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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 (85)
Abstract (67)
Letter (6)
Review (3)
Article in Press (3)
Note (1)
Editorial Material (1)
Unpublished (1)
Year Start - End:
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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: 167
151
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
|
CIÊNCIAVITAE
152
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
|
CIÊNCIAVITAE
153
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
|
CIÊNCIAVITAE
154
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
|
CIÊNCIAVITAE
155
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
|
CIÊNCIAVITAE
156
TITLE:
Early destructive spondyloarthropathy from combined beta(2)-microglobulin and transthyretin Met30 amyloidosis in a dialysed patient
AUTHORS:
Beirao, I
;
Lobato, L
; Guimaraes, SM; Cardoso, P;
Costa, PMP
;
Coelho, T
;
Rocha, G
; Guimaraes, S;
PUBLISHED:
1998
,
SOURCE:
NEPHROLOGY DIALYSIS TRANSPLANTATION,
VOLUME:
13,
ISSUE:
12
INDEXED IN:
Scopus
WOS
CrossRef
:
2
IN MY:
ORCID
|
CIÊNCIAVITAE
157
TITLE:
Study of an anti-human transthyretin immunoadsorbent - Influence of coupling chemistry on binding capacity and ligand leakage
Full Text
AUTHORS:
Riedstra, S;
Ferreira, JPM
;
Costa, PMP
;
PUBLISHED:
1998
,
SOURCE:
JOURNAL OF CHROMATOGRAPHY B,
VOLUME:
705,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
CIÊNCIAVITAE
158
TITLE:
The future of selective apheresis in FAP. Editorial
AUTHORS:
Costa, PMP
;
Costa, PP
;
PUBLISHED:
1998
,
SOURCE:
AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS,
VOLUME:
5,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
CIÊNCIAVITAE
159
TITLE:
IMMUNOADSORPTION PROCEDURE AS A POTENTIAL METHOD FOR THE SPECIFIC BETA-2-MICROGLOBULIN REMOVAL FROM PLASMA OF PATIENTS WITH CHRONIC-RENAL-FAILURE
Full Text
AUTHORS:
VALLAR, L
;
COSTA, PMP
; TEIXEIRA, A; PFISTER, M; BARROIS, R;
COSTA, PP
; RIVAT, C;
PUBLISHED:
1995
,
SOURCE:
5th Symposium of the European-Society-for-Bio-Chromatography on Bio-Chromatography and Bio-Engineering
in
JOURNAL OF CHROMATOGRAPHY B-BIOMEDICAL APPLICATIONS,
VOLUME:
664,
ISSUE:
1
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
CIÊNCIAVITAE
160
TITLE:
GEOGRAPHICAL-DISTRIBUTION OF TTR MET(30) CARRIERS IN NORTHERN SWEDEN - DISCREPANCY BETWEEN CARRIER FREQUENCY AND PREVALENCE RATE
AUTHORS:
HOLMGREN, G;
COSTA, PMP
; ANDERSSON, C; ASPLUND, K; STEEN, L; BEEKMAN, L; NYLANDER, PO; TEIXEIRA, A;
SARAIVA, MJM
; COSTA, PP;
PUBLISHED:
1994
,
SOURCE:
JOURNAL OF MEDICAL GENETICS,
VOLUME:
31,
ISSUE:
5
INDEXED IN:
Scopus
WOS
CrossRef
:
119
IN MY:
ORCID
|
CIÊNCIAVITAE
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