Serial Learning < Serine < Serine Endopeptidases

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List of bibliographic references

Number of relevant bibliographic references: 32.
[0-20] [0 - 20][0 - 32][20-31][20-40]

Ident.	Authors (with country if any)	Title
001080 (2005)	Lorraine N. Clark [États-Unis] ; Angelique Nicolai ; Shehla Afridi ; Juliette Harris ; Helen Mejia-Santana ; Lisa Strug ; Lucien J. Cote ; Elan D. Louis ; Howard Andrews ; Cheryl Waters ; Blair Ford ; Steven Frucht ; Stanley Fahn ; Richard Mayeux ; Ruth Ottman ; K. Marder	Pilot association study of the beta-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity.
001263 (2005)	Aideen Mcinerney-Leo	Genetic testing in Parkinson's disease.
001311 (2005)	Denise M. Kay ; Patricia Kramer ; Don Higgins ; Cyrus P. Zabetian ; Haydeh Payami	Escaping Parkinson's disease: a neurologically healthy octogenarian with the LRRK2 G2019S mutation.
001428 (2005)	Jose Miguel Bras [Portugal] ; Rita Joao Guerreiro ; Maria Helena Ribeiro ; Cristina Januario ; Ana Morgadinho ; Catarina Resende Oliveira ; Luis Cunha ; John Hardy ; Andrew Singleton	G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort.
001516 (2006)	Denise M. Kay [États-Unis] ; Cyrus P. Zabetian ; Stewart A. Factor ; John G. Nutt ; Ali Samii ; Alida Griffith ; Tom D. Bird ; Patricia Kramer ; Donald S. Higgins ; Haydeh Payami	Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics.
001586 (2006)	David A. Grimes [Canada] ; Fabin Han ; Michel Panisset ; Lemuel Racacho ; Fengxia Xiao ; Ruobing Zou ; Kelly Westaff ; Dennis E. Bulman	Translated mutation in the Nurr1 gene as a cause for Parkinson's disease.
001736 (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.
001873 (2006)	Hui-Fang Shang [République populaire de Chine] ; Xiao-Feng Jiang ; Jean-Marc Burgunder ; Qin Chen ; Dong Zhou	Novel mutation in the ceruloplasmin gene causing a cognitive and movement disorder with diabetes mellitus.
001899 (2006)	Sofya N. Pchelina [Russie] ; Andrei F. Yakimovskii ; Olga N. Ivanova ; Anton K. Emelianov ; Andrei H. Zakharchuk ; Alexander L. Schwarzman	G2019S LRRK2 mutation in familial and sporadic Parkinson's disease in Russia.
001913 (2006)	Nathan Pankratz [États-Unis] ; Michael W. Pauciulo ; Veronika E. Elsaesser ; Diane K. Marek ; Cheryl A. Halter ; Alice Rudolph ; Clifford W. Shults ; Tatiana Foroud ; William C. Nichols	Mutations in LRRK2 other than G2019S are rare in a north American-based sample of familial Parkinson's disease.
001921 (2007)	Michael Schüpbach [France] ; Ebba Lohmann ; Mathieu Anheim ; Suzanne Lesage ; Virginie Czernecki ; Sadek Yaici ; Yulia Worbe ; Perrine Charles ; Marie-Laure Welter ; Pierre Pollak ; Alexandra Dürr ; Yves Agid [France] ; Alexis Brice	Subthalamic nucleus stimulation is efficacious in patients with Parkinsonism and LRRK2 mutations.
001933 (2007)	Eng-King Tan [Singapour] ; Lisa Skipper ; Louis Tan ; Jian-Jun Liu	LRRK2 G2019S founder haplotype in the Chinese population.
001960 (2007)	Lianna Ishihara [Royaume-Uni] ; Rachel A. Gibson ; Liling Warren ; Rim Amouri ; Kelly Lyons ; Catherine Wielinski ; Christine Hunter ; Jina E. Swartz ; Ramu Elango ; P Anthony Akkari ; David Leppert ; Linda Surh ; Kevin H. Reeves ; Siwan Thomas ; Leigh Ragone ; Nobutaka Hattori ; Rajesh Pahwa ; Joseph Jankovic [États-Unis] ; Martha Nance ; Alan Freeman ; Neziha Gouider-Khouja ; Mounir Kefi ; Mourad Zouari ; Samia Ben Sassi ; Samia Ben Yahmed ; Ghada El Euch-Fayeche ; Lefkos Middleton ; David J. Burn ; Ray L. Watts ; Faycal Hentati	Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families.
001B67 (2007)	Yue Huang [Australie] ; Glenda M. Halliday ; Himesha Vandebona ; George D. Mellick ; Frank Mastaglia ; Julia Stevens ; John Kwok ; Michael Garlepp ; Peter A. Silburn ; Malcolm K. Horne ; Katya Kotschet ; Alison Venn ; Dominic B. Rowe ; Justin P. Rubio ; Carolyn M. Sue	Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease.
001C52 (2007)	Dietrich Haubenberger [Autriche] ; Silvia Bonelli ; Christoph Hotzy ; Petra Leitner ; Peter Lichtner ; Doris Samal ; Regina Katzenschlager ; Atbin Djamshidian ; Thomas Brücke ; Michaela Steffelbauer ; Christian Bancher ; Josef Grossmann ; Gerhard Ransmayr ; Tim M. Strom ; Thomas Meitinger ; Thomas Gasser ; Eduard Auff ; Alexander Zimprich	A novel LRRK2 mutation in an Austrian cohort of patients with Parkinson's disease.
001F23 (2008)	Renato P. Munhoz [Brésil] ; Yosuke Wakutani ; Connie Marras ; Helio A. Teive ; Salmo Raskin ; Lineu C. Werneck ; Danielle Moreno ; Christine Sato ; Anthony E. Lang ; Ekaterina Rogaeva	The G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: phenotype in monozygotic twins.
001F71 (2008)	Elvira V. De Marco [Italie] ; Grazia Annesi ; Patrizia Tarantino ; Francesca E. Rocca ; Giovanni Provenzano ; Donatella Civitelli ; Innocenza C. Cir Candiano ; Ferdinanda Annesi ; Sara Carrideo ; Francesca Condino ; Giuseppe Nicoletti ; Demetrio Messina ; Fabiana Novellino ; Maurizio Morelli ; Aldo Quattrone	Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy.
002181 (2008)	Sebastian Paus [Allemagne] ; Gabor Zsurka ; Miriam Baron ; Marcus Deschauer ; Christian Bamberg ; Thomas Klockgether ; Wolfram S. Kunz ; Cornelia Kornblum	Apraxia of lid opening mimicking ptosis in compound heterozygosity for A467T and W748S POLG1 mutations.
002438 (2009)	Renato P. Munhoz ; Helio A. Teive ; Alexandre N. Francisco ; Salmo Raskin ; Ekaterina Rogaeva	Unilateral pallidotomy in a patient with parkinsonism and G2019S LRRK2 mutation.
002606 (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.
002763 (2009)	Elena García-Martín [Espagne] ; Carmen Martínez ; Hortensia Alonso-Navarro ; Julián Benito-Le N ; Inmaculada Puertas ; Lluisa Rubio ; Tomás L Pez-Alburquerque ; José A G. Agúndez ; Félix Javier Jiménez-Jiménez	Dopamine receptor D3 (DRD3) genotype and allelic variants and risk for essential tremor.

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