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8. Distinctive MRI findings in pallidopontonigral degeneration (PPND). Frank AR; Wszolek ZK; Jack CR; Boeve BF Neurology; 2007 Feb; 68(8):620-1. PubMed ID: 17310038 [No Abstract] [Full Text] [Related]
9. Presynaptic nigrostriatal function in genetically tested asymptomatic relatives from the pallido-ponto-nigral degeneration family. Kishore A; Wszolek ZK; Snow BJ; de la Fuente-Fernandez R; Arwert F; Wijker M; Schulzer M; Calne DB; Vingerhoets FJ Neurology; 1996 Dec; 47(6):1588-90. PubMed ID: 8960754 [TBL] [Abstract][Full Text] [Related]
10. Physiologic assessment of autonomic dysfunction in pallidopontonigral degeneration with N279K mutation in the tau gene on chromosome 17. Cheshire WP; Tsuboi Y; Wszolek ZK Auton Neurosci; 2002 Nov; 102(1-2):71-7. PubMed ID: 12492138 [TBL] [Abstract][Full Text] [Related]
11. A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration. Yasuda M; Kawamata T; Komure O; Kuno S; D'Souza I; Poorkaj P; Kawai J; Tanimukai S; Yamamoto Y; Hasegawa H; Sasahara M; Hazama F; Schellenberg GD; Tanaka C Neurology; 1999 Sep; 53(4):864-8. PubMed ID: 10489057 [TBL] [Abstract][Full Text] [Related]
12. Anatomy of disturbed sleep in pallido-ponto-nigral degeneration. Spector AR; Dugger BN; Wszolek ZK; Uitti RJ; Fredrickson P; Kaplan J; Boeve BF; Dickson DW; Strongosky A; Lin SC Ann Neurol; 2011 Jun; 69(6):1014-1025. PubMed ID: 21681797 [TBL] [Abstract][Full Text] [Related]
18. [Characteristic clinicopathological and genetic features of frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17): in particular consideration for a large family of pallido-ponto-nigral degeneration (PPND)]. Yamada T No To Shinkei; 1999 Sep; 51(9):761-9. PubMed ID: 10511953 [No Abstract] [Full Text] [Related]
19. Linkage of frontotemporal dementia to chromosome 17: clinical and neuropathological characterization of phenotype. Yamaoka LH; Welsh-Bohmer KA; Hulette CM; Gaskell PC; Murray M; Rimmler JL; Helms BR; Guerra M; Roses AD; Schmechel DE; Pericak-Vance MA Am J Hum Genet; 1996 Dec; 59(6):1306-12. PubMed ID: 8940276 [TBL] [Abstract][Full Text] [Related]
20. Familial neuroaxonal dystrophy with principal lesions of nigro-pallido-subthalamic degeneration. Nakamura Y Folia Psychiatr Neurol Jpn; 1982; 36(2):151-62. PubMed ID: 6290357 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]