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Journal Abstract Search

179 related items for PubMed ID: 22177342

  • 1. 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. PubMed ID: 22177342
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  • 5. Association analysis of the major histocompatibility complex, class II, DQ β1 gene, HLA-DQB1, with narcolepsy in Han Chinese patients from Taiwan.
    Chen YH, Huang YS, Chien WH, Chen CH.
    Sleep Med; 2013 Dec; 14(12):1393-7. PubMed ID: 24157097
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  • 6. Evaluation of polygenic risks for narcolepsy and essential hypersomnia.
    Yamasaki M, Miyagawa T, Toyoda H, Khor SS, Liu X, Kuwabara H, Kano Y, Shimada T, Sugiyama T, Nishida H, Sugaya N, Tochigi M, Otowa T, Okazaki Y, Kaiya H, Kawamura Y, Miyashita A, Kuwano R, Kasai K, Tanii H, Sasaki T, Honda Y, Honda M, Tokunaga K.
    J Hum Genet; 2016 Oct; 61(10):873-878. PubMed ID: 27305985
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  • 7. EIF3G is associated with narcolepsy across ethnicities.
    Holm A, Lin L, Faraco J, Mostafavi S, Battle A, Zhu X, Levinson DF, Han F, Gammeltoft S, Jennum P, Mignot E, Kornum BR.
    Eur J Hum Genet; 2015 Nov; 23(11):1573-80. PubMed ID: 25669430
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  • 8. Narcolepsy-cataplexy and schizophrenia in adolescents.
    Huang YS, Guilleminault C, Chen CH, Lai PC, Hwang FM.
    Sleep Med; 2014 Jan; 15(1):15-22. PubMed ID: 24268496
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  • 9. The role of cerebrospinal fluid hypocretin measurement in the diagnosis of narcolepsy and other hypersomnias.
    Mignot E, Lammers GJ, Ripley B, Okun M, Nevsimalova S, Overeem S, Vankova J, Black J, Harsh J, Bassetti C, Schrader H, Nishino S.
    Arch Neurol; 2002 Oct; 59(10):1553-62. PubMed ID: 12374492
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  • 10. HLA-DQ association and allele competition in Chinese narcolepsy.
    Han F, Lin L, Li J, Dong SX, An P, Zhao L, Liu NY, Li QY, Yan H, Gao ZC, Faraco J, Strohl KP, Liu X, Miyadera H, Mignot E.
    Tissue Antigens; 2012 Oct; 80(4):328-35. PubMed ID: 22862152
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  • 11. A study of the diagnostic utility of HLA typing, CSF hypocretin-1 measurements, and MSLT testing for the diagnosis of narcolepsy in 163 Korean patients with unexplained excessive daytime sleepiness.
    Hong SC, Lin L, Jeong JH, Shin YK, Han JH, Lee JH, Lee SP, Zhang J, Einen M, Mignot E.
    Sleep; 2006 Nov; 29(11):1429-38. PubMed ID: 17162989
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  • 12. [Positivity analysis of human leukocyte histocompatibility antigen-DQB1*0602 allele in Chinese patients with narcolepsy].
    Li J, Dong X, Yan H, Liu Y, An P, Zhao L, Li Q, Zhang X, Gao Z, Han F.
    Zhonghua Yi Xue Za Zhi; 2014 Mar 18; 94(10):763-5. PubMed ID: 24844961
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  • 13. Narcolepsy in African Americans.
    Kawai M, O'Hara R, Einen M, Lin L, Mignot E.
    Sleep; 2015 Nov 01; 38(11):1673-81. PubMed ID: 26158891
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  • 14. Nocturnal rapid eye movement sleep latency for identifying patients with narcolepsy/hypocretin deficiency.
    Andlauer O, Moore H, Jouhier L, Drake C, Peppard PE, Han F, Hong SC, Poli F, Plazzi G, O'Hara R, Haffen E, Roth T, Young T, Mignot E.
    JAMA Neurol; 2013 Jul 01; 70(7):891-902. PubMed ID: 23649748
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  • 15. Emergent Coordination of the CHKB and CPT1B Genes in Eutherian Mammals: Implications for the Origin of Brown Adipose Tissue.
    Patel BV, Yao F, Howenstine A, Takenaka R, Hyatt JA, Sears KE, Shewchuk BM.
    J Mol Biol; 2020 Nov 20; 432(23):6127-6145. PubMed ID: 33058877
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  • 16. Rare missense mutations in P2RY11 in narcolepsy with cataplexy.
    Degn M, Dauvilliers Y, Dreisig K, Lopez R, Pfister C, Pradervand S, Rahbek Kornum B, Tafti M.
    Brain; 2017 Jun 01; 140(6):1657-1668. PubMed ID: 28460015
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  • 17. HLA DQB1*06:02 negative narcolepsy with hypocretin/orexin deficiency.
    Han F, Lin L, Schormair B, Pizza F, Plazzi G, Ollila HM, Nevsimalova S, Jennum P, Knudsen S, Winkelmann J, Coquillard C, Babrzadeh F, Strom TM, Wang C, Mindrinos M, Fernandez Vina M, Mignot E.
    Sleep; 2014 Oct 01; 37(10):1601-8. PubMed ID: 25197808
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  • 18. Abnormally low serum acylcarnitine levels in narcolepsy patients.
    Miyagawa T, Miyadera H, Tanaka S, Kawashima M, Shimada M, Honda Y, Tokunaga K, Honda M.
    Sleep; 2011 Mar 01; 34(3):349-53A. PubMed ID: 21358852
    [Abstract] [Full Text] [Related]

  • 19. 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, 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 01; 43(1):66-71. PubMed ID: 21170044
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  • 20. Correlation between HLA-DQB1*06:02 and narcolepsy with and without cataplexy: approving a safe and sensitive genetic test in four major ethnic groups. A systematic meta-analysis.
    Capittini C, De Silvestri A, Terzaghi M, Scotti V, Rebuffi C, Pasi A, Manni R, Martinetti M, Tinelli C.
    Sleep Med; 2018 Dec 01; 52():150-157. PubMed ID: 30321823
    [Abstract] [Full Text] [Related]

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