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Volumn 25, Issue 137, 1997, Pages 86-88

Congenital hyperekplexia as a cause of neonatal hypertonia;Hiperekplexia congenita como causa de hipertonia neonatal

Author keywords

Hyperekplexia; Infant; Muscle hypertonia; Newborn; Startle reaction

Indexed keywords

CLONAZEPAM; ANTICONVULSIVE AGENT;

EID: 0030637532     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (5)

References (13)
  • 1
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    • Hyperexplexia: A hereditary startle syndrome
    • Suhren AL, Bruyn GW, Tuynman JA. Hyperexplexia: a hereditary startle syndrome. J Neurol Sci 1966; 3: 577-586.
    • (1966) J Neurol Sci , vol.3 , pp. 577-586
    • Suhren, A.L.1    Bruyn, G.W.2    Tuynman, J.A.3
  • 2
    • 0000266703 scopus 로고
    • An unidentified hereditary disease
    • Kok O, Bruyn GW. An unidentified hereditary disease. Lancet 1962; 1: 1359.
    • (1962) Lancet , vol.1 , pp. 1359
    • Kok, O.1    Bruyn, G.W.2
  • 3
    • 0014151623 scopus 로고
    • The startle disease or hyperekplexia. Pathological surprise reaction
    • Gastaut H, Villeneuve A. The startle disease or hyperekplexia. Pathological surprise reaction. J Neurol Sci 1967; 5: 523-542.
    • (1967) J Neurol Sci , vol.5 , pp. 523-542
    • Gastaut, H.1    Villeneuve, A.2
  • 4
    • 0027437603 scopus 로고
    • Startle disease or Hyperekplexia
    • Gordon N. Startle disease or Hyperekplexia. Dev Med Child Neur 1993; 35: 1015-1024.
    • (1993) Dev Med Child Neur , vol.35 , pp. 1015-1024
    • Gordon, N.1
  • 5
    • 0026651547 scopus 로고
    • 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, et al. Startle disease or Hyperekplexia: response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis. Ann Neurol 1992; 21: 663-668.
    • (1992) Ann Neurol , vol.21 , pp. 663-668
    • Ryan, S.G.1    Sherman, S.L.2    Terry, J.C.3
  • 6
    • 0026683048 scopus 로고
    • Lowcerebrospinal fluid concentration of free gamma-aminobutyric acid in startle disease
    • Dubowitz LMS, Bousa H, Hird MF, Jaeken J. Lowcerebrospinal fluid concentration of free gamma-aminobutyric acid in startle disease. Lancet 1992; 340: 80-81.
    • (1992) Lancet , vol.340 , pp. 80-81
    • Dubowitz, L.M.S.1    Bousa, H.2    Hird, M.F.3    Jaeken, J.4
  • 7
    • 0028342827 scopus 로고
    • Possible involment of a gamma-hydroxybutyric acid receptor in startle disease
    • Berthier M, Bouneau D, Desbordes JM, et al. Possible involment of a gamma-hydroxybutyric acid receptor in startle disease. Acta Paediatr 1994; 83: 678-640.
    • (1994) Acta Paediatr , vol.83 , pp. 678-640
    • Berthier, M.1    Bouneau, D.2    Desbordes, J.M.3
  • 8
    • 0019225609 scopus 로고
    • Startle disease or hyperekplexia: Further delineation of the syndrome
    • Anderman F, Kleen DL, Anderman E, Quesney LF. Startle disease or hyperekplexia: further delineation of the syndrome. Brain 1980; 103: 985-97.
    • (1980) Brain , vol.103 , pp. 985-997
    • Anderman, F.1    Kleen, D.L.2    Anderman, E.3    Quesney, L.F.4
  • 12
  • 13
    • 0026006850 scopus 로고
    • Nose taping test inducing a generalized flexor spasm: A hallmark of hyperekplexia
    • Shahar E, Brand N, Uziel Y, Barak Y. Nose taping test inducing a generalized flexor spasm: a hallmark of hyperekplexia. Acta Paediatr Scand 1991; 80: 1073-1077.
    • (1991) Acta Paediatr Scand , vol.80 , pp. 1073-1077
    • Shahar, E.1    Brand, N.2    Uziel, Y.3    Barak, Y.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.