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Results: 18

1.

History of narcolepsy at Stanford University.

Mignot EJ.

Immunol Res. 2014 May;58(2-3):315-39. doi: 10.1007/s12026-014-8513-4.

PMID:
24825774
[PubMed - in process]
Free PMC Article
2.

DQB1 locus alone explains most of the risk and protection in narcolepsy with cataplexy in Europe.

Tafti M, Hor H, Dauvilliers Y, Lammers GJ, Overeem S, Mayer G, Javidi S, Iranzo A, Santamaria J, Peraita-Adrados R, Vicario JL, Arnulf I, Plazzi G, Bayard S, Poli F, Pizza F, Geisler P, Wierzbicka A, Bassetti CL, Mathis J, Lecendreux M, Donjacour CE, van der Heide A, Heinzer R, Haba-Rubio J, Feketeova E, Högl B, Frauscher B, Benetó A, Khatami R, Cañellas F, Pfister C, Scholz S, Billiard M, Baumann CR, Ercilla G, Verduijn W, Claas FH, Dubois V, Nowak J, Eberhard HP, Pradervand S, Hor CN, Testi M, Tiercy JM, Kutalik Z.

Sleep. 2014 Jan 1;37(1):19-25. doi: 10.5665/sleep.3300.

PMID:
24381371
[PubMed - in process]
Free PMC Article
3.

DQB1*06:02 allele-specific expression varies by allelic dosage, not narcolepsy status.

Weiner Lachmi K, Lin L, Kornum BR, Rico T, Lo B, Aran A, Mignot E.

Hum Immunol. 2012 Apr;73(4):405-10. doi: 10.1016/j.humimm.2012.01.004. Epub 2012 Jan 31.

PMID:
22326585
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

TCRA, P2RY11, and CPT1B/CHKB associations in Chinese narcolepsy.

Han F, Lin L, Li J, Aran A, Dong SX, An P, Zhao L, Li QY, Yan H, Wang JS, Gao HY, Li M, Gao ZC, Strohl KP, Mignot E.

Sleep Med. 2012 Mar;13(3):269-72. doi: 10.1016/j.sleep.2011.06.020. Epub 2011 Dec 15.

PMID:
22177342
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Towards universal structure-based prediction of class II MHC epitopes for diverse allotypes.

Bordner AJ.

PLoS One. 2010 Dec 20;5(12):e14383. doi: 10.1371/journal.pone.0014383.

PMID:
21187956
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Common variants in P2RY11 are associated with narcolepsy.

Kornum BR, Kawashima M, Faraco J, Lin L, Rico TJ, Hesselson S, Axtell RC, Kuipers H, Weiner K, Hamacher A, Kassack MU, Han F, Knudsen S, Li J, Dong X, Winkelmann J, Plazzi G, Nevsimalova S, Hong SC, Honda Y, Honda M, Högl B, Ton TG, Montplaisir J, Bourgin P, Kemlink D, Huang YS, Warby S, Einen M, Eshragh JL, Miyagawa T, Desautels A, Ruppert E, Hesla PE, Poli F, Pizza F, Frauscher B, Jeong JH, Lee SP, Strohl KP, Longstreth WT Jr, Kvale M, Dobrovolna M, Ohayon MM, Nepom GT, Wichmann HE, Rouleau GA, Gieger C, Levinson DF, Gejman PV, Meitinger T, Peppard P, Young T, Jennum P, Steinman L, Tokunaga K, Kwok PY, Risch N, Hallmayer J, Mignot E.

Nat Genet. 2011 Jan;43(1):66-71. doi: 10.1038/ng.734. Epub 2010 Dec 19. Erratum in: Nat Genet. 2011 Oct;43(10):1040.

PMID:
21170044
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Clinical and therapeutic aspects of childhood narcolepsy-cataplexy: a retrospective study of 51 children.

Aran A, Einen M, Lin L, Plazzi G, Nishino S, Mignot E.

Sleep. 2010 Nov;33(11):1457-64.

PMID:
21102987
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

MultiRTA: a simple yet reliable method for predicting peptide binding affinities for multiple class II MHC allotypes.

Bordner AJ, Mittelmann HD.

BMC Bioinformatics. 2010 Sep 24;11:482. doi: 10.1186/1471-2105-11-482.

PMID:
20868497
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Whole genome association studies in complex diseases: where do we stand?

Need AC, Goldstein DB.

Dialogues Clin Neurosci. 2010;12(1):37-46. Review.

PMID:
20373665
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

The type 1 diabetes - HLA susceptibility interactome--identification of HLA genotype-specific disease genes for type 1 diabetes.

Brorsson C, Tue Hansen N, Bergholdt R, Brunak S, Pociot F.

PLoS One. 2010 Mar 5;5(3):e9576. doi: 10.1371/journal.pone.0009576.

PMID:
20221424
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Regulation of major histocompatibility complex class II gene expression, genetic variation and disease.

Handunnetthi L, Ramagopalan SV, Ebers GC, Knight JC.

Genes Immun. 2010 Mar;11(2):99-112. doi: 10.1038/gene.2009.83. Epub 2009 Nov 5. Review.

PMID:
19890353
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Association of narcolepsy-cataplexy with HLA-DRB1 and DQB1 in Mexican patients: a relationship between HLA and gender is suggested.

Alaez C, Lin L, Flores-A H, Vazquez M, Munguia A, Mignot E, Haro R, Baker H, Gorodezky C.

BMC Med Genet. 2008 Aug 15;9:79. doi: 10.1186/1471-2350-9-79.

PMID:
18706091
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

History of the development of sleep medicine in the United States.

Shepard JW Jr, Buysse DJ, Chesson AL Jr, Dement WC, Goldberg R, Guilleminault C, Harris CD, Iber C, Mignot E, Mitler MM, Moore KE, Phillips BA, Quan SF, Rosenberg RS, Roth T, Schmidt HS, Silber MH, Walsh JK, White DP.

J Clin Sleep Med. 2005 Jan 15;1(1):61-82.

PMID:
17561617
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Clinical and neurobiological aspects of narcolepsy.

Nishino S.

Sleep Med. 2007 Jun;8(4):373-99. Epub 2007 Apr 30. Review.

PMID:
17470414
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Crystal structure of HLA-DQ0602 that protects against type 1 diabetes and confers strong susceptibility to narcolepsy.

Siebold C, Hansen BE, Wyer JR, Harlos K, Esnouf RE, Svejgaard A, Bell JI, Strominger JL, Jones EY, Fugger L.

Proc Natl Acad Sci U S A. 2004 Feb 17;101(7):1999-2004. Epub 2004 Feb 9.

PMID:
14769912
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Complex HLA-DR and -DQ interactions confer risk of narcolepsy-cataplexy in three ethnic groups.

Mignot E, Lin L, Rogers W, Honda Y, Qiu X, Lin X, Okun M, Hohjoh H, Miki T, Hsu S, Leffell M, Grumet F, Fernandez-Vina M, Honda M, Risch N.

Am J Hum Genet. 2001 Mar;68(3):686-99. Epub 2001 Feb 13.

PMID:
11179016
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

"Cataplexy" and muscle ultrasound abnormalities in Coffin-Lowry syndrome.

Crow YJ, Zuberi SM, McWilliam R, Tolmie JL, Hollman A, Pohl K, Stephenson JB.

J Med Genet. 1998 Feb;35(2):94-8.

PMID:
9507386
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Genetics of narcolepsy and other sleep disorders.

Mignot E.

Am J Hum Genet. 1997 Jun;60(6):1289-302. Review. No abstract available.

PMID:
9199548
[PubMed - indexed for MEDLINE]
Free PMC Article

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