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Volumn 5, Issue 2, 2003, Pages 108-114

Dropped head presentation of mitochondrial myopathy

Author keywords

Dropped head; Mitochondrial; Muscle biopsy; Myopathy; Ragged red fibers

Indexed keywords

ACETYLSALICYLIC ACID; ATORVASTATIN; CARNITINE; CERIVASTATIN; CREATINE KINASE; CYTOCHROME C OXIDASE; FUROSEMIDE; LACTIC ACID; NICOTINIC ACID; POTASSIUM CHLORIDE; SUCCINATE DEHYDROGENASE;

EID: 4644253662     PISSN: 15220443     EISSN: None     Source Type: Journal    
DOI: 10.1097/00131402-200312000-00007     Document Type: Review
Times cited : (12)

References (37)
  • 1
    • 0026726204 scopus 로고
    • The dropped head syndrome
    • Suarez GA, Kelly JJ Jr. The dropped head syndrome. Neurology. 1992;42:1625-1627.
    • (1992) Neurology , vol.42 , pp. 1625-1627
    • Suarez, G.A.1    Kelly Jr., J.J.2
  • 2
    • 0030006283 scopus 로고    scopus 로고
    • Isolated neck extensor myopathy: A common cause of dropped head syndrome
    • Katz JS, Wolfe GI, Burns DK, et al. Isolated neck extensor myopathy: a common cause of dropped head syndrome. Neurology. 1996;46:917-921.
    • (1996) Neurology , vol.46 , pp. 917-921
    • Katz, J.S.1    Wolfe, G.I.2    Burns, D.K.3
  • 4
    • 0031133478 scopus 로고    scopus 로고
    • Dropped head syndrome: Diagnostic discussion apropos of 3 cases
    • Petiot P, Vial C, de Saint Victor JF, et al. Dropped head syndrome: diagnostic discussion apropos of 3 cases. Rev Neurol (Paris). 1997;153:251-255.
    • (1997) Rev, Neurol, (Paris) , vol.153 , pp. 251-255
    • Petiot, P.1    Vial, C.2    de Saint Victor, J.F.3
  • 5
    • 0033860795 scopus 로고    scopus 로고
    • Myopathic dropped head syndrome: A syndrome of mixed etiology
    • Gob KJ, Wong KT, Tan CT. Myopathic dropped head syndrome: a syndrome of mixed etiology. J Clin Neurosci. 2000;7:334-336.
    • (2000) J. Clin. Neurosci. , vol.7 , pp. 334-336
    • Gob, K.J.1    Wong, K.T.2    Tan, C.T.3
  • 6
    • 0038638022 scopus 로고    scopus 로고
    • Early or late appearance of 'dropped head syndrome' in amyotrophic lateral sclerosis
    • Gourie-Devi M, Nalini A, Sandhya S. Early or late appearance of 'dropped head syndrome' in amyotrophic lateral sclerosis. J Neurol Neurosurg Psychiatry. 2003;74:683-686.
    • (2003) J. Neurol. Neurosurg. Psychiatry , vol.74 , pp. 683-686
    • Gourie-Devi, M.1    Nalini, A.2    Sandhya, S.3
  • 7
    • 0028287450 scopus 로고
    • The dropped head syndrome with chronic inflammatory demyelinating polyneuropathy
    • Hoffman D, Gutmann L. The dropped head syndrome with chronic inflammatory demyelinating polyneuropathy. Muscle Nerve. 1994;17:808-810.
    • (1994) Muscle Nerve , vol.17 , pp. 808-810
    • Hoffman, D.1    Gutmann, L.2
  • 8
    • 0026335673 scopus 로고
    • Diagnostic criteria for fascioscapulohumeral muscular dystrophy
    • Padberg GW, Lunt PW, Koch M, et al. Diagnostic criteria for fascioscapulohumeral muscular dystrophy. Neuromuscul Disord. 1991;1:231-234.
    • (1991) Neuromuscul. Disord. , vol.1 , pp. 231-234
    • Padberg, G.W.1    Lunt, P.W.2    Koch, M.3
  • 9
    • 0030482285 scopus 로고    scopus 로고
    • Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle dystrophy
    • Sewry CA, Taylor J, Anderson LV, et al. Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle dystrophy. Neuromuscul Disord. 1996;6:467-474.
    • (1996) Neuromuscul. Disord. , vol.6 , pp. 467-474
    • Sewry, C.A.1    Taylor, J.2    Anderson, L.V.3
  • 10
    • 0027516962 scopus 로고
    • Dropped head syndrome
    • Bleck TP. Dropped head syndrome. Neurology. 1993;43:846.
    • (1993) Neurology , vol.43 , pp. 846
    • Bleck, T.P.1
  • 11
    • 0037004899 scopus 로고    scopus 로고
    • Dropped head as the presenting symptom of primary hyperparathyroidism
    • Beekman R, Tijssen CC, Visser LH, et al. Dropped head as the presenting symptom of primary hyperparathyroidism. J Neurol. 2002;249:1738-1739.
    • (2002) J. Neurol. , vol.249 , pp. 1738-1739
    • Beekman, R.1    Tijssen, C.C.2    Visser, L.H.3
  • 12
    • 0032806575 scopus 로고    scopus 로고
    • Adult-onset nemaline myopathy: Another cause of dropped head
    • Lomen-Hoerth C, Simmons ML, DeArmond SJ, et al. Adult-onset nemaline myopathy: Another cause of dropped head. Muscle Nerve. 1999;22:1146-1150.
    • (1999) Muscle Nerve , vol.22 , pp. 1146-1150
    • Lomen-Hoerth, C.1    Simmons, M.L.2    DeArmond, S.J.3
  • 13
    • 0034718584 scopus 로고    scopus 로고
    • Treatable dropped head syndrome in hypothyroidism
    • Askmark H, Olsson Y, Rossini S. Treatable dropped head syndrome in hypothyroidism. Neurology. 2000;55:896-897.
    • (2000) Neurology , vol.55 , pp. 896-897
    • Askmark, H.1    Olsson, Y.2    Rossini, S.3
  • 14
    • 0029376749 scopus 로고
    • Profiles of neuromuscular diseases. Becker's muscular dystrophy
    • McDonald CM, Abresch RT, Carter GT, et al. Profiles of neuromuscular diseases. Becker's muscular dystrophy. Am J Phys Med Rehabil. 1995;74(suppl): S93-103.
    • (1995) Am. J. Phys. Med. Rehabil. , vol.74 , Issue.SUPPL.
    • McDonald, C.M.1    Abresch, R.T.2    Carter, G.T.3
  • 15
    • 0005978509 scopus 로고
    • Inclusion body myositis (IBM) presenting as the 'dropped head syndrome'
    • (DHS) [Abstract]
    • Luque FA, Rosenkilde C, Valsamis M, et al. Inclusion body myositis (IBM) presenting as the 'dropped head syndrome' (DHS) [Abstract]. Brain Pathol. 1994;4:568.
    • (1994) Brain Pathol. , vol.4 , pp. 568
    • Luque, F.A.1    Rosenkilde, C.2    Valsamis, M.3
  • 16
    • 0031828024 scopus 로고    scopus 로고
    • Dropped head syndrome and bent spine syndrome: Two separate clinical entities or different manifestations of axial myopathy?
    • Oerlemans WG, de Visser M. Dropped head syndrome and bent spine syndrome: two separate clinical entities or different manifestations of axial myopathy? J Neurol Neurosurg Psychiatry. 1998;65: 258-259.
    • (1998) J. Neurol. Neurosurg. Psychiatry , vol.65 , pp. 258-259
    • Oerlemans, W.G.1    de Visser, M.2
  • 17
    • 0036080334 scopus 로고    scopus 로고
    • Axial myopathy - An unrecognised entity
    • Mahjneh I, Marconi G, Paetau A, et al. Axial myopathy - an unrecognised entity. J Neurol. 2002;249: 730-734.
    • (2002) J. Neurol. , vol.249 , pp. 730-734
    • Mahjneh, I.1    Marconi, G.2    Paetau, A.3
  • 18
    • 0028934051 scopus 로고
    • Is camptocormia a primary muscular disease?
    • Laroche M, Delisle MB, Aziza R, et al. Is camptocormia a primary muscular disease? Spine. 1995;20: 1011-1016.
    • (1995) Spine , vol.20 , pp. 1011-1016
    • Laroche, M.1    Delisle, M.B.2    Aziza, R.3
  • 19
    • 0036163531 scopus 로고    scopus 로고
    • Bent spine syndrome: Computed tomographic study and isokinetic evaluation
    • Laroche M, Ricq G, Delisle MB, et al. Bent spine syndrome: computed tomographic study and isokinetic evaluation. Muscle Nerve. 2002;25:189-193.
    • (2002) Muscle Nerve , vol.25 , pp. 189-193
    • Laroche, M.1    Ricq, G.2    Delisle, M.B.3
  • 21
    • 0037964141 scopus 로고    scopus 로고
    • Severe forward flexion of the trunk in Parkinson's disease: Focal myopathy of the paraspinal muscles mimicking camptocormia
    • Schabitz WR, Glatz K, Schuhan C, et al. Severe forward flexion of the trunk in Parkinson's disease: focal myopathy of the paraspinal muscles mimicking camptocormia. Mov Disord. 2003;18:408-414.
    • (2003) Mov. Disord. , vol.18 , pp. 408-414
    • Schabitz, W.R.1    Glatz, K.2    Schuhan, C.3
  • 22
    • 0026091344 scopus 로고
    • Mitochondrial oxidative phosphorylation defects in Parkinson's disease
    • Shoffner JM, Watts RL, Juncos JL, et al. Mitochondrial oxidative phosphorylation defects in Parkinson's disease. Ann Neurol. 1991;30:332-339.
    • (1991) Ann. Neurol. , vol.30 , pp. 332-339
    • Shoffner, J.M.1    Watts, R.L.2    Juncos, J.L.3
  • 23
    • 0029396976 scopus 로고
    • Generalized mitochondrial dysfunction in Parkinson's disease detected by magnetic resonance spectroscopy of muscle
    • Penn AM, Roberts T, Hodder J, et al. Generalized mitochondrial dysfunction in Parkinson's disease detected by magnetic resonance spectroscopy of muscle. Neurology. 1995;45:2097-2099.
    • (1995) Neurology , vol.45 , pp. 2097-2099
    • Penn, A.M.1    Roberts, T.2    Hodder, J.3
  • 24
    • 0023180605 scopus 로고
    • McArdle's disease in two generations: Autosomal recessive transmission with manifesting heterozygote
    • Schmidt B, Servidei S, Gabbai AA, et al. McArdle's disease in two generations: autosomal recessive transmission with manifesting heterozygote. Neurology. 1987;37:1558-1561.
    • (1987) Neurology , vol.37 , pp. 1558-1561
    • Schmidt, B.1    Servidei, S.2    Gabbai, A.A.3
  • 25
    • 0027513089 scopus 로고
    • Manifesting heterozygotes in McArdle's disease: Clinical, morphological, and biochemical studies in a family
    • Manfredi G, Silvestri G, Servidei S, et al. Manifesting heterozygotes in McArdle's disease: clinical, morphological, and biochemical studies in a family. J Neurol Sci. 1993;115:91-94.
    • (1993) J. Neurol. Sci. , vol.115 , pp. 91-94
    • Manfredi, G.1    Silvestri, G.2    Servidei, S.3
  • 26
    • 0029809426 scopus 로고    scopus 로고
    • Diagnosis of McArdle's disease by molecular genetic analysis of blood
    • el-Schahawi M, Tsujino S, Shanske S, et al. Diagnosis of McArdle's disease by molecular genetic analysis of blood. Neurology. 1996;47:579-580.
    • (1996) Neurology , vol.47 , pp. 579-580
    • el-Schahawi, M.1    Tsujino, S.2    Shanske, S.3
  • 28
    • 0344595467 scopus 로고    scopus 로고
    • Neck extensor myopathy: A mitochondrial disease
    • Baquis GD, Moral L, Sorrell M. Neck extensor myopathy: a mitochondrial disease. Neurology. 1997; 48:A443.
    • (1997) Neurology , vol.48
    • Baquis, G.D.1    Moral, L.2    Sorrell, M.3
  • 29
    • 0035109637 scopus 로고    scopus 로고
    • Parkinsonism and neck extensor myopathy: A new syndrome or coincidental findings?
    • Askmark H, Eeg-Olofsson K, Johansson A, et al. Parkinsonism and neck extensor myopathy: a new syndrome or coincidental findings? Arch Neurol. 2001; 58:232-237.
    • (2001) Arch. Neurol. , vol.58 , pp. 232-237
    • Askmark, H.1    Eeg-Olofsson, K.2    Johansson, A.3
  • 30
    • 0032888967 scopus 로고    scopus 로고
    • The dropped head plus syndrome: Quantification of response to corticosteroids
    • Rose MR, Levin KH, Griggs RC. The dropped head plus syndrome: quantification of response to corticosteroids. Muscle Nerve. 1999;22:115-118.
    • (1999) Muscle Nerve , vol.22 , pp. 115-118
    • Rose, M.R.1    Levin, K.H.2    Griggs, R.C.3
  • 31
    • 0032992927 scopus 로고    scopus 로고
    • Focal, steroid responsive myositis causing dropped head syndrome
    • Biran I, Cohen O, Diment J, et al. Focal, steroid responsive myositis causing dropped head syndrome. Muscle Nerve. 1999;22:769-771.
    • (1999) Muscle Nerve , vol.22 , pp. 769-771
    • Biran, I.1    Cohen, O.2    Diment, J.3
  • 33
    • 0027311193 scopus 로고
    • Phenotypic heterogeneity in families with the myoclonic epilepsy and ragged-red fiber disease point mutation in mitochondrial DNA
    • Graf WD, Sumi SM, Copass MK, et al. Phenotypic heterogeneity in families with the myoclonic epilepsy and ragged-red fiber disease point mutation in mitochondrial DNA. Ann Neurol. 1993;33:640-645.
    • (1993) Ann. Neurol. , vol.33 , pp. 640-645
    • Graf, W.D.1    Sumi, S.M.2    Copass, M.K.3
  • 34
    • 0027161003 scopus 로고
    • A mitochondrial tRNA anticodon swap associated with a muscle disease
    • Moraes CT, Ciacci F, Bonilla E, et al. A mitochondrial tRNA anticodon swap associated with a muscle disease. Nat Genet. 1993;4:284-288.
    • (1993) Nat. Genet. , vol.4 , pp. 284-288
    • Moraes, C.T.1    Ciacci, F.2    Bonilla, E.3
  • 35
    • 0031020420 scopus 로고    scopus 로고
    • A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle
    • Weber K, Wilson JN, Taylor L, et al. A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle. Am J Hum Genet. 1997; 60:373-380.
    • (1997) Am. J. Hum. Genet. , vol.60 , pp. 373-380
    • Weber, K.1    Wilson, J.N.2    Taylor, L.3
  • 36
    • 0031801084 scopus 로고    scopus 로고
    • A new mitochondrial tRNA (Met) gene mutation in a patient with dystrophic muscle and exercise intolerance
    • Vissing J, Salamon MB, Arlien-Soborg P, et al. A new mitochondrial tRNA (Met) gene mutation in a patient with dystrophic muscle and exercise intolerance. Neurology. 1998;50:1875-1878.
    • (1998) Neurology , vol.50 , pp. 1875-1878
    • Vissing, J.1    Salamon, M.B.2    Arlien-Soborg, P.3
  • 37
    • 0032923074 scopus 로고    scopus 로고
    • Adult onset limb-girdle type mitochondrial myopathy with a mitochondrial DNA np8291 A to G substitution
    • Hirata K, Nakagawa N, Higuchi I, et al. Adult onset limb-girdle type mitochondrial myopathy with a mitochondrial DNA np8291 A to G substitution. J Hum Genet. 1999;44:210-214.
    • (1999) J. Hum. Genet. , vol.44 , pp. 210-214
    • Hirata, K.1    Nakagawa, N.2    Higuchi, I.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.