These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
173 related items for PubMed ID: 18550428
1. Sleep and temperature rhythms in two sisters with P102L Gerstmann-Sträussler-Scheinker (GSS) disease. Provini F, Vetrugno R, Pierangeli G, Cortelli P, Rizzo G, Filla A, Strisciuglio C, Gallassi R, Montagna P. Sleep Med; 2009 Mar; 10(3):374-7. PubMed ID: 18550428 [Abstract] [Full Text] [Related]
2. Normal sleep-wake and circadian rhythms in a case of Gerstmann-Sträussler-Sheinker (GSS) disease. Pierangeli G, Bono F, Aguglia U, Maltoni P, Montagna P, Lugaresi E, Quattrone A, Cortelli P. Clin Auton Res; 2004 Feb; 14(1):39-41. PubMed ID: 15045600 [Abstract] [Full Text] [Related]
3. Gerstmann-Sträussler-Scheinker syndrome with variable phenotype in a new kindred with PRNP-P102L mutation. Riudavets MA, Sraka MA, Schultz M, Rojas E, Martinetto H, Begué C, Noher de Halac I, Poleggi A, Equestre M, Pocchiari M, Sevlever G, Taratuto AL. Brain Pathol; 2014 Mar; 24(2):142-7. PubMed ID: 23944754 [Abstract] [Full Text] [Related]
12. A Chinese patient of P102L Gerstmann-Sträussler-Scheinker disease contains three other disease-associated mutations in SYNE1. Wang J, Xiao K, Zhou W, Gao C, Chen C, Shi Q, Dong XP. Prion; 2018 Mar 04; 12(2):150-155. PubMed ID: 29509064 [Abstract] [Full Text] [Related]
15. A previously undiagnosed case of Gerstmann-Sträussler-Scheinker disease revealed by PRNP gene analysis in patients with adult-onset ataxia. Cagnoli C, Brussino A, Sbaiz L, Di Gregorio E, Atzori C, Caroppo P, Orsi L, Migone N, Buffa C, Imperiale D, Brusco A. Mov Disord; 2008 Jul 30; 23(10):1468-71. PubMed ID: 18566986 [Abstract] [Full Text] [Related]
19. [Gerstmann-Sträussler-Scheinker disease, fatal familial insomnia and less common human prion diseases]. Kawashima T. Nihon Rinsho; 2003 Mar 30; 61 Suppl 3():17-21. PubMed ID: 12717941 [No Abstract] [Full Text] [Related]
20. Gerstmann-Sträussler-Scheinker disease with the PRNP P102L mutation and valine at codon 129. Young K, Clark HB, Piccardo P, Dlouhy SR, Ghetti B. Brain Res Mol Brain Res; 1997 Feb 30; 44(1):147-50. PubMed ID: 9030710 [Abstract] [Full Text] [Related] Page: [Next] [New Search]