Author:
Baldin Elisa,Capellari Sabina,Provini Federica,Corrado Patrizia,Liguori Rocco,Parchi Piero,Montagna Pasquale,Cortelli Pietro
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Reference7 articles.
1. Bosque PJ, Vnencak-Jones CL, Johnson MD, Whitlock JA, McLean MJ (1992) A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt–Jakob disease. Neurology 42(10):1864–1870
2. Cervenakova L, Brown P, Piccardo P, Cummings JL, Nagle J, Vinters HV, Kaur P, Ghetti B, Chapman J, Gajdusek DC, Goldfarb LG (1996) 24-nucleotide deletion in the PRNP gene: analysis of associated phenotypes in transmissible subacute spongiform encephalopathies. In: Court L, Dodet B (eds) Elsevier, Paris, pp 433–444
3. Krasnianski A, Bartl M, Sanchez Juan PJ, Heinemann U, Meissner B, Varges D, Schulze-Sturm U, Kretzschmar HA, Schulz-Schaeffer WJ, Zerr I (2008) Fatal familial insomnia: Clinical features and early identification. Ann Neurol 63(5):658–661
4. Montagna P, Gambetti P, Cortelli P, Lugaresi E (2003) Familial and sporadic fatal insomnia. Lancet Neurol 2(3):167–176
5. Montagna P (2005) Fatal familial insomnia: a model disease in sleep physiopathology. Sleep Med Rev 9(5):339–353
Cited by
11 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