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Volumn 40, Issue 6, 2005, Pages 351-353

Alternating hemiplegia of childhood treated as epilepsy. Two new cases;Hemiplejía alternante de la infancia tratada como epilepsia. Dos nuevos casos

Author keywords

Alternating hemiplegia; Convulsions; Flunarizine

Indexed keywords

ANTICONVULSIVE AGENT; FLUNARIZINE;

EID: 24344477575     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: 10.33588/rn.4006.2004494     Document Type: Article
Times cited : (7)

References (25)
  • 1
    • 0015047406 scopus 로고
    • Alternating hemiplegia in childhood: Report of eight patients with complicated migraine beginning in infancy
    • Verret S, Seteele JC. Alternating hemiplegia in childhood: report of eight patients with complicated migraine beginning in infancy. Pediatrics 1971; 47: 675-80.
    • (1971) Pediatrics , vol.47 , pp. 675-680
    • Verret, S.1    Seteele, J.C.2
  • 2
    • 0019135555 scopus 로고
    • Alternating hemiplegia in infants: Report of five cases
    • Krakelog I, Aicardi J. Alternating hemiplegia in infants: report of five cases. Dev Med Child Neurol 1980; 22: 784-91.
    • (1980) Dev Med Child Neurol , vol.22 , pp. 784-791
    • Krakelog, I.1    Aicardi, J.2
  • 4
    • 0026460358 scopus 로고
    • Alternating hemiplegia in childhood: 23 cases in Japan
    • Sakuragawa N. Alternating hemiplegia in childhood: 23 cases in Japan. Brain Dev 1992; 14: 283-8.
    • (1992) Brain Dev , vol.14 , pp. 283-288
    • Sakuragawa, N.1
  • 7
    • 1942504308 scopus 로고    scopus 로고
    • Alternating hemiplegia of childhood: Presentation of two cases regarding the extent of variability
    • Saltik S, Cokar O, Uslu T, Uludz D, Dervent A. Alternating hemiplegia of childhood: presentation of two cases regarding the extent of variability. Epileptic Disord 2004; 1: 45-8.
    • (2004) Epileptic Disord , vol.1 , pp. 45-48
    • Saltik, S.1    Cokar, O.2    Uslu, T.3    Uludz, D.4    Dervent, A.5
  • 8
    • 0033804586 scopus 로고    scopus 로고
    • Alternating hemiplegia of childhood: Clinical manifestations and long-term outcome
    • Mikati MA, Kramer U, Zupanc ML, Shanahan RJ. Alternating hemiplegia of childhood: clinical manifestations and long-term outcome. Pediatr Neurol 2000; 23: 134-41.
    • (2000) Pediatr Neurol , vol.23 , pp. 134-141
    • Mikati, M.A.1    Kramer, U.2    Zupanc, M.L.3    Shanahan, R.J.4
  • 9
    • 0009971069 scopus 로고
    • Alternating hemiplegia of childhood: Epilepsy and electroencephalographic investigations
    • Andermann F, Aicardi J, Vivegano F, eds, New York: Raven Press;
    • Dalla Bernardina B, Fontana R, Colomaría V. Alternating hemiplegia of childhood: epilepsy and electroencephalographic investigations. In Andermann F, Aicardi J, Vivegano F, eds. Alternating hemiplegia of childhood. New York: Raven Press; 1995. p. 75-88.
    • (1995) Alternating hemiplegia of childhood , pp. 75-88
    • Dalla Bernardina, B.1    Fontana, R.2    Colomaría, V.3
  • 10
    • 0025264955 scopus 로고
    • Reversible changes of somatosensory-evoked potentials in a child with alternating hemiplegia
    • Imani T, Minami R, Ishikawa Y, Okabe M, Matsumoto H. Reversible changes of somatosensory-evoked potentials in a child with alternating hemiplegia. J Child Neurol 1990; 5: 71-2.
    • (1990) J Child Neurol , vol.5 , pp. 71-72
    • Imani, T.1    Minami, R.2    Ishikawa, Y.3    Okabe, M.4    Matsumoto, H.5
  • 11
    • 0025372629 scopus 로고
    • Hemiplejía alternante en la infancia: Forma de presentación, evolución y tratamiento en tres observaciones
    • Campistol J, Sans A, Pineda M, Fernández-Álvarez E. Hemiplejía alternante en la infancia: forma de presentación, evolución y tratamiento en tres observaciones. An Esp Pediatr 1990; 32: 336-8.
    • (1990) An Esp Pediatr , vol.32 , pp. 336-338
    • Campistol, J.1    Sans, A.2    Pineda, M.3    Fernández-Álvarez, E.4
  • 12
    • 0001942496 scopus 로고    scopus 로고
    • Nonepileptic neurologic paroxysmal disorders and episodic symptoms in infants
    • Engel J Jr, Pedley T, eds, Philadelphia: Lippincott-Raven;
    • Fejerman N. Nonepileptic neurologic paroxysmal disorders and episodic symptoms in infants. In Engel J Jr, Pedley T, eds. Epilepsy: a comprehensive textbook. Philadelphia: Lippincott-Raven; 1997. p. 2745-56.
    • (1997) Epilepsy: A comprehensive textbook , pp. 2745-2756
    • Fejerman, N.1
  • 13
    • 0001834981 scopus 로고    scopus 로고
    • Hemiplejía aguda y trastornos vasculares
    • Fejerman N, Fernández E, eds, Buenos Aires: Panamericana;
    • Grippo J. Hemiplejía aguda y trastornos vasculares. In Fejerman N, Fernández E, eds. Neurología pediátrica. Buenos Aires: Panamericana; 1997. p. 421-33.
    • (1997) Neurología pediátrica , pp. 421-433
    • Grippo, J.1
  • 15
    • 0035811775 scopus 로고    scopus 로고
    • The clinical spectrum of hemiplegic migraine associated with mutations in a neuronal calcium channel
    • Ducros A, Denier C, Joutel A, Cecillon M, Lescoat C, Vahedi K, et al. The clinical spectrum of hemiplegic migraine associated with mutations in a neuronal calcium channel. N Engl J Med 2001; 345: 17-24.
    • (2001) N Engl J Med , vol.345 , pp. 17-24
    • Ducros, A.1    Denier, C.2    Joutel, A.3    Cecillon, M.4    Lescoat, C.5    Vahedi, K.6
  • 16
    • 2542575651 scopus 로고    scopus 로고
    • Alternating hemiplegia of childhood or familial hemiplegic migraine?: A novel ATP1A2 mutation
    • Swoboda KJ, Kanavakis E, Xaidara A, Johnson JE. Alternating hemiplegia of childhood or familial hemiplegic migraine?: a novel ATP1A2 mutation. Ann Neurol 2004; 55: 884-7.
    • (2004) Ann Neurol , vol.55 , pp. 884-887
    • Swoboda, K.J.1    Kanavakis, E.2    Xaidara, A.3    Johnson, J.E.4
  • 17
    • 0030799454 scopus 로고    scopus 로고
    • Calcium channels in neurological disease
    • Greenberg DA. Calcium channels in neurological disease. Ann Neurol 1997; 42: 275-82.
    • (1997) Ann Neurol , vol.42 , pp. 275-282
    • Greenberg, D.A.1
  • 18
    • 0036237839 scopus 로고    scopus 로고
    • Japanese cases of familial hemiplegic migraine with cerebellar ataxia carrying a T666M mutation in the CACNA1A gene
    • Takahashi T, Igarashi S, Kimura T, Hozumi I, Kawachi I, Onodera O, et al. Japanese cases of familial hemiplegic migraine with cerebellar ataxia carrying a T666M mutation in the CACNA1A gene. J Neurol Neurosurg Psychiatry 2002; 72: 676-7.
    • (2002) J Neurol Neurosurg Psychiatry , vol.72 , pp. 676-677
    • Takahashi, T.1    Igarashi, S.2    Kimura, T.3    Hozumi, I.4    Kawachi, I.5    Onodera, O.6
  • 19
    • 0038076033 scopus 로고    scopus 로고
    • Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: A description of 5 families with familial hemiplegic migraine
    • Kors E, Haan J, Giffin N, Pazdera L, Schnittger C, Lennox G, et al. Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine. Arch Neurol 2003; 60: 684-8.
    • (2003) Arch Neurol , vol.60 , pp. 684-688
    • Kors, E.1    Haan, J.2    Giffin, N.3    Pazdera, L.4    Schnittger, C.5    Lennox, G.6
  • 20
    • 3042854209 scopus 로고    scopus 로고
    • Familial alternating hemiplegia of childhood or channelopathy? A report with valuable pathophysiological implications
    • Auvin A, Joriot-Chekaf S, Chrisrophe-Cuvellier J, Vallèe L. Familial alternating hemiplegia of childhood or channelopathy? A report with valuable pathophysiological implications. Dev Med Child Neurol 2004; 46: 500.
    • (2004) Dev Med Child Neurol , vol.46 , pp. 500
    • Auvin, A.1    Joriot-Chekaf, S.2    Chrisrophe-Cuvellier, J.3    Vallèe, L.4
  • 21
    • 2942741093 scopus 로고    scopus 로고
    • Recurrent hemiplegia, normal MRI, and NOTCH3 mutation year-old: Is this early CADASIL?
    • Golomb MR, Sokol DK, Walsh LE, Christensen CK, Garg BP. Recurrent hemiplegia, normal MRI, and NOTCH3 mutation year-old: is this early CADASIL? Neurology 2004; 62: 2331-2.
    • (2004) Neurology , vol.62 , pp. 2331-2332
    • Golomb, M.R.1    Sokol, D.K.2    Walsh, L.E.3    Christensen, C.K.4    Garg, B.P.5
  • 22
    • 10744233032 scopus 로고    scopus 로고
    • Guidetti D, Casali B, Mazzei R, Cenacchi G, De Berti G, Zuccoli G, et al. An Italian case of CASADIL with mutation CGC-TCG in codon 1006, exon 19 Notch3 gene. Neurol Sci 2004; 24: 401-6.
    • Guidetti D, Casali B, Mazzei R, Cenacchi G, De Berti G, Zuccoli G, et al. An Italian case of CASADIL with mutation CGC-TCG in codon 1006, exon 19 Notch3 gene. Neurol Sci 2004; 24: 401-6.
  • 23
    • 0036393522 scopus 로고    scopus 로고
    • CADASIL syndrome in a large Turkish kindred caused by the mutation in the Notch3 receptor
    • Utku U, Celik Y, Uyguner O, Yuksel-Apak M, Wollnik B. CADASIL syndrome in a large Turkish kindred caused by the mutation in the Notch3 receptor. Eur J Neurol 2002; 9: 23-8.
    • (2002) Eur J Neurol , vol.9 , pp. 23-28
    • Utku, U.1    Celik, Y.2    Uyguner, O.3    Yuksel-Apak, M.4    Wollnik, B.5
  • 24
    • 0023513855 scopus 로고
    • Flunarizine in alternanting hemiplegia in childhood: An international study in 12 children
    • Casaer P. Flunarizine in alternanting hemiplegia in childhood: an international study in 12 children. Neuropediatrics 1987; 18: 191-5.
    • (1987) Neuropediatrics , vol.18 , pp. 191-195
    • Casaer, P.1
  • 25
    • 0027391849 scopus 로고
    • Alternating hemiplegia of childhood: A study of 10 patients and results of flunarizine treatment
    • Silver K, Andermann F. Alternating hemiplegia of childhood: a study of 10 patients and results of flunarizine treatment. Neurology 1993; 43: 36-41.
    • (1993) Neurology , vol.43 , pp. 36-41
    • Silver, K.1    Andermann, F.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.