| Ident. | Authors (with country if any) | Title |
|---|
| 000479 (2014) |
Lucia Ricciardi [Italie] ; Simona Petrucci ; Arianna Guidubaldi ; Tamara Ialongo ; Laura Serra ; Alessandro Ferraris ; Barbara Span ; Marco Bozzali ; Enza Maria Valente ; Anna Rita Bentivoglio | Phenotypic variability of PINK1 expression: 12 Years' clinical follow-up of two Italian families. |
| 000486 (2014) |
Darius Ebrahimi-Fakhari [États-Unis] ; Lara Wahlster ; Mustafa Sahin | Parkinson's disease: A disorder of axonal mitophagy? |
| 000693 (2014) |
Paolo Calabresi [Italie] ; Veronica Ghiglieri | "Lazy" nigrostriatal synapses in the heterozygous PINK1 mouse model of familial Parkinson's disease. |
| 000926 (2013) |
Benjamin Dehay [France] ; Marta Martinez-Vicente ; Guy A. Caldwell ; Kim A. Caldwell ; Zhenyue Yue ; Mark R. Cookson ; Christine Klein ; Miquel Vila ; Erwan Bezard | Lysosomal impairment in Parkinson's disease. |
| 000B43 (2013) |
G. Madeo [Italie] ; T. Schirinzi [Italie] ; G. Martella [Italie] ; E. C. Latagliata [Italie] ; F. Puglisi [Italie] ; J. Shen [États-Unis] ; E. M. Valente [Italie] ; M. Federici [Italie] ; N. B. Mercuri [Italie] ; S. Puglisi-Allegra [Italie] ; P. Bonsi [Italie] ; A. Pisani [Italie] | PINK1 heterozygous mutations induce subtle alterations in dopamine-dependent synaptic plasticity |
| 000B95 (2012) |
Laura L. Kilarski [Royaume-Uni] ; Justin P. Pearson ; Victoria Newsway ; Elisa Majounie ; M Duleeka W. Knipe ; Anjum Misbahuddin ; Patrick F. Chinnery ; David J. Burn ; Carl E. Clarke ; Marie-Helene Marion ; Alistair J. Lewthwaite ; David J. Nicholl ; Nicholas W. Wood ; Karen E. Morrison ; Caroline H. Williams-Gray ; Jonathan R. Evans ; Stephen J. Sawcer ; Roger A. Barker ; Mirdhu M. Wickremaratchi ; Yoav Ben-Shlomo ; Nigel M. Williams ; Huw R. Morris | Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease. |
| 001267 (2011) |
Taku Hatano [Japon] | A novel protein degradation system in young-onset Parkinson's disease: mitophagy is a therapeutic target as a quality control for damaged mitochondria. |
| 001334 (2011) |
Christine Klein [Canada, Allemagne] ; Rosalind Chuang [Canada] ; Connie Marras [Canada] ; Anthony E. Lang [Canada] | The curious case of phenocopies in families with genetic Parkinson's disease |
| 001497 (2011) |
Farzaneh Ghazavi [Iran] ; Zeinab Fazlali [Iran] ; Setareh Sadat Banihosseini [Iran] ; Sayed-Rzgar Hosseini [Iran] ; Mohammad Hossein Kazemi [Iran] ; Seyedmehdi Shojaee [Iran] ; Khosro Parsa [Iran] ; Homa Sadeghi [Iran] ; Farzad Sina [Iran] ; Mohammad Rohani [Iran] ; Gholam-Ali Shahidi [Iran] ; Nasser Ghaemi [Iran] ; Mostafa Ronaghi [États-Unis] ; Elahe Elahi [Iran] | PRKN, DJ‐1, and PINK1 screening identifies novel splice site mutation in PRKN and two novel DJ‐1 mutations |
| 001D67 (2010) |
Mark R. Cookson [États-Unis] | DJ‐1, PINK1, and their effects on mitochondrial pathways |
| 001D92 (2010) |
Christian Wider [États-Unis] ; Tatiana Foroud [États-Unis] ; Zbigniew K. Wszolek [États-Unis] | Clinical implications of gene discovery in Parkinson's disease and parkinsonism |
| 001D97 (2010) |
Meike Kasten [Allemagne] ; Charlotte Weichert [Allemagne] ; Katja Lohmann [Allemagne] ; Christine Klein [Allemagne] | Clinical and demographic characteristics of PINK1 mutation carriers—A meta‐analysis |
| 002161 (2009) |
Clecio Godeiro-Junior [Brésil] ; Patricia M. De Carvalho-Aguiar [Brésil] ; Andre C. Felício [Brésil] ; Orlando G. P. Barsottini [Brésil] ; Sonia M. A. Silva [Brésil] ; Vanderci Borges [Brésil] ; Luiz Augusto F. Andrade [Brésil] ; Henrique Ballalai Ferraz [Brésil] | PINK1 mutations in a Brazilian cohort of early‐onset Parkinson's disease patients |
| 002169 (2009) |
Alessandro Ferraris [Italie] ; Tamara Ialongo [Italie] ; Giulio Cesare Passali [Italie] ; Maria Teresa Pellecchia [Italie] ; Livia Brusa [Italie] ; Marianna Laruffa [Italie] ; Arianna Guidubaldi [Italie] ; Gaetano Paludetti [Italie] ; Alberto Albanese [Italie] ; Paolo Barone [Italie] ; Bruno Dallapiccola [Italie] ; Enza Maria Valente [Italie] ; Anna Rita Bentivoglio [Italie] | Olfactory dysfunction in Parkinsonism caused by PINK1 mutations |
| 002219 (2009) |
Bart F. L. Van Nuenen [Pays-Bas, Allemagne] ; Thilo Van Eimeren [Canada] ; Joyce P. M. Van Der Vegt [Pays-Bas, Allemagne] ; Carsten Buhmann [Allemagne] ; Christine Klein [Allemagne] ; Bastiaan R. Bloem [Pays-Bas] ; Hartwig R. Siebner [Allemagne, Danemark] | Mapping preclinical compensation in Parkinson's disease: An imaging genomics approach |
| 002288 (2009) |
Maria G. Macedo [Pays-Bas] ; Dagmar Verbaan [Pays-Bas] ; Yue Fang [Pays-Bas] ; Stephanie M. Van Rooden [Pays-Bas] ; Martine Visser [Pays-Bas] ; Burcu Anar [Pays-Bas] ; Antonella Uras [Pays-Bas] ; Justus L. Groen [Pays-Bas] ; Patrizia Rizzu [Pays-Bas] ; Jacobus J. Van Hilten [Pays-Bas] ; Peter Heutink [Pays-Bas] | Genotypic and phenotypic characteristics of Dutch patients with early onset Parkinson's disease |
| 002289 (2009) |
Ming-Jen Lee [Taïwan] ; Ignacio F. Mata [États-Unis] ; Chin-Hsien Lin [Taïwan] ; Kai-Yuan Tzen [Taïwan] ; Sarah J. Lincoln [États-Unis] ; Rebecca Bounds [États-Unis] ; Paul J. Lockhart [Australie] ; Mary M. Hulihan [États-Unis] ; Matthew J. Farrer [États-Unis] ; Ruey-Meei Wu [Taïwan] | Genotype–phenotype correlates in Taiwanese patients with early‐onset recessive parkinsonism |
| 002298 (2009) |
Stephanie A. Cobb [États-Unis] ; Christian Wider [États-Unis] ; Owen A. Ross [États-Unis] ; Ignacio F. Mata [États-Unis] ; Charles H. Adler [États-Unis] ; Alex Rajput [Canada] ; Ali H. Rajput [Canada] ; Ruey-Meei Wu [Taïwan] ; Robert Hauser [États-Unis] ; Keith A. Josephs [États-Unis] ; Jonathan Carr [Afrique du Sud] ; Katrina Gwinn [États-Unis] ; Michael G. Heckman [États-Unis] ; Jan O. Aasly [Norvège] ; Timothy Lynch [Irlande (pays)] ; Ryan J. Uitti [États-Unis] ; Zbigniew K. Wszolek [États-Unis] ; Gregory Kapatos [États-Unis] ; Matthew J. Farrer [États-Unis] | GCH1 in early‐onset Parkinson's disease |
| 002304 (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 |
| 002351 (2009) |
Greg T. Sutherland [Australie] ; Glenda M. Halliday [Australie] ; Peter A. Silburn [Australie] ; Frank L. Mastaglia [Australie] ; Dominic B. Rowe [Australie] ; Richard S. Boyle [Australie] ; John D. O'Sullivan [Australie] ; Tina Ly [Australie] ; Steve D. Wilton [Australie] ; George D. Mellick [Australie] | Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease? |
| 002378 (2009) |
Susanne A. Schneider [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] ; John Hardy [Royaume-Uni] | Complicated recessive dystonia parkinsonism syndromes |
