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Paulo Manuel de Castro Pinho e Costa
AuthID:
R-000-EHG
Publications
Confirmed
To Validate
Document Source:
All
Document Type:
All Document Types
Article (81)
Abstract (67)
Letter (6)
Review (3)
Article in Press (2)
Note (1)
Editorial Material (1)
Unpublished (1)
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Order:
Year Dsc
Year Asc
Cit. WOS Dsc
IF WOS Dsc
Cit. Scopus Dsc
IF Scopus Dsc
Title Asc
Title Dsc
Results:
10
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Confirmed Publications: 162
141
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
142
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
143
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
144
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
145
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
146
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
147
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
148
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
149
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
150
TITLE:
Detection of a variant protein in hair: new diagnostic method in Portuguese type familial amyloid polyneuropathy Commentary: A new hair test for rare antigens
AUTHORS:
Ando, Y; Anan, I; Suhr, O; Holmgren, G;
Costa, PMP
; Pereira, RS;
PUBLISHED:
1998
,
SOURCE:
BMJ,
VOLUME:
316,
ISSUE:
7143
INDEXED IN:
CrossRef
:
3
IN MY:
ORCID
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