnold Munnich; Jorge Sequeiros;
PUBLISHED: 1993, SOURCE: Genomics, VOLUME: 17, ISSUE: 3
36
TITLE: LINKAGE STUDIES IN MACHADO-JOSEPH DISEASE
AUTHORS: CARSON, WJ; MACLEOD, PL; VINCENT, D; NEXARATI, M; RADVANY, J; SEQUEIROS, J ; COUTINHO, P; WHITE, B; FORSE, RA; ROSENBERG, RN; ROULEAU, GA;
PUBLISHED: 1991, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 49, ISSUE: 4
AUTHORS: CARSON, WJ; MACLEOD, PL; VINCENT, D; NEXARATI, M; RADVANY, J; SEQUEIROS, J ; COUTINHO, P; WHITE, B; FORSE, RA; ROSENBERG, RN; ROULEAU, GA;
PUBLISHED: 1991, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 49, ISSUE: 4
INDEXED IN: WOS
WOS37
TITLE: PATHOLOGICAL, GENETIC, AND CLINICAL ASPECTS OF MACHADO-JOSEPHS DISEASE
AUTHORS: COUTINHO, P; SEQUEIROS, J ;
PUBLISHED: 1981, SOURCE: JOURNAL DE GENETIQUE HUMAINE, VOLUME: 29, ISSUE: 3
AUTHORS: COUTINHO, P; SEQUEIROS, J ;
PUBLISHED: 1981, SOURCE: JOURNAL DE GENETIQUE HUMAINE, VOLUME: 29, ISSUE: 3
INDEXED IN: WOS
WOS