J Sequeiros
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Explore the profile of J Sequeiros including associated specialties, affiliations and a list of published articles.
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64
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1445
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Recent Articles
1.
Zhou X, Wang C, Ding D, Chen Z, Peng Y, Peng H, et al.
Sci Rep
. 2018 Mar;
8(1):3889.
PMID: 29497168
Multiple system atrophy (MSA) is a complex and multifactorial neurodegenerative disease, and its pathogenesis remains uncertain. Patients with MSA or spinocerebellar ataxia (SCA) show overlapping clinical phenotypes. Previous studies have...
2.
Gheno T, Furtado G, Saute J, Donis K, Fontanari A, Emmel V, et al.
Eur J Neurol
. 2017 Jun;
24(7):892-e36.
PMID: 28560845
Background And Purpose: Spinocerebellar ataxia type 10 is a neurodegenerative disorder that is due to an expanded ATTCT repeat tract in the ATXN10 gene. Our aim was to describe clinical...
3.
Alves-Ferreira M, Pinho T, Sousa A, Sequeiros J, Lemos C, Alonso I
Bull Group Int Rech Sci Stomatol Odontol
. 2014 Dec;
51(2):e17.
PMID: 25460790
Short Communication selected from the Oral Presentations of the 56th Congress of the Groupèment International pour la Recherche Scientifique en Stomatologie et Odontologie, Peñafiel (Portugal) May 2012.
4.
Paneque M, Mendes A, Guimaraes L, Sequeiros J, Skirton H
J Genet Couns
. 2014 Nov;
24(4):616-25.
PMID: 25363284
Quality assessment of genetic counseling practice for improving healthcare is a challenge for genetic services worldwide; however, there is scarce literature regarding quality issues in genetic counseling in the context...
5.
Alves-Ferreira M, Pinho T, Sousa A, Sequeiros J, Lemos C, Alonso I
J Dent Res
. 2014 Feb;
93(5):452-8.
PMID: 24554542
Tooth agenesis affects 20% of the world population, and maxillary lateral incisors agenesis (MLIA) is one of the most frequent subtypes, characterized by the absence of formation of deciduous or...
6.
Castilhos R, Souza A, Furtado G, Gheno T, Silva A, Vargas F, et al.
Clin Genet
. 2013 Oct;
86(4):373-7.
PMID: 24102565
The aim of this study was to identify the relative frequency of Huntington's disease (HD) and HD-like (HDL) disorders HDL1, HDL2, spinocerebellar ataxia type 2 (SCA2), SCA17, dentatorubral-pallidoluysian degeneration (DRPLA),...
7.
Lee J, Ramos E, Lee J, Gillis T, Mysore J, Hayden M, et al.
Neurology
. 2012 Feb;
78(10):690-5.
PMID: 22323755
Objective: Age at onset of diagnostic motor manifestations in Huntington disease (HD) is strongly correlated with an expanded CAG trinucleotide repeat. The length of the normal CAG repeat allele has...
8.
Emmel V, Alonso I, Jardim L, Saraiva-Pereira M, Sequeiros J
Clin Genet
. 2010 Dec;
79(1):100-2.
PMID: 21143471
No abstract available.
9.
Lemos C, Neto J, Pereira-Monteiro J, Mendonca D, Barros J, Sequeiros J, et al.
Eur J Neurol
. 2010 Oct;
18(4):649-55.
PMID: 20964792
Background And Purpose: Migraine is a common neurological disabling disorder, and anomalies of vascular function have been implied in its pathophysiology. Several findings point to a possible role of the...
10.
Sequeiros J, Ramos E, Cerqueira J, Costa M, Sousa A, Pinto-Basto J, et al.
Clin Genet
. 2010 Mar;
78(4):381-7.
PMID: 20236117
Large normal ('intermediate') alleles may produce de novo expansions in Huntington disease; nevertheless, there is very little evidence about their population prevalence and impact in daily practice, and there are...