Ident. | Authors (with country if any) | Title |
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000266 (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 |
000C88 (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 |
000E22 (2008) |
Ji-Feng Guo [République populaire de Chine] ; Bin Xiao [République populaire de Chine] ; Bing Liao [République populaire de Chine] ; Xue-Wei Zhang [République populaire de Chine] ; Li-Luo Nie [République populaire de Chine] ; Yu-Hu Zhang [République populaire de Chine] ; Lu Shen [République populaire de Chine] ; Hong Jiang [République populaire de Chine] ; Kun Xia [République populaire de Chine] ; Qian Pan [République populaire de Chine] ; Xin-Xiang Yan [République populaire de Chine] ; Bei-Sha Tang [République populaire de Chine] | Mutation analysis of Parkin, PINK1, DJ‐1 and ATP13A2 genes in Chinese patients with autosomal recessive early‐onset Parkinsonism |
000F65 (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 |
001095 (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 |
001216 (2006) |
Shin-Ichiro Kubo [Japon] ; Nobutaka Hattori [Japon] ; Yoshikuni Mizuno [Japon] | Recessive Parkinson's disease |
001639 (2008) |
Manabu Funayama [Japon] ; Yuanzhe Li [Japon] ; Tak-Hong Tsoi [République populaire de Chine] ; Ching-Wan Lam [République populaire de Chine] ; Takekazu Ohi [Japon] ; Shogo Yazawa [Japon] ; Eiichiro Uyama [Japon] ; Ruth Djaldetti [Israël] ; Eldad Melamed [Israël] ; Hiroyo Yoshino [Japon] ; Yoko Imamichi [Japon] ; Hiroshi Takashima [Japon] ; Kenya Nishioka [Japon] ; Kenichi Sato [Japon] ; Hiroyuki Tomiyama [Japon] ; Shin-Ichiro Kubo [Japon] ; Yoshikuni Mizuno [Japon] ; Nobutaka Hattori [Japon] | Familial Parkinsonism with digenic parkin and PINK1 mutations |
001A87 (2009) |
Sarah Teixeira Camargos [Brésil] ; Leonardo Oliveira Dornas [Brésil] ; Parastoo Momeni [États-Unis] ; Andrew Lees [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 |
001B45 (2006) |
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 |
001B84 (2010) |
Ted M. Dawson [États-Unis] ; Valina L. Dawson [États-Unis] | The role of parkin in familial and sporadic Parkinson's disease |
002096 (2010) |
Mark R. Cookson [États-Unis] | DJ‐1, PINK1, and their effects on mitochondrial pathways |
002E47 (2007) |
Lilach Ephraty [Israël] ; Omer Porat [Israël] ; David Israeli [Israël] ; Oren S. Cohen [Israël] ; Olga Tunkel [Israël] ; Shinar Yael [Israël] ; Yasaku Hatano [Japon] ; Nobutaka Hattori [Japon] ; Sharon Hassin-Baer [Israël] | Neuropsychiatric and cognitive features in autosomal‐recessive early parkinsonism due to PINK1 mutations |
002F59 (2006) |
Cindy Zadikoff [Canada] ; Ekaterina Rogaeva [Canada] ; Ana Djarmati [Allemagne] ; Christine Sato [Canada] ; Shabnam Salehi-Rad [Canada] ; Peter St. George-Hyslop [Canada] ; Christine Klein [Canada, Allemagne] ; Anthony E. Lang [Canada] | Homozygous and heterozygous PINK1 mutations: Considerations for diagnosis and care of Parkinson's disease patients |
002F86 (2008) |
Vania Gelmetti [Italie] ; Alessandro Ferraris [Italie] ; Livia Brusa [Italie] ; Francesca Romano [Italie] ; Federica Lombardi [Italie] ; Chiara Barzaghi [Italie] ; Paolo Stanzione [Italie] ; Barbara Garavaglia [Italie] ; Bruno Dallapiccola [Italie] ; Enza Maria Valente [Italie] | Late onset sporadic Parkinson's disease caused by PINK1 mutations: Clinical and functional study |
003422 (2006) |
Ana Djarmati [Allemagne, Serbie] ; Katja Hedrich [Allemagne] ; Marina Svetel [Serbie] ; Thora Lohnau [Allemagne] ; Eberhard Schwinger [Allemagne] ; Stanka Romac [Serbie] ; Peter P. Pramstaller [Italie] ; Vladimir Kosti [Serbie] ; Christine Klein [Allemagne] | Heterozygous PINK1 mutations: A susceptibility factor for Parkinson disease? |
003715 (2006) |
Chiara Criscuolo [Italie] ; Giampiero Volpe [Italie] ; Anna De Rosa [Italie] ; Andrea Varrone [Italie] ; Roberta Marongiu [Italie] ; Pietro Mancini [Italie] ; Elena Salvatore [Italie] ; Bruno Dallapiccola [Italie] ; Alessandro Filla [Italie] ; Enza Maria Valente [Italie] ; Giuseppe De Michele [Italie] | PINK1 homozygous W437X mutation in a patient with apparent dominant transmission of parkinsonism |
003789 (2007) |
Anja Hiller [Allemagne] ; Johann M. Hagenah [Allemagne] ; Ana Djarmati [Allemagne] ; Katja Hedrich [Allemagne] ; Kathrin Reetz [Allemagne] ; Christiane Schneider-Gold [Allemagne] ; Wolfgang Kress [Allemagne] ; Alexander Münchau [Allemagne] ; Christine Klein [Allemagne] | Phenotypic spectrum of PINK1‐associated parkinsonism in 15 mutation carriers from 1 family |