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Ana Paula Costa Santos Peralta Leandro
AuthID:
R-000-19T
Publications
Confirmed
To Validate
Document Source:
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Document Type:
All Document Types
Article (14)
Review (3)
Article in Press (2)
Note (1)
Proceedings Paper (1)
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Order:
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Cit. WOS Dsc
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IF Scopus Dsc
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Results:
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Confirmed Publications: 21
11
TITLE:
The lytic cassette of mycobacteriophage Ms6 encodes an enzyme with lipolytic activity
AUTHORS:
Filipa Gil;
Maria Joao Catalao
;
Jose Moniz Pereira
;
Paula Leandro
;
Michael McNeil
;
Madalena Pimentel
;
PUBLISHED:
2008
,
SOURCE:
MICROBIOLOGY-SGM,
VOLUME:
154,
ISSUE:
5
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
12
TITLE:
Co-expression of different subunits of human phenylalanine hydroxylase: Evidence of negative interallelic complementation
Full Text
AUTHORS:
Leandro, J
;
Nascimento, C
;
de Almeida, IT
;
Leandro, P
;
PUBLISHED:
2006
,
SOURCE:
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE,
VOLUME:
1762,
ISSUE:
5
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
13
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
14
TITLE:
Glycerol increases the yield and activity of human phenylalanine hydroxylase mutant enzymes produced in a prokaryotic expression system
Full Text
AUTHORS:
Leandro, P
;
Lechner, MC
;
de Almeida, IT
; Konecki, D;
PUBLISHED:
2001
,
SOURCE:
MOLECULAR GENETICS AND METABOLISM,
VOLUME:
73,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
15
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
|
ResearcherID
16
TITLE:
The V388M mutation results in a kinetic variant form of phenylalanine hydroxylase
Full Text
AUTHORS:
Leandro, P
;
Rivera, I
;
Lechner, MC
;
de Almeida, IT
; Konecki, D;
PUBLISHED:
2000
,
SOURCE:
MOLECULAR GENETICS AND METABOLISM,
VOLUME:
69,
ISSUE:
3
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
17
TITLE:
Population genetics of hyperphenylalaninaemia resulting from phenylalanine hydroxylase deficiency in Portugal
AUTHORS:
Rivera, I
;
Leandro, P
; Lichter Konecki, U;
de Almeida, IT
;
Lechner, MC
;
PUBLISHED:
1998
,
SOURCE:
JOURNAL OF MEDICAL GENETICS,
VOLUME:
35,
ISSUE:
4
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
18
TITLE:
Relative frequency of IVS10nt546 mutation in a Portuguese phenylketonuric population
Full Text
AUTHORS:
Rivera, I
;
Leandro, P
; LichterKonecki, U;
deAlmeida, IT
;
Lechner, MC
;
PUBLISHED:
1997
,
SOURCE:
HUMAN MUTATION,
VOLUME:
9,
ISSUE:
3
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
19
TITLE:
MUTATION ANALYSIS OF PHENYLKETONURIA IN SOUTH AND CENTRAL PORTUGAL - PREVELANCE OF V388M MUTATION
AUTHORS:
LEANDRO, P
;
RIVERA, I
;
RIBEIRO, V
;
DEALMEIDA, IT
; DASILVEIRA, CL; LECHNER, MC;
PUBLISHED:
1995
,
SOURCE:
HUMAN MUTATION,
VOLUME:
6,
ISSUE:
2
INDEXED IN:
Scopus
WOS
IN MY:
ORCID
|
ResearcherID
20
TITLE:
TETRAHYDROBIOPTERIN DEFICIENCY IN PORTUGAL - RESULTS OF THE SCREENING FOR HYPERPHENYLALANINEMIA
AUTHORS:
DEALMEIDA, IT
;
LEANDRO, PP
; PORTEL, R; CABRAL, A; EUSEBIO, F; TASSO, T; MATASOVIC, A; BLAU, N;
PUBLISHED:
1993
,
SOURCE:
10TH INTERNATIONAL SYMP ON CHEMISTRY AND BIOLOGY OF PTERIDINES
in
CHEMISTRY AND BIOLOGY OF PTERIDINES AND FOLATES,
VOLUME:
338
INDEXED IN:
Scopus
WOS
IN MY:
ORCID
|
ResearcherID
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