Movement Disorders (revue) - Curation (Ncbi)

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Glycine (cerebrospinal fluid) < Glycine (genetics) < Glycine (metabolism)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 35.
[0-20] [0 - 20][0 - 35][20-34][20-40]
Ident.Authors (with country if any)Title
001186 (2005) Yu-Hu Zhang [République populaire de Chine] ; Bei-Sha Tang [République populaire de Chine] ; Ai-Ling Zhao [République populaire de Chine] ; Kun Xia [République populaire de Chine] ; Zhi-Gao Long [République populaire de Chine] ; Ji-Feng Guo [République populaire de Chine] ; Shawn K. Westaway [États-Unis] ; Susan J. Hayflick [États-Unis]Novel Compound Heterozygous Mutations in the PANK2 Gene in a Chinese Patient With Atypical Pantothenate Kinase-Associated Neurodegeneration
001263 (2005) Aideen Mcinerney-LeoGenetic testing in Parkinson's disease.
001311 (2005) Denise M. Kay ; Patricia Kramer ; Don Higgins ; Cyrus P. Zabetian ; Haydeh PayamiEscaping 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 SingletonG2019S 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 PayamiParkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics.
001557 (2006) Tsao-Wei Liang [États-Unis] ; Adam C. Truax ; John Q. Trojanowski ; Virginia M-Y Lee ; Matthew B. Stern ; Paul T. KotzbauerPartial deficit of pantothenate kinase 2 catalytic activity in a case of tremor-predominant neurodegeneration with brain iron accumulation.
001828 (2006) Ina Schmitt ; Ullrich Wüllner ; Daniel G. Healy ; Nicholas W. Wood ; Heike Kölsch ; Reinhard HeunThe ADH1C stop mutation in multiple system atrophy patients and healthy probands in the United Kingdom and Germany.
001855 (2006) Javier Sim N-Sánchez [Espagne] ; José-Félix Martí-Mass ; José Vicente Sánchez-Mut ; Coro Paisán-Ruiz ; Angel Martínez-Gil ; Javier Ruiz-Martínez ; Amets Sáenz ; Andrew B. Singleton ; Adolfo L Pez De Munain ; Jordi Pérez-TurParkinson's disease due to the R1441G mutation in Dardarin: a founder effect in the Basques.
001899 (2006) Sofya N. Pchelina [Russie] ; Andrei F. Yakimovskii ; Olga N. Ivanova ; Anton K. Emelianov ; Andrei H. Zakharchuk ; Alexander L. SchwarzmanG2019S 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. NicholsMutations 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 BriceSubthalamic nucleus stimulation is efficacious in patients with Parkinsonism and LRRK2 mutations.
001933 (2007) Eng-King Tan [Singapour] ; Lisa Skipper ; Louis Tan ; Jian-Jun LiuLRRK2 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 HentatiScreening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families.
001B05 (2007) Eng-King Tan ; Stephanie Fook-Chong ; Zhao YiComparing LRRK2 Gly2385Arg carriers with noncarriers.
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. SuePrevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease.
001D79 (2007) Eng-King Tan [Singapour] ; Yi Zhao ; Louis Tan ; Hui-Qin Lim ; Jasinda Lee ; Yih Yuen ; Ratnagopal Pavanni ; Meng-Cheong Wong ; Stephanie Fook-Chong ; Jian-Jun LiuAnalysis of LRRK2 Gly2385Arg genetic variant in non-Chinese Asians.
001D99 (2007) Friedrich Asmus [Allemagne] ; Anita Devlin ; Marita Munz ; Alexander Zimprich ; Thomas Gasser ; Patrick F. ChinneryClinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia.
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 RogaevaThe G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: phenotype in monozygotic twins.
002438 (2009) Renato P. Munhoz ; Helio A. Teive ; Alexandre N. Francisco ; Salmo Raskin ; Ekaterina RogaevaUnilateral pallidotomy in a patient with parkinsonism and G2019S LRRK2 mutation.
002566 (2009) Yih-Ru Wu ; Chiung-Mei Chen ; Chih-Ying Chao ; Ron-Kuo Lyu ; Guey-Jen Lee-ChenPantothenate kinase-associated neurodegeneration in two Taiwanese siblings: identification of a novel PANK2 gene mutation.
002600 (2009) Cyrus P. Zabetian [États-Unis] ; Mitsutoshi Yamamoto [Japon] ; Alexis N. Lopez [États-Unis] ; Hiroshi Ujike [Japon] ; Ignacio F. Mata [États-Unis] ; Yuishin Izumi [Japon] ; Ryuji Kaji [Japon] ; Hirofumi Maruyama [Japon] ; Hiroyuki Morino [Japon] ; Masaya Oda [Japon] ; Carolyn M. Hutter [États-Unis] ; Karen L. Edwards [États-Unis] ; Gerard D. Schellenberg [États-Unis] ; Debby W. Tsuang [États-Unis] ; Dora Yearout [États-Unis] ; Eric B. Larson [États-Unis] ; Hideshi Kawakami [Japon]LRRK2 Mutations and Risk Variants in Japanese Patients with Parkinson’s Disease

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