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Maria Paula Mourao do Amaral Coutinho
AuthID:
R-000-CFK
Publications
Confirmed
To Validate
Document Source:
All
Document Type:
All Document Types
Article (67)
Letter (4)
Note (2)
Erratum (1)
Proceedings Paper (1)
Abstract (1)
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Order:
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Results:
10
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Confirmed Publications: 76
41
TITLE:
Ancestral origins of the Machado-Joseph disease mutation: A worldwide haplotype study
AUTHORS:
Gaspar, C; Lopes Cendes, I; Hayes, S; Goto, J;
Arvidsson, K
; Dias, A;
Silveira, I
;
Maciel, P
;
Coutinho, P
;
Lima, M
; Zhou, YX; Soong, BW; Watanabe, M; Giunti, P;
Stevanin, G
; Riess, O; Sasaki, H; Hsieh, M; Nicholson, GA; Brunt, E;
Higgins, JJ;
Lauritzen, M;
Tranebjaerg, L;
Volpini, V;
Wood, N;
Ranum, L;
Tsuji, S;
Brice, A;
Sequeiros, J
;
Rouleau, GA;
...More
PUBLISHED:
2001
,
SOURCE:
AMERICAN JOURNAL OF HUMAN GENETICS,
VOLUME:
68,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
42
TITLE:
Homozygosity mapping of portuguese and Japanese forms of ataxia-oculomotor apraxia to 9p13, and evidence for genetic heterogeneity
AUTHORS:
Moreira, MD;
Barbot, C
; Tachi, N; Kozuka, N; Mendonca, P;
Barros, José
;
Coutinho, P
;
Sequeiros, J
; Koenig, M;
PUBLISHED:
2001
,
SOURCE:
AMERICAN JOURNAL OF HUMAN GENETICS,
VOLUME:
68,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
43
TITLE:
Improvement in the molecular diagnosis of Machado-Joseph disease
AUTHORS:
Maciel, P
;
Costa, MDC
; Ferro, A; Rousseau, M;
Santos, CS
; Gaspar, C;
Barros, José
; Rouleau, GA;
Coutinho, P
;
Sequeiros, J
;
PUBLISHED:
2001
,
SOURCE:
ARCHIVES OF NEUROLOGY,
VOLUME:
58,
ISSUE:
11
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
44
TITLE:
Natural selection at the MJD locus: Phenotypic diversity, survival and fertility among Machado-Joseph Disease patients from the Azores
AUTHORS:
Lima, M
; Smith, MT; Silva, C; Abade, A; Mayer, FM;
Coutinho, P
;
PUBLISHED:
2001
,
SOURCE:
JOURNAL OF BIOSOCIAL SCIENCE,
VOLUME:
33,
ISSUE:
3
INDEXED IN:
Scopus
WOS
45
TITLE:
Recessive ataxia with ocular apraxia - Review of 22 Portuguese patients
AUTHORS:
Barbot, C
;
Coutinho, P
; Chorao, R; Ferreira, C;
Barros, José
; Fineza, I; Dias, K; Monteiro, JP; Guimaraes, A; Mendonca, P; Moreira, MD;
Sequeiros, J
;
PUBLISHED:
2001
,
SOURCE:
ARCHIVES OF NEUROLOGY,
VOLUME:
58,
ISSUE:
2
INDEXED IN:
Scopus
WOS
IN MY:
ORCID
46
TITLE:
The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin
Full Text
AUTHORS:
Moreira, MC
;
Barbot, C
; Tachi, N; Kozuka, N; Uchida, E; Gibson, T; Mendonca, P; Costa, M;
Barros, José
;
Yanagisawa, T
; Watanabe, M; Ikeda, Y; Aoki, M; Nagata, T;
Coutinho, P
;
Sequeiros, J
; Koenig, M;
PUBLISHED:
2001
,
SOURCE:
NATURE GENETICS,
VOLUME:
29,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
:
307
IN MY:
ORCID
47
TITLE:
High germinal instability of the (CTG)(n) at the SCA8 locus of both expanded and normal alleles
AUTHORS:
Silveira, I
;
Alonso, I
;
Guimaraes, L
; Mendonca, P;
Santos, C
;
Maciel, P
; de Matos, JMF;
Costa, M
;
Barbot, C
; Tuna, A;
Barros, José
; Jardim, L;
Coutinho, P
;
Sequeiros, J
;
PUBLISHED:
2000
,
SOURCE:
AMERICAN JOURNAL OF HUMAN GENETICS,
VOLUME:
66,
ISSUE:
3
INDEXED IN:
Scopus
WOS
CrossRef
:
65
IN MY:
ORCID
48
TITLE:
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia
AUTHORS:
Fonknechten, N; Mavel, D; Byrne, P; Davoine, CS; Cruaud, C; Boentsch, D; Samson, D;
Coutinho, P
; Hutchinson, M; McMonagle, P; Burgunder, JM; Tartaglione, A; Heinzlef, O; Feki, I; Deufel, T; Parfrey, N; Brice, A; Fontaine, B; Prud'homme, JF; Weissenbach, J;
Durr, A;
Hazan, J;
...More
PUBLISHED:
2000
,
SOURCE:
HUMAN MOLECULAR GENETICS,
VOLUME:
9,
ISSUE:
4
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
49
TITLE:
Clinical heterogeneity of autosomal recessive spastic paraplegias - Analysis of 106 patients in 46 families. Analysis of 106 Patients in 46 Families
AUTHORS:
Coutinho, P
;
Barros, José
; Zemmouri, R; Guimaraes, J;
Alves, C
; Chorao, R; Lourenco, E; Ribeiro, P;
Loureiro, JL
;
Santos, JV
; Hamri, A; Paternotte, C; Hazan, J;
Silva, MC
; Prud'homme, JF;
Grid, D
;
PUBLISHED:
1999
,
SOURCE:
ARCHIVES OF NEUROLOGY,
VOLUME:
56,
ISSUE:
8
INDEXED IN:
Scopus
WOS
CrossRef
:
59
IN MY:
ORCID
50
TITLE:
Analysis of SCA1, DRPLA, MJD, SCA2, and SCA6 CAG repeats in 48 Portuguese ataxia families
Full Text
AUTHORS:
Silveira, I
;
Coutinho, P
;
Maciel, P
; Gaspar, C; Hayes, S; Dias, A; Guimaraes, J; Loureiro, L;
Sequeiros, J
; Rouleau, GA;
PUBLISHED:
1998
,
SOURCE:
AMERICAN JOURNAL OF MEDICAL GENETICS,
VOLUME:
81,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
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