Genomics < Genotype < Geriatric Assessment

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 214.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000003 (1999)	D C Wan [Hong Kong] ; L K Law ; D T Ip ; W T Cheung ; W K Ho ; K W Tsim ; R. Kay ; J. Woo ; C P Pang	Lack of allelic association of dopamine D4 receptor gene polymorphisms with Parkinson's disease in a Chinese population.
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.
000130 (1999)	L. Baum [République populaire de Chine] ; Z Y Dong ; H K Ng ; L K Law ; J. Woo ; C P Pang	Low-density lipoprotein receptor-related protein (LRP) gene 766T polymorphism and Parkinson's disease.
000173 (1999)	M G Sieberer [Allemagne] ; P. Vieregge ; C. Klein ; L J Ozelius ; K P Wandinger	Concordant late onset of craniocervical dystonia in a pair of monozygotic twins.
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.
000285 (2000)	J J Higgins [États-Unis] ; K. Kluetzman ; J. Berciano ; O. Combarros ; J M Loveless	Posterior column ataxia and retinitis pigmentosa: a distinct clinical and genetic disorder.
000310 (2000)	D M Maraganore [États-Unis] ; M J Farrer ; J A Hardy ; S K Mcdonnell ; D J Schaid ; W A Rocca	Case-control study of debrisoquine 4-hydroxylase, N-acetyltransferase 2, and apolipoprotein E gene polymorphisms in Parkinson's disease.
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.
000362 (2000)	I. Mizuta [Japon] ; E. Mizuta ; S. Yamasaki ; S. Kuno ; M. Yasuda ; C. Tanaka	Meta-analysis of polymorphism of the catechol-O-methyltransferase gene in relation to the etiology of Parkinson's disease in Japan.
000366 (2000)	S N Illarioshkin [Russie] ; I A Ivanova-Smolenskaya ; R A Rahmonov ; E D Markova ; G. Stevanin ; A. Brice	Clinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan.
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.
000473 (2001)	B S Harhangi [Pays-Bas] ; B A Oostra ; P. Heutink ; C M Van Duijn ; A. Hofman ; M M Breteler	CYP2D6 polymorphism in Parkinson's disease: the Rotterdam Study.
000501 (2001)	L I Golbe [États-Unis] ; A M Lazzarini ; J R Spychala ; W G Johnson ; E S Stenroos ; M H Mark ; J I Sage	The tau A0 allele in Parkinson's disease.
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.
000837 (2002)	Andrea Carmine [Suède] ; Silvia Buervenich ; Olof Sydow ; Maria Anvret ; Lars Olson	Further evidence for an association of the paraoxonase 1 (PON1) Met-54 allele with Parkinson's disease.
000838 (2002)	Jian Wang [République populaire de Chine] ; Chun-Ying Zhao ; Yan-Mei Si ; Zhuo-Lin Liu ; Biao Chen ; Long Yu	ACT and UCH-L1 polymorphisms in Parkinson's disease and age of onset.
000846 (2002)	Masataka Nishimura [Japon] ; Hideshi Kawakami ; Osamu Komure ; Hirofumi Maruyama ; Hiroyuki Morino ; Yuishin Izumi ; Shigenobu Nakamura ; Ryuji Kaji ; Sadako Kuno	Contribution of the interleukin-1beta gene polymorphism in multiple system atrophy.
000851 (2002)	Masataka Nishimura [Japon] ; Ryuji Kaji ; Mitsuhiro Ohta ; Ikuko Mizuta ; Sadako Kuno	Association between dopamine transporter gene polymorphism and susceptibility to Parkinson's disease in Japan.
000907 (2002)	Chin-Song Lu [Taïwan] ; Yah-Huei Wu Chou ; Tzu-Chen Yen ; Chon-Haw Tsai ; Rou-Shayn Chen ; Hsiu-Chen Chang	Dopa-responsive parkinsonism phenotype of spinocerebellar ataxia type 2.

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