Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 18

1.

The startle syndromes: physiology and treatment.

Dreissen YE, Tijssen MA.

Epilepsia. 2012 Dec;53 Suppl 7:3-11. doi: 10.1111/j.1528-1167.2012.03709.x. Review.

PMID:
23153204
[PubMed - indexed for MEDLINE]
2.

Exaggerated startle reactions.

Dreissen YE, Bakker MJ, Koelman JH, Tijssen MA.

Clin Neurophysiol. 2012 Jan;123(1):34-44. doi: 10.1016/j.clinph.2011.09.022. Epub 2011 Oct 26. Review.

PMID:
22033030
[PubMed - indexed for MEDLINE]
3.

Startle syndromes.

Bakker MJ, van Dijk JG, van den Maagdenberg AM, Tijssen MA.

Lancet Neurol. 2006 Jun;5(6):513-24. Review.

PMID:
16713923
[PubMed - indexed for MEDLINE]
4.

Startle and its disorders.

Meinck HM.

Neurophysiol Clin. 2006 Sep-Dec;36(5-6):357-64. Epub 2007 Jan 26. Review.

PMID:
17336782
[PubMed - indexed for MEDLINE]
5.

Hyperekplexia in neonates.

Praveen V, Patole SK, Whitehall JS.

Postgrad Med J. 2001 Sep;77(911):570-2. Review.

PMID:
11524514
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Hyperekplexia: abnormal startle response due to glycine receptor mutations.

Andrew M, Owen MJ.

Br J Psychiatry. 1997 Feb;170:106-8. Review.

PMID:
9093496
[PubMed - indexed for MEDLINE]
7.

From the jumping Frenchmen of Maine to post-traumatic stress disorder: the startle response in neuropsychiatry.

Howard R, Ford R.

Psychol Med. 1992 Aug;22(3):695-707. Review.

PMID:
1410093
[PubMed - indexed for MEDLINE]
8.

[A study of pathogenesis and symptoms of Tourette's syndrome--mainly on the importance of "startle reflex" through Latah reaction].

Nishida H, Shinbo Y, Motomura H.

Seishin Shinkeigaku Zasshi. 1994;96(1):26-47. Review. Japanese.

PMID:
8190811
[PubMed - indexed for MEDLINE]
9.

The role of glycine and glycine receptors in myoclonus and startle syndromes.

Schofield PR.

Adv Neurol. 2002;89:263-74. Review. No abstract available.

PMID:
11968453
[PubMed - indexed for MEDLINE]
10.

[Familial hyperekplexia: startle disease. Clinical, electrophysiological and genetic study of a family].

Bernasconi A, Regli F, Schorderet DF, Pescia G.

Rev Neurol (Paris). 1996 Jun-Jul;152(6-7):447-50. Review. French.

PMID:
8944241
[PubMed - indexed for MEDLINE]
11.

Molecular mechanisms of inherited startle syndromes.

Rajendra S, Schofield PR.

Trends Neurosci. 1995 Feb;18(2):80-2. Review.

PMID:
7537418
[PubMed - indexed for MEDLINE]
12.

Neurophysiology of the startle syndrome and hyperekplexia.

Brown P.

Adv Neurol. 2002;89:153-9. Review. No abstract available.

PMID:
11968441
[PubMed - indexed for MEDLINE]
13.

Assessment of excitability in brainstem circuits mediating the blink reflex and the startle reaction.

Valls-Sole J.

Clin Neurophysiol. 2012 Jan;123(1):13-20. doi: 10.1016/j.clinph.2011.04.029. Epub 2011 Oct 24. Review.

PMID:
22030138
[PubMed - indexed for MEDLINE]
14.

Physiology of startle phenomena.

Brown P.

Adv Neurol. 1995;67:273-87. Review.

PMID:
8848974
[PubMed - indexed for MEDLINE]
15.

Brainstem encephalopathy with stimulus-sensitive myoclonus leading to respiratory arrest, but with recovery: a description of two cases and review of the literature.

Kullmann DM, Howard RS, Miller DH, Hirsch NP, Brown P, Marsden CD.

Mov Disord. 1996 Nov;11(6):715-8. Review.

PMID:
8914099
[PubMed - indexed for MEDLINE]
16.

Debate: Does genetic information in humans help us treat patients? PRO--genetic information in humans helps us treat patients. CON--genetic information does not help at all.

Delgado-Escueta AV, Bourgeois BF.

Epilepsia. 2008 Dec;49 Suppl 9:13-24. doi: 10.1111/j.1528-1167.2008.01922.x. Review.

PMID:
19087113
[PubMed - indexed for MEDLINE]
17.

Hyperekplexia: treatment of a severe phenotype and review of the literature.

Mineyko A, Whiting S, Graham GE.

Can J Neurol Sci. 2011 May;38(3):411-6. Review.

PMID:
21515498
[PubMed - indexed for MEDLINE]
18.

Hyperekplexia: a treatable neurogenetic disease.

Zhou L, Chillag KL, Nigro MA.

Brain Dev. 2002 Oct;24(7):669-74. Review.

PMID:
12427512
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk