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Volumn 50, Issue SUPPL. 5, 2009, Pages 37-40

Familial benign nonprogressive myoclonic epilepsies

Author keywords

ADCME; BAFME; Epilepsy; FIME; Genetics; Myoclonus

Indexed keywords

ANTICONVULSIVE AGENT; PHENOBARBITAL; VALPROIC ACID;

EID: 65549153633     PISSN: 00139580     EISSN: 15281167     Source Type: Journal    
DOI: 10.1111/j.1528-1167.2009.02118.x     Document Type: Article
Times cited : (16)

References (18)
  • 4
    • 23944448356 scopus 로고    scopus 로고
    • Absence of linkage to 8q23.3-q24.1 and 2p11.1-q12.2 in a new BAFME pedigree in China: Indication of a third locus for BAFME
    • DOI 10.1016/j.eplepsyres.2005.05.006, PII S0920121105000938
    • Deng FY, Gong J, Zhang YC, Wang K, Xiao SM, Li YN, Lei SF, Chen XD, Xiao B, Deng HW 2005) Absence of linkage to 8q23.3-q24.1 and 2p11.1-q12.2 in a new BAFME pedigree in China: indication of a third locus for BAFME. Epilepsy Res 65 : 147 152. (Pubitemid 41187567)
    • (2005) Epilepsy Research , vol.65 , Issue.3 , pp. 147-152
    • Deng, F.-Y.1    Gong, J.2    Zhang, Y.-C.3    Wang, K.4    Xiao, S.-M.5    Li, Y.-N.6    Lei, S.-F.7    Chen, X.-D.8    Xiao, B.9    Deng, H.-W.10
  • 5
    • 0035669199 scopus 로고    scopus 로고
    • Familial infantile myoclonic epilepsy: Clinical features in a large kindred with autosomal recessive inheritance
    • DOI 10.1046/j.1528-1157.2001.26701.x
    • de Falco FA, Majello L, Santangelo R, Stabile M, Dagna Bricarelli F, Zara F 2001) Familial infantile myoclonic epilepsy. Clinical features in a large kindred with autosomal recessive inheritance. Epilepsia 42 : 1541 1548. (Pubitemid 34020091)
    • (2001) Epilepsia , vol.42 , Issue.12 , pp. 1541-1548
    • De Falco, F.A.1    Majello, L.2    Santangelo, R.3    Stabile, M.4    Bricarelli, F.D.5    Zara, F.6
  • 8
    • 0035208272 scopus 로고    scopus 로고
    • Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial and generalized seizures: A newly recognized epilepsy syndrome with linkage to chromosome 2p11.1-q12.2
    • Guerrini R, Bonanni P, Patrignani A, Brown P, Parmeggiani L, Grosse P, Brovedani P, Moro F, Aridon P, Carrozzo R, Casari G 2001) Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial seizures and generalized seizures. A newly recognized epilepsy syndrome with linkage to chromosome 2p11.1-q12.2. Brain 124 : 2459 2475. (Pubitemid 33134935)
    • (2001) Brain , vol.124 , Issue.12 , pp. 2459-2475
    • Guerrini, R.1    Bonanni, P.2    Patrignani, A.3    Brown, P.4    Parmeggiani, L.5    Grosse, P.6    Brovedani, P.7    Moro, F.8    Aridon, P.9    Carrozzo, R.10    Casari, G.11
  • 9
    • 0025043869 scopus 로고
    • Cortical tremor: A variant of cortical reflex myoclonus
    • Ikeda A, Kakigi R, Funai N, Neshige R, Kuroda Y, Shibasaki H 1990) Cortical tremor: a variant of cortical reflex myoclonus. Neurology 40 : 1561 1565. (Pubitemid 20351350)
    • (1990) Neurology , vol.40 , Issue.10 , pp. 1561-1565
    • Ikeda, A.1    Kakigi, R.2    Funai, N.3    Neshige, R.4    Kuroda, Y.5    Shibasaki, H.6
  • 13
    • 0842268282 scopus 로고    scopus 로고
    • A New Benign Adult Familial Myoclonic Epilepsy (BAFME) Pedigree Suggesting Linkage to Chromosome 2p11.1-q12.2
    • DOI 10.1111/j.0013-9580.2004.39903.x
    • Striano P, Chifari R, Striano S, de Fusco M, Elia M, Guerrini R, Casari G, Canevini MP 2004) A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2. Epilepsia 45 : 190 192. (Pubitemid 38174127)
    • (2004) Epilepsia , vol.45 , Issue.2 , pp. 190-192
    • Striano, P.1    Chifari, R.2    Striano, S.3    De Fusco, M.4    Elia, M.5    Guerrini, R.6    Casari, G.7    Canevini, M.P.8
  • 14
    • 15044365677 scopus 로고    scopus 로고
    • Autosomal dominant cortical tremor, myoclonus and epilepsy: Many syndromes, one phenotype
    • DOI 10.1111/j.1600-0404.2005.00385.x
    • Striano P, Zara F, Striano S 2005) Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype. Acta Neurol Scand 111 : 211 217. (Pubitemid 40380454)
    • (2005) Acta Neurologica Scandinavica , vol.111 , Issue.4 , pp. 211-217
    • Striano, P.1    Zara, F.2    Striano, S.3
  • 15
    • 65549150278 scopus 로고    scopus 로고
    • 1H MR spectroscopy indicates prominent cerebellar dysfunction in benign adult familial myoclonic epilepsy
    • Nov 22. [Epub ahead of print].
    • Striano P, Caranci F, Di Benedetto R, Tortora F, Zara F, Striano S 2009) 1H MR spectroscopy indicates prominent cerebellar dysfunction in benign adult familial myoclonic epilepsy. Epilepsia Nov 22. [Epub ahead of print].
    • (2009) Epilepsia
    • Striano, P.1    Caranci, F.2    Di Benedetto, R.3    Tortora, F.4    Zara, F.5    Striano, S.6
  • 17
    • 16544376293 scopus 로고    scopus 로고
    • Familial adult myoclonic epilepsy (FAME)
    • In. Delgado-Escueta, A.V. Guerrini, R. Medina, M.T. Genton, P. Bureau, M. Dravet, C. Eds). Vol. Ch. 22. Lippincott Williams & Wilkins. Philadelphia. pp.
    • Uyama MD, Fu YH, Ptacek L 2005) Familial adult myoclonic epilepsy (FAME). In Delgado-Escueta AV, Guerrini R, Medina MT, Genton P, Bureau M, Dravet C (Eds) Advances in neurology. Myoclonic epilepsies. Vol. 95. Ch. 22. Lippincott Williams & Wilkins, Philadelphia, pp. 281 288.
    • (2005) Advances in Neurology. Myoclonic Epilepsies. , vol.95 , pp. 281-288
    • Uyama, M.D.1    Fu, Y.H.2    Ptacek, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.