Gyrus précentral < Gène < Gène CACNA1A

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List of bibliographic references indexed by Gène

Number of relevant bibliographic references: 39.
[0-20] [0 - 20][0 - 39][20-38][20-40]

Ident.	Authors (with country if any)	Title
003F39 (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
004031 (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
004045 (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
004062 (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
004095 (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
004179 (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 ϵ‐sarcoglycan gene in familial and sporadic myoclonus‐dystonia: Evidence for genetic heterogeneity
004216 (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
004394 (2002)	Marina A. J. Tijssen [Pays-Bas] ; Monique N. Vergouwe [Pays-Bas] ; J. Gert Van Dijk [Pays-Bas] ; Michelle Rees [Royaume-Uni] ; Rune R. Frants [Pays-Bas] ; Peter Brown [Royaume-Uni]	Major and minor form of hereditary hyperekplexia
004530 (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
004547 (2002)	Demetrius M. Maraganore [États-Unis] ; Matthew J. Farrer [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
004614 (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
004636 (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
004713 (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
004739 (2001)	J. Hoenicka [Espagne] ; L. Vidal [Espagne] ; M. Godoy [Espagne] ; J. J. Ochoa [Espagne] ; J. García De Yébenes [Espagne]	New nonsense mutation in the GTP‐cyclohydrolase I gene in L‐DOPA responsive dystonia‐parkinsonism
004751 (2001)	Massimo Pandolfo [Canada]	Molecular basis of Friedreich ataxia
004842 (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
004844 (2001)	C. Lu [Taïwan] ; J. Wu [Taïwan] ; C. Tsai [Taïwan] ; R. Chen [Taïwan] ; Y. 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
004A31 (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
004A32 (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
004A48 (2000)	Louise C. Abbott [États-Unis] ; Melissa Bump [États-Unis] ; Amy Brandl [États-Unis] ; Scarlett De Laune [États-Unis]	Investigation of the role of the cerebellum in the myoclonic‐like movement disorder exhibited by tottering mice
004B07 (2000)	Sergei N. Illarioshkin [Russie] ; Irina A. Ivanova-Smolenskaya [Russie] ; Rahmatullo A. Rahmonov [Russie] ; Elena D. Markova [Russie] ; Giovanni Stevanin [France] ; Alexis Brice [France]	Clinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan

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