Movement Disorders (revue) - Merge (PascalFrancis)

Index « FA11s1.i » - entrée « FARRER (Matthew J.) »
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List of bibliographic references

Number of relevant bibliographic references: 22.
[0-20] [0 - 20][0 - 22][20-21][20-40]
Ident.Authors (with country if any)Title
000742 (2002) John L. Goudreau ; Demetrius M. Maraganore ; Matthew J. Farrer ; Timothy G. Lesnick ; Andrew B. Singleton ; James H. Bower ; John A. Hardy ; Walter A. RoccaCase-control study of dopamine transporter-1, monoamine oxidase-B, and catechol-O-methyl transferase polymorphisms in Parkinson's disease
000841 (2003) Demetrius M. Maraganore ; Mariza De Andrade ; Timothy G. Lesnick ; Matthew J. Farrer ; James H. Bower ; John A. Hardy ; Walter A. RoccaComplex interactions in Parkinson's disease: A two-phased approach
000A05 (2003) Sarah J. Lincoln ; Demetrius M. Maraganore ; Timothy G. Lesnick ; Rebecca Bounds ; Mariza De Andrade ; James H. Bower ; John A. Hardy ; Matthew J. FarrerParkin variants in North American Parkinson's disease: Cases and controls
000A17 (2003) Demetrius M. Maraganore ; Matthew J. Farrer ; Timothy G. Lesnick ; Mariza De Andrade ; James H. Bower ; Dena Hernandez ; John A. Hardy ; Walter A. RoccaCase-control study of the α-synuclein interacting protein gene and Parkinson's disease
000A96 (2004) Paul J. Lockhart ; Casey A. O'Farrell ; Matthew J. FarrerIt's a double knock-out! The Quaking mouse is a spontaneous deletion of Parkin and Parkin co-regulated gene (PACRG)
000B88 (2004) Joseph Wiley ; Timothy Lynch ; Sarah Lincoln ; Lisa Skipper ; Mary Hulihan ; David Gosal ; Gina Bisceglio ; Jennifer Kachergus ; John Hardy ; Matthew J. FarrerParkinson's disease in Ireland: Clinical presentation and genetic heterogeneity in patients with Parkin mutations
000C59 (2004) Paul J. Lockhart ; Rebecca Bounds ; Mary Hulihan ; Jennifer Kachergus ; Sarah Lincoln ; Chin-Hsien Lin ; Ruey-Meei Wu ; Matthew J. FarrerLack of mutations in DJ-1 in a cohort of Taiwanese ethnic Chinese with early-onset parkinsonism
000D48 (2005) Mathias Toft ; Jan Aasly ; Gina Bisceglio ; Charles H. Adler ; Ryan J. Uitti ; Anna Krygowska-Wajs ; Timothy Lynch ; Zbigniew K. Wszolek ; Matthew J. FarrerParkinsonism, FXTAS, and FMR1 premutations
001259 (2006) Hiroyuki Tomiyama ; YUANZHE LI ; Manabu Funayama ; Kazuko Hasegawa ; Hiroyo Yoshino ; Shin-Ichiro Kubo ; Kenichi Sato ; Tatsuya Hattori ; Chin-Song Lu ; Rivka Inzelberg ; Ruth Djaldetti ; Eldad Melamed ; Rim Amouri ; Neziha Gouider-Khouja ; Faycal Hentati ; Yasuko Hatano ; MEI WANG ; Yoko Imamichi ; Koichi Mizoguchi ; Hiroaki Miyajima ; Fumiya Obata ; Tatsushi Toda ; Matthew J. Farrer ; Yoshikuni Mizuno ; Nobutaka HattoriClinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries
001548 (2007) Mathias Toft ; Ignacio F. Mata ; Owen A. Ross ; Jennifer Kachergus ; Mary M. Hulihan ; Kristoffer Haugarvoll ; Jeremy T. Stone ; Marta Blazquez ; J. Mark Gibson ; Jan O. Aasly ; Linda R. White ; Timothy Lynch ; Charles H. Adler ; Katrina Gwinn-Hardy ; Matthew J. FarrerPathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease
001586 (2007) Kristoffer Haugarvoll ; Mathias Toft ; Owen A. Ross ; Jeremy T. Stone ; Michael G. Heckman ; Linda R. White ; Timothy Lynch ; John Mark Gibson ; Zbigniew K. Wszolek ; Ryan J. Uitti ; Jan O. Aasly ; Matthew J. FarrerELAVL4, PARK10, and the celts
001D20 (2009) Ming-Jen Lee ; Ignacio F. Mata ; Chin-Hsien Lin ; Kai-Yuan Tzen ; Sarah J. Lincoln ; Rebecca Bounds ; Paul J. Lockhart ; Mary M. Hulihan ; Matthew J. Farrer ; Ruey-Meei WuGenotype-Phenotype Correlates in Taiwanese Patients with Early-Onset Recessive Parkinsonism
001D70 (2009) Christian Wider ; Justus C. Dachsel ; Alexandra I. Soto ; Michael G. Heckman ; Nancy N. Diehl ; MEI YUE ; Sarah Lincoln ; Jan O. Aasly ; Kristoffer Haugarvoll ; John Q. Trojanowski ; Spiridon Papapetropoulos ; Deborah Mash ; Alex Rajput ; Ali H. Rajput ; J. Mark Gibson ; Timothy Lynch ; Dennis W. Dickson ; Ryan J. Uitti ; Zbigniew K. Wszolek ; Matthew J. Farrer ; Owen A. RossFGF20 and Parkinson's Disease : No Evidence of Association or Pathogenicity via oc-Synuclein Expression
001F61 (2009) Kenya Nishioka ; Owen A. Ross ; Kenji Ishii ; Jennifer M. Kachergus ; Kiichi Ishiwata ; Mayumi Kitagawa ; Satoshi Kono ; Tomokazu Obi ; Koichi Mizoguchi ; Yuichi Inoue ; Hisamasa Imai ; Masashi Takanashi ; Yoshikuni Mizuno ; Matthew J. Farrer ; Nobutaka HattoriExpanding the Clinical Phenotype of SNCA Duplication Carriers
001F85 (2009) Stephanie A. Cobb ; Christian Wider ; Owen A. Ross ; Ignacio F. Mata ; Charles H. Adler ; Alex Rajput ; Ali H. Rajput ; Ruey-Meei Wu ; Robert Hauser ; Keith A. Josephs ; Jonathan Carr ; Katrina Gwinn ; Michael G. Heckman ; Jan O. Aasly ; Timothy Lynch ; Ryan J. Uitti ; Zbigniew K. Wszolek ; Gregory Kapatos ; Matthew J. FarrerGCH1 in Early-Onset Parkinson's Disease
002048 (2009) Alex Rajput ; Carles Vilarino-Güell ; Michele L. Rajput ; Owen A. Ross ; Alexandra I. Soto-Ortolaza ; Sarah J. Lincoln ; Stephanie A. Cobb ; Michael G. Heckman ; Matthew J. Farrer ; Ali RajputAlpha-Synuclein Polymorphisms are Associated with Parkinson's Disease in a Saskatchewan Population
002403 (2010) Owen A. Ross ; Greggory J. Wilhoite ; Justin A. Bacon ; Alexandra Soto-Ortolaza ; Jennifer Kachergus ; Stephanie A. Cobb ; Andreas Puschmann ; Carles Vilarino-Güell ; Matthew J. Farrer ; Neill Graff-Radford ; James F. Meschia ; Zbigniew K. WszolekLRRK2 Variation and Parkinson's Disease in African Americans
002445 (2010) Barbara Jasinska-Myga ; Jennifer Kachergus ; Carles Vilarino-Güell ; Christian Wider ; Alexandra I. Soto-Ortolaza ; Mounir Kefi ; Lefkos T. Middleton ; Lianna Ishihara-Paul ; Rachel A. Gibson ; Rim Amouri ; SAMIA BEN YAHMED ; SAMIA BEN SASSI ; Mourad Zouari ; Ghada El Euch ; Owen A. Ross ; Faycal Hentati ; Matthew J. FarrerComprehensive Sequencing of the LRRK2 Gene in Patients with Familial Parkinson's Disease from North Africa
002456 (2010) Jan O. Aasly ; Carles Vilarino-Güell ; Justus C. Dachsel ; Philip J. Webber ; Andrew B. West ; Kristoffer Haugarvoll ; Krisztina K. Johansen ; Mathias Toft ; John G. Nutt ; Haydeh Payami ; Jennifer M. Kachergus ; Sarah J. Lincoln ; Amela Felic ; Christian Wider ; Alexandra I. Soto-Ortolaza ; Stephanie A. Cobb ; Linda R. White ; Owen A. Ross ; Matthew J. FarrerNovel Pathogenic LRRK2 p.Asn1437His Substitution in Familial Parkinson's Disease
002533 (2010) Vesna Sossi ; Raul De La Fuente-Fernandez ; Ramachandiran Nandhagopal ; Michael Schulzer ; Jessamyn Mckenzie ; Thomas J. Ruth ; Jan O. Aasly ; Matthew J. Farrer ; Zbigniew K. Wszolek ; Jon A. StoesslDopamine Turnover Increases in Asymptomatic LRRK2 Mutations Carriers
002609 (2011) SUN JU CHUNG ; Sebastian M. Armasu ; Joanna M. Biernacka ; Timothy G. Lesnick ; David N. Rider ; Sarah J. Lincoln ; Alexandra I. Ortolaza ; Matthew J. Farrer ; Julie M. Cunningham ; Walter A. Rocca ; Demetrius M. MaraganoreCommon Variants in PARK Loci and Related Genes and Parkinson's Disease

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