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António Jorge dos Santos Pereira de Sequeiros
AuthID:
R-000-23K
Publications
Confirmed
To Validate
Document Source:
All
Document Type:
All Document Types
Article (139)
Abstract (65)
Letter (12)
Review (6)
Proceedings Paper (5)
Article in Press (5)
Note (2)
Correction (2)
Editorial Material (2)
Biographical-Item (2)
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Order:
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Year Asc
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IF WOS Dsc
Cit. Scopus Dsc
IF Scopus Dsc
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Title Dsc
Results:
10
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Confirmed Publications: 240
91
TITLE:
The C677T polymorphism in MTHFR is not associated with migraine in Portugal
Full Text
AUTHORS:
Ferro, A; Castro, MJ;
Lemos, C
;
Santos, M
;
Sousa, A
;
Pereira Monteiro, J
;
Sequeiros, J
;
Maciel, P
;
PUBLISHED:
2008
,
SOURCE:
DISEASE MARKERS,
VOLUME:
25,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
92
TITLE:
Two novel functional mutations in the Na+,K+-ATPase alpha 2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes
Full Text
AUTHORS:
Castro, MJ; Nunes, B; de Vries, B;
Lemos, C
;
Vanmolkot, KRJ
;
van den Heuvel, JJMW
;
Temudo, T
; Barros, J;
Sequeiros, J
; Frants, RR; Koenderink, JB;
Pereira Monteiro, JM
;
van den Maagdenberg, AMJM
;
PUBLISHED:
2008
,
SOURCE:
CLINICAL GENETICS,
VOLUME:
73,
ISSUE:
1
INDEXED IN:
Scopus
WOS
CrossRef
:
17
IN MY:
ORCID
93
TITLE:
What is ideal genetic counselling? A survey of current international guidelines
Full Text
AUTHORS:
Elina Rantanen
;
Marja Hietala
;
Ulf Kristoffersson
; Irmgard Nippert; Joerg Schmidtke;
Jorge Sequeiros
;
Helena Kaariainen
;
PUBLISHED:
2008
,
SOURCE:
EUROPEAN JOURNAL OF HUMAN GENETICS,
VOLUME:
16,
ISSUE:
4
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
94
TITLE:
Abnormal movements in Rett syndrome are present before the regression period: A case study
Full Text
AUTHORS:
Teresa Temudo;
Patricia Maciel
;
Jorge Sequeiros
;
PUBLISHED:
2007
,
SOURCE:
MOVEMENT DISORDERS,
VOLUME:
22,
ISSUE:
15
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
95
TITLE:
Asian origin for the worldwide-spread mutational event in Machado-Joseph disease
AUTHORS:
Sandra Martins
; Francesc Calafell; Claudia Gaspar;
Virginia C N Wong
;
Isabel Silveira
; Garth A Nicholson; Ewout R Brunt;
Lisbeth Tranebjaerg
;
Giovanni Stevanin
; Mingli Hsieh; Bing Wen Soong;
Leal Loureiro
; Alexandra Duerr; Shoji Tsuji; Mitsunori Watanabe;
Laura B Jardim
; Paola Giunti;
Olaf Riess
;
Laura P W Ranum
; Alexis Brice;
Guy A Rouleau;
Paula Coutinho
;
Amorim, Antonio
;
Jorge Sequeiros
;
...More
PUBLISHED:
2007
,
SOURCE:
ARCHIVES OF NEUROLOGY,
VOLUME:
64,
ISSUE:
10
INDEXED IN:
Scopus
WOS
CrossRef
:
54
IN MY:
ORCID
96
TITLE:
Depressive symptoms in Machado-Joseph disease (SCA3) patients and their relatives
AUTHORS:
Cecchin, CR; Pires, AP; Rieder, CR; Monte, TL;
Silveira, I
; Carvalho, T; Saraiva Pereira, ML;
Sequeiros, J
;
Jardim, LB
;
PUBLISHED:
2007
,
SOURCE:
COMMUNITY GENETICS,
VOLUME:
10,
ISSUE:
1
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
97
TITLE:
Functional genomics and biochemical characterization of the C-elegans orthologue of the Machado-Joseph disease protein ataxin-3
AUTHORS:
Ana Joao Rodrigues
; Giovanni Coppola;
Claudia Santos
;
Maria do Carmo Costa
;
Michael Ailion
;
Jorge Sequeiros
; Daniel H Geschwind;
Patricia Maciel
;
PUBLISHED:
2007
,
SOURCE:
FASEB JOURNAL,
VOLUME:
21,
ISSUE:
4
INDEXED IN:
Scopus
WOS
CrossRef
:
58
IN MY:
ORCID
98
TITLE:
NEDD8: A new ataxin-3 interactor
Full Text
AUTHORS:
Ferro, A;
Carvalho, AL
;
Teixeira Castro, A
; Almeida, C; Tome, RJ;
Cortes, L
;
Rodrigues, AJ
;
Logarinho, E
;
Sequeiros, J
;
Macedo Ribeiro, S
;
Maciel, P
;
PUBLISHED:
2007
,
SOURCE:
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH,
VOLUME:
1773,
ISSUE:
11
INDEXED IN:
Scopus
WOS
CrossRef
Handle
IN MY:
ORCID
99
TITLE:
Psychological follow-up of presymptomatic genetic testing for spinocerebellar ataxia type 2 (SCA2) in Cuba
Full Text
AUTHORS:
Paneque, M
;
Lemos, C
; Escalona, K; Prieto, L; Reynaldo, R; Velazquez, M; Quevedo, J; Santos, N; Almaguer, LE; Velazquez, L;
Sousa, A
;
Fleming, M
;
Sequeiros, J
;
PUBLISHED:
2007
,
SOURCE:
Journal of Genetic Counseling,
VOLUME:
16,
ISSUE:
4
INDEXED IN:
Scopus
CrossRef
:
11
IN MY:
ORCID
100
TITLE:
Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine
Full Text
AUTHORS:
Maria Jose Castro; Anine H Stam;
Carolina Lemos
;
Barros, José
;
Raquel G Gouveia
;
Isabel Pavao Martins
; Jan B Koenderink;
Kaate R J Vanmolkot
; Alexandre P Mendes; Rune R Frants; Michel D Ferrari;
Jorge Sequeiros
;
Jose M Pereira Monteiro
;
Arn M J M van den Maagdenberg
;
PUBLISHED:
2007
,
SOURCE:
JOURNAL OF HUMAN GENETICS,
VOLUME:
52,
ISSUE:
12
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
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