Polyethylene Glycols (therapeutic use) < Polymerase Chain Reaction < Polymerase Chain Reaction (methods)

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 65.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000002 (1999)	G D Mellick [Australie] ; D D Buchanan ; S J Mccann ; K M James ; A G Johnson ; D R Davis ; N. Liyou ; D. Chan ; D G Le Couteur	Variations in the monoamine oxidase B (MAOB) gene are associated with Parkinson's disease.
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.
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.
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.
000371 (2000)	M. Tanaka ; K. Endo ; T. Suzuki ; A. Kakita ; H. Takahashi ; T. Sata	Parkinsonism in HIV encephalopathy.
000423 (2001)	D A Grimes [Canada] ; D. Bulman ; P S George-Hyslop ; A E Lang	Inherited myoclonus-dystonia: evidence supporting genetic heterogeneity.
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.
000799 (2002)	Pau Pastor [Espagne] ; Mario Ezquerra ; Eduardo Tolosa ; Esteban Mu Oz ; María José Martí ; Francesc Valldeoriola ; José Luís Molinuevo ; Matilde Calopa ; Rafael Oliva	Further extension of the H1 haplotype associated with progressive supranuclear palsy.
000831 (2002)	Sian D. Spacey [Royaume-Uni] ; Enza-Maria Valente ; Gurusidheshwar M. Wali ; Thomas T. Warner ; Paul R. Jarman ; Anthony H V. Schapira ; Peter H. Dixon ; Mary B. Davis ; Kailash P. Bhatia ; Nicholas W. Wood	Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene.
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.
000A04 (2003)	Giovanni Defazio [Italie] ; Francesco Brancati ; Enza Maria Valente ; Viviana Caputo ; Antonio Pizzuti ; Davide Martino ; Giovanni Abbruzzese ; Paolo Livrea ; Alfredo Berardelli ; Bruno Dallapiccola	Familial blepharospasm is inherited as an autosomal dominant trait and relates to a novel unassigned gene.
000B01 (2003)	David R. Lynch [États-Unis] ; P David Mozley ; Set Sokol ; Nicole M C. Maas ; Laura J. Balcer ; Andrew D. Siderowf	Lack of effect of polymorphisms in dopamine metabolism related genes on imaging of TRODAT-1 in striatum of asymptomatic volunteers and patients with Parkinson's disease.
000B70 (2003)	Enza-Maria Valente [Italie] ; Anjum Misbahuddin ; Francesco Brancati ; Mark R. Placzek ; Barbara Garavaglia ; Sergio Salvi ; Andrea Nemeth ; Charles Shaw-Smith ; Nardo Nardocci ; Anna-Rita Bentivoglio ; Alfredo Berardelli ; Roberto Eleopra ; Bruno Dallapiccola ; Thomas T. Warner	Analysis of the epsilon-sarcoglycan gene in familial and sporadic myoclonus-dystonia: evidence for genetic heterogeneity.
000B75 (2003)	Hyun Sook Kim [Corée du Sud] ; Myung Sik Lee	Frequencies of single nucleotide polymorphism in alcohol dehydrogenase7 gene in patients with multiple system atrophy and controls.
000C18 (2003)	Aida M. Bertoli-Avella [Pays-Bas] ; Jose L. Giroud-Benitez ; Vincenzo Bonifati ; Eduardo Alvarez-Gonzalez ; Luis Heredero-Baute ; Cornelia M. Van Duijn ; Peter Heutink	Suggestive linkage to chromosome 19 in a large Cuban family with late-onset Parkinson's disease.
000C27 (2003)	Sarah J. Lincoln [États-Unis] ; Demetrius M. Maraganore ; Timothy G. Lesnick ; Rebecca Bounds ; Mariza De Andrade ; James H. Bower ; John A. Hardy ; Matthew J. Farrer	Parkin variants in North American Parkinson's disease: cases and controls.
000C93 (2004)	Alex Desautels [Canada] ; Gustavo Turecki ; Lan Xiong ; Daniel Rochefort ; Jacques Montplaisir ; Guy A. Rouleau	Mutational analysis of neurotensin in familial restless legs syndrome.
000C97 (2004)	Susan Hollán [Hongrie] ; Lászl Vécsei ; Kálmán Magyar	Adverse effects of dopamine potentiation by long-term treatment with selegiline.
000D38 (2004)	Francesca Romana Pezzella [Italie] ; Maria Grazia Paglia ; Carlo Colosimo	Cerebrospinal fluid analysis for Whipple's disease in patients with progressive supranuclear palsy.
000E05 (2004)	Anthony C. Pereira [Royaume-Uni] ; Mark J. Edwards ; Philip C. Buttery ; Christopher H. Hawkes ; Niall P. Quinn ; Gavin Giovannoni ; Marios Hadjivassiliou ; Kailash P. Bhatia	Choreic syndrome and coeliac disease: a hitherto unrecognised association.

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