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Page 1
Unraveling the role of relative telomere length and CAG expansion on initial symptoms of juvenile Huntington disease.
PerezGrovas-Saltijeral A, Ochoa-Morales A, Jara-Prado A, Velázquez-Cruz R, Rivera-Paredez B, Dávila-OrtizdeMontellano D, Benítez-Alonso EO, Santamaría-Olmedo M, Sevilla-Montoya R, Marfil-Marín E, Valdés-Flores M, Martínez-Ruano L, Camacho-Molina A, Hidalgo-Bravo A. PerezGrovas-Saltijeral A, et al. Eur J Neurol. 2023 Mar;30(3):612-621. doi: 10.1111/ene.15644. Epub 2022 Dec 8. Eur J Neurol. 2023. PMID: 36421025
Juvenile Huntington disease in Argentina.
Gatto EM, Parisi V, Etcheverry JL, Sanguinetti A, Cordi L, Binelli A, Persi G, Squitieri F. Gatto EM, et al. Arq Neuropsiquiatr. 2016 Jan;74(1):50-4. doi: 10.1590/0004-282X20150192. Epub 2015 Nov 24. Arq Neuropsiquiatr. 2016. PMID: 26602194 Free article.
We analyzed demographic, clinical and genetic characteristics of juvenile Huntington disease (JHD) and it frequency in an Argentinean cohort. ...
We analyzed demographic, clinical and genetic characteristics of juvenile Huntington disease (JHD) and it frequency in …
Juvenile Huntington disease in the Netherlands.
Siesling S, Vegter-van der Vlis M, Roos RA. Siesling S, et al. Pediatr Neurol. 1997 Jul;17(1):37-43. doi: 10.1016/s0887-8994(97)00069-6. Pediatr Neurol. 1997. PMID: 9308974
Juvenile Huntington disease (JHD) patients are distinguished from adult patients by an age at onset of less than 20 years. ...
Juvenile Huntington disease (JHD) patients are distinguished from adult patients by an age at onset of less than 20 yea …
Psychiatric and cognitive difficulties as indicators of juvenile huntington disease onset in 29 patients.
Ribaï P, Nguyen K, Hahn-Barma V, Gourfinkel-An I, Vidailhet M, Legout A, Dodé C, Brice A, Dürr A. Ribaï P, et al. Arch Neurol. 2007 Jun;64(6):813-9. doi: 10.1001/archneur.64.6.813. Arch Neurol. 2007. PMID: 17562929
BACKGROUND: Juvenile Huntington disease (JHD) is a rare clinical entity characterized by an age at onset younger than 20 years. ...
BACKGROUND: Juvenile Huntington disease (JHD) is a rare clinical entity characterized by an age at onset younger than 2 …
The gender effect in juvenile Huntington disease patients of Italian origin.
Cannella M, Gellera C, Maglione V, Giallonardo P, Cislaghi G, Muglia M, Quattrone A, Pierelli F, Di Donato S, Squitieri F. Cannella M, et al. Am J Med Genet B Neuropsychiatr Genet. 2004 Feb 15;125B(1):92-8. doi: 10.1002/ajmg.b.20110. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 14755452
We analyzed a population of juvenile Huntington disease (HD) subjects of Italian origin (n = 57). ...
We analyzed a population of juvenile Huntington disease (HD) subjects of Italian origin (n = 57). ...
Clinical presentation of juvenile Huntington disease.
Ruocco HH, Lopes-Cendes I, Laurito TL, Li LM, Cendes F. Ruocco HH, et al. Arq Neuropsiquiatr. 2006 Mar;64(1):5-9. doi: 10.1590/s0004-282x2006000100002. Epub 2006 Apr 5. Arq Neuropsiquiatr. 2006. PMID: 16622544 Free article.
Early testing for Huntington disease in children: pros and cons.
Toufexis M, Gieron-Korthals M. Toufexis M, et al. J Child Neurol. 2010 Apr;25(4):482-4. doi: 10.1177/0883073809343315. Epub 2009 Oct 6. J Child Neurol. 2010. PMID: 19808987
Premature testing of a child or fetus carries complex medical and psychological issues to both the child and the family that need to be considered and explored more than in an adult with Huntington disease. We suggest that a child at risk for juvenile Huntington …
Premature testing of a child or fetus carries complex medical and psychological issues to both the child and the family that need to be cons …
Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent.
Telenius H, Kremer HP, Theilmann J, Andrew SE, Almqvist E, Anvret M, Greenberg C, Greenberg J, Lucotte G, Squitieri F, et al. Telenius H, et al. Hum Mol Genet. 1993 Oct;2(10):1535-40. doi: 10.1093/hmg/2.10.1535. Hum Mol Genet. 1993. PMID: 8268906
Juvenile Huntington disease (HD), characterised by onset of symptoms before the age of 20 with rigidity and intellectual decline, is associated with a predominance of affected fathers. ...This study demonstrates that the sex of transmitting parent is the majo …
Juvenile Huntington disease (HD), characterised by onset of symptoms before the age of 20 with rigidity and intellectua …