Ident. | Authors (with country if any) | Title |
---|
000190 |
Fernando Cardona [Espagne] ; Jose Vicente Sánchez-Mut [Espagne] ; Hernán Dopazo [Espagne] ; Jordi Pérez-Tur [Espagne] | Phylogenetic and in silico structural analysis of the Parkinson disease‐related kinase PINK1 |
000200 |
K. K. Johansen [Norvège] ; J. V. J Rgensen [Norvège] ; L. R. White [Norvège] ; M. J. Farrer [États-Unis] ; J. O. Aasly [Norvège] | Parkinson‐related genetics in patients treated with deep brain stimulation |
000212 |
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 |
000506 |
Ted M. Dawson [États-Unis] ; Valina L. Dawson [États-Unis] | The role of parkin in familial and sporadic Parkinson's disease |
000704 |
Karen Nuytemans [Belgique] ; Jessie Theuns [Belgique] ; Marc Cruts [Belgique] ; Christine Van Broeckhoven [Belgique] | Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update |
000762 |
Mark R. Cookson [États-Unis] | DJ‐1, PINK1, and their effects on mitochondrial pathways |
000A08 |
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 |
000A12 |
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 |
000A76 |
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 |
000A86 |
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 |
000B40 |
Eng-King Tan [Singapour] ; F. Shaffra Refai [Singapour] ; Mobin Siddique [Singapour] ; Karen Yap [Singapour] ; Patrick Ho [Singapour] ; Stephanie Fook-Chong [Singapour] ; Yi Zhao [Singapour] | Clinically reported heterozygous mutations in the PINK1 kinase domain exert a gene dosage effect |
000C22 |
Helene Plun-Favreau [Royaume-Uni] ; Sonia Gandhi [Royaume-Uni] ; Alison Wood-Kaczmar [Royaume-Uni] ; Emma Deas [Royaume-Uni] ; Zhi Yao [Royaume-Uni] ; Nicholas W. Wood [Royaume-Uni] | What Have PINK1 and HtrA2 Genes Told Us about the Role of Mitochondria in Parkinson's Disease? |
000D73 |
Andrew B. Knott [États-Unis] ; Ella Bossy-Wetzel [États-Unis] | Impairing the Mitochondrial Fission and Fusion Balance: A New Mechanism of Neurodegeneration |
000F13 |
Roberta Marongiu [Italie] ; Francesco Brancati [Italie] ; Angelo Antonini [Italie] ; Tamara Ialongo [Italie] ; Caterina Ceccarini [Italie] ; Oronzo Scarciolla [Italie] ; Anna Capalbo [Italie] ; Riccardo Benti [Italie] ; Gianni Pezzoli [Italie] ; Bruno Dallapiccola [Italie] ; Stefano Goldwurm [Italie] ; Enza Maria Valente [Italie] | Whole gene deletion and splicing mutations expand the PINK1 genotypic spectrum |
001210 |
Shin-Ichiro Kubo [Japon] ; Nobutaka Hattori [Japon] ; Yoshikuni Mizuno [Japon] | Recessive Parkinson's disease |
001244 |
Eng-King Tan [Singapour] ; Kenneth Yew [Singapour] ; Eva Chua [Singapour] ; K. Puvan [Singapour] ; Hui Shen [Singapour] ; Esther Lee [Singapour] ; Kim-Yoong Puong [Singapour] ; Yi Zhao [Singapour] ; Ratnagopal Pavanni [Singapour] ; Meng-Cheong Wong [Singapour] ; Dominic Jamora [Singapour] ; Deidre De Silva [Singapour] ; Kyaw-Thu Moe [Singapour] ; Fung-Peng Woon [Singapour] ; Yih Yuen [Singapour] ; Louis Tan [Singapour] | PINK1 mutations in sporadic early‐onset Parkinson's disease |
001257 |
Pablo Iba N Ez ; Suzanne Lesage ; Ebba Lohmann ; Ste Phane Thobois ; Giuseppe De Michele [Italie] ; Michel Borg ; Yves Agid [France] ; Alexandra Du Rr ; Alexis Brice | Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa |