Paulo Manuel de Castro Pinho e Costa


AuthID: R-000-EHG

Confirmed Publications: 167



131
TITLE: GABBR1 polymorphisms in portuguese mesial temporal lobe epilepsy patients
AUTHORS: Pereira, C; Chaves, J; Leal, B; Carvalho, A; Bettencourt, C; Costa, P ; Monteiro, L; Lima, J; Silva, A; Pinto, D; Silva, B;
PUBLISHED: 2006, SOURCE: 7th European Congress on Epileptology in EPILEPSIA, VOLUME: 47
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
132
TITLE: HLA-A*02 allele as a modulating factor in multiple sclerosis: Implications for susceptibility and severity  Full Text
AUTHORS: Silva, AM ; Bettencourt, A; Pereira, C; Carvalho, C; Casimiro, S; Costa, PP ; Monteiro, L; Silva, BM;
PUBLISHED: 2006, SOURCE: EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 13
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
133
TITLE: Protective influence on Multiple Sclerosis by HLA-A*02: a study in the Portuguese population  Full Text
AUTHORS: Bettencourt, A; Pereira, C; Silva, AM; Carvalho, C; Quintas, Z; Costa, PP ; Monteiro, L;
PUBLISHED: 2006, SOURCE: 20th European Immunogenetics and Histocompatibility Conference in TISSUE ANTIGENS, VOLUME: 67, ISSUE: 6
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
134
TITLE: The molecular diagnosis in familial amyloidotic polyneuropathy [Diagnóstico molecular da polineuropatia amiloidótica familiar]
AUTHORS: Costa, PP ;
PUBLISHED: 2006, SOURCE: Sinapse, VOLUME: 6, ISSUE: 1 SUPPL. 1
INDEXED IN: Scopus
IN MY: ORCID | CIÊNCIAVITAE
135
TITLE: The role of PTPN22 1858T autoimmunity risk variant in a Portuguese multiple sclerosis population
AUTHORS: Pereira, C; Martins da Silva, A; Pinto, D; Bettencourt, A; Costa, P ; Koeleman, B; Martins da Silva, B;
PUBLISHED: 2006, SOURCE: 22nd Congress of the European-Committee-for-the-Treatment-and-Resarch-in-Multiple-Sclerosis in MULTIPLE SCLEROSIS, VOLUME: 12
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
136
TITLE: The role of PTPN22 1858T autoimmunity risk variant in Multiple Sclerosis Portuguese population  Full Text
AUTHORS: Pereira, C; Silva, AM; Pinto, D; Bettencourt, A; Costa, PP ; Koeleman, B; Silva, BM;
PUBLISHED: 2006, SOURCE: 20th European Immunogenetics and Histocompatibility Conference in TISSUE ANTIGENS, VOLUME: 67, ISSUE: 6
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
137
TITLE: Vitamin D deficiency and serum levels of parathyroid hormone in Portuguese patients with familial amyloidotic polyneuropathy (FAP, TTR V30M)  Full Text
AUTHORS: Fonseca, I; Lobato, L; Santos, J; Beirao, I; Cunha, C; Oliveira, JC; Cabrita, A; Costa, PP ;
PUBLISHED: 2006, SOURCE: 11th International Symposium on Amyloidosis in AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, VOLUME: 13
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
138
TITLE: Birth of two healthy females after preimplantation genetic diagnosis for familial amyloid polyneuropathy  Full Text
AUTHORS: Almeida, VM ; Costa, PM ; Moreira, P; Goncalves, J; Braga, J;
PUBLISHED: 2005, SOURCE: REPRODUCTIVE BIOMEDICINE ONLINE, VOLUME: 10, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 10
IN MY: ORCID | CIÊNCIAVITAE
139
140
TITLE: DR/DQ antigens in papillary thyroid tumors  Full Text
AUTHORS: Pereira, C; Silva, AM; Carvalho, C; Bettencourt, A; Casimiro, S; Quintas, Z; Costa, PM ; Monteiro, L; Silva, BM;
PUBLISHED: 2005, SOURCE: 19th European Immunogenetics and Histocompatibility Conference in GENES AND IMMUNITY, VOLUME: 6
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
Page 14 of 17. Total results: 167.

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