Lemos C - Search Results

1

Overcoming artefact: anticipation in 284 Portuguese kindreds with familial amyloid polyneuropathy (FAP) ATTRV30M.

Lemos C, Coelho T, Alves-Ferreira M, Martins-da-Silva A, Sequeiros J, Mendonça D, Sousa A. Lemos C, et al. J Neurol Neurosurg Psychiatry. 2014 Mar;85(3):326-30. doi: 10.1136/jnnp-2013-305383. Epub 2013 Sep 17. J Neurol Neurosurg Psychiatry. 2014. PMID: 24046394

2

Psychological follow-up of presymptomatic genetic testing for spinocerebellar ataxia type 2 (SCA2) in Cuba.

Paneque M, Lemos C, Escalona K, Prieto L, Reynaldo R, Velázquez M, Quevedo J, Santos N, Almaguer LE, Velázquez L, Sousa A, Fleming M, Sequeiros J. Paneque M, et al. Among authors: lemos c. J Genet Couns. 2007 Aug;16(4):469-79. doi: 10.1007/s10897-006-9083-y. Epub 2007 Feb 23. J Genet Couns. 2007. PMID: 17318452

3

Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine.

Castro MJ, Stam AH, Lemos C, Barros J, Gouveia RG, Martins IP, Koenderink JB, Vanmolkot KRJ, Mendes AP, Frants RR, Ferrari MD, Sequeiros J, Pereira-Monteiro JM, van den Maagdenberg AMJM. Castro MJ, et al. Among authors: lemos c. J Hum Genet. 2007;52(12):990-998. doi: 10.1007/s10038-007-0205-7. Epub 2007 Oct 19. J Hum Genet. 2007. PMID: 17952365

4

Two novel functional mutations in the Na+,K+-ATPase alpha2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes.

Castro MJ, Nunes B, de Vries B, Lemos C, Vanmolkot KR, van den Heuvel JJ, Temudo T, Barros J, Sequeiros J, Frants RR, Koenderink JB, Pereira-Monteiro JM, van den Maagdenberg AM. Castro MJ, et al. Among authors: lemos c. Clin Genet. 2008 Jan;73(1):37-43. doi: 10.1111/j.1399-0004.2007.00918.x. Epub 2007 Nov 19. Clin Genet. 2008. PMID: 18028456

5

Familial clustering of migraine: further evidence from a Portuguese study.

Lemos C, Castro MJ, Barros J, Sequeiros J, Pereira-Monteiro J, Mendonça D, Sousa A. Lemos C, et al. Headache. 2009 Mar;49(3):404-11. doi: 10.1111/j.1526-4610.2008.01177.x. Epub 2008 Jul 1. Headache. 2009. PMID: 18624713 Free article.

6

The C677T polymorphism in MTHFR is not associated with migraine in Portugal.

Ferro A, Castro MJ, Lemos C, Santos M, Sousa A, Pereira-Monteiro J, Sequeiros J, Maciel P. Ferro A, et al. Among authors: lemos c. Dis Markers. 2008;25(2):107-13. doi: 10.1155/2008/178679. Dis Markers. 2008. PMID: 18957721 Free PMC article.

7

First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy.

Castro MJ, Stam AH, Lemos C, de Vries B, Vanmolkot KR, Barros J, Terwindt GM, Frants RR, Sequeiros J, Ferrari MD, Pereira-Monteiro JM, van den Maagdenberg AM. Castro MJ, et al. Among authors: lemos c. Cephalalgia. 2009 Mar;29(3):308-13. doi: 10.1111/j.1468-2982.2008.01721.x. Cephalalgia. 2009. PMID: 19220312

8

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.

Paneque M, Lemos C, Sousa A, Velázquez L, Fleming M, Sequeiros J. Paneque M, et al. Among authors: lemos c. J Genet Couns. 2009 Oct;18(5):483-93. doi: 10.1007/s10897-009-9240-1. J Genet Couns. 2009. PMID: 19731000

9

Evidence of syntaxin 1A involvement in migraine susceptibility: a Portuguese study.

Lemos C, Pereira-Monteiro J, Mendonça D, Ramos EM, Barros J, Sequeiros J, Alonso I, Sousa A. Lemos C, et al. Arch Neurol. 2010 Apr;67(4):422-7. doi: 10.1001/archneurol.2010.37. Arch Neurol. 2010. PMID: 20385907

10

Familial aggregation of maxillary lateral incisor agenesis.

Pinho T, Maciel P, Lemos C, Sousa A. Pinho T, et al. Among authors: lemos c. J Dent Res. 2010 Jun;89(6):621-5. doi: 10.1177/0022034510364486. Epub 2010 Apr 16. J Dent Res. 2010. PMID: 20400722 Free article.

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