Genetic Markers < Genetic Predisposition to Disease < Genetic Research

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 195.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000004 (1999)	N. Sabbagh [France] ; A. Brice ; D. Marez ; A. Dürr ; M. Legrand ; J M Lo Guidice ; A. Destée ; Yves Agid [France] ; F. Broly	CYP2D6 polymorphism and Parkinson's disease susceptibility.
000078 (1999)	O. Joost [États-Unis] ; C A Taylor ; C A Thomas ; L A Cupples ; M H Saint-Hilaire ; R G Feldman ; C T Baldwin ; R H Myers	Absence of effect of seven functional mutations in the CYP2D6 gene in Parkinson's disease.
000127 (1999)	A H Németh [Royaume-Uni] ; K R Mills ; J S Elston ; A. Williams ; E. Dunne ; N M Hyman	Do the same genes predispose to Gilles de la Tourette syndrome and dystonia? Report of a new family and review of the literature.
000162 (1999)	D L Picchietti [États-Unis] ; D J Underwood ; W A Farris ; A S Walters ; M M Shah ; R E Dahl ; L J Trubnick ; M A Bertocci ; M. Wagner ; W A Hening	Further studies on periodic limb movement disorder and restless legs syndrome in children with attention-deficit hyperactivity disorder.
000169 (1999)	A. Minguez-Castellanos [Espagne] ; C. Carnero-Pardo ; A. G Mez-Camello ; A. Ortega-Moreno ; T. García-G Mez ; V. Arjona ; J M Martin-Linares	Primary writing tremor treated by chronic thalamic stimulation.
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.
000199 (2000)	R L Oliveri [Italie] ; G. Annesi ; M. Zappia ; D. Civitelli ; E V De Marco ; A A Pasqua ; F. Annesi ; P. Spadafora ; A. Gambardella ; G. Nicoletti ; D. Branca ; M. Caracciolo ; U. Aguglia ; A. Quattrone	The dopamine D2 receptor gene is a susceptibility locus for Parkinson's disease.
000330 (2000)	S. Buervenich [Suède] ; O. Sydow ; A. Carmine ; Z. Zhang ; M. Anvret ; L. Olson	Alcohol dehydrogenase alleles in Parkinson's disease.
000341 (2000)	S. Hayashi [Japon] ; K. Wakabayashi ; A. Ishikawa ; H. Nagai ; M. Saito ; M. Maruyama ; T. Takahashi ; T. Ozawa ; S. Tsuji ; H. Takahashi	An autopsy case of autosomal-recessive juvenile parkinsonism with a homozygous exon 4 deletion in the parkin gene.
000351 (2000)	F. Masuhr [Allemagne] ; J. Wissel ; J. Müller ; U. Scholz ; Werner Poewe [Autriche]	Quantification of sensory trick impact on tremor amplitude and frequency in 60 patients with head tremor.
000369 (2000)	F. Cardoso [Brésil] ; J T De Oliveira ; M. Puccioni-Sohler ; A R Fernandes ; J P De Mattos ; I. Lopes-Cendes	Eyelid dystonia in Machado-Joseph disease.
000372 (2000)	H S Singer [États-Unis]	Current issues in Tourette syndrome.
000398 (2000)	C. Kamm [Allemagne] ; M. Naumann ; J. Mueller ; N. Mai ; L. Riedel ; J. Wissel ; T. Gasser	The DYT1 GAG deletion is infrequent in sporadic and familial writer' s cramp.
000405 (2000)	J. Wang [République populaire de Chine] ; Z. Liu	No association between paraoxonase 1 (PON1) gene polymorphisms and susceptibility to Parkinson's disease in a Chinese population.
000406 (2000)	J. Wang [République populaire de Chine] ; Z. Liu ; P. Chan	Lack of association between cytochrome P450 2E1 gene polymorphisms and Parkinson's disease in a Chinese population.
000496 (2001)	A. Lees	Jumpers.
000508 (2001)	P C Jedynak [France] ; C. Tranchant ; D Z De Beyl	Prospective clinical study of writer's cramp.
000516 (2001)	D A Mcfarling [États-Unis]	The "Ragin' Cajuns" of Louisiana.
000578 (2001)	E D Louis [États-Unis]	Etiology of essential tremor: should we be searching for environmental causes?
000620 (2001)	P. Pastor [Espagne] ; E. Mu Oz ; M. Ezquerra ; V. Obach ; M J Martí ; F. Valldeoriola ; E. Tolosa ; R. Oliva	Analysis of the coding and the 5' flanking regions of the alpha-synuclein gene in patients with Parkinson's disease.
000727 (2002)	Puneet Opal [États-Unis] ; Ron Tintner ; Joseph Jankovic [États-Unis] ; Joanne Leung ; Xandra O. Breakefield ; Jennifer Friedman ; Laurie Ozelius	Intrafamilial phenotypic variability of the DYT1 dystonia: from asymptomatic TOR1A gene carrier status to dystonic storm.

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