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Isabel Maria Antolin Martins de Carvalho Croce Rivera
AuthID:
R-000-69F
Publications
Confirmed
To Validate
Document Source:
All
Document Type:
All Document Types
Article (22)
Review (2)
Note (1)
Letter (1)
Article in Press (1)
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Order:
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Year Asc
Cit. WOS Dsc
IF WOS Dsc
Cit. Scopus Dsc
IF Scopus Dsc
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Results:
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Confirmed Publications: 27
11
TITLE:
The TCN2 776C > G polymorphism correlates with vitamin B-12 cellular delivery in healthy adult populations
Full Text
AUTHORS:
Rita Castro
;
Madalena Barroso
;
Monica Rocha
;
Ruben Esse
; Ruben Ramos;
Paula Ravasco
;
Isabel Rivera
;
Isabel Tavares de Almeida
;
PUBLISHED:
2010
,
SOURCE:
CLINICAL BIOCHEMISTRY,
VOLUME:
43,
ISSUE:
7-8
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
12
TITLE:
Pyruvate dehydrogenase deficiency: identification of a novel mutation in the PDHA1 gene which responds to amino acid supplementation
Full Text
AUTHORS:
Maria Joao Silva
; Ana Pinheiro;
Filomena Eusebio
;
Ana Gaspar
;
Isabel Tavares de Almeida
;
Isabel Rivera
;
PUBLISHED:
2009
,
SOURCE:
EUROPEAN JOURNAL OF PEDIATRICS,
VOLUME:
168,
ISSUE:
1
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
13
TITLE:
Association of A313 G polymorphism (GSTP1*B) in the glutathione-S-transferase P1 gene with sporadic Parkinson's disease
Full Text
AUTHORS:
Vilar, R
;
Coelho, H
;
Rodrigues, E
;
Gama, MJ
;
Rivera, I
;
Taioli, E
;
Lechner, MC
;
PUBLISHED:
2007
,
SOURCE:
EUROPEAN JOURNAL OF NEUROLOGY,
VOLUME:
14,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
14
TITLE:
Homocysteine metabolism, hyperhomocysteinaemia and vascular disease: An overview
Full Text
AUTHORS:
Castro, R
;
Rivera, I
; Blom, HJ; Jakobs, C;
de Almeida, IT
;
PUBLISHED:
2006
,
SOURCE:
JOURNAL OF INHERITED METABOLIC DISEASE,
VOLUME:
29,
ISSUE:
1
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
15
TITLE:
Mutational spectrum of classical galactosaemia in Spain and Portugal
Full Text
AUTHORS:
Gort, L;
Boleda, MD
; Tyfield, L; Vilarinho, L;
Rivera, I
; Cardoso, ML; Santos Leite, M; Giros, M; Briones, P;
PUBLISHED:
2006
,
SOURCE:
JOURNAL OF INHERITED METABOLIC DISEASE,
VOLUME:
29,
ISSUE:
6
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
16
TITLE:
Phenylketonuria revisited [Fenilcetonúria revisitada]
AUTHORS:
Vilarinho, L; Queiros, A;
Leandro, P
;
De Almeida, IT
;
Rivera, I
;
PUBLISHED:
2006
,
SOURCE:
Arquivos de Medicina,
VOLUME:
20,
ISSUE:
5-6
INDEXED IN:
Scopus
IN MY:
ORCID
17
TITLE:
Intracellular S-adenosylhomocysteine increased levels are associated with DNA hypomethylation in HUVEC
Full Text
AUTHORS:
Castro, R
;
Rivera, I
;
Martins, C
; Struys, EA; Jansen, EEW;
Clode, N
;
Graca, LM
; Blom, HJ; Jakobs, C;
de Almeida, IT
;
PUBLISHED:
2005
,
SOURCE:
JOURNAL OF MOLECULAR MEDICINE-JMM,
VOLUME:
83,
ISSUE:
10
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
18
TITLE:
5,10-methylenetetrahydrofolate reductase (MTHFR) 677C -> T and 1298A -> C mutations are associated with DNA hypomethylation
AUTHORS:
Castro, R
;
Rivera, I
;
Ravasco, P
;
Camilo, ME
; Jakobs, C;
Blom, HJ
;
de Almeida, IT
;
PUBLISHED:
2004
,
SOURCE:
JOURNAL OF MEDICAL GENETICS,
VOLUME:
41,
ISSUE:
6
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
19
TITLE:
5,10-Methylenetetrahydrofolate reductase 677C -> T and 1298A -> C mutations are genetic determinants of elevated homocysteine
AUTHORS:
Castro, R
;
Rivera, I
;
Ravasco, P
; Jakobs, C; Blom, HJ;
Camilo, ME
;
de Almeida, IT
;
PUBLISHED:
2003
,
SOURCE:
QJM-AN INTERNATIONAL JOURNAL OF MEDICINE,
VOLUME:
96,
ISSUE:
4
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
20
TITLE:
Increased, homocysteine and S-adenosylhomocysteine concentrations and DNA hypomethylation in vascular disease
AUTHORS:
Castro, R
;
Rivera, I
; Struys, EA;
Jansen, EEW
;
Ravasco, P
;
Camilo, ME
; Blom, HJ; Jakobs, C;
de Almeida, IT
;
PUBLISHED:
2003
,
SOURCE:
CLINICAL CHEMISTRY,
VOLUME:
49,
ISSUE:
8
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
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