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Esmeralda Emilia Gomes Martins
AuthID:
R-00J-QTW
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Document Source:
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Document Type:
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Article (73)
Review (5)
Book Chapter (4)
Letter (2)
Note (2)
Proceedings Paper (2)
Article in Press (2)
Correction (2)
Abstract (1)
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Cit. WOS Dsc
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Results:
10
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Confirmed Publications: 93
81
TITLE:
Liver transplantation in a case of argininaemia
Full Text
AUTHORS:
Silva, ES;
Martins, E
; Cardoso, ML;
Barbot, C
; Vilarinho, L; Medina, M;
PUBLISHED:
2001
,
SOURCE:
JOURNAL OF INHERITED METABOLIC DISEASE,
VOLUME:
24,
ISSUE:
8
INDEXED IN:
Scopus
WOS
CrossRef
:
12
IN MY:
ORCID
82
TITLE:
Central diabetes insipidus - A case report [Diabetes insipida central - Um caso clinico]
AUTHORS:
Madalena, C; Sameiro Faria, M; Coelho, B;
Martins, E
; Mota, C; Pereira, E;
PUBLISHED:
2000
,
SOURCE:
Nascer e Crescer,
VOLUME:
9,
ISSUE:
2
INDEXED IN:
Scopus
IN MY:
ORCID
83
TITLE:
Sjörgren - Larsson syndrome [Síndrome de Sjögren-larsson - Caso clínico]
AUTHORS:
Oliveira, T; Rosario, C; Selores, M;
Martins, E
;
Barbot, C
;
PUBLISHED:
2000
,
SOURCE:
Nascer e Crescer,
VOLUME:
9,
ISSUE:
4
INDEXED IN:
Scopus
IN MY:
ORCID
84
TITLE:
The correlation of genotype and phenotype in Portuguese hyperphenylalaninemic patients
Full Text
AUTHORS:
Rivera, I
; Cabral, A; Almeida, M;
Leandro, P
; Carmona, C; Eusebio, F; Tasso, T; Vilarinho, L;
Martins, E
;
Lechner, MC
;
de Almeida, IT
; Konecki, DS; Lichter Konecki, U;
PUBLISHED:
2000
,
SOURCE:
MOLECULAR GENETICS AND METABOLISM,
VOLUME:
69,
ISSUE:
3
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
85
TITLE:
Diagnostic approach to inborn errors of metabolism [Principios gerais da abordagem diagnostica nas doencas metabolicas hereditarias]
AUTHORS:
Martins, E
;
Barbot, C
;
PUBLISHED:
1999
,
SOURCE:
Nascer e Crescer,
VOLUME:
8,
ISSUE:
2
INDEXED IN:
Scopus
IN MY:
ORCID
86
TITLE:
Glycogen storage disease type IV presenting as hydrops fetalis
Full Text
AUTHORS:
Alegria, A;
Martins, E
; Dias, M; Cunha, A; Cardoso, ML; Maire, I;
PUBLISHED:
1999
,
SOURCE:
JOURNAL OF INHERITED METABOLIC DISEASE,
VOLUME:
22,
ISSUE:
3
INDEXED IN:
Scopus
WOS
CrossRef
:
27
IN MY:
ORCID
87
TITLE:
Identification of a novel R21X mutation in the liver-type arginase gene (ARG1) in four Portuguese patients with argininemia.
Full Text
AUTHORS:
Cardoso, ML;
Martins, E
; Vasconcelos, R; Vilarinho, L; Rocha, J;
PUBLISHED:
1999
,
SOURCE:
Human mutation,
VOLUME:
14,
ISSUE:
4
INDEXED IN:
Scopus
IN MY:
ORCID
88
TITLE:
Sialuria in a Portuguese girl: Clinical, biochemical, and molecular characteristics
Full Text
AUTHORS:
Ferreira, H;
Seppala, R
; Pinto, R; Huizing, M;
Martins, E
; Braga, AC; Gomes, L;
Krasnewich, DM
;
Miranda, MCS
; Gahl, WA;
PUBLISHED:
1999
,
SOURCE:
MOLECULAR GENETICS AND METABOLISM,
VOLUME:
67,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
89
TITLE:
What is your diagnosis? Microcytic anaemia refractory to iron therapy [Qual o seu diagnostico? Anemia microcitica sem resposta ao tratamento com ferro]
AUTHORS:
Martins, E
; Barbot, J; Carrapato, R;
PUBLISHED:
1999
,
SOURCE:
Nascer e Crescer,
VOLUME:
8,
ISSUE:
1
INDEXED IN:
Scopus
IN MY:
ORCID
90
TITLE:
What is your diagnosis? [Qual o seu diagnostico? Elevacao persistente da aspartato aminotransferase]
AUTHORS:
Martins, E
; Carvalho, A; Silva, E;
PUBLISHED:
1999
,
SOURCE:
Nascer e Crescer,
VOLUME:
8,
ISSUE:
4
INDEXED IN:
Scopus
IN MY:
ORCID
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