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Neurology, ISSN 0028-3878, 03/2012, Volume 78, Issue 10, pp. 690 - 695
Objective: Age at onset of diagnostic motor manifestations in Huntington disease (HD) is strongly correlated with an expanded CAG trinucleotide repeat. The... 
HOMOZYGOSITY | ALLELE | OF-ONSET | GENE | LENGTH | MUTATION | CHROMOSOMES | CLINICAL NEUROLOGY | TRINUCLEOTIDE REPEAT | Humans | Age of Onset | Alleles | Huntington Disease - genetics | Adult | Female | Genotype | Huntington Disease - diagnosis | Male | Trinucleotide Repeat Expansion | 164
Journal Article
Clinical Genetics, ISSN 0009-9163, 03/2016, Volume 89, Issue 3, pp. 275 - 284
Journal Article
NATURE REVIEWS NEUROLOGY, ISSN 1759-4758, 11/2015, Volume 11, Issue 11, pp. 618 - 619
Since 2005, we have made substantial progress in understanding the pathophysiology and natural history of movement disorders such as Parkinson disease and... 
DIAGNOSIS | HUNTINGTONS-DISEASE | PROGRESSION | ONSET | CLINICAL NEUROLOGY | PARKINSONS-DISEASE | Complications and side effects | Care and treatment | Neurotransmitters | Parkinson's disease | Influence | Research | Movement disorders | Risk factors
Journal Article
Neurogenetics, ISSN 1364-6745, 2013, Volume 14, Issue 3-4, pp. 173 - 179
Journal Article
Journal Article
by Braisch, U and Muche, R and Rothenbacher, D and Landwehrmeyer, GB and Long, JD and Orth, M and Bachoud-Levi, AC and Bentivoglio, AR and Biunno, I and Bonelli, RM and Burgunder, JM and Dunnett, SB and Ferreira, JJ and Handley, OJ and Heiberg, A and Illmann, T and Levey, J and Ramos-Arroyo, M and Nielsen, JE and Koivisto, SP and Paivarinta, M and Roos, RAC and Sebastian, AR and Tabrizi, SJ and Vandenberghe, W and Verellen-Dumoulin, C and Uhrova, T and Wahlstrom, J and Zaremba, J and Baake, V and Barth, K and Bos, R and Come, A and Guedes, LC and Finisterra, AM and Garde, MB and Betz, S and Callaghan, J and Capodarca, S and Wildson, SC and da Silva, V and Di Renzo, M and Ecker, D and Finisterra, M and Fullam, R and Genoves, C and Gilling, M and Hvalstedt, C and Held, C and Koppers, K and Lamanna, C and Laura, M and Descals, AM and Martinez-Horta, S and Mestre, T and Minster, S and Monza, D and Mutze, L and Oehmen, M and Padieu, H and Paterski, L and Peppa, N and Rindal, B and Roren, N and Sasinkova, P and Seliverstov, Y and Timewell, E and Townhill, J and Cubillo, PT and van Walsem, MR and Witjes-Ane, MN and Witkowski, G and Wright, A and Yudina, E and Zielonka, D and Zielonka, E and Zinzi, P and Braunwarth, EM and Brugger, F and Buratti, L and Hametner, EM and Hepperger, C and Holas, C and Hotter, A and Hussl, A and Larcher, B and Mahlknecht, P and Muller, C and Pinter, B and Poewe, W and Seppi, K and Sprenger, F and Wenning, G and Dupuis, M and Minet, C and Ribai, P and Van Paemel, D and Klempir, J and Majerova, V and Roth, J and ...
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, ISSN 1552-485X, 2019, Volume 180, Issue 3, p. 232
Journal Article
Journal Article
Cell, ISSN 0092-8674, 02/2018, Volume 172, Issue 5, pp. 924 - 936.e11
Journal Article
Parkinsonism and Related Disorders, ISSN 1353-8020, 2006, Volume 13, Issue 8, pp. 535 - 536
Journal Article
Journal Article
Movement Disorders, ISSN 0885-3185, 04/2015, Volume 30, Issue 4, pp. 500 - 509
Journal Article