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Journal Abstract Search

194 related items for PubMed ID: 6830476

  • 1. Hyperekplexia.
    Kurczynski TW.
    Arch Neurol; 1983 Apr; 40(4):246-8. PubMed ID: 6830476
    [Abstract] [Full Text] [Related]

  • 2. [Hyperekplexia -- a treatable neuropediatric disease].
    Freilinger M, Jalowetz S, Reiter E, Schubert MT, Seidl R.
    Klin Padiatr; 2005 Apr; 217(4):220-1. PubMed ID: 16032547
    [Abstract] [Full Text] [Related]

  • 3. [Startle disease: growing rigid with fear].
    Tijssen MA, van Dijk JG, Roos RA, Padberg GW.
    Ned Tijdschr Geneeskd; 1995 Sep 23; 139(38):1940-3. PubMed ID: 7477535
    [Abstract] [Full Text] [Related]

  • 4. Hyperekplexia phenotype due to compound heterozygosity for GLRA1 gene mutations.
    Vergouwe MN, Tijssen MA, Peters AC, Wielaard R, Frants RR.
    Ann Neurol; 1999 Oct 23; 46(4):634-8. PubMed ID: 10514101
    [Abstract] [Full Text] [Related]

  • 5. Hyperekplexia-like syndromes without mutations in the GLRA1 gene.
    Vergouwe MN, Tijssen MA, Shiang R, van Dijk JG, al Shahwan S, Ophoff RA, Frants RR.
    Clin Neurol Neurosurg; 1997 Aug 23; 99(3):172-8. PubMed ID: 9350397
    [Abstract] [Full Text] [Related]

  • 6. Hyperekplexia and stiff-baby syndrome: an identical neurological disorder?
    Cioni G, Biagioni E, Bottai P, Castellacci AM, Paolicelli PB.
    Ital J Neurol Sci; 1993 Mar 23; 14(2):145-52. PubMed ID: 8509269
    [Abstract] [Full Text] [Related]

  • 7. Hyperekplexia: pedigree studies in two families.
    Hayashi T, Tachibana H, Kajii T.
    Am J Med Genet; 1991 Aug 01; 40(2):138-43. PubMed ID: 1897565
    [Abstract] [Full Text] [Related]

  • 8. Hyperekplexia and sudden neonatal death.
    Nigro MA, Lim HC.
    Pediatr Neurol; 1992 Aug 01; 8(3):221-5. PubMed ID: 1622521
    [Abstract] [Full Text] [Related]

  • 9. Exaggerated startle reactions.
    Dreissen YE, Bakker MJ, Koelman JH, Tijssen MA.
    Clin Neurophysiol; 2012 Jan 01; 123(1):34-44. PubMed ID: 22033030
    [Abstract] [Full Text] [Related]

  • 10. Hyperekplexia in neonates.
    Praveen V, Patole SK, Whitehall JS.
    Postgrad Med J; 2001 Sep 01; 77(911):570-2. PubMed ID: 11524514
    [Abstract] [Full Text] [Related]

  • 11. Hyperekplexia in the first year of life.
    Koning-Tijssen MA, Brouwer OF.
    Mov Disord; 2000 Nov 01; 15(6):1293-6. PubMed ID: 11104232
    [No Abstract] [Full Text] [Related]

  • 12. Startle disease or hyperekplexia: further delineation of the syndrome.
    Andermann F, Keene DL, Andermann E, Quesney LF.
    Brain; 1980 Dec 01; 103(4):985-97. PubMed ID: 6777025
    [Abstract] [Full Text] [Related]

  • 13. Startle disease, or hyperekplexia: response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis.
    Ryan SG, Sherman SL, Terry JC, Sparkes RS, Torres MC, Mackey RW.
    Ann Neurol; 1992 Jun 01; 31(6):663-8. PubMed ID: 1355335
    [Abstract] [Full Text] [Related]

  • 14. Complete heart block in nonfamilial hyperekplexia.
    McAbee GN, Kadakia SK, Sisley KC, Delfiner JS.
    Pediatr Neurol; 1995 Feb 01; 12(2):149-51. PubMed ID: 7779213
    [Abstract] [Full Text] [Related]

  • 15. Jumping Frenchmen, Miryachit, and Latah: Culture-Specific Hyperstartle-Plus Syndromes.
    Lanska DJ.
    Front Neurol Neurosci; 2018 Feb 01; 42():122-131. PubMed ID: 29151096
    [Abstract] [Full Text] [Related]

  • 16. Startle disease--hyperekplexia (two sibling cases).
    Altunbaşak S, Baytok V.
    Seizure; 1996 Dec 01; 5(4):313-5. PubMed ID: 8952019
    [Abstract] [Full Text] [Related]

  • 17. Hyperekplexia and other startle syndromes.
    Saini AG, Pandey S.
    J Neurol Sci; 2020 Sep 15; 416():117051. PubMed ID: 32721683
    [Abstract] [Full Text] [Related]

  • 18. Novel mutation of GLRA1 in Omani families with hyperekplexia and mild mental retardation.
    Al-Futaisi AM, Al-Kindi MN, Al-Mawali AM, Koul RL, Al-Adawi S, Al-Yahyaee SA.
    Pediatr Neurol; 2012 Feb 15; 46(2):89-93. PubMed ID: 22264702
    [Abstract] [Full Text] [Related]

  • 19. [Familial hyperekplexia: startle disease. Clinical, electrophysiological and genetic study of a family].
    Bernasconi A, Regli F, Schorderet DF, Pescia G.
    Rev Neurol (Paris); 1996 Feb 15; 152(6-7):447-50. PubMed ID: 8944241
    [Abstract] [Full Text] [Related]

  • 20. A novel GLRA1 mutation associated with an atypical hyperekplexia phenotype.
    Gregory ML, Guzauskas GF, Edgar TS, Clarkson KB, Srivastava AK, Holden KR.
    J Child Neurol; 2008 Dec 15; 23(12):1433-8. PubMed ID: 19073849
    [Abstract] [Full Text] [Related]

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