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Maria Paula Duarte Faustino Gonçalves
AuthID:
R-000-CF7
Publications
Confirmed
To Validate
Document Source:
All
Document Type:
All Document Types
Article (24)
Letter (7)
Note (2)
Review (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
20
30
40
50
Confirmed Publications: 34
21
TITLE:
Asymptomatic homozygous in an African deletional beta(0)-thalassemia individual
Full Text
AUTHORS:
Faustino, P
; Reis, AB; Feliciano, H; Ferrao, L; Pereira, P; Picanco, I; Miranda, A; Seixas, T;
Romao, L
; Correia, E; Lavinha, J;
PUBLISHED:
2002
,
SOURCE:
AMERICAN JOURNAL OF HEMATOLOGY,
VOLUME:
70,
ISSUE:
3
INDEXED IN:
Scopus
WOS
IN MY:
ORCID
22
TITLE:
Compound heterozygosity for Hb Spanish Town [alpha 27(B8)Glu -> Val], Hb S [beta 6(A3)Glu -> 4Val] and the -alpha(3.7 kb) thalassemia deletion
Full Text
AUTHORS:
Faustino, P
; Picanco, I; Miranda, A; Seixas, T; Ferrao, A; Morais, A; Lavinha, J;
Romao, L
;
PUBLISHED:
2002
,
SOURCE:
HEMOGLOBIN,
VOLUME:
26,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
23
TITLE:
The peopling of Sao Tome (Gulf of Guinea): Origins of slave settlers and admixture with the Portuguese
AUTHORS:
Tomas, G; Seco, L;
Seixas, S
;
Faustino, P
;
Lavinha, J
;
Rocha, J
;
PUBLISHED:
2002
,
SOURCE:
HUMAN BIOLOGY,
VOLUME:
74,
ISSUE:
3
INDEXED IN:
Scopus
WOS
CrossRef
:
22
IN MY:
ORCID
24
TITLE:
Nonsense mutations in the human beta-globin gene lead to unexpected levels of cytoplasmic mRNA accumulation
AUTHORS:
Romao, L
;
Inacio, A
; Santos, S; Avila, M;
Faustino, P
; Pacheco, P; Lavinha, J;
PUBLISHED:
2000
,
SOURCE:
BLOOD,
VOLUME:
96,
ISSUE:
8
INDEXED IN:
Scopus
WOS
IN MY:
ORCID
25
TITLE:
The geographic pattern of beta-thalassaemia mutations in the Portuguese population
Full Text
AUTHORS:
Faustino, P
;
Pacheco, P
; Loureiro, P;
Nogueira, PJ
;
Lavinha, J
;
PUBLISHED:
1999
,
SOURCE:
BRITISH JOURNAL OF HAEMATOLOGY,
VOLUME:
107,
ISSUE:
4
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
26
TITLE:
The molecular basis of dominantly inherited beta-thalassemia [Base molecular de uma beta-talassémia de transmissão dominante.]
AUTHORS:
Faustino, P
; Barbot, J;
Goncalves, J
; Peres, MJ;
Lavinha, J
;
PUBLISHED:
1999
,
SOURCE:
Acta medica portuguesa,
VOLUME:
12,
ISSUE:
7-11
INDEXED IN:
Scopus
IN MY:
ORCID
27
TITLE:
Dominantly transmitted beta-thalassemia arising from the production of several aberrant mRNA species and one abnormal peptide
AUTHORS:
Faustino, P
; Osorio Almeida, L;
Romao, L
;
Barbot, J
; Fernandes, B; Justica, B; Lavinha, J;
PUBLISHED:
1998
,
SOURCE:
BLOOD,
VOLUME:
91,
ISSUE:
2
INDEXED IN:
Scopus
WOS
IN MY:
ORCID
28
TITLE:
beta-thalassemia mutation at -90C->T impairs the interaction of the proximal CACCC box with both erythroid and nonerythroid factors
AUTHORS:
Faustino, P
; Lavinha, J; Marini, MG; Moi, P;
PUBLISHED:
1996
,
SOURCE:
BLOOD,
VOLUME:
88,
ISSUE:
8
INDEXED IN:
Scopus
WOS
IN MY:
ORCID
29
TITLE:
Haplotypic heterogeneity of beta-thalassaemia IVS I-1(G->A) mutation in southern Portugal
AUTHORS:
Pacheco, P; Loureiro, P;
Faustino, P
; Lavinha, J;
PUBLISHED:
1996
,
SOURCE:
BRITISH JOURNAL OF HAEMATOLOGY,
VOLUME:
94,
ISSUE:
4
INDEXED IN:
Scopus
WOS
IN MY:
ORCID
30
TITLE:
BETA-THALASSEMIA UNLINKED TO THE BETA-GLOBIN GENE INTERACTS WITH SICKLE-CELL TRAIT IN A PORTUGUESE FAMILY
AUTHORS:
PACHECO, P; PERES, MJ;
FAUSTINO, P
; PISCHEDDA, C;
GONCALVES, J
; CARVAJALESRAMOS, M; SEIXAS, T; MARTINS, MC; MOI, P; LAVINHA, J;
PUBLISHED:
1995
,
SOURCE:
BRITISH JOURNAL OF HAEMATOLOGY,
VOLUME:
91,
ISSUE:
1
INDEXED IN:
Scopus
WOS
IN MY:
ORCID
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