Januário C - Search Results

1

Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practice.

Costa MC, Magalhães P, Ferreirinha F, Guimarães L, Januário C, Gaspar I, Loureiro L, Vale J, Garrett C, Regateiro F, Magalhães M, Sousa A, Maciel P, Sequeiros J. Costa MC, et al. Among authors: januario c. Eur J Hum Genet. 2003 Nov;11(11):872-8. doi: 10.1038/sj.ejhg.5201055. Eur J Hum Genet. 2003. PMID: 14571273

2

Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.

Silveira I, Miranda C, Guimarães L, Moreira MC, Alonso I, Mendonça P, Ferro A, Pinto-Basto J, Coelho J, Ferreirinha F, Poirier J, Parreira E, Vale J, Januário C, Barbot C, Tuna A, Barros J, Koide R, Tsuji S, Holmes SE, Margolis RL, Jardim L, Pandolfo M, Coutinho P, Sequeiros J. Silveira I, et al. Among authors: januario c. Arch Neurol. 2002 Apr;59(4):623-9. doi: 10.1001/archneur.59.4.623. Arch Neurol. 2002. PMID: 11939898

3

Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY.

Orth M; European Huntington's Disease Network; Handley OJ, Schwenke C, Dunnett S, Wild EJ, Tabrizi SJ, Landwehrmeyer GB. Orth M, et al. J Neurol Neurosurg Psychiatry. 2011 Dec;82(12):1409-12. doi: 10.1136/jnnp.2010.209668. Epub 2010 Nov 19. J Neurol Neurosurg Psychiatry. 2011. PMID: 21097549 No abstract available.

4

Independent patterns of damage within magno-, parvo- and koniocellular pathways in Parkinson's disease.

Silva MF, Faria P, Regateiro FS, Forjaz V, Januário C, Freire A, Castelo-Branco M. Silva MF, et al. Among authors: januario c. Brain. 2005 Oct;128(Pt 10):2260-71. doi: 10.1093/brain/awh581. Epub 2005 Jul 6. Brain. 2005. PMID: 16000338 Free article.

5

Parkinson's disease and mitochondrial DNA NADH dehydrogenase subunit 1 nucleotides 3337-3340: study in a population from the central region of Portugal (Coimbra).

Grazina M, Silva F, Januário C, Oliveira M, Cunha L, Oliveira C. Grazina M, et al. Among authors: januario c. Eur Neurol. 2003;50(1):60-1. doi: 10.1159/000070863. Eur Neurol. 2003. PMID: 12824717 No abstract available.

6

Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study.

McNulty P, Pilcher R, Ramesh R, Necuiniate R, Hughes A, Farewell D, Holmans P, Jones L; REGISTRY Investigators of the European Huntington's Disease Network. McNulty P, et al. J Huntingtons Dis. 2018;7(3):209-222. doi: 10.3233/JHD-170263. J Huntingtons Dis. 2018. PMID: 30103338

7

Prevalence of Parkinson's disease: a population-based study in Portugal.

Ferreira JJ, Gonçalves N, Valadas A, Januário C, Silva MR, Nogueira L, Vieira JLM, Lima AB. Ferreira JJ, et al. Among authors: januario c. Eur J Neurol. 2017 May;24(5):748-750. doi: 10.1111/ene.13273. Epub 2017 Mar 2. Eur J Neurol. 2017. PMID: 28251720

8

Apathy Profile in Parkinson's and Huntington's Disease: A Comparative Cross-Sectional Study.

Sousa M, Moreira F, Jesus-Ribeiro J, Marques I, Cunha F, Canário N, Freire A, Januário C. Sousa M, et al. Among authors: januario c. Eur Neurol. 2018;79(1-2):13-20. doi: 10.1159/000481981. Epub 2017 Nov 13. Eur Neurol. 2018. PMID: 29131091

9

The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients.

Metzger S, Walter C, Riess O, Roos RA, Nielsen JE, Craufurd D; REGISTRY Investigators of the European Huntington’s Disease Network; Nguyen HP. Metzger S, et al. PLoS One. 2013 Jul 22;8(7):e68951. doi: 10.1371/journal.pone.0068951. Print 2013. PLoS One. 2013. PMID: 23894380 Free PMC article.

10

G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort.

Bras JM, Guerreiro RJ, Ribeiro MH, Januario C, Morgadinho A, Oliveira CR, Cunha L, Hardy J, Singleton A. Bras JM, et al. Among authors: januario c. Mov Disord. 2005 Dec;20(12):1653-5. doi: 10.1002/mds.20682. Mov Disord. 2005. PMID: 16149095

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