Paulo Manuel de Castro Pinho e Costa


AuthID: R-000-EHG

Confirmed Publications: 163



141
TITLE: TNFA promoter polymrphisms in Portuguese multiple sclerosis patients  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
142
TITLE: Association studies with GABA[B]R1 polymorphisms and idiopathic generalised epilepsy in Portuguese patients
AUTHORS: Pereira, C; Paulo, P; Costa, PPE ; Barbot, C; Santos, M; Ramalheira, J; Lopes, J; Lima, JL; Monteiro, L; Silva, AM; Martins, B;
PUBLISHED: 2004, SOURCE: 6th European Congress on Epileptology in EPILEPSIA, VOLUME: 45
INDEXED IN: WOS
IN MY: ORCID
143
TITLE: GABA(B)R1 polymorphisms and idiopathic generalized epilepsy in Portuguese patients  Full Text
AUTHORS: Paulo, P; Pereira, C; Carvalho, C; Costa, PP ; Lima, J; Casimiro, S; Quintas, Z; Silva, AM; Martins, B;
PUBLISHED: 2004, SOURCE: 18th European Histocompatibility Conference in GENES AND IMMUNITY, VOLUME: 5
INDEXED IN: WOS
IN MY: ORCID
144
TITLE: Kidney and anemia in familial amyloidosis type I  Full Text
AUTHORS: Beirao, I ; Lobato, L ; Costa, PMP ; Fonseca, I ; Mendes, P; Silva, M; Bravo, F; Cabrita, A; Porto, G ;
PUBLISHED: 2004, SOURCE: KIDNEY INTERNATIONAL, VOLUME: 66, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 17
IN MY: ORCID
145
TITLE: A whole genome association study in multiple sclerosis patients from north Portugal  Full Text
AUTHORS: Silva, BM ; Thorlacius, T; Benediktsson, K; Pereira, C; Fossdal, R; Jonsson, HH; Silva, A; Leite, I; Cerqueira, J; Costa, PP ; Marta, M; Foltynie, T; Sawcer, S; Compston, A; Jonasdottir, A;
PUBLISHED: 2003, SOURCE: JOURNAL OF NEUROIMMUNOLOGY, VOLUME: 143, ISSUE: 1-2
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
146
TITLE: Evidence of oxidative stress in familial amyloidotic polyneuropathy type 1
AUTHORS: Fiszman, ML; Di Egidio, M; Ricart, KC; Repetto, MG; Borodinsky, LN; Llesuy, SF; Saizar, RD; Trigo, PL; Riedstra, S; Costa, PP ; Villa, AM; Katz, N; Lendoire, JC; Sica, REP;
PUBLISHED: 2003, SOURCE: ARCHIVES OF NEUROLOGY, VOLUME: 60, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
147
TITLE: Psoriasis and psoriatic arthritis: A possible modifying influence of a non-HLA gene in an HLA class I associated disease
AUTHORS: Pereira, C; Pinto, D; Pereira, O; Farinha, F; Massa, A; Cerqueira, J; Pauperio, S; Casimiro, S; Barbosa, P; Vasconcelos, C ; Costa, PM ; Cardoso, MF ; Mendonca, D ; Martins Da Silva, B ;
PUBLISHED: 2001, SOURCE: European Journal of Immunogenetics, VOLUME: 28, ISSUE: 2
INDEXED IN: Scopus
IN MY: ORCID
148
TITLE: The course and prognostic factors of familial amyloid polyneuropathy after liver transplantation  Full Text
AUTHORS: Adams, D; Samuel, D; Goulon Goeau, C; Nakazato, M; Costa, PMP ; Feray, C; Plante, V; Ducot, B; Ichai, P; Lacroix, C; Metral, S; Bismuth, H; Said, G;
PUBLISHED: 2000, SOURCE: BRAIN, VOLUME: 123, ISSUE: 7
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
149
TITLE: Ineffectiveness of dialysis in transthyretin (TTR) clearance in Familial Amyloid Polyneuropathy type I, in spite of lower stability of the TTR Met30 variant
AUTHORS: Beirao, I ; Lobato, L ; Riedstra, S; Costa, PMP ; Pimentel, S; Guimaraes, S;
PUBLISHED: 1999, SOURCE: CLINICAL NEPHROLOGY, VOLUME: 51, ISSUE: 1
INDEXED IN: Scopus WOS
IN MY: ORCID
150
TITLE: Detection of a variant protein in hair: new diagnostic method in Portuguese type familial amyloid polyneuropathy
AUTHORS: Ando, Y; Anan, I; Suhr, O; Holmgren, G; Costa, PMP ;
PUBLISHED: 1998, SOURCE: BRITISH MEDICAL JOURNAL, VOLUME: 316, ISSUE: 7143
INDEXED IN: Scopus WOS
IN MY: ORCID
Page 15 of 17. Total results: 163.

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