Huntington Disease (etiology) < Huntington Disease (genetics) < Huntington Disease (history)

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List of bibliographic references

Number of relevant bibliographic references: 109.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000017 (1999)	N. Georgiou [Australie] ; J L Bradshaw ; E. Chiu ; A. Tudor ; L. O'Gorman ; J G Phillips	Differential clinical and motor control function in a pair of monozygotic twins with Huntington's disease.
000171 (1999)	E D Louis [États-Unis] ; K. Marder ; C. Moskowitz ; P. Greene	Arm elevation in Huntington's disease: dystonia or levitation?
000187 (2000)	O. Bandmann [Royaume-Uni] ; J R Vaughan ; P. Holmans ; C D Marsden ; N W Wood	Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's disease.
000211 (2000)	E K Tan [États-Unis] ; Joseph Jankovic [États-Unis] ; W. Ondo	Bruxism in Huntington's disease.
000282 (2000)	E H Aylward [États-Unis] ; A M Codori ; A. Rosenblatt ; M. Sherr ; J. Brandt ; O C Stine ; P E Barta ; G D Pearlson ; C A Ross	Rate of caudate atrophy in presymptomatic and symptomatic stages of Huntington's disease.
000347 (2000)	R J Carter [Royaume-Uni] ; M J Hunt ; A J Morton	Environmental stimulation increases survival in mice transgenic for exon 1 of the Huntington's disease gene.
000358 (2000)	A. Destée [France] ; I. Delalande ; I. Vuillaume ; S. Schraen-Maschke ; L. Defebvre ; B. Sablonnière	The first identified French family with dentatorubral-pallidoluysian atrophy.
000491 (2001)	J. Müller [Autriche] ; G K Wenning ; J. Wissel ; Werner Poewe [Autriche]	Intrafamilial heterogeneity of facial hyperkinesias: chance association of tics, cranial dystonia, and Huntington's disease?
000517 (2001)	S. Bohlega [Arabie saoudite] ; A. Al-Tahan ; M. Kambouris ; M. Divakaran	Neurodegenerative Huntington-like disorder.
000569 (2001)	E D Louis ; E. Tampone	Bruxism in Huntington's disease.
000725 (2002)	Eric K. Richfield [États-Unis] ; Jean-Paul Vonsattel ; Marcy E. Macdonald ; Zhiqiang Sun ; Yun-Ping P. Deng ; Anton Reiner	Selective loss of striatal preprotachykinin neurons in a phenocopy of Huntington's disease.
000835 (2002)	Johannes Schiefer [Allemagne] ; G Bernhard Landwehrmeyer ; Hans-Gerd Lüesse ; Arne Sprünken ; Christiane Puls ; Anna Milkereit ; Eva Milkereit ; Christoph M. Kosinski	Riluzole prolongs survival time and alters nuclear inclusion formation in a transgenic mouse model of Huntington's disease.
000943 (2002)	Jean-Pascal Lefaucheur [France] ; Anne-Catherine Bachoud-Levi ; Catherine Bourdet ; Thierry Grandmougin ; Philippe Hantraye ; Pierre Cesaro ; Jean-Denis Degos ; Marc Peschanski ; Fabrice Lisovoski	Clinical relevance of electrophysiological tests in the assessment of patients with Huntington's disease.
000A09 (2003)	Stefan Evers [Allemagne] ; Florian Stögbauer	Genetic association of Huntington's disease and restless legs syndrome? A family report.
000B66 (2003)	Brian F. O'Donnell [États-Unis] ; Marcia A. Wilt ; Ann Marie Hake ; Julie C. Stout ; Sandra C. Kirkwood ; Tatiana Foroud	Visual function in Huntington's disease patients and presymptomatic gene carriers.
000B68 (2003)	Ruth H. Walker [États-Unis] ; Paul F. Good ; P. Shashidharan	TorsinA immunoreactivity in inclusion bodies in trinucleotide repeat diseases.
000C68 (2003)	Ruth H. Walker [États-Unis] ; Joseph Jankovic [États-Unis] ; Elizabeth O'Hearn ; Russell L. Margolis	Phenotypic features of Huntington's disease-like 2.
000E19 (2004)	Patrice Péran [France] ; Jean-François Démonet ; Cyril Pernet ; Dominique Cardebat	Verb and noun generation tasks in Huntington's disease.
000E86 (2004)	Shih-Ching Wang [Taïwan] ; Guey-Jen Lee-Chen ; Cheng-Kung Wang ; Chiung-Mei Chen ; Lok-Ming Tang ; Yih-Ru Wu	Markedly asymmetrical parkinsonism as a leading feature of adult-onset Huntington's disease.
001042 (2004)	Marina De Tommaso [Italie] ; Nicola Specchio ; Vittorio Sciruicchio ; Olimpia Difruscolo ; Luigi Maria Specchio	Effects of rivastigmine on motor and cognitive impairment in Huntington's disease.
001075 (2005)	Aideen Mcinerney-Leo [États-Unis] ; Donald W. Hadley ; Katrina Gwinn-Hardy ; John Hardy	Genetic testing in Parkinson's disease.

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