Literature DB >> 11198287

Hypocretin deficiency in familial symptomatic narcolepsy.

A Melberg, B Ripley, L Lin, J Hetta, E Mignot, S Nishino.   

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Year:  2001        PMID： 11198287

Source DB:  PubMed          Journal:  Ann Neurol        ISSN： 0364-5134            Impact factor:   10.422


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  4 in total

1.  Age- and gender-specific changes of hypocretin immunopositive neurons in C57Bl/6 mice.

Authors:  Sara E Brownell; Bruno Conti
Journal:  Neurosci Lett       Date:  2010-02-01       Impact factor: 3.046

2.  A novel de novo exon 21 DNMT1 mutation causes cerebellar ataxia, deafness, and narcolepsy in a Brazilian patient.

Authors:  José Luiz Pedroso; Orlando Graziani Povoas Barsottini; Ling Lin; Atle Melberg; Acary S B Oliveira; Emmanuel Mignot
Journal:  Sleep       Date:  2013-08-01       Impact factor: 5.849

3.  Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy.

Authors:  Juliane Winkelmann; Ling Lin; Barbara Schormair; Birgitte R Kornum; Juliette Faraco; Giuseppe Plazzi; Atle Melberg; Ferdinando Cornelio; Alexander E Urban; Fabio Pizza; Francesca Poli; Fabian Grubert; Thomas Wieland; Elisabeth Graf; Joachim Hallmayer; Tim M Strom; Emmanuel Mignot
Journal:  Hum Mol Genet       Date:  2012-02-09       Impact factor: 6.150

Review 4.  The hypocretin/orexin system.

Authors:  I O Ebrahim; R S Howard; M D Kopelman; M K Sharief; A J Williams
Journal:  J R Soc Med       Date:  2002-05       Impact factor: 18.000
  4 in total

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