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Volumn 21, Issue 5, 2012, Pages 316-321

Epilepsy in mitochondrial disorders

Author keywords

Antiepileptic drugs; Central nervous system involvement; EEG; Epilepsy; Mitochondrial disorder; Seizure

Indexed keywords

CARBAMAZEPINE; VALPROIC ACID;

EID: 84860698221     PISSN: 10591311     EISSN: 15322688     Source Type: Journal    
DOI: 10.1016/j.seizure.2012.03.003     Document Type: Review
Times cited : (62)

References (68)
  • 1
    • 33748377123 scopus 로고    scopus 로고
    • Central nervous system manifestations of mitochondrial disorders
    • DOI 10.1111/j.1600-0404.2006.00671.x
    • J. Finsterer Central nervous system manifestations of mitochondrial disorders Acta Neurol Scand 114 2006 217 238 (Pubitemid 44337240)
    • (2006) Acta Neurologica Scandinavica , vol.114 , Issue.4 , pp. 217-238
    • Finsterer, J.1
  • 3
    • 81855192225 scopus 로고    scopus 로고
    • POLG-related disorders
    • Mar 16. In: Pagon RA, Bird TD, Dolan CR, Stephens K, editors [Internet]. Seattle (WA): University of Washington, Seattle; 1993
    • Cohen BH, Chinnery PF, Copeland WC. POLG-related disorders. 2010 Mar 16. In: Pagon RA, Bird TD, Dolan CR, Stephens K, editors. GeneReviews [Internet]. Seattle (WA): University of Washington, Seattle; 1993. Available from http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=alpers.
    • (2010) GeneReviews
    • Cohen, B.H.1    Chinnery, P.F.2    Copeland, W.C.3
  • 5
    • 0034910899 scopus 로고    scopus 로고
    • High mitochondrial DNA T8993G mutation (>90%) without typical features of leigh's and NARP syndromes
    • C.Y. Tsao, J.R. Mendell, and D. Bartholomew High mitochondrial DNA T8993G mutation (<90%) without typical features of Leigh's and NARP syndromes J Child Neurol 16 2001 533 535 (Pubitemid 32725393)
    • (2001) Journal of Child Neurology , vol.16 , Issue.7 , pp. 533-535
    • Tsao, C.-Y.1    Mendell, J.R.2    Bartholomew, D.3
  • 6
    • 0027197011 scopus 로고
    • A T-to-G mutation at nucleotide pair 8993 in mitochondrial tDNA in a patient with Leigh's Syndrome
    • H. Yoshinaga, T. Ogino, S. Ohtahara, R. Sakuta, I. Nonaka, and S. Horai A T-to-G mutation at nucleotide pair 8993 in mitochondrial DNA in a patient with Leigh's syndrome J Child Neurol 8 1993 129 133 (Pubitemid 23170746)
    • (1993) Journal of Child Neurology , vol.8 , Issue.2 , pp. 129-133
    • Yoshinaga, H.1    Ogino, T.2    Ohtahara, S.3    Sakuta, R.4    Nonaka, I.5    Horai, S.6
  • 8
    • 0021143782 scopus 로고
    • Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome
    • S.G. Pavlakis, P.C. Phillips, S. DiMauro, D.C. De Vivo, and L.P. Rowland Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome Ann Neurol 16 1984 481 488 (Pubitemid 14021826)
    • (1984) Annals of Neurology , vol.16 , Issue.4 , pp. 481-488
    • Pavlakis, S.G.1    Phillips, P.C.2    DiMauro, S.3
  • 14
    • 84860662825 scopus 로고    scopus 로고
    • Infantile-onset spinocerebellar ataxia
    • Jan 27 [updated 2010 Jul 22]. In: Pagon RA, Bird TD, Dolan CR, Stephens K, editors [Internet]. Seattle (WA): University of Washington, Seattle; 1993
    • Nikali K, Lönnqvist T. Infantile-onset spinocerebellar ataxia. 2009 Jan 27 [updated 2010 Jul 22]. In: Pagon RA, Bird TD, Dolan CR, Stephens K, editors. GeneReviews [Internet]. Seattle (WA): University of Washington, Seattle; 1993. Available from http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi? book=gene&part=sca-io.
    • (2009) GeneReviews
    • Nikali Lönnqvist K, T.1
  • 15
    • 0031464918 scopus 로고    scopus 로고
    • A case of incomplete Kearns-Sayre syndrome with a stroke like episode
    • H. Furuya, T. Sugimura, T. Yamada, K. Hayashi, and T. Kobayashi A case of incomplete Kearns-Sayre syndrome with a stroke like episode Rinsho Shinkeigaku 37 1997 680 684 (Pubitemid 28011481)
    • (1997) Clinical Neurology , vol.37 , Issue.8 , pp. 680-684
    • Furuya, H.1    Sugimura, T.2    Yamada, T.3    Hayashi, K.4    Kobayashi, T.5
  • 16
    • 0029127326 scopus 로고
    • Evidence for cardioembolic stroke in a case of Kearns-Sayre syndrome
    • C. Kosinski, M. Mull, H. Lethen, and R. Töpper Evidence for cardioembolic stroke in a case of Kearns-Sayre syndrome Stroke 26 1995 1950 1952
    • (1995) Stroke , vol.26 , pp. 1950-1952
    • Kosinski, C.1    Mull, M.2    Lethen, H.3    Töpper, R.4
  • 19
    • 80955140618 scopus 로고    scopus 로고
    • Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation
    • May 25. In: Pagon RA, Bird TD, Dolan CR, Stephens K, editors [Internet]. Seattle (WA): University of Washington, Seattle; 1993
    • Van der Knaap MS, Scheper GC. Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation. 2010 May 25. In: Pagon RA, Bird TD, Dolan CR, Stephens K, editors. GeneReviews [Internet]. Seattle (WA): University of Washington, Seattle; 1993. Available from http://www.ncbi.nlm.nih. gov/bookshelf/br.fcgi?book=gene&part=lbsl.
    • (2010) GeneReviews
    • Van Der Knaap, M.S.1    Scheper, G.C.2
  • 20
    • 33749596336 scopus 로고    scopus 로고
    • NARP syndrome and adult-onset generalised seizures
    • T. Keränen, and H. Kuusisto NARP syndrome and adult-onset generalised seizures Epileptic Disord 8 2006 200 203 (Pubitemid 44546252)
    • (2006) Epileptic Disorders , vol.8 , Issue.3 , pp. 200-203
    • Keranen, T.1    Kuusisto, H.2
  • 21
    • 33751110611 scopus 로고    scopus 로고
    • Alpers syndrome: Progressive neuronal degeneration of children with liver disease
    • DOI 10.1017/S0012162206002209, PII S0012162206002209
    • N. Gordon Alpers syndrome: progressive neuronal degeneration of children with liver disease Dev Med Child Neurol 48 2006 1001 1003 (Pubitemid 44768806)
    • (2006) Developmental Medicine and Child Neurology , vol.48 , Issue.12 , pp. 1001-1003
    • Gordon, N.1
  • 22
    • 79960914601 scopus 로고    scopus 로고
    • Palliative functional hemispherectomy for treatment of refractory status epilepticus associated with Alpers' disease
    • S. Lupashko, S. Malik, D. Donahue, A. Hernandez, and M.S. Perry Palliative functional hemispherectomy for treatment of refractory status epilepticus associated with Alpers' disease Childs Nerv Syst 27 2011 1321 1323
    • (2011) Childs Nerv Syst , vol.27 , pp. 1321-1323
    • Lupashko, S.1    Malik, S.2    Donahue, D.3    Hernandez, A.4    Perry, M.S.5
  • 24
    • 35649024143 scopus 로고    scopus 로고
    • Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion
    • DOI 10.1093/brain/awm242
    • A.H. Hakonen, P. Isohanni, A. Paetau, R. Herva, A. Suomalainen, and T. Lönnqvist Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion Brain 130 2007 3032 3040 (Pubitemid 350033977)
    • (2007) Brain , vol.130 , Issue.11 , pp. 3032-3040
    • Hakonen, A.H.1    Isohanni, P.2    Paetau, A.3    Herva, R.4    Suomalainen, A.5    Lonnqvist, T.6
  • 25
    • 52049087584 scopus 로고    scopus 로고
    • Leigh and Leigh-like syndrome in children and adults
    • J. Finsterer Leigh and Leigh-like syndrome in children and adults Pediatr Neurol 39 2008 223 235
    • (2008) Pediatr Neurol , vol.39 , pp. 223-235
    • Finsterer, J.1
  • 26
    • 0030872164 scopus 로고    scopus 로고
    • Subacute necrotizing encephalomyelopathy (Leigh's disease): A clinicopathologic study of ten cases
    • E. Agapitos, P.M. Pavlopoulos, E. Patsouris, and P. Davaris Subacute necrotizing encephalomyelopathy (Leigh's disease): a clinicopathologic study of ten cases Gen Diagn Pathol 142 1997 335 341 (Pubitemid 27308220)
    • (1997) General and Diagnostic Pathology , vol.142 , Issue.5-6 , pp. 335-341
    • Agapitos, E.1    Pavlopoulos, P.M.2    Patsouris, E.3    Davaris, P.4
  • 27
    • 0030152946 scopus 로고    scopus 로고
    • Leigh syndrome and partial deficit of cytochrome c oxidase associated with epilepsia partialis continua
    • DOI 10.1016/0387-7604(95)00126-3
    • M. Elia, S.A. Musumeci, R. Ferri, V. Colamaria, G. Azan, and D. Greco Leigh syndrome and partial deficit of cytochrome c oxidase associated with epilepsia partialis continua Brain Dev 18 1996 207 211 (Pubitemid 26253927)
    • (1996) Brain and Development , vol.18 , Issue.3 , pp. 207-211
    • Elia, M.1    Musumeci, S.A.2    Ferri, R.3    Colamaria, V.4    Azan, G.5    Greco, D.6    Stefanini, M.C.7
  • 31
    • 79954622177 scopus 로고    scopus 로고
    • Juvenile Leigh syndrome, optic atrophy, ataxia, dystonia, and epilepsy due to T14487C mutation in the mtDNA-ND6 gene: A mitochondrial syndrome presenting from birth to adolescence
    • E. Leshinsky-Silver, R. Shuvalov, S. Inbar, S. Cohen, D. Lev, and T. Lerman-Sagie Juvenile Leigh syndrome, optic atrophy, ataxia, dystonia, and epilepsy due to T14487C mutation in the mtDNA-ND6 gene: a mitochondrial syndrome presenting from birth to adolescence J Child Neurol 26 2011 476 481
    • (2011) J Child Neurol , vol.26 , pp. 476-481
    • Leshinsky-Silver, E.1    Shuvalov, R.2    Inbar, S.3    Cohen, S.4    Lev, D.5    Lerman-Sagie, T.6
  • 32
    • 77952926538 scopus 로고    scopus 로고
    • A novel presentation of inappropriate antidiuretic hormone secretion in Leigh syndrome with the myoclonic epilepsy and ragged red fibers, mitochondrial DNA 8344A>G mutation
    • N. Swiderska, R. Appleton, A. Morris, D. Isherwood, and A. Selby A novel presentation of inappropriate antidiuretic hormone secretion in Leigh syndrome with the myoclonic epilepsy and ragged red fibers, mitochondrial DNA 8344A>G mutation J Child Neurol 25 2010 782 785
    • (2010) J Child Neurol , vol.25 , pp. 782-785
    • Swiderska, N.1    Appleton, R.2    Morris, A.3    Isherwood, D.4    Selby, A.5
  • 33
    • 65749096440 scopus 로고    scopus 로고
    • A case of Leigh syndrome associated with respiratory chain complex i deficiency due to mitochondrial gene 13513G>A mutation
    • X.Q. Wei, Q.P. Kong, Y. Zhang, Y.L. Yang, X.Z. Chang, and Y. Qi A case of Leigh syndrome associated with respiratory chain complex I deficiency due to mitochondrial gene 13513G>A mutation Zhongguo Dang Dai Er Ke Za Zhi 11 2009 333 336
    • (2009) Zhongguo Dang Dai Er Ke Za Zhi , vol.11 , pp. 333-336
    • Wei, X.Q.1    Kong, Q.P.2    Zhang, Y.3    Yang, Y.L.4    Chang, X.Z.5    Qi, Y.6
  • 34
    • 77955576599 scopus 로고    scopus 로고
    • MELAS with recurrent complex partial seizures, nonconvulsive status epilepticus, psychosis, and behavioral disturbances: Case analysis with literature review
    • K.R. Kaufman, N. Zuber, M.A. Rueda-Lara, and A. Tobia MELAS with recurrent complex partial seizures, nonconvulsive status epilepticus, psychosis, and behavioral disturbances: case analysis with literature review Epilepsy Behav 18 2010 494 497
    • (2010) Epilepsy Behav , vol.18 , pp. 494-497
    • Kaufman, K.R.1    Zuber, N.2    Rueda-Lara, M.A.3    Tobia, A.4
  • 35
    • 55449118855 scopus 로고    scopus 로고
    • Seizure frequency in adults with Wolf-Hirschhorn syndrome
    • J.C. Worthington, A.S. Rigby, and O.W. Quarrell Seizure frequency in adults with Wolf-Hirschhorn syndrome Am J Med Genet A 146A 2008 2528 2531
    • (2008) Am J Med Genet A , vol.146 A , pp. 2528-2531
    • Worthington, J.C.1    Rigby, A.S.2    Quarrell, O.W.3
  • 36
    • 0031720931 scopus 로고    scopus 로고
    • Maternally-inherited diabetes and deafness: Report of two affected German families with the A3243G mitochondrial DNA mutation
    • C. Thorns, A. Widjaja, N. Boeck, C. Skamira, and H. Zühlke Maternally-inherited diabetes and deafness: report of two affected German families with the A3243G mitochondrial DNA mutation Exp Clin Endocrinol Diabetes 106 1998 384 388 (Pubitemid 28491203)
    • (1998) Experimental and Clinical Endocrinology and Diabetes , vol.106 , Issue.5 , pp. 384-388
    • Thorns, C.1    Widjaja, A.2    Boeck, N.3    Skamira, C.4    Zuhlke, H.5
  • 37
    • 0034051849 scopus 로고    scopus 로고
    • Maternally inherited diabetes and deafness (MIDD): Unusual occult exocrine pancreatic manifestation in an affected German family
    • DOI 10.1055/s-2000-5800
    • T. Schleiffer, L.M. 't Hart, C. Schürfeld, K. Kraatz, and J.F. Riemann Maternally inherited diabetes and deafness (MIDD): unusual occult exocrine pancreatic manifestation in an affected German family Exp Clin Endocrinol Diabetes 108 2000 81 85 (Pubitemid 30234969)
    • (2000) Experimental and Clinical Endocrinology and Diabetes , vol.108 , Issue.2 , pp. 81-85
    • Schleiffer, T.1    'T Hart, L.M.2    Schurfeld, C.3    Kraatz, K.4    Riemann, J.F.5
  • 39
    • 70349488018 scopus 로고    scopus 로고
    • Encephalomyopathies caused by abnormal nuclear-mitochondrial intergenomic cross-talk
    • C. Lamperti, and M. Zeviani Encephalomyopathies caused by abnormal nuclear-mitochondrial intergenomic cross-talk Acta Myol 28 2009 2 11
    • (2009) Acta Myol , vol.28 , pp. 2-11
    • Lamperti, C.1    Zeviani, M.2
  • 40
    • 0032569825 scopus 로고    scopus 로고
    • Infantile onset spinocerebellar ataxia with sensory neuropathy (IOSCA): Neuropathological features
    • DOI 10.1016/S0022-510X(98)00249-4, PII S0022510X98002494
    • T. Lönnqvist, A. Paetau, K. Nikali, K. von Boguslawski, and H. Pihko Infantile onset spinocerebellar ataxia with sensory neuropathy (IOSCA): neuropathological features J Neurol Sci 161 1998 57 65 (Pubitemid 28559184)
    • (1998) Journal of the Neurological Sciences , vol.161 , Issue.1 , pp. 57-65
    • Lonnqvist, T.1    Paetau, A.2    Nikali, K.3    Von Boguslawski, K.4    Pihko, H.5
  • 41
    • 0025785934 scopus 로고
    • EEG findings in children and adolescents with mitochondrial encephalomyopathies: A study of 25 cases
    • M.H. Tulinius, and I. Hagne EEG findings in children and adolescents with mitochondrial encephalomyopathies: a study of 25 cases Brain Dev 13 1991 167 173
    • (1991) Brain Dev , vol.13 , pp. 167-173
    • Tulinius, M.H.1    Hagne, I.2
  • 43
    • 78651248711 scopus 로고    scopus 로고
    • Mitochondrial dysfunction due to Leber's hereditary optic neuropathy as a cause of visual loss during assessment for epilepsy surgery
    • P. Niehusmann, R. Surges, R.D. von Wrede, C.E. Elger, J. Wellmer, and J. Reimann Mitochondrial dysfunction due to Leber's hereditary optic neuropathy as a cause of visual loss during assessment for epilepsy surgery Epilepsy Behav 20 2011 38 43
    • (2011) Epilepsy Behav , vol.20 , pp. 38-43
    • Niehusmann, P.1    Surges, R.2    Von Wrede, R.D.3    Elger, C.E.4    Wellmer, J.5    Reimann, J.6
  • 44
    • 33847234224 scopus 로고    scopus 로고
    • Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G>A point mutation - A case report
    • M.M. Grazina, L.M. Diogo, P.C. Garcia, E.D. Silva, T.D. Garcia, and C.B. Robalo Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G>A point mutation - a case report Eur J Paediatr Neurol 11 2007 115 118
    • (2007) Eur J Paediatr Neurol , vol.11 , pp. 115-118
    • Grazina, M.M.1    Diogo, L.M.2    Garcia, P.C.3    Silva, E.D.4    Garcia, T.D.5    Robalo, C.B.6
  • 45
    • 9144224757 scopus 로고    scopus 로고
    • Familial mtDNA T8993C transition causing both the NARP and the MILS phenotype in the same generation: A morphological, genetic and spectroscopic study [4]
    • DOI 10.1007/s00415-003-0246-6
    • M. Sciacco, A. Prelle, E. D'Adda, C. Lamperti, A. Bordoni, and M. Rango Familial mtDNA T8993C transition causing both the NARP and the MILS phenotype in the same generation. A morphological, genetic and spectroscopic study J Neurol 250 2003 1498 1500 (Pubitemid 38121852)
    • (2003) Journal of Neurology , vol.250 , Issue.12 , pp. 1498-1500
    • Sciacco, M.1    Prelle, A.2    D'Adda, E.3    Lamperti, C.4    Bordoni, A.5    Rango, M.6    Crimi, M.7    Comi, G.P.8    Bresolin, N.9    Moggio, M.10
  • 46
    • 34247473345 scopus 로고    scopus 로고
    • NARP mitochondriopathy: An unusual cause of progressive myoclonic epilepsy
    • DOI 10.1212/01.wnl.0000264019.53959.10, PII 0000611420070424000018
    • J. Jung, F. Mauguière, P. Clerc-Renaud, E. Ollagnon, B. Mousson de Camaret, and P. Ryvlin NARP mitochondriopathy: an unusual cause of progressive myoclonic epilepsy Neurology 68 2007 1429 1430 (Pubitemid 46659096)
    • (2007) Neurology , vol.68 , Issue.17 , pp. 1429-1430
    • Jung, J.1    Mauguiere, F.2    Clerc-Renaud, P.3    Ollagnon, E.4    De Camaret, B.M.5    Ryvlin, P.6
  • 47
    • 67649718862 scopus 로고    scopus 로고
    • Mitochondrial diseases
    • J. Engel, T.A. Pedley, Lippincott Williams & Wilkins Philadelphia
    • M. Hirano, W.S. Kunz, and S. DiMauro Mitochondrial diseases J. Engel, T.A. Pedley, Epilepsy - a comprehensive textbook, III. Part 2008 Lippincott Williams & Wilkins Philadelphia 2621 2630
    • (2008) Epilepsy - A Comprehensive Textbook, III. Part , pp. 2621-2630
    • Hirano, M.1    Kunz, W.S.2    Dimauro, S.3
  • 48
    • 67349196844 scopus 로고    scopus 로고
    • Mitochondrial DNA G8363A mutation in the tRNA Lys gene: Clinical, biochemical and pathological study
    • R. Virgilio, D. Ronchi, A. Bordoni, E. Fassone, S. Bonato, and C. Donadoni Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological study J Neurol Sci 281 2009 85 92
    • (2009) J Neurol Sci , vol.281 , pp. 85-92
    • Virgilio, R.1    Ronchi, D.2    Bordoni, A.3    Fassone, E.4    Bonato, S.5    Donadoni, C.6
  • 49
    • 84860413554 scopus 로고    scopus 로고
    • Variable phenotypes in a family with mitochondrial encephalomyopathy harboring a 3291T > C mutation in mitochondrial DNA
    • Y. Sunami, K. Sugaya, N. Chihara, Y. Goto, and S. Matsubara Variable phenotypes in a family with mitochondrial encephalomyopathy harboring a 3291T > C mutation in mitochondrial DNA Neurol Sci 32 2011 861 864
    • (2011) Neurol Sci , vol.32 , pp. 861-864
    • Sunami, Y.1    Sugaya, K.2    Chihara, N.3    Goto, Y.4    Matsubara, S.5
  • 51
    • 34648840669 scopus 로고    scopus 로고
    • Nonspecific mitochondrial disease with epilepsy in children: Diagnostic approaches and epileptic phenotypes
    • DOI 10.1007/s00381-007-0369-7
    • H.C. Kang, J.W. Kwon, Y.M. Lee, H.D. Kim, H.J. Lee, and S.H. Hahn Nonspecific mitochondrial disease with epilepsy in children: diagnostic approaches and epileptic phenotypes Childs Nerv Syst 23 2007 1301 1307 (Pubitemid 47456681)
    • (2007) Child's Nervous System , vol.23 , Issue.11 , pp. 1301-1307
    • Kang, H.-C.1    Kwon, J.W.2    Lee Y.M.Young Mock3    Kim, H.D.4    Lee, H.J.5    Hahn, S.H.6
  • 52
    • 80051531713 scopus 로고    scopus 로고
    • Epileptic seizures in infants and children with mitochondrial diseases
    • H.F. Lee, C.S. Chi, C.R. Tsai, and C.H. Chen Epileptic seizures in infants and children with mitochondrial diseases Pediatr Neurol 45 2011 169 174
    • (2011) Pediatr Neurol , vol.45 , pp. 169-174
    • Lee, H.F.1    Chi, C.S.2    Tsai, C.R.3    Chen, C.H.4
  • 54
    • 79953700540 scopus 로고    scopus 로고
    • Drug-resistant epilepsia and fulminant valproate liver toxicity Alpers-Huttenlocher syndrome in two children confirmed post mortem by identification of p. W748S mutation in POLG gene
    • E. Pronicka, A. Weglewska-Jurkiewicz, M. Pronicki, J. Sykut-Cegielska, P. Kowalski, and M. Pajdowska Drug-resistant epilepsia and fulminant valproate liver toxicity Alpers-Huttenlocher syndrome in two children confirmed post mortem by identification of p. W748S mutation in POLG gene Med Sci Monit 17 2011 CR203 CR209
    • (2011) Med Sci Monit , vol.17
    • Pronicka, E.1    Weglewska-Jurkiewicz, A.2    Pronicki, M.3    Sykut-Cegielska, J.4    Kowalski, P.5    Pajdowska, M.6
  • 55
    • 77649188407 scopus 로고    scopus 로고
    • POLG DNA testing as an emerging standard of care before instituting valproic acid therapy for pediatric seizure disorders
    • R.P. Saneto, I.C. Lee, M.K. Koenig, X. Bao, S.W. Weng, and R.K. Naviaux POLG DNA testing as an emerging standard of care before instituting valproic acid therapy for pediatric seizure disorders Seizure 19 2010 140 146
    • (2010) Seizure , vol.19 , pp. 140-146
    • Saneto, R.P.1    Lee, I.C.2    Koenig, M.K.3    Bao, X.4    Weng, S.W.5    Naviaux, R.K.6
  • 56
    • 84255167255 scopus 로고    scopus 로고
    • Mitochondrial toxicity of antiepileptic drugs and their tolerability in mitochondrial disorders
    • J. Finsterer, and S. Zarrouk Mahjoub Mitochondrial toxicity of antiepileptic drugs and their tolerability in mitochondrial disorders Expert Opin Drug Metab Toxicol 8 2012 71 79
    • (2012) Expert Opin Drug Metab Toxicol , vol.8 , pp. 71-79
    • Finsterer, J.1    Zarrouk Mahjoub, S.2
  • 57
    • 79952462096 scopus 로고    scopus 로고
    • Regression of stroke-like lesions in MELAS-syndrome after seizure control
    • J. Finsterer, and P. Barton Regression of stroke-like lesions in MELAS-syndrome after seizure control Epileptic Disord 12 2010 330 334
    • (2010) Epileptic Disord , vol.12 , pp. 330-334
    • Finsterer, J.1    Barton, P.2
  • 58
    • 33846498389 scopus 로고    scopus 로고
    • Usefulness of L-arginine infusion for status epilepticus in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
    • Y. Toribe, K. Tominaga, K. Ogawa, and Y. Suzuki Usefulness of L-arginine infusion for status epilepticus in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes No To Hattatsu 39 2007 38 43 (Pubitemid 46154142)
    • (2007) No To Hattatsu , vol.39 , Issue.1 , pp. 38-43
    • Toribe, Y.1    Tominaga, K.2    Ogawa, K.3    Suzuki, Y.4
  • 59
    • 84855573842 scopus 로고    scopus 로고
    • Beneficial effect of pyruvate therapy on Leigh syndrome due to a novel mutation in PDH E1α gene
    • Y. Koga, N. Povalko, K. Katayama, N. Kakimoto, T. Matsuishi, and E. Naito Beneficial effect of pyruvate therapy on Leigh syndrome due to a novel mutation in PDH E1α gene Brain Dev 34 2012 87 91
    • (2012) Brain Dev , vol.34 , pp. 87-91
    • Koga, Y.1    Povalko, N.2    Katayama, K.3    Kakimoto, N.4    Matsuishi, T.5    Naito, E.6
  • 60
    • 56449103912 scopus 로고    scopus 로고
    • Ketamine successfully terminates malignant status epilepticus
    • H. Prüss, and M. Holtkamp Ketamine successfully terminates malignant status epilepticus Epilepsy Res 82 2008 219 222
    • (2008) Epilepsy Res , vol.82 , pp. 219-222
    • Prüss, H.1    Holtkamp, M.2
  • 63
    • 33746336630 scopus 로고    scopus 로고
    • Landau-Kleffner Syndrome with Mitochondrial Respiratory Chain-Complex I Deficiency
    • DOI 10.1016/j.pediatrneurol.2006.01.012, PII S088789940600083X
    • H.C. Kang, H.D. Kim, Y.M. Lee, and S.H. Han Landau-Kleffner syndrome with mitochondrial respiratory chain-complex I deficiency Pediatr Neurol 35 2006 158 161 (Pubitemid 44109956)
    • (2006) Pediatric Neurology , vol.35 , Issue.2 , pp. 158-161
    • Kang, H.-C.1    Kim, H.D.2    Lee, Y.M.3    Han, S.H.4
  • 64
    • 43349098636 scopus 로고    scopus 로고
    • Mitochondrial respiratory chain defects: Underlying etiology in various epileptic conditions
    • DOI 10.1111/j.1528-1167.2007.01522.x
    • Y.M. Lee, H.C. Kang, J.S. Lee, S.H. Kim, E.Y. Kim, and S.K. Lee Mitochondrial respiratory chain defects: underlying etiology in various epileptic conditions Epilepsia 49 2008 685 690 (Pubitemid 351661064)
    • (2008) Epilepsia , vol.49 , Issue.4 , pp. 685-690
    • Lee, Y.M.1    Kang, H.C.2    Lee, J.S.3    Kim, S.H.4    Kim, E.Y.5    Lee, S.K.6    Slama, A.7    Kim, H.D.8
  • 65
    • 77649191276 scopus 로고    scopus 로고
    • A case of Ohtahara syndrome with mitochondrial respiratory chain complex i deficiency
    • J.H. Seo, Y.M. Lee, J.S. Lee, S.H. Kim, and H.D. Kim A case of Ohtahara syndrome with mitochondrial respiratory chain complex I deficiency Brain Dev 32 2010 253 257
    • (2010) Brain Dev , vol.32 , pp. 253-257
    • Seo, J.H.1    Lee, Y.M.2    Lee, J.S.3    Kim, S.H.4    Kim, H.D.5
  • 68
    • 0029886656 scopus 로고    scopus 로고
    • Mitochondrial cytopathy presenting as hereditary sensory neuropathy with progressive external ophthalmoplegia, ataxia and fatal myoclonic epileptic status
    • DOI 10.1093/brain/119.3.997
    • P.H. van Domburg, A.A. Gabreëls-Festen, F.J. Gabreëls, R. de Coo, W. Ruitenbeek, and P. Wesseling Mitochondrial cytopathy presenting as hereditary sensory neuropathy with progressive external ophthalmoplegia, ataxia and fatal myoclonic epileptic status Brain 119 1996 997 1010 (Pubitemid 26237193)
    • (1996) Brain , vol.119 , Issue.3 , pp. 997-1010
    • Van Domburg, P.H.1    Gabreels-Festen, A.A.2    Gabreels, F.J.3    De Coo, R.4    Ruitenbeek, W.5    Wesseling, P.6    Ter Laak, H.7


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