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Carolina Luísa Cardoso Lemos
AuthID:
R-000-JQQ
Publications
Confirmed
To Validate
Document Source:
All
Document Type:
All Document Types
Article (52)
Abstract (6)
Article in Press (5)
Unpublished (3)
Review (2)
Letter (1)
Correction (1)
Year Start - End:
2006
2007
2008
2009
2010
2011
2012
2013
2014
2015
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2017
2018
2019
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2025
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2018
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2012
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2007
2006
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: 70
61
TITLE:
Familial Aggregation of Maxillary Lateral Incisor Agenesis
AUTHORS:
Pinho, T
;
Maciel, P
;
Lemos, C
;
Sousa, A
;
PUBLISHED:
2010
,
SOURCE:
JOURNAL OF DENTAL RESEARCH,
VOLUME:
89,
ISSUE:
6
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
62
TITLE:
Familial Clustering of Migraine: Further Evidence From a Portuguese Study
Full Text
AUTHORS:
Carolina Lemos
; Maria Jose Castro;
Barros, José
;
Jorge Sequeiros
;
Jose Pereira Monteiro
;
Denisa Mendonca
;
Alda Sousa
;
PUBLISHED:
2009
,
SOURCE:
HEADACHE,
VOLUME:
49,
ISSUE:
3
INDEXED IN:
Scopus
WOS
CrossRef
:
23
IN MY:
ORCID
|
ResearcherID
63
TITLE:
First mutation in the voltage-gated Na(V)1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy
Full Text
AUTHORS:
Castro, MJ; Stam, AH;
Lemos, C
; de Vries, B;
Vanmolkot, KRJ
;
Barros, José
;
Terwindt, GM
; Frants, RR;
Sequeiros, J
; Ferrari, MD;
Pereira Monteiro, JM
;
van den Maagdenberg, AMJM
;
PUBLISHED:
2009
,
SOURCE:
CEPHALALGIA,
VOLUME:
29,
ISSUE:
3
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
64
TITLE:
Role of the Disease in the Psychological Impact of Pre-Symptomatic Testing for SCA2 and FAP ATTRV30M: Experience with the Disease, Kinship and Gender of the Transmitting Parent
Full Text
AUTHORS:
Milena Paneque
;
Carolina Lemos
;
Alda Sousa
; Luis Velazquez;
Manuela Fleming
;
Jorge Sequeiros
;
PUBLISHED:
2009
,
SOURCE:
JOURNAL OF GENETIC COUNSELING,
VOLUME:
18,
ISSUE:
5
INDEXED IN:
Scopus
WOS
CrossRef
:
19
IN MY:
ORCID
|
ResearcherID
65
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
|
ResearcherID
66
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
|
ResearcherID
67
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
68
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
|
ResearcherID
69
TITLE:
Migraine: Familial distribution in a Portuguese population [Enxaqueca: Distribuição familiar numa população portuguesa]
AUTHORS:
Lemos, C
; Castro, MJ; Mendonca, T;
Barros, José
;
Pereira Monteiro, JM
;
PUBLISHED:
2006
,
SOURCE:
Sinapse,
VOLUME:
6,
ISSUE:
1
INDEXED IN:
Scopus
IN MY:
ORCID
70
TITLE:
Novel recurrent mutation in ATP1A2 gene in a Portuguese family with familiar hemiplegic migraine type 2 [Nova mutação recorrente no gene ATP1A2 numa familia portuguesa com enxaqueca hemiplégica familiar tipo 2]
AUTHORS:
Castro, MJ; Barros, J;
Lemos, C
; Mendes, A; Vanmolkot, K; Frants, R;
Sequeiros, J
; Monteiro, JP; van den Maagdenberg, A;
PUBLISHED:
2006
,
SOURCE:
Sinapse,
VOLUME:
6,
ISSUE:
2
INDEXED IN:
Scopus
IN MY:
ORCID
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