Jorge António Gonçalves Pinto Basto
AuthID: R-000-7NH
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TITLE: Prostate cancer in Cowden syndrome: somatic loss and germline mutation of the PTEN gene Full Text
AUTHORS: Mafalda Barbosa; Martinha Henrique; Jorge Pinto Basto; Kathleen Claes; Gabriela Soares;
PUBLISHED: 2011, SOURCE: CANCER GENETICS, VOLUME: 204, ISSUE: 4
AUTHORS: Mafalda Barbosa; Martinha Henrique; Jorge Pinto Basto; Kathleen Claes; Gabriela Soares;
PUBLISHED: 2011, SOURCE: CANCER GENETICS, VOLUME: 204, ISSUE: 4
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TITLE: Sensory neuronopathy in ataxia with oculomotor apraxia type 2 Full Text
AUTHORS: Jose Gazulla; Isabel Benavente; Isabel P Perez Lopez Fraile; Carlos Tordesillas; Pedro Modrego; Isabel Alonso ; Jorge Pinto Basto;
PUBLISHED: 2010, SOURCE: JOURNAL OF THE NEUROLOGICAL SCIENCES, VOLUME: 298, ISSUE: 1-2
AUTHORS: Jose Gazulla; Isabel Benavente; Isabel P Perez Lopez Fraile; Carlos Tordesillas; Pedro Modrego; Isabel Alonso ; Jorge Pinto Basto;
PUBLISHED: 2010, SOURCE: JOURNAL OF THE NEUROLOGICAL SCIENCES, VOLUME: 298, ISSUE: 1-2
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TITLE: Large normal and reduced penetrance alleles in Huntington disease: instability in families and frequency at the laboratory, at the clinic and in the population Full Text
AUTHORS: Sequeiros, J ; Ramos, EM; Cerqueira, J; Costa, MC; Sousa, A ; Pinto Basto, J; Alonso, I ;
PUBLISHED: 2010, SOURCE: CLINICAL GENETICS, VOLUME: 78, ISSUE: 4
AUTHORS: Sequeiros, J ; Ramos, EM; Cerqueira, J; Costa, MC; Sousa, A ; Pinto Basto, J; Alonso, I ;
PUBLISHED: 2010, SOURCE: CLINICAL GENETICS, VOLUME: 78, ISSUE: 4
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TITLE: A NONSENSE PORCN MUTATION IN SEVERE FOCAL DERMAL HYPOPLASIA WITH NATAL TEETH Full Text
AUTHORS: Cristina Dias; Jorge Basto; Odilia Pinho; Carla Barbedo; Marcia Martins; Dorothea Bornholdt; Ana Fortuna; Karl Heinz Grzeschik; Margarida Lima;
PUBLISHED: 2010, SOURCE: FETAL AND PEDIATRIC PATHOLOGY, VOLUME: 29, ISSUE: 5
AUTHORS: Cristina Dias; Jorge Basto; Odilia Pinho; Carla Barbedo; Marcia Martins; Dorothea Bornholdt; Ana Fortuna; Karl Heinz Grzeschik; Margarida Lima;
PUBLISHED: 2010, SOURCE: FETAL AND PEDIATRIC PATHOLOGY, VOLUME: 29, ISSUE: 5
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TITLE: Osteopathia Striata With Cranial Sclerosis Owing to WTX Gene Defect Full Text
AUTHORS: Bram Perdu; Fenna de Freitas; Suzanne G M Frints; Meyke Schouten; Connie Schrander Stumpel; Mafalda Barbosa; Jorge Pinto Basto; Margarida Reis Lima; Marie Christine de Vernejoul; Kristin Becker; Marie Louise Freckmann; Kathlijn Keymolen; Eric Haan; Ravi Savarirayan; Rainer Koenig; Bernhard Zabel; Filip M Vanhoenacker; Wim Van Hul;
PUBLISHED: 2010, SOURCE: JOURNAL OF BONE AND MINERAL RESEARCH, VOLUME: 25, ISSUE: 1
AUTHORS: Bram Perdu; Fenna de Freitas; Suzanne G M Frints; Meyke Schouten; Connie Schrander Stumpel; Mafalda Barbosa; Jorge Pinto Basto; Margarida Reis Lima; Marie Christine de Vernejoul; Kristin Becker; Marie Louise Freckmann; Kathlijn Keymolen; Eric Haan; Ravi Savarirayan; Rainer Koenig; Bernhard Zabel; Filip M Vanhoenacker; Wim Van Hul;
PUBLISHED: 2010, SOURCE: JOURNAL OF BONE AND MINERAL RESEARCH, VOLUME: 25, ISSUE: 1
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TITLE: Muenke Syndrome With Osteochondroma Full Text
AUTHORS: Mafalda Barbosa; Maria do Rosario Almeida; Margarida Reis Lima; Jorge Pinto Basto; Heloisa Goncalves dos Santos;
PUBLISHED: 2009, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 149A, ISSUE: 2
AUTHORS: Mafalda Barbosa; Maria do Rosario Almeida; Margarida Reis Lima; Jorge Pinto Basto; Heloisa Goncalves dos Santos;
PUBLISHED: 2009, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 149A, ISSUE: 2
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TITLE: Genotypes at the APOE and SCA2 loci do not predict the course of multiple sclerosis in patients of Portuguese origin
AUTHORS: Santos, M; Costa, MD; Rio, ME; Sa, MJ; Monteiro, M; Valenca, A; Sa, A; Dinis, J; Figueiredo, J; de Almeida, LB; Valongueiro, A; Coelho, I; Matama, MT ; Pinto Basto, J; Sequeiros, J ; Maciel, P ;
PUBLISHED: 2004, SOURCE: MULTIPLE SCLEROSIS, VOLUME: 10, ISSUE: 2
AUTHORS: Santos, M; Costa, MD; Rio, ME; Sa, MJ; Monteiro, M; Valenca, A; Sa, A; Dinis, J; Figueiredo, J; de Almeida, LB; Valongueiro, A; Coelho, I; Matama, MT ; Pinto Basto, J; Sequeiros, J ; Maciel, P ;
PUBLISHED: 2004, SOURCE: MULTIPLE SCLEROSIS, VOLUME: 10, ISSUE: 2
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TITLE: A whole genome screen for association with multiple sclerosis in Portuguese patients Full Text
AUTHORS: Santos, M; Pinto Basto, J; Rio, ME; Sa, MJ ; Valenca, A; Sa, A; Dinis, J; Figueiredo, J; de Almeida, LB; Coelho, I; Sawcer, S; Setakis, E; Compston, A; Sequeiros, J ; Maciel, P ;
PUBLISHED: 2003, SOURCE: JOURNAL OF NEUROIMMUNOLOGY, VOLUME: 143, ISSUE: 1-2
AUTHORS: Santos, M; Pinto Basto, J; Rio, ME; Sa, MJ ; Valenca, A; Sa, A; Dinis, J; Figueiredo, J; de Almeida, LB; Coelho, I; Sawcer, S; Setakis, E; Compston, A; Sequeiros, J ; Maciel, P ;
PUBLISHED: 2003, SOURCE: JOURNAL OF NEUROIMMUNOLOGY, VOLUME: 143, ISSUE: 1-2
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TITLE: Inherited and acquired risk factors and their combined effects in pediatric stroke Full Text
AUTHORS: Barreirinho, S; Ferro, A; Santos, M; Costa, E ; Pinto Basto, J; Sousa, A ; Sequeiros, J ; Maciel, P ; Barbot, C ; Barbot, J;
PUBLISHED: 2003, SOURCE: PEDIATRIC NEUROLOGY, VOLUME: 28, ISSUE: 2
AUTHORS: Barreirinho, S; Ferro, A; Santos, M; Costa, E ; Pinto Basto, J; Sousa, A ; Sequeiros, J ; Maciel, P ; Barbot, C ; Barbot, J;
PUBLISHED: 2003, SOURCE: PEDIATRIC NEUROLOGY, VOLUME: 28, ISSUE: 2
