Author:
Akcakaya Nihan Hande,Iseri Sibel Ugur,Bilir Birdal,Battaloglu Esra,Tekturk Pinar,Gultekin Murat,Akar Gokcen,Yigiter Remzi,Hanagasi Hasmet,Alp Recep,Cagirici Sultan,Eraksoy Mefkure,Ozbek Ugur,Yapici Zuhal
Funder
Scientific Research Projects Coordination Unit of Istanbul University
Istanbul Development Agency
Subject
Neurology (clinical),General Medicine,Surgery
Reference18 articles.
1. Syndromes of neurodegeneration with brain iron accumulation (NBIA): an update on clinical presentations, histological and genetic underpinnings, and treatment considerations;Schneider;Mov. Disord.,2012
2. Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome;Hayflick;N. Eng. J. Med.,2003
3. A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome;Zhou;Nat. Genet.,2001
4. An isoform of hPANK2, deficient in pantothenate kinase-associated neurodegeneration, localizes to mitochondria;Hortnagel;Hum. Mol. Genet.,2003
5. Mitochondrial localization of human PANK2 and hypotheses of secondary iron accumulation in pantothenate kinase associated neurodegeneration;Johnson;Ann. N. Y. Acad. Sci.,2004
Cited by
17 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献