Gène And NotAlexis Brice

List of bibliographic references

Number of relevant bibliographic references: 37.

Ident.	Authors (with country if any)	Title
002319	Yoshiki Sekijima [Japon] ; Takao Hashimoto [Japon] ; Osam Onodera [Japon] ; Hidetoshi Date [Japon] ; Tomomi Okano [Japon] ; Kosuke Naito [Japon] ; Shoji Tsuji [Japon] ; Shu-Ichi Ikeda [Japon]	Severe generalized dystonia as a presentation of a patient with aprataxin gene mutation
002412	Marina A. J. Tijssen [Pays-Bas, Royaume-Uni] ; Peter Brown [Royaume-Uni] ; David Macmanus [Royaume-Uni] ; Mary A. Mclean [Royaume-Uni] ; Charles Davie [Royaume-Uni]	Magnetic resonance spectroscopy of cerebral cortex is normal in hereditary hyperekplexia due to mutations in the GLRA1 gene
002428	Masataka Nishimura [Japon] ; Sadako Kuno [Japon] ; Ikuko Mizuta [Japon] ; Mitsuhiro Ohta [Japon] ; Hirofumi Maruyama [Japon] ; Ryuji Kaji [Japon] ; Hideshi Kawakami [Japon]	Influence of monocyte chemoattractant protein 1 gene polymorphism on age at onset of sporadic Parkinson's disease
002447	HYUN SOOK KIM [Corée du Sud] ; MYUNG SIK LEE [Corée du Sud]	Frequencies of single nucleotide polymorphism in alcohol dehydrogenase7 gene in patients with multiple system atrophy and controls
002460	Simona Pigullo [Italie] ; Emilio Di Maria [Italie] ; Roberta Marchese [Italie] ; Emilia Bellone [Italie] ; Rossella Gulli [Italie] ; Cesa Scaglione [Italie] ; Stella Battaglia [Italie] ; Paolo Barone [Italie] ; Paolo Martinelli [Italie] ; Giovanni Abbruzzese [Italie] ; Franco Ajmar [Italie] ; Paola Mandich [Italie]	Essential tremor is not associated with α-synuclein gene haplotypes
002538	Enza-Maria Valente [Italie] ; Anjum Misbahuddin [Royaume-Uni] ; Francesco Brancati [Italie] ; Mark R. Placzek [Royaume-Uni] ; Barbara Garavaglia [Italie] ; Sergio Salvi [Italie] ; Andrea Nemeth [Royaume-Uni] ; Charles Shaw-Smith [Royaume-Uni] ; Nardo Nardocci [Italie] ; Anna-Rita Bentivoglio [Italie] ; Alfredo Berardelli [Italie] ; Roberto Eleopra [Italie] ; Bruno Dallapiccola [Italie] ; Thomas T. Warner [Royaume-Uni]	Analysis of the ∈-sarcoglycan gene in familial and sporadic myoclonus-dystonia: Evidence for genetic heterogeneity
002698	Marina A. J. Tijssen [Pays-Bas] ; Monique N. Vergouwe [Pays-Bas] ; J. Gert Van Dijk [Pays-Bas] ; Michelle Rees [Royaume-Uni] ; Rune R. Fronts [Pays-Bas] ; Peter Brown [Royaume-Uni]	Major and minor form of hereditary hyperekplexia
002749	DANQING ZHU [Australie] ; Christopher Burke [Australie] ; Anthony Leslie [Australie] ; Garth A. Nicholson [Australie]	Friedreich's ataxia with chorea and myoclonus caused by a compound heterozygosity for a novel deletion and the trinucleotide GAA expansion
002820	Masataka Nishimura [Japon] ; Hideshi Kawakami [Japon] ; Osamu Komure [Japon] ; Hirofumi Maruyama [Japon] ; Hiroyuki Morino [Japon] ; Yuishin Izumi [Japon] ; Shigenobu Nakamura [Japon] ; Ryuji Kaji [Japon] ; Sadako Kuno [Japon]	Contribution of the interleukin-1β gene polymorphism in multiple system atrophy
002828	Ruey-Meei Wu [Taïwan] ; Din-E Shan [Taïwan] ; Chen-Ming Sun [Taïwan] ; Ren-Shyan Liu [Taïwan] ; Wuh-Liang Hwu [Taïwan] ; Chun-Hwei Tai [Taïwan] ; Jennifer Hussey [États-Unis] ; Andrew West [États-Unis] ; Katrina Gwinn-Hardy [États-Unis] ; John Hardy [États-Unis] ; Judy Chen [États-Unis] ; Matt Farrer [États-Unis] ; Sarah Lincoln [États-Unis]	Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and parkin gene mutations
002835	Demetrius M. Maraganore [États-Unis] ; Matthew J. Fairer [États-Unis] ; Shannon K. Mcdonnell [États-Unis] ; Alexis Elbaz [États-Unis] ; Daniel J. Schaid [États-Unis] ; John A. Hardy [États-Unis] ; Walter A. Rocca [États-Unis]	Case-control study of estrogen receptor gene polymorphisms in Parkinson's disease
002923	Hiroshi Ujike [Japon] ; Mitsutoshi Yamamoto [Japon] ; Akihiro Kanzaki [Japon] ; Kazuya Okumura [Japon] ; Manabu Takaki [Japon] ; Shigetoshi Kuroda [Japon]	Prevalence of homozygous deletions of the parkin gene in a cohort of patients with sporadic and familial Parkinson's disease
002946	J. Hoenicka [Espagne] ; L. Vidal [Espagne] ; M. Godoy [Espagne] ; J. J. Ochoa [Espagne] ; J. Garcia De Yebenes [Espagne]	New nonsense mutation in the GTP-cyclohydrolase I gene in L-DOPA responsive dystonia-parkinsonism
002957	Massimo Pandolfo [Canada]	Molecular basis of friedreich ataxia
002A34	S. Bostantjopoulou [Grèce] ; Z. Katsarou [Grèce] ; A. Papadimitriou [Grèce] ; V. Veletza [Grèce] ; G. Hatzigeorgiou [Grèce] ; A. Lees [Royaume-Uni]	Clinical features of parkinsonian patients with the α-synuclein (G209A) mutation
002A35	C.-S. Lu [Taïwan] ; J.-C. Wu [Taïwan] ; C.-H. Tsai [Taïwan] ; R.-S. Chen [Taïwan] ; Y.-H. Wu Chou [Taïwan] ; N. Hattori [Japon] ; H. Yoshino [Japon] ; Y. Mizuno [Japon]	Clinical and genetic studies on familial parkinsonism : The first report on a Parkin gene mutation in a Taiwanese family
002B56	JIAN WANG [République populaire de Chine] ; ZHUOLIN LIU [République populaire de Chine]	No association between paraoxonase 1 (PON1) gene polymorphisms and susceptibility to Parkinson's disease in a chinese population
002B70	Ikuko Mizuta [Japon] ; Eiji Mizuta [Japon] ; Shunzou Yamasaki [Japon] ; Sadako Kuno [Japon] ; Minoru Yasuda [Japon] ; Chikako Tanaka [Japon]	Meta-analysis of polymorphism of the catechol-O-methyltransferase gene in relation to the etiology of Parkinson's disease in Japan
002B71	Maria Teresa Dotti [Italie] ; Carla Battisti [Italie] ; Alessandro Malandrini [Italie] ; Antonio Federico [Italie] ; Justin P. Rubio [Australie] ; Giuseppe Circiarello [Italie] ; Anthony P. Monaco [Royaume-Uni]	Mcleod syndrome and neuroacanthocytosis with a novel mutation in the XK gene
002B79	JIAN WANG [République populaire de Chine] ; ZHUOLIN LIU [République populaire de Chine] ; PIU CHAN [États-Unis]	Lack of association between cytochrome P450 2E1 gene polymorphisms and Parkinson's disease in a chinese population
002B86	L. C. Abbott [États-Unis] ; M. Bump [États-Unis] ; A. Brandl [États-Unis] ; S. De Laune [États-Unis]	Investigation of the role of the cerebellum in the myoclonic-like movement disorder exhibited by tottering mice
002C66	Shintaro Hayashi [Japon] ; Koichi Wakabayashi [Japon] ; Atsushi Ishikawa [Japon] ; Hiroko Nagai [Japon] ; Masaaki Saito [Japon] ; Mieko Maruyama [Japon] ; Toshiaki Takahashi [Japon] ; Tetsutaro Ozawa [Japon] ; Shoji Tsuji [Japon] ; Hitoshi Takahashi [Japon]	An autopsy case of autosomal-recessive juvenile parkinsonism with a homozygous exon 4 deletion in the parkin gene
002C69	L. Grevle [Norvège] ; C. Güzey [Norvège] ; H. Hadidi [Norvège] ; R. Brennersted [Norvège] ; J. R. Idle [Norvège] ; J. Aasly [Norvège]	Allelic association between the DRD2 TaqI A polymorphism and Parkinson's disease
002C70	Silvia Buervenich [Suède] ; Olof Sydow [Suède] ; Andrea Carmine [Suède] ; ZHIPING ZHANG [Suède] ; Maria Anvret [Suède] ; Lars Olson [Suède]	Alcohol dehydrogenase alleles in Parkinson's disease
002C91	G. D. Mellick [Australie] ; D. D. Buchanan [Australie] ; S. J. Mccann [Australie] ; K. M. James [Australie] ; A. G. Johnson [Australie] ; D. R. Davis [Australie] ; N. Liyou [Australie] ; D. Chan [Australie] ; D. G. Le Couteur [Australie]	Variations in the monoamine oxidase B (MAOB) gene are associated with Parkinson's disease
002D73	H. R. Morris [Royaume-Uni] ; Andrew Lees (neurologue) [Royaume-Uni] ; N. W. Wood [Royaume-Uni]	Neurofibrillary tangle Parkinsonian disorders : Tau pathology and Tau genetics
002D95	D. C. C. Wan [Hong Kong] ; L. K. Law [Hong Kong] ; D. T. M. Ip [Hong Kong] ; W. T. Cheung [Hong Kong] ; W. K. K. Ho [Hong Kong] ; K. W. K. Tsim [Hong Kong] ; R. Kay [Hong Kong] ; J. Woo [Hong Kong] ; C. P. Pang [Hong Kong]	Lack of allelic association of dopamine D4 receptor gene polymorphisms with Parkinson's disease in a chinese population
002E57	N. Sabbagh [France] ; A. Brice [France] ; D. Marez [France] ; A. Dürr [France] ; M. Legrand [France] ; J.-M. Lo Guidice [France] ; A. Destee [France] ; Yves Agid [France] ; F. Broly [France]	CYP2D6 polymorphism and Parkinson's disease susceptibility
002E75	O. Joost [États-Unis] ; C. A. Taylor [États-Unis] ; C. A. Thomas [États-Unis] ; L. A. Cupples [États-Unis] ; M. H. Saint-Hilaire [États-Unis] ; R. G. Feldman [États-Unis] ; C. T. Baldwin [États-Unis] ; R. H. Myers [États-Unis]	Absence of effect of seven functional mutations in the CYP2D6 gene in Parkinson's disease
002F33	C. P. Pang [Hong Kong] ; JUN ZHANG [Hong Kong] ; T. Woo [Hong Kong] ; D. Chan [Hong Kong] ; L. K. Law [Hong Kong] ; S. F. Tong [Hong Kong] ; T. Kwok [Hong Kong] ; T. Kay [Hong Kong]	Rarity of debrisoquine hydroxylase gene polymorphism in chinese patients with Parkinson's disease
003007	M. G. Hanna [Royaume-Uni] ; M. B. Davis [Royaume-Uni] ; M. G. Sweeney [Royaume-Uni] ; M. Noursadeghi [Royaume-Uni] ; C. J. Ellis [Royaume-Uni] ; P. Elliot [Royaume-Uni] ; N. W. Wood [Royaume-Uni] ; C. D. Marsden [Royaume-Uni]	Generalized chorea in two patients harboring the Friedreich's ataxia gene trinucleotide repeat expansion
003176	E. S. Simon [États-Unis]	Phenotypic heterogeneity and disease course in three murine strains with mutations in genes encoding for α1 and β glycine receptor subunits
003224	T. Xie [Hong Kong] ; S. L. Ho [Hong Kong] ; L. S. W. Li [Hong Kong] ; O. C. K. Ma [Hong Kong]	G/A1947 polymorphism in catechol-O-methyltransferase (COMT) gene in Parkinson's disease
003276	D. G. Le Couteur [Australie] ; P. W. Leighton [Australie] ; S. J. Mccann [Australie] ; S. M. Pond [Australie]	Association of a polymorphism in the dopamine-transporter gene with Parkinson's disease
003293	J. J. Higgins [États-Unis] ; L. T. Pho [États-Unis] ; L. E. Nee [États-Unis]	A gene (ETM) for essential tremor maps to chromosome 2p22-p25
003298	T. Hanihara [Japon] ; K. Inoue [Japon] ; C. Kawanishi [Japon] ; N. Sugiyama [Japon] ; T. Miyakawa [Japon] ; H. Onishi [Japon] ; Y. Yamada [Japon] ; H. Osaka [Japon] ; K. Kosaka [Japon] ; K. Iwabuchi [Japon] ; M. Owada [Japon]	6-Pyruvoyl-tetrahydropterin synthase deficiency with generalized dystonia and diurnal fluctuation of symptoms : A clinical and molecular study
003515	V. Plante-Bordeneuve [Royaume-Uni] ; O. Bandmann ; G. Wenning ; N. P. Quinn ; S. E. Daniel ; A. E. Harding	CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy

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	Movement Disorders (revue)
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Movement Disorders (revue)

Gène And NotAlexis Brice

List of bibliographic references