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Susana Moreira Ferreira
AuthID:
R-000-KNQ
Publications
Confirmed
To Validate
Document Source:
All
Document Type:
All Document Types
Article (6)
Review (1)
Abstract (1)
Year Start - End:
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
-
2024
2023
2022
2021
2020
2019
2018
2017
2016
2015
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: 8
1
TITLE:
Evaluation of Cerebral Microvascular Regulatory Mechanisms with Transcranial Doppler in Fabry Disease
Full Text
AUTHORS:
Pedro Castro
; Mariana Gutierres; Gilberto Pereira;
Susana Ferreira
;
Oliveira, JP
;
Elsa Azevedo
;
PUBLISHED:
2020
,
SOURCE:
BRAIN SCIENCES,
VOLUME:
10,
ISSUE:
8
INDEXED IN:
Scopus
WOS
CrossRef
:
7
2
TITLE:
Fabry disease caused by the GLA p.Phe113Leu (p.F113L) variant: Natural history in males
AUTHORS:
Oliveira, JP
; Albina Nowak;
Frederic Barbey
;
Marcia Torres
;
Jose P Nunes
;
Fernando Teixeira e Costa
; Fernanda Carvalho;
Susana Sampaio
;
Isabel Tavares
; Odete Pereira; Ana L Soares;
Catia Carmona
;
Maria Teresa Cardoso
;
Iulia E Jurca Simina
; Marco Spada;
Susana Ferreira
; Dominique P Germain;
PUBLISHED:
2020
,
SOURCE:
EUROPEAN JOURNAL OF MEDICAL GENETICS,
VOLUME:
63,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
:
19
3
TITLE:
Fabry disease associated with the GLA p.Phe113Leu variant: Evidence for a common ancestor between Portuguese and Italians
Full Text
AUTHORS:
Diana Martins;
Susana Ferreira
; Luisa Pereira; Nicoletta Chiesa; Joao Oliveira;
PUBLISHED:
2019
,
SOURCE:
22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH)
in
MEDICINE,
VOLUME:
98,
ISSUE:
26
INDEXED IN:
WOS
4
TITLE:
Multiple phenotypic domains of Fabry disease and their relevance for establishing genotype-phenotype correlations
Full Text
AUTHORS:
Oliveira, JP
;
Susana Ferreira
;
PUBLISHED:
2019
,
SOURCE:
APPLICATION OF CLINICAL GENETICS,
VOLUME:
12
INDEXED IN:
Scopus
WOS
CrossRef
:
38
5
TITLE:
Primary involvement of neurovascular coupling in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Full Text
AUTHORS:
Andrea Jokumsen Cabral
;
Ana Aires
;
Susana Ferreira
;
Elsa Azevedo
;
Pedro Castro
;
PUBLISHED:
2019
,
SOURCE:
JOURNAL OF NEUROLOGY,
VOLUME:
266,
ISSUE:
7
INDEXED IN:
Scopus
WOS
CrossRef
:
13
6
TITLE:
Individuals With Normal GLA Gene Sequence May Present Abnormally Spliced Alpha-Galactosidase mRNA Transcripts
AUTHORS:
Susana Ferreira
; Miguel Viana-Baptista; Daniel Rodrigues;
Oliveira, JP
;
PUBLISHED:
2015
,
SOURCE:
Gene, Cell and Tissue,
VOLUME:
3,
ISSUE:
1
INDEXED IN:
CrossRef
7
TITLE:
The alpha-galactosidase A p.Arg118Cys variant does not cause a Fabry disease phenotype: Data from individual patients and family studies
Full Text
AUTHORS:
Susana Ferreira
; Alberto Ortiz; Dominique P Germain;
Miguel Viana Baptista
; Antonio Caldeira Gomes;
Marta Camprecios
;
Maria Fenollar Cortes
;
Angel Gallegos Villalobos
; Diego Garcia; Jose A Antonio Garcia Robles; Jesus Egido; Eduardo Gutierrez Rivas; Jose A Antonio Herrero; Sebastian Mas; Raluca Oancea; Paloma Peres; Luis M Manuel Salazar Martin; Jesus Solera Garcia; Helena Alves; Scott C Garman;
Oliveira, JP
;
...More
PUBLISHED:
2015
,
SOURCE:
MOLECULAR GENETICS AND METABOLISM,
VOLUME:
114,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
:
67
8
TITLE:
Variations in the GLA gene correlate with globotriaosylceramide and globotriaosylsphingosine analog levels in urine and plasma
Full Text
AUTHORS:
Susana Ferreira
;
Christiane Auray Blais
; Michel Boutin; Pamela Lavoie;
Jose Pedro Nunes
;
Elisabete Martins
; Scott Garman;
Oliveira, JP
;
PUBLISHED:
2015
,
SOURCE:
CLINICA CHIMICA ACTA,
VOLUME:
447
INDEXED IN:
Scopus
WOS
CrossRef
:
19
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