Neurogenetics,volume 14,issue 3-4  (11-2013)

Period of time: 2013年3-4期

Publisher: Springer Publishing Company

Founded in: 1997

Total resources: 16

ISSN: 1364-6745

Subject: R74 Neurology and Psychiatry

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Neurogenetics,volume 14,issue 3-4

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Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington’s disease motor onset

By Ramos Eliana,Latourelle Jeanne,Gillis Tammy,Mysore Jayalakshmi,Squitieri Ferdinando,Pardo Alba,Donato Stefano,Gellera Cinzia,Hayden Michael,Morrison Patrick,Nance Martha,Ross Christopher,Margolis Russell,Gomez-Tortosa Estrella,Ayuso Carmen,Suchowersky Oksana,Trent Ronald,McCusker Elizabeth,Novelletto Andrea,Frontali Marina,Jones Randi,Ashizawa Tetsuo,Frank Samuel,Saint-Hilaire Marie-Helene,Hersch Steven,Rosas Herminia,Lucente Diane,Harrison Madaline,Zanko Andrea,Abramson Ruth,Marder Karen,Gusella James,Lee Jong-Min,Alonso Isabel,Sequeiros Jorge,Myers Richard,MacDonald Marcy in (2013)

Neurogenetics,volume 14,issue 3-4 , Vol. 14, Iss. 3-4, 2013-11 , pp. 173-179

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Autosomal recessive hereditary spastic paraplegia—clinical and genetic characteristics of a well-defined cohort

By Yoon G.,Baskin B.,Tarnopolsky M.,Boycott K.,Geraghty M.,Sell E.,Goobie S.,Meschino W.,Banwell B.,Ray P. in (2013)

Neurogenetics,volume 14,issue 3-4 , Vol. 14, Iss. 3-4, 2013-11 , pp. 181-188

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Homozygous dystroglycan mutation associated with a novel muscle–eye–brain disease-like phenotype with multicystic leucodystrophy

By Geis Tobias,Marquard Klaus,Rödl Tanja,Reihle Christof,Schirmer Sophie,Kalle Thekla,Bornemann Antje,Hehr Ute,Blankenburg Markus in (2013)

Neurogenetics,volume 14,issue 3-4 , Vol. 14, Iss. 3-4, 2013-11 , pp. 205-213

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Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyria

By Valence Stéphanie,Poirier Karine,Lebrun Nicolas,Saillour Yoann,Sonigo Pascale,Bessières Bettina,Attié-Bitach Tania,Benachi Alexandra,Masson Cécile,Encha-Razavi Ferechté,Chelly Jamel,Bahi-Buisson Nadia in (2013)

Neurogenetics,volume 14,issue 3-4 , Vol. 14, Iss. 3-4, 2013-11 , pp. 215-224

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Diagnostic utility of whole exome sequencing in patients showing cerebellar and/or vermis atrophy in childhood

By Ohba Chihiro,Osaka Hitoshi,Iai Mizue,Yamashita Sumimasa,Suzuki Yume,Aida Noriko,Shimozawa Nobuyuki,Takamura Ayumi,Doi Hiroshi,Tomita-Katsumoto Atsuko,Nishiyama Kiyomi,Tsurusaki Yoshinori,Nakashima Mitsuko,Miyake Noriko,Eto Yoshikatsu,Tanaka Fumiaki,Matsumoto Naomichi,Saitsu Hirotomo in (2013)

Neurogenetics,volume 14,issue 3-4 , Vol. 14, Iss. 3-4, 2013-11 , pp. 225-232

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