Movement Disorders (revue) - Checkpoint (PascalFrancis)

Index « FC03.fr.i » - entrée « Gène »
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List of bibliographic references

Number of relevant bibliographic references: 39.
[0-20] [0 - 20][0 - 39][20-38][20-40]
Ident.Authors (with country if any)Title
002319 (2003) 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
002398 (2003) Sergei N. Illarioshkin [Russie] ; Magali Periquet [France] ; Nina Rawal [France] ; Christoph B. Lücking [France] ; Tatyana B. Zagorovskaya [Russie] ; Pyotr A. Slominsky [Russie] ; Olga V. Miloserdova [Russie] ; Elena D. Markova [Russie] ; Svetlana A. Limborska [Russie] ; Irina A. Ivanova-Smolenskaya [Russie] ; Alexis Brice [France]Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism
002412 (2003) 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 (2003) 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 (2003) 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 (2003) 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 (2003) 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 (2002) 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 (2002) 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 (2002) 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 (2002) 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 (2002) 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 (2001) 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 (2001) 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 (2001) Massimo Pandolfo [Canada]Molecular basis of friedreich ataxia
002A34 (2001) 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 (2001) 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 (2000) 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 (2000) 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 (2000) 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 (2000) 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

List of associated Author.i

Nombre de
documents
Descripteur
3Sadako Kuno
2Alexis Brice
2C. P. Pang
2D. Chan
2D. G. Le Couteur
2Elena D. Markova
2Hideshi Kawakami
2Hirofumi Maruyama
2Ikuko Mizuta
2Irina A. Ivanova-Smolenskaya
2JIAN WANG
2L. K. Law
2Marina A. J. Tijssen
2Masataka Nishimura
2N. W. Wood
2Peter Brown
2Ryuji Kaji
2S. J. Mccann
2Sergei N. Illarioshkin
2Shoji Tsuji
2ZHUOLIN LIU
1A. Brandl
1A. Brice
1A. Destee
1A. Dürr
1A. E. Harding
1A. G. Johnson
1A. Lees
1A. Papadimitriou
1Akihiro Kanzaki
1Alessandro Malandrini
1Alexis Elbaz
1Alfredo Berardelli
1Andrea Carmine
1Andrea Nemeth
1Andrew Lees (neurologue)
1Andrew West
1Anjum Misbahuddin
1Anna-Rita Bentivoglio
1Anthony Leslie
1Anthony P. Monaco
1Antonio Federico
1Atsushi Ishikawa
1Barbara Garavaglia
1Bruno Dallapiccola
1C. A. Taylor
1C. A. Thomas
1C. D. Marsden
1C. Güzey
1C. J. Ellis
1C. Kawanishi
1C. T. Baldwin
1C.-H. Tsai
1C.-S. Lu
1Carla Battisti
1Cesa Scaglione
1Charles Davie
1Charles Shaw-Smith
1Chen-Ming Sun
1Chikako Tanaka
1Christoph B. Lücking
1Christopher Burke
1Chun-Hwei Tai
1D. C. C. Wan
1D. D. Buchanan
1D. Marez
1D. R. Davis
1D. T. M. Ip
1DANQING ZHU
1Daniel J. Schaid
1David Macmanus
1Demetrius M. Maraganore
1Din-E Shan
1E. S. Simon
1Eiji Mizuta
1Emilia Bellone
1Emilio Di Maria
1Enza-Maria Valente
1F. Broly
1Francesco Brancati
1Franco Ajmar
1G. D. Mellick
1G. Hatzigeorgiou
1G. Wenning
1Garth A. Nicholson
1Giovanni Abbruzzese
1Giovanni Stevanin
1Giuseppe Circiarello
1H. Hadidi
1H. Onishi
1H. Osaka
1H. R. Morris
1H. Yoshino
1HYUN SOOK KIM
1Hidetoshi Date
1Hiroko Nagai
1Hiroshi Ujike
1Hiroyuki Morino
1Hitoshi Takahashi
1J. Aasly

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