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João Paulo Ferreira da Silva Oliveira
AuthID:
R-000-7B1
Affiliation
Degree
Publications
Confirmed
To Validate
Document Source:
All
Document Type:
All Document Types
Article (59)
Abstract (28)
Review (7)
Letter (4)
Book Chapter (4)
Note (2)
Correction (2)
Unpublished (1)
Article in Press (1)
Proceedings Paper (1)
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Order:
Year Dsc
Year Asc
Cit. WOS Dsc
IF WOS Dsc
Cit. Scopus Dsc
IF Scopus Dsc
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Title Dsc
Results:
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Confirmed Publications: 109
81
TITLE:
Nephropathy in Fabry disease: Baseline characteristics of 1262 patients in the Fabry Registry
Full Text
AUTHORS:
Christine Eng; Alberto Ortiz;
Oliveira, JP
;
Steven Waldek
; David Warnock;
Bruno Cianciaruso
; Christoph Wanner;
PUBLISHED:
2008
,
SOURCE:
4th Annual World Symposium of the Lysosomal-Disease-Network
in
MOLECULAR GENETICS AND METABOLISM,
VOLUME:
93,
ISSUE:
2
INDEXED IN:
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
|
CIÊNCIAVITAE
82
TITLE:
Nephropathy in Fabry disease: Baseline characteristics of a cohort of 1262 female and male patients in the Fabry registry
AUTHORS:
Ortiz, A;
Oliveira, JP
; Waldek, S; Warnock, DG; Cianciaruso, B; Wanner, C;
PUBLISHED:
2008
,
SOURCE:
8th Annual European Round Table on Fabry Disease
in
CLINICAL THERAPEUTICS,
VOLUME:
30
INDEXED IN:
WOS
IN MY:
ORCID
|
ResearcherID
|
CIÊNCIAVITAE
83
TITLE:
Nephropathy in males and females with Fabry disease: cross-sectional description of patients before treatment with enzyme replacement therapy
AUTHORS:
Alberto Ortiz;
Oliveira, JP
;
Steven Waldek
; David G Warnock;
Bruno Cianciaruso
; Christoph Wanner;
PUBLISHED:
2008
,
SOURCE:
NEPHROLOGY DIALYSIS TRANSPLANTATION,
VOLUME:
23,
ISSUE:
5
INDEXED IN:
Scopus
WOS
CrossRef
:
161
IN MY:
ORCID
|
ResearcherID
|
CIÊNCIAVITAE
84
TITLE:
PORTYSTROKE: SCREENING GENETIC CONDITIONS IN PORTUGUESE YOUNG STROKE PATIENTS
AUTHORS:
Viana Baptista, M; Ferreira, S; Melo, TP; Carvalho, M;
Cruz, VT
; Carmona, C; Tuna, A; Rodrigues, M; Ferreira, C; Pinto, AN; Silva, FA; Leitao, A; Gabriel, JP; Calado, S;
Oliveira, JP
; Ferro, JM;
PUBLISHED:
2008
,
SOURCE:
5th Symposium on Lysosomal Storage Disorders
in
CLINICAL THERAPEUTICS,
VOLUME:
30
INDEXED IN:
WOS
IN MY:
ORCID
|
ResearcherID
|
CIÊNCIAVITAE
85
TITLE:
Recommendations and guidelines for the diagnosis and treatment of Fabry nephropathy in adults
AUTHORS:
Alberto Ortiz;
Oliveira, JP
; Christoph Wanner; Barry M Brenner;
Stephen Waldek
; David G Warnock;
PUBLISHED:
2008
,
SOURCE:
NATURE CLINICAL PRACTICE NEPHROLOGY,
VOLUME:
4,
ISSUE:
6
INDEXED IN:
Scopus
WOS
CrossRef
:
64
IN MY:
ORCID
|
ResearcherID
|
CIÊNCIAVITAE
86
TITLE:
Significant proteinuria reduction in Fabry disease after a short period of combined enzyme replacement therapy and angiotensin-converting enzyme inhibitor
AUTHORS:
Soares, C
; Faria, B; Sousa, T; Garrido, J; Lemos, S;
Oliveira, JP
;
PUBLISHED:
2008
,
SOURCE:
8th Annual European Round Table on Fabry Disease
in
CLINICAL THERAPEUTICS,
VOLUME:
30
INDEXED IN:
WOS
IN MY:
ORCID
|
ResearcherID
|
CIÊNCIAVITAE
87
TITLE:
Splenomegaly, hypersplenism and peripheral blood cytopaenias in patients with classical Anderson-Fabry disease
Full Text
AUTHORS:
Oliveira, JP
;
Carmen Valbuena
; Antonio Baldaia Moreira;
Elsa Fonseca
;
Carlos Soares
; Elisa Leao Teles;
Stephen Waldek
;
PUBLISHED:
2008
,
SOURCE:
VIRCHOWS ARCHIV,
VOLUME:
453,
ISSUE:
3
INDEXED IN:
Scopus
WOS
CrossRef
:
8
IN MY:
ORCID
|
ResearcherID
|
CIÊNCIAVITAE
88
TITLE:
The g.1170C > T polymorphism of the 5 ' untranslated region of the human alpha-galactosidase gene is associated with decreased enzyme expression-Evidence from a family study
Full Text
AUTHORS:
Oliveira, JP
;
Ferreira, S
;
Reguenga, C
;
Carvalho, F
; Mansson, JE;
PUBLISHED:
2008
,
SOURCE:
JOURNAL OF INHERITED METABOLIC DISEASE,
VOLUME:
31,
ISSUE:
S2
INDEXED IN:
Scopus
WOS
CrossRef
:
17
IN MY:
ORCID
|
ResearcherID
|
CIÊNCIAVITAE
89
TITLE:
Evidence for selective low leukocyte enzyme activity levels associated with the G1170C > T 5 ' untranslated polymorphism of the alpha-galactosidase A gene
Full Text
AUTHORS:
Ferreira, S; Barcelo, J;
Carvalho, F
; Mansson, JE;
Oliveira, JP
;
PUBLISHED:
2007
,
SOURCE:
7th Annual European Round Table on Fabry Disease
in
CLINICAL THERAPEUTICS,
VOLUME:
29
INDEXED IN:
WOS
CrossRef
IN MY:
ORCID
|
CIÊNCIAVITAE
90
TITLE:
Fabry disease: Worsening of hearing loss with enzyme replacement therapy
Full Text
AUTHORS:
Moura, C;
Soares, C
;
Seixas, D
; Ayres Bastos, M;
Pais Clemente, M
;
Oliveira, JP
;
PUBLISHED:
2007
,
SOURCE:
7th Annual European Round Table on Fabry Disease
in
CLINICAL THERAPEUTICS,
VOLUME:
29
INDEXED IN:
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
|
CIÊNCIAVITAE
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