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Luísa Cristina da Costa Azevedo
AuthID:
R-000-9VD
Publications
Confirmed
To Validate
Document Source:
All
Document Type:
All Document Types
Article (47)
Review (11)
Abstract (6)
Book Chapter (3)
Editorial Material (3)
Article in Press (2)
Letter (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
Title Asc
Title Dsc
Results:
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Confirmed Publications: 74
61
TITLE:
Late onset carbamoylphosphate synthetase deficiency
Full Text
AUTHORS:
Ferreira, AC; Moco, C; Quental, R;
Azevedo, L
; Sequeira, S;
PUBLISHED:
2008
,
SOURCE:
JOURNAL OF INHERITED METABOLIC DISEASE,
VOLUME:
31
INDEXED IN:
WOS
62
TITLE:
Ornithine transcarbamylase deficiency: Phenotype and genotype characterization in 25 patients - Experience from a Portuguese tertiary center
Full Text
AUTHORS:
Teles E Leao
; Rodrigues, E; Soares, S; Trindade, E; Vilarinho, L; Cardoso, ML;
Azevedo, L
;
PUBLISHED:
2008
,
SOURCE:
JOURNAL OF INHERITED METABOLIC DISEASE,
VOLUME:
31
INDEXED IN:
WOS
63
TITLE:
Congenital disorder of glycosylation type Ia: Searching for the origin of common mutations in PMM2. Origin(s) of PMM2 Gene Mutations
Full Text
AUTHORS:
Quelhas, D
;
Quental, R
;
Vilarinho, L
;
Amorim, Antonio
;
Azevedo, L
;
PUBLISHED:
2007
,
SOURCE:
ANNALS OF HUMAN GENETICS,
VOLUME:
71,
ISSUE:
3
INDEXED IN:
Scopus
WOS
CrossRef
:
13
IN MY:
ORCID
|
ResearcherID
64
TITLE:
In vitro demonstration of intra-locus compensation using the ornithine transcarbamylase protein as model
AUTHORS:
Gianpaolo Suriano
;
Luisa Azevedo
; Marta Novais; Barbara Boscolo;
Raquel Seruca
;
Amorim, Antonio
; Elena Maria Ghibaudi;
PUBLISHED:
2007
,
SOURCE:
HUMAN MOLECULAR GENETICS,
VOLUME:
16,
ISSUE:
18
INDEXED IN:
Scopus
WOS
CrossRef
:
14
IN MY:
ORCID
|
ResearcherID
65
TITLE:
Epistatic interactions: how strong in disease and evolution?
Full Text
AUTHORS:
Luisa Azevedo
;
Gianpaolo Suriano
;
Barbara van Asch
; Rosalind M Harding;
Amorim, Antonio
;
PUBLISHED:
2006
,
SOURCE:
TRENDS IN GENETICS,
VOLUME:
22,
ISSUE:
11
INDEXED IN:
Scopus
WOS
CrossRef
:
37
IN MY:
ORCID
|
ResearcherID
66
TITLE:
Mutational spectrum and linkage disequilibrium patterns at the ornithine transcarbamylase gene (OTC)
Full Text
AUTHORS:
Azevedo, L
;
Soares, PA
;
Quental, R
;
Vilarinho, L
; Teles, EL;
Martins, E
; Diogo, L; Garcia, P; Cenni, B;
Wermuth, B
;
Amorim, Antonio
;
PUBLISHED:
2006
,
SOURCE:
ANNALS OF HUMAN GENETICS,
VOLUME:
70,
ISSUE:
6
INDEXED IN:
Scopus
WOS
CrossRef
:
8
IN MY:
ORCID
|
ResearcherID
67
TITLE:
NOVEL MUTATIONS IN 21 PATIENTS WITH L-2-HYDROXYGLUTARIC ACIDURIA OF PORTUGUESE ORIGIN
Full Text
AUTHORS:
Vilarinho, L
; Cardoso, ML;
Gaspar, P
;
Barbot, C
;
Azevedo, L
; Diogo, L;
Santos, M
; Carrilho, I; Fineza, I; Kok, F; Chorao, R; Alegria, P;
Martins, E
;
Teixeira, J
;
Cabral C Fernandes
;
Verhoeven, NM
; Salomons, GS; Santorelli, FM; Cabral, P;
Amorim, Antonio
;
Jakobs, C;
...More
PUBLISHED:
2005
,
SOURCE:
JOURNAL OF INHERITED METABOLIC DISEASE,
VOLUME:
28,
ISSUE:
4
INDEXED IN:
Scopus
WOS
CrossRef
:
26
IN MY:
ORCID
68
TITLE:
Evidence for mutational cis-acting factors affecting mutagenesis in the ornithine transcarbamylase gene.
AUTHORS:
Azevedo, L
; Climent, C; Vilarinho, L; Calafell, F;
Amorim, Antonio
;
PUBLISHED:
2004
,
SOURCE:
Human mutation,
VOLUME:
24,
ISSUE:
3
INDEXED IN:
Scopus
CrossRef
:
4
IN MY:
ORCID
69
TITLE:
Analysis of polymorphic sites within ornithine transcarbamylase (OTC) gene improves mutation analysis in females with OTC deficiency
AUTHORS:
Dvorakova, L;
Stolnaja, L
;
Tietzeova, E
;
Azevedo, L
;
Vilarinho, L
;
Amorim, Antonio
;
Hruba, E
;
Hrebicek, M
;
PUBLISHED:
2003
,
SOURCE:
Annual Meeting of the American-Society-of-Human-Genetics
in
AMERICAN JOURNAL OF HUMAN GENETICS,
VOLUME:
73,
ISSUE:
5
INDEXED IN:
WOS
70
TITLE:
New polymorphic sites within ornithine transcarbamylase gene: population genetics studies and implications for diagnosis
Full Text
AUTHORS:
Azevedo, L
;
Stolnaja, L
;
Tietzeova, E
; Hrebicek, M; Hruba, E;
Vilarinho, L
;
Amorim, Antonio
; Dvorakova, L;
PUBLISHED:
2003
,
SOURCE:
MOLECULAR GENETICS AND METABOLISM,
VOLUME:
78,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
:
10
IN MY:
ORCID
|
ResearcherID
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