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Concomitant loss of dynorphin, NARP, and orexin in narcolepsy.
Crocker A, España RA, Papadopoulou M, Saper CB, Faraco J, Sakurai T, Honda M, Mignot E, Scammell TE. Crocker A, et al. Among authors: faraco j. Neurology. 2005 Oct 25;65(8):1184-8. doi: 10.1212/01.wnl.0000168173.71940.ab. Epub 2005 Sep 14. Neurology. 2005. PMID: 16247044 Free PMC article.
Genetic studies in the sleep disorder narcolepsy.
Kadotani H, Faraco J, Mignot E. Kadotani H, et al. Among authors: faraco j. Genome Res. 1998 May;8(5):427-34. doi: 10.1101/gr.8.5.427. Genome Res. 1998. PMID: 9582188 Free article. Review.
A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains.
Peyron C, Faraco J, Rogers W, Ripley B, Overeem S, Charnay Y, Nevsimalova S, Aldrich M, Reynolds D, Albin R, Li R, Hungs M, Pedrazzoli M, Padigaru M, Kucherlapati M, Fan J, Maki R, Lammers GJ, Bouras C, Kucherlapati R, Nishino S, Mignot E. Peyron C, et al. Among authors: faraco j. Nat Med. 2000 Sep;6(9):991-7. doi: 10.1038/79690. Nat Med. 2000. PMID: 10973318
Kleine-Levin syndrome: a systematic study of 108 patients.
Arnulf I, Lin L, Gadoth N, File J, Lecendreux M, Franco P, Zeitzer J, Lo B, Faraco JH, Mignot E. Arnulf I, et al. Among authors: faraco jh. Ann Neurol. 2008 Apr;63(4):482-93. doi: 10.1002/ana.21333. Ann Neurol. 2008. PMID: 18438947
Variant between CPT1B and CHKB associated with susceptibility to narcolepsy.
Miyagawa T, Kawashima M, Nishida N, Ohashi J, Kimura R, Fujimoto A, Shimada M, Morishita S, Shigeta T, Lin L, Hong SC, Faraco J, Shin YK, Jeong JH, Okazaki Y, Tsuji S, Honda M, Honda Y, Mignot E, Tokunaga K. Miyagawa T, et al. Among authors: faraco j. Nat Genet. 2008 Nov;40(11):1324-8. doi: 10.1038/ng.231. Epub 2008 Sep 28. Nat Genet. 2008. PMID: 18820697
37 results