Movement Disorders (revue) - Checkpoint (Ncbi)

Index « Mesh.i » - entrée « Protein Kinases »
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Protein Kinase C < Protein Kinases < Protein Phosphatase 2  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 36.
[0-20] [0 - 20][0 - 36][20-35][20-40]
Ident.Authors (with country if any)Title
001075 (2005) Aideen Mcinerney-Leo [États-Unis] ; Donald W. Hadley ; Katrina Gwinn-Hardy ; John HardyGenetic testing in Parkinson's disease.
001113 (2005) Aida M. Bertoli-Avella [Pays-Bas] ; José L. Giroud-Benitez ; Ali Akyol ; Egberto Barbosa ; Onno Schaap ; Herma C. Van Der Linde ; Emilia Martignoni ; Leonardo Lopiano ; Paolo Lamberti ; Emiliana Fincati ; Angelo Antonini ; Fabrizio Stocchi ; Pasquale Montagna ; Ferdinando Squitieri ; Paolo Marini ; Giovanni Abbruzzese ; Giovanni Fabbrini ; Roberto Marconi ; Alessio Dalla Libera ; Giorgio Trianni ; Marco Guidi ; Antonio De Gaetano ; Gustavo Boff Maegawa ; Antonino De Leo ; Virgilio Gallai ; Giulia De Rosa ; Nicola Vanacore ; Giuseppe Meco ; Cornelia M. Van Duijn ; Ben A. Oostra ; Peter Heutink ; Vincenzo BonifatiNovel parkin mutations detected in patients with early-onset Parkinson's disease.
001576 (2006) Eng-King Tan [Singapour] ; Kenneth Yew ; Eva Chua ; K. Puvan ; Hui Shen ; Esther Lee ; Kim-Yoong Puong ; Yi Zhao ; Ratnagopal Pavanni ; Meng-Cheong Wong ; Dominic Jamora ; Deidre De Silva ; Kyaw-Thu Moe ; Fung-Peng Woon ; Yih Yuen ; Louis TanPINK1 mutations in sporadic early-onset Parkinson's disease.
001612 (2006) Cindy Zadikoff [Canada] ; Ekaterina Rogaeva ; Ana Djarmati ; Christine Sato ; Shabnam Salehi-Rad ; Peter St George-Hyslop ; Christine Klein ; Anthony E. LangHomozygous and heterozygous PINK1 mutations: considerations for diagnosis and care of Parkinson's disease patients.
001635 (2006) Shin-Ichiro Kubo [Japon] ; Nobutaka Hattori ; Yoshikuni MizunoRecessive Parkinson's disease.
001691 (2006) Chiara Criscuolo [Italie] ; Giampiero Volpe ; Anna De Rosa ; Andrea Varrone ; Roberta Marongiu ; Pietro Mancini ; Elena Salvatore ; Bruno Dallapiccola ; Alessandro Filla ; Enza Maria Valente ; Giuseppe De MichelePINK1 homozygous W437X mutation in a patient with apparent dominant transmission of parkinsonism.
001719 (2006) Ana Djarmati [Allemagne] ; Katja Hedrich ; Marina Svetel ; Thora Lohnau ; Eberhard Schwinger ; Stanka Romac ; Peter P. Pramstaller ; Vladimir Kosti ; Christine KleinHeterozygous PINK1 mutations: a susceptibility factor for Parkinson disease?
001869 (2007) Anja Hiller [Allemagne] ; Johann M. Hagenah ; Ana Djarmati ; Katja Hedrich ; Kathrin Reetz ; Christiane Schneider-Gold ; Wolfgang Kress ; Alexander Münchau ; Christine KleinPhenotypic spectrum of PINK1-associated parkinsonism in 15 mutation carriers from 1 family.
001A59 (2007) Lilach Ephraty [Israël] ; Omer Porat ; David Israeli ; Oren S. Cohen ; Olga Tunkel ; Shinar Yael ; Yasaku Hatano ; Nobutaka Hattori ; Sharon Hassin-BaerNeuropsychiatric and cognitive features in autosomal-recessive early parkinsonism due to PINK1 mutations.
001E60 (2007) Oronzo Scarciolla [Italie] ; Francesco Brancati ; Enza Maria Valente ; Alessandro Ferraris ; Maria Vittoria De Angelis ; Stefano Valbonesi ; Barbara Garavaglia ; Antonino Uncini ; Giandomenico Palka ; Liborio Stuppia ; Bruno DallapiccolaMultiplex ligation-dependent probe amplification assay for simultaneous detection of Parkinson's disease gene rearrangements.
001E90 (2008) Aldo Quattrone [Italie] ; Antonio Bagnato ; Grazia Annesi ; Fabiana Novellino ; Letterio Morgante ; Giovanni Savettieri ; Mario Zappia ; Patrizia Tarantino ; Innocenza Claudia Cir Candiano ; Ferdinanda Annesi ; Donatella Civitelli ; Francesca Emanuela Rocca ; Marco D'Amelio ; Giuseppe Nicoletti ; Maurizio Morelli ; Alfredo Petrone ; Piercostanzo Loizzo ; Francesca CondinoMyocardial 123metaiodobenzylguanidine uptake in genetic Parkinson's disease.
002012 (2007) Thomas Gasser [Allemagne]Update on the genetics of Parkinson's disease.
002056 (2008) Vania Gelmetti [Italie] ; Alessandro Ferraris ; Livia Brusa ; Francesca Romano ; Federica Lombardi ; Chiara Barzaghi ; Paolo Stanzione ; Barbara Garavaglia ; Bruno Dallapiccola ; Enza Maria ValenteLate onset sporadic Parkinson's disease caused by PINK1 mutations: clinical and functional study.
002164 (2008) Manabu Funayama [Japon] ; Yuanzhe Li ; Tak-Hong Tsoi ; Ching-Wan Lam ; Takekazu Ohi ; Shogo Yazawa ; Eiichiro Uyama ; Ruth Djaldetti ; Eldad Melamed ; Hiroyo Yoshino ; Yoko Imamichi ; Hiroshi Takashima ; Kenya Nishioka ; Kenichi Sato ; Hiroyuki Tomiyama ; Shin-Ichiro Kubo ; Yoshikuni Mizuno ; Nobutaka HattoriFamilial Parkinsonism with digenic parkin and PINK1 mutations.
002325 (2008) Ji-Feng Guo [République populaire de Chine] ; Bin Xiao ; Bing Liao ; Xue-Wei Zhang ; Li-Luo Nie ; Yu-Hu Zhang ; Lu Shen ; Hong Jiang ; Kun Xia ; Qian Pan ; Xin-Xiang Yan ; Bei-Sha TangMutation analysis of Parkin, PINK1, DJ-1 and ATP13A2 genes in Chinese patients with autosomal recessive early-onset Parkinsonism.
002418 (2009) Maria G. Macedo [Pays-Bas] ; Dagmar Verbaan ; Yue Fang ; Stephanie M. Van Rooden ; Martine Visser ; Burcu Anar ; Antonella Uras ; Justus L. Groen ; Patrizia Rizzu ; Jacobus J. Van Hilten ; Peter HeutinkGenotypic and phenotypic characteristics of Dutch patients with early onset Parkinson's disease.
002437 (2009) Ming-Jen Lee [Taïwan] ; 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.
002510 (2009) Susanne A. Schneider [Royaume-Uni] ; Kailash P. Bhatia ; John HardyComplicated recessive dystonia parkinsonism syndromes.
002533 (2009) Sarah Teixeira Camargos [Brésil] ; Leonardo Oliveira Dornas [Brésil] ; Parastoo Momeni [États-Unis] ; Andrew Lees (neurologue) [Royaume-Uni] ; John Hardy [Royaume-Uni] ; Andrew Singleton [États-Unis] ; Francisco Cardoso [Brésil]Familial Parkinsonism and early onset Parkinson's disease in a Brazilian Movement Disorders clinic: Phenotypic characterization and frequency of SNCA, PRKN, PINK1 and LRRK2 mutations
002568 (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. MellickDo polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease?
002747 (2009) Clecio Godeiro-Junior [Brésil] ; Patricia M. De Carvalho-Aguiar ; Andre C. Felício ; Orlando G P. Barsottini ; Sonia M A. Silva ; Vanderci Borges ; Luiz Augusto F. Andrade ; Henrique Ballalai FerrazPINK1 mutations in a Brazilian cohort of early-onset Parkinson's disease patients.

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