Polymethyl Methacrylate < Polymorphism, Genetic < Polymorphism, Restriction Fragment Length

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List of bibliographic references

Number of relevant bibliographic references: 78.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000F11 (2012)	Masahiko Suzuki [Japon] ; Masayuki Yoshioka ; Masaya Hashimoto ; Maiko Murakami ; Keiichi Kawasaki ; Miki Noya ; Daisuke Takahashi ; Mitsuyoshi Urashima	25-hydroxyvitamin D, vitamin D receptor gene polymorphisms, and severity of Parkinson's disease.
000F65 (2012)	Lonneke M L. De Lau [Pays-Bas] ; Dagmar Verbaan ; Johan Marinus ; Peter Heutink ; Jacobus J. Van Hilten	Catechol-O-methyltransferase Val158Met and the risk of dyskinesias in Parkinson's disease.
001432 (2011)	Thilo Herzfeld ; Rudolf Korinthenberg ; Ulrich Müller	D216H polymorphism within TOR1A does not affect penetrance in DRD and is not a general modifier in primary dystonia.
001514 (2011)	Jee-Young Lee [Corée du Sud] ; Jinwhan Cho ; Eun-Kyung Lee ; Sung-Sup Park ; Beom S. Jeon	Differential genetic susceptibility in diphasic and peak-dose dyskinesias in Parkinson's disease.
001830 (2010)	Giuseppe De Palma [Italie] ; Finlay D. Dick ; Stefano Calzetti ; Neil W. Scott ; Gordon J. Prescott ; Aileen Osborne ; Neva Haites ; Paola Mozzoni ; Anna Negrotti ; Augusto Scaglioni ; Antonio Mutti	A case-control study of Parkinson's disease and tobacco use: gene-tobacco interactions.
001C92 (2009)	Maria C. Rodriguez-Oroz [Espagne] ; Pablo Martínez Lage ; Jose Sanchez-Mut ; Isabel Lamet ; Javier Pagonabarraga ; Jon B. Toledo ; David García-Garcia ; Pedro Clavero ; Lluis Samaranch ; Cecilia Irurzun ; Juan M. Matsubara ; Jaione Irigoien ; Emilia Bescos ; Jaime Kulisevsky ; Jordi Pérez-Tur ; Jose A. Obeso	Homocysteine and cognitive impairment in Parkinson's disease: a biochemical, neuroimaging, and genetic study.
001D71 (2009)	Sebastian Paus [Allemagne] ; Franziska Gadow ; Michael Knapp ; Christine Klein ; Thomas Klockgether ; Ullrich Wüllner	Motor complications in patients form the German Competence Network on Parkinson's disease and the DRD3 Ser9Gly polymorphism.
001E09 (2009)	Greg T. Sutherland [Australie] ; Glenda M. Halliday ; Peter A. Silburn ; Frank L. Mastaglia ; Dominic B. Rowe ; Richard S. Boyle ; John D. O'Sullivan ; Tina Ly ; Steve D. Wilton ; George D. Mellick	Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease?
001F19 (2009)	Jan Edler [Allemagne] ; Brit Mollenhauer ; Uta Heinemann ; Daniela Varges ; Carola Werner ; Inga Zerr ; Walter J. Schulz-Schaeffer	Movement disturbances in the differential diagnosis of Creutzfeldt-Jakob disease.
002231 (2008)	Patricia De Carvalho Aguiar [Brésil] ; Patricia Silva Lessa ; Clecio Godeiro ; Orlando Barsottini ; Andre Carvalho Felício ; Vanderci Borges ; Sonia Maria De Azevedo Silva ; Roberta Arb Saba ; Henrique Ballalai Ferraz ; Carlos A. Moreira-Filho ; Luiz Augusto F. Andrade	Genetic and environmental findings in early-onset Parkinson's disease Brazilian patients.
002319 (2008)	Eng-King Tan [Singapour] ; Hui-Qin Lim ; Yih Yuen ; Yi Zhao	Pathogenicity of LRRK2 P755L variant in Parkinson's disease.
002347 (2007)	Thomas Gasser [Allemagne]	Update on the genetics of Parkinson's disease.
002363 (2008)	Sebastian Paus [Allemagne] ; Anne Grünewald ; Christine Klein ; Michael Knapp ; Alexander Zimprich ; Bernd Janetzky ; Jens C. Möller ; Thomas Klockgether ; Ullrich Wüllner	The DRD2 TaqIA polymorphism and demand of dopaminergic medication in Parkinson's disease.
002969 (2007)	David Kemlink [Allemagne] ; Olli Polo ; Pasquale Montagna ; Federica Provini ; Karin Stiasny-Kolster ; Wolfgang Oertel ; Al De Weerd ; Sona Nevsimalova ; Karel Sonka ; Birgit Högl ; Birgit Frauscher ; Werner Poewe ; Claudia Trenkwalder ; Peter P. Pramstaller ; Luigi Ferini-Strambi ; Marco Zucconi ; Eric Konofal ; Isabelle Arnulf ; Georgios M. Hadjigeorgiou ; Svenja Happe ; Christine Klein ; Anja Hiller ; Peter Lichtner ; Thomas Meitinger ; Betram Müller-Myshok ; Juliane Winkelmann	Family-based association study of the restless legs syndrome loci 2 and 3 in a European population.
002972 (2007)	Jordi Clarimon [États-Unis] ; Francesco Brancati ; Elizabeth Peckham ; Enza Maria Valente ; Bruno Dallapiccola ; Giovanni Abruzzese ; Paolo Girlanda ; Giovanni Defazio ; Alfredo Berardelli ; Mark Hallett ; Andrew B. Singleton	Assessing the role of DRD5 and DYT1 in two different case-control series with primary blepharospasm.
002A33 (2006)	Hideaki Kobayashi [Japon] ; Hiroshi Ujike ; Junko Hasegawa ; Mitsutoshi Yamamoto ; Akihiro Kanzaki ; Ichiro Sora	Identification of a risk haplotype of the alpha-synuclein gene in Japanese with sporadic Parkinson's disease.
002A47 (2006)	Sun J. Kang [États-Unis] ; William K. Scott ; Yi-Ju Li ; Michael A. Hauser ; Joelle M. Van Der Walt ; Kenichiro Fujiwara ; Gregory M. Mayhew ; Sandra G. West ; Jeffery M. Vance ; Eden R. Martin	Family-based case-control study of MAOA and MAOB polymorphisms in Parkinson disease.
002B24 (2006)	Eng-King Tan [Singapour] ; Kim-Yoong Puong ; Stephanie Fook-Chong ; Eva Chua ; Hui Shen ; Yih Yuen ; Ratnagopal Pavanni ; Meng-Cheong Wong ; Kathiravelu Puvan ; Yi Zhao	Case-control study of UCHL1 S18Y variant in Parkinson's disease.
002C00 (2006)	Keiko Hiramoto [Japon] ; Hideshi Kawakami ; Kimiko Inoue ; Takahiro Seki ; Hirofumi Maruyama ; Hiroyuki Morino ; Masayasu Matsumoto ; Kaoru Kurisu ; Norio Sakai	Identification of a new family of spinocerebellar ataxia type 14 in the Japanese spinocerebellar ataxia population by the screening of PRKCG exon 4.
002C21 (2006)	Shaochun Ma [États-Unis] ; Thomas L. Davis ; Marcia A. Blair ; John Y. Fang ; Yuki Bradford ; Jonathan L. Haines ; Peter Hedera	Familial essential tremor with apparent autosomal dominant inheritance: should we also consider other inheritance modes?
002C51 (2006)	Florian D. Vogl [Italie] ; Irene Pichler ; Susanna Adel ; Gerd K. Pinggera ; Stefano Bracco ; Alessandro De Grandi ; Claudia Beu Volpato ; Paolo Aridon ; Thomas Mayer ; Thomas Meitinger ; Christine Klein ; Giorgio Casari ; Peter P. Pramstaller	Restless legs syndrome: epidemiological and clinicogenetic study in a South Tyrolean population isolate.

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