List of bibliographic references
Number of relevant bibliographic references: 6.
Ident. | Authors (with country if any) | Title |
---|
000100 (2010) |
Coro Paisán-Ruiz [Royaume-Uni] ; Rocio Guevara [Royaume-Uni] ; Monica Federoff [Royaume-Uni] ; Hasmet Hanagasi [Turquie] ; Fardaz Sina [Iran] ; Elahe Elahi [Iran] ; Susanne A. Schneider [Royaume-Uni, Allemagne] ; Petra Schwingenschuh [Allemagne] ; Nin Bajaj [Royaume-Uni] ; Murat Emre [Turquie] ; Andrew B. Singleton [États-Unis] ; John Hardy [Royaume-Uni] ; Kailash P. Bhatia [Allemagne] ; Sebastian Brandner [Royaume-Uni] ; Andrew J. Lees [Royaume-Uni] ; Henry Houlden [Royaume-Uni] | Early‐onset L‐dopa‐responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations |
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 |
000E14 (2008) |
Maria G. Motlagh [États-Unis, Iran] ; Arshia Seddigh [Iran, Royaume-Uni] ; Behnoosh Dashti [Iran] ; James F. Leckman [États-Unis] ; Javad Alaghband-Rad [Iran, Canada] | Consanguineous Iranian kindreds with severe Tourette syndrome |
002A20 (2009) |
Behzad Elahi [Canada] ; Behrad Elahi [Iran] ; Robert Chen [Canada] | Effect of transcranial magnetic stimulation on Parkinson motor function—Systematic review of controlled clinical trials |
002B93 (2009) |
Seyedmehdi Shojaee [Iran] ; Farzad Sina [Iran] ; Niloofar Farboodi [Iran] ; Zeinab Fazlali [Iran] ; Farzaneh Ghazavi [Iran] ; Seyed Ali Ghorashi [Iran] ; Khosro Parsa [Iran] ; Homa Sadeghi [Iran] ; Gholam-Ali Shahidi [Iran] ; Mostafa Ronaghi [États-Unis, Iran] ; Elahe Elahi [Iran] | A clinic‐based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients |
003158 (2011) |
Susanne A. Schneider [Allemagne, Royaume-Uni] ; Alfredo Ramirez [Allemagne] ; Kaveh Shafiee [Iran] ; Frank J. Kaiser [Allemagne] ; Alev Erogullari [Allemagne] ; Norbert Brüggemann [Allemagne] ; Susen Winkler [Allemagne] ; Ideh Bahman [Iran] ; Alma Osmanovic [Allemagne] ; Mohammad A. Shafa [Iran] ; Kailish P. Bhatia [Royaume-Uni] ; Hossein Najmabadi [Iran] ; Christine Klein [Allemagne] ; Katja Lohmann [Allemagne] | Homozygous THAP1 mutations as cause of early‐onset generalized dystonia |
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