Literature DB >> 2563117

Startle disease: an avoidable cause of sudden infant death.

F Vigevano, M Di Capua, B Dalla Bernardina.   

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Year:  1989        PMID: 2563117     DOI: 10.1016/s0140-6736(89)91226-9

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


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  14 in total

1.  Hyperexplexia or stiff baby syndrome.

Authors:  C Tohier; J C Roze; A David; M F Veccierini; P Renaud; A Mouzard
Journal:  Arch Dis Child       Date:  1991-04       Impact factor: 3.791

2.  Hyperekplexia masquerading as epilepsy.

Authors:  Jitendra Kumar Sahu; Anita Choudhary; Indranil Ghosh; Sheffali Gulati; Madhulika Kabra; Takeshi Taketani; Veena Kalra
Journal:  Indian J Pediatr       Date:  2011-01-09       Impact factor: 1.967

Review 3.  Myoclonus and epilepsies.

Authors:  N Fejerman
Journal:  Indian J Pediatr       Date:  1997 Sep-Oct       Impact factor: 1.967

4.  Congenital hyperekplexia: five sporadic cases.

Authors:  Serge Rivera; Frédéric Villega; Anne de Saint-Martin; Jacqueline Matis; Benoît Escande; Denys Chaigne; Dominique Astruc
Journal:  Eur J Pediatr       Date:  2005-10-07       Impact factor: 3.183

Review 5.  Hyperekplexia in neonates.

Authors:  V Praveen; S K Patole; J S Whitehall
Journal:  Postgrad Med J       Date:  2001-09       Impact factor: 2.401

6.  Properties of human glycine receptors containing the hyperekplexia mutation alpha1(K276E), expressed in Xenopus oocytes.

Authors:  T M Lewis; L G Sivilotti; D Colquhoun; R M Gardiner; R Schoepfer; M Rees
Journal:  J Physiol       Date:  1998-02-15       Impact factor: 5.182

7.  The glycinergic system in human startle disease: a genetic screening approach.

Authors:  Jeff S Davies; Seo-Kyung Chung; Rhys H Thomas; Angela Robinson; Carrie L Hammond; Jonathan G L Mullins; Eloisa Carta; Brian R Pearce; Kirsten Harvey; Robert J Harvey; Mark I Rees
Journal:  Front Mol Neurosci       Date:  2010-03-23       Impact factor: 5.639

8.  Evolution and the sudden infant death syndrome (SIDS) : Part III: Infant arousal and parent-infant co-sleeping.

Authors:  J J McKenna; S Mosko
Journal:  Hum Nat       Date:  1990-09

9.  Hyperekplexia and stiff-baby syndrome: an identical neurological disorder?

Authors:  G Cioni; E Biagioni; P Bottai; A M Castellacci; P B Paolicelli
Journal:  Ital J Neurol Sci       Date:  1993-03

10.  Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease.

Authors:  Eloisa Carta; Seo-Kyung Chung; Victoria M James; Angela Robinson; Jennifer L Gill; Nathalie Remy; Jean-François Vanbellinghen; Cheney J G Drew; Sophie Cagdas; Duncan Cameron; Frances M Cowan; Mireria Del Toro; Gail E Graham; Adnan Y Manzur; Amira Masri; Serge Rivera; Emmanuel Scalais; Rita Shiang; Kate Sinclair; Catriona A Stuart; Marina A J Tijssen; Grahame Wise; Sameer M Zuberi; Kirsten Harvey; Brian R Pearce; Maya Topf; Rhys H Thomas; Stéphane Supplisson; Mark I Rees; Robert J Harvey
Journal:  J Biol Chem       Date:  2012-06-14       Impact factor: 5.157

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