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Journal Abstract Search

95 related items for PubMed ID: 7477535

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor.
    Rees MI, Andrew M, Jawad S, Owen MJ.
    Hum Mol Genet; 1994 Dec; 3(12):2175-9. PubMed ID: 7881416
    [Abstract] [Full Text] [Related]

  • 23. Startle disease--hyperekplexia (two sibling cases).
    Altunbaşak S, Baytok V.
    Seizure; 1996 Dec; 5(4):313-5. PubMed ID: 8952019
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  • 24.
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  • 25. Mutations within the human GLYT2 (SLC6A5) gene associated with hyperekplexia.
    Eulenburg V, Becker K, Gomeza J, Schmitt B, Becker CM, Betz H.
    Biochem Biophys Res Commun; 2006 Sep 22; 348(2):400-5. PubMed ID: 16884688
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  • 26. Startle epilepsy complicating aspartylglucosaminuria.
    Labate A, Barone R, Gambardella A, Civitelli D, Fiumara A, Annesi G, Zappia M, Pavone L, Quattrone A.
    Brain Dev; 2004 Mar 22; 26(2):130-3. PubMed ID: 15036433
    [Abstract] [Full Text] [Related]

  • 27. Fear-potentiated startle in two strains of inbred mice.
    Falls WA, Carlson S, Turner JG, Willott JF.
    Behav Neurosci; 1997 Aug 22; 111(4):855-61. PubMed ID: 9267664
    [Abstract] [Full Text] [Related]

  • 28. Hyperekplexia: a non-epileptic startle disorder.
    Rajadhyaksha SB, Bahl VB.
    Indian Pediatr; 2002 Aug 22; 39(8):773-6. PubMed ID: 12196692
    [No Abstract] [Full Text] [Related]

  • 29. Recurrence of major depressive disorder is predicted by inhibited startle magnitude while recovered.
    O'Brien-Simpson L, Di Parsia P, Simmons JG, Allen NB.
    J Affect Disord; 2009 Jan 22; 112(1-3):243-9. PubMed ID: 18495249
    [Abstract] [Full Text] [Related]

  • 30. [Hyperekplexia -- a treatable neuropediatric disease].
    Freilinger M, Jalowetz S, Reiter E, Schubert MT, Seidl R.
    Klin Padiatr; 2005 Jan 22; 217(4):220-1. PubMed ID: 16032547
    [Abstract] [Full Text] [Related]

  • 31. [Startle disease].
    Okino S, Yamada M.
    Ryoikibetsu Shokogun Shirizu; 2002 Jan 22; (37 Pt 6):403-5. PubMed ID: 12483911
    [No Abstract] [Full Text] [Related]

  • 32. Hyperekplexia in neonates.
    Praveen V, Patole SK, Whitehall JS.
    Postgrad Med J; 2001 Sep 22; 77(911):570-2. PubMed ID: 11524514
    [Abstract] [Full Text] [Related]

  • 33. Clinical and genetic investigation of 17 Japanese patients with hyperekplexia.
    Mine J, Taketani T, Yoshida K, Yokochi F, Kobayashi J, Maruyama K, Nanishi E, Ono M, Yokoyama A, Arai H, Tamaura S, Suzuki Y, Otsubo S, Hayashi T, Kimura M, Kishi K, Yamaguchi S.
    Dev Med Child Neurol; 2015 Apr 22; 57(4):372-7. PubMed ID: 25356525
    [Abstract] [Full Text] [Related]

  • 34. Frontal lobe dysfunction in sporadic hyperekplexia--case study and literature review.
    Gaitatzis A, Kartsounis LD, Gacinovic S, Costa DC, Harvey K, Harvey RJ, de Silva RN.
    J Neurol; 2004 Jan 22; 251(1):91-8. PubMed ID: 14999495
    [Abstract] [Full Text] [Related]

  • 35. Exaggerated startle reflexes in an elderly woman.
    Colebatch JG, Barrett G, Lees AJ.
    Mov Disord; 1990 Jan 22; 5(2):167-9. PubMed ID: 2325679
    [Abstract] [Full Text] [Related]

  • 36. Startle disease or hyperekplexia: further delineation of the syndrome.
    Andermann F, Keene DL, Andermann E, Quesney LF.
    Brain; 1980 Dec 22; 103(4):985-97. PubMed ID: 6777025
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  • 37.
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  • 38.
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  • 40. Molecular genetic reevaluation of the Dutch hyperekplexia family.
    Tijssen MA, Shiang R, van Deutekom J, Boerman RH, Wasmuth JJ, Sandkuijl LA, Frants RR, Padberg GW.
    Arch Neurol; 1995 Jun 22; 52(6):578-82. PubMed ID: 7763205
    [Abstract] [Full Text] [Related]

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