메뉴 건너뛰기




Volumn 162, Issue HS2, 2006, Pages

Clinical characteristics of ALS subsets;Quels sont les critères cliniques de la sclérose latérale amyotrophique en fonction des formes cliniques?

Author keywords

ALS; Primary lateral sclerosis; Progressive bulbar palsy; Progressive muscular atrophy

Indexed keywords

AMYOTROPHIC LATERAL SCLEROSIS; CLINICAL FEATURE; CLINICAL PRACTICE; CONFERENCE PAPER; DISEASE ASSOCIATION; HUMAN; ONSET AGE; PROGNOSIS; CLASSIFICATION; CONSENSUS DEVELOPMENT;

EID: 33750032901     PISSN: 00353787     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper
Times cited : (8)

References (49)
  • 1
    • 0029983886 scopus 로고    scopus 로고
    • Clinical characteristics of familial amyotrophic lateral sclerosis with Cu/Zn superoxide dismutase gene mutations
    • ABE K, AOKI M, IKEDA M, WATANABE M, HIRAI S,ITOYAMA Y. (1996). Clinical characteristics of familial amyotrophic lateral sclerosis with Cu/Zn superoxide dismutase gene mutations. J Neurol Sci, 136: 108-116.
    • (1996) J Neurol Sci , vol.136 , pp. 108-116
    • Abe, K.1    Aoki, M.2    Ikeda, M.3    Watanabe, M.4    Hirai, S.5    Itoyama, Y.6
  • 5
    • 9544236295 scopus 로고    scopus 로고
    • Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patients
    • ANDERSEN PM, FORSGREN L, BINZER M, NILSSON P, ALA-HURULA V, KERANEN ML, BERGMARK L et al. (1996). Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patients. Brain, 119: 1153-1172.
    • (1996) Brain , vol.119 , pp. 1153-1172
    • Andersen, P.M.1    Forsgren, L.2    Binzer, M.3    Nilsson, P.4    Ala-Hurula, V.5    Keranen, M.L.6    Bergmark, L.7
  • 8
    • 0032801298 scopus 로고    scopus 로고
    • Diagnostic dilemmas in amyotrophic lateral sclerosis
    • BROOKS BR. (1999). Diagnostic dilemmas in amyotrophic lateral sclerosis. J Neurol Sci, 165 Suppl 1: S1-S9.
    • (1999) J Neurol Sci , vol.165 , Issue.SUPPL. 1
    • Brooks, B.R.1
  • 12
    • 84859674288 scopus 로고    scopus 로고
    • La sclérose latérale amyotrophique: Une maladie d'origine génétique et environnementale
    • DUPRÉ N, PRADAT PF, BOUCHARD GA, MEININGER V. (2005). La sclérose latérale amyotrophique: une maladie d'origine génétique et environnementale. La Lettre du Neurologue, 9: 139-142.
    • (2005) La Lettre du Neurologue , vol.9 , pp. 139-142
    • Dupré, N.1    Pradat, P.F.2    Bouchard, G.A.3    Meininger, V.4
  • 14
    • 0017756670 scopus 로고
    • Amyotrophic lateral sclerosis presenting with respiratory failure. Diaphragmatic paralysis and dependence on mechanical ventilation in two patients
    • FROMM GB, WISDOM PJ, BLOCK AJ. (1977). Amyotrophic lateral sclerosis presenting with respiratory failure. Diaphragmatic paralysis and dependence on mechanical ventilation in two patients. Chest, 71: 612-614.
    • (1977) Chest , vol.71 , pp. 612-614
    • Fromm, G.B.1    Wisdom, P.J.2    Block, A.J.3
  • 16
  • 17
    • 0024449824 scopus 로고
    • Respiratory complications and their management in motor neuron disease
    • HOWARD RS, WILES CM, LOH L. (1989). Respiratory complications and their management in motor neuron disease. Brain, 112 (Pt 5): 1155-1170.
    • (1989) Brain , vol.112 , Issue.PART 5 , pp. 1155-1170
    • Howard, R.S.1    Wiles, C.M.2    Loh, L.3
  • 18
    • 1542374575 scopus 로고    scopus 로고
    • Les anomalies du gène superoxyde dismutase 1 dans le sclérose latérale amyotrophique familiale: Corrélations phénotype/génotype et implications pratiques. L'expérience française et revue de la littérature
    • JAFARI-SCHLUEP HF, KHORIS J, MAYEUX-PORTAS V, HAND C, ROULEAU G, CAMU W. (2004). Les anomalies du gène superoxyde dismutase 1 dans le sclérose latérale amyotrophique familiale: corrélations phénotype/génotype et implications pratiques. L'expérience française et revue de la littérature. Rev Neurol (Paris), 160: 44-50.
    • (2004) Rev Neurol (Paris) , vol.160 , pp. 44-50
    • Jafari-Schluep, H.F.1    Khoris, J.2    Mayeux-Portas, V.3    Hand, C.4    Rouleau, G.5    Camu, W.6
  • 20
    • 0031458389 scopus 로고    scopus 로고
    • Prominent sensory and autonomic disturbances in familial amyotrophic lateral sclerosis with a Gly93Ser mutation in the SOD1 gene
    • KAWATA A, KATO S, HAYASHI H, HIRAI S. (1997). Prominent sensory and autonomic disturbances in familial amyotrophic lateral sclerosis with a Gly93Ser mutation in the SOD1 gene. J Neurol Sci, 153: 82-85.
    • (1997) J Neurol Sci , vol.153 , pp. 82-85
    • Kawata, A.1    Kato, S.2    Hayashi, H.3    Hirai, S.4
  • 21
    • 0034463339 scopus 로고    scopus 로고
    • Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same country
    • KHORIS J, MOULARD B, BRIOLOTTI V, HAYER M, DURIEUX A, CLAVELOU P, MALAFOSSE A et al. (2000). Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same country. Eur J Neurol, 7: 207-211.
    • (2000) Eur J Neurol , vol.7 , pp. 207-211
    • Khoris, J.1    Moulard, B.2    Briolotti, V.3    Hayer, M.4    Durieux, A.5    Clavelou, P.6    Malafosse, A.7
  • 22
    • 0035069990 scopus 로고    scopus 로고
    • Familial amyotrophic lateral sclerosis and parkinsonism-dementia complex of the Kii Peninsula of Japan: Clinical and neuropathological study and tau analysis
    • KUZUHARA S, KOKUBO Y, SASAKI R, NARITA Y, YABANA T, HASEGAWA M, IWATSUBO T. (2001). Familial amyotrophic lateral sclerosis and parkinsonism-dementia complex of the Kii Peninsula of Japan: clinical and neuropathological study and tau analysis. Ann Neurol, 49: 501-511.
    • (2001) Ann Neurol , vol.49 , pp. 501-511
    • Kuzuhara, S.1    Kokubo, Y.2    Sasaki, R.3    Narita, Y.4    Yabana, T.5    Hasegawa, M.6    Iwatsubo, T.7
  • 26
    • 0025695793 scopus 로고
    • Clinical features and associations of 560 cases of motor neuron disease
    • LI TM, ALBERMAN E, SWASH M. (1990). Clinical features and associations of 560 cases of motor neuron disease. J Neurol Neurosurg Psychiatry, 53: 1043-1045.
    • (1990) J Neurol Neurosurg Psychiatry , vol.53 , pp. 1043-1045
    • Li, T.M.1    Alberman, E.2    Swash, M.3
  • 27
    • 0036234975 scopus 로고    scopus 로고
    • Disease progression in amyotrophic lateral sclerosis: Predictors of survival
    • MAGNUS T, BECK M, GIESS R, PULS I, NAUMANN M, TOYKA KV. (2002). Disease progression in amyotrophic lateral sclerosis: predictors of survival. Muscle Nerve, 25: 709-714.
    • (2002) Muscle Nerve , vol.25 , pp. 709-714
    • Magnus, T.1    Beck, M.2    Giess, R.3    Puls, I.4    Naumann, M.5    Toyka, K.V.6
  • 28
    • 0021954533 scopus 로고
    • Amyotrophic lateral sclerosis presenting with respiratory insufficiency as the primary complaint. Clinicopathological study of a case
    • MEYRIGNAC C, POIRIER J, DEGOS JD. (1985). Amyotrophic lateral sclerosis presenting with respiratory insufficiency as the primary complaint. Clinicopathological study of a case. Eur Neurol, 24: 115-120.
    • (1985) Eur Neurol , vol.24 , pp. 115-120
    • Meyrignac, C.1    Poirier, J.2    Degos, J.D.3
  • 29
    • 0000589688 scopus 로고    scopus 로고
    • Clinical features: Signs and symptoms
    • H. Mitsumoto, D.A. Chad, and E. P. Pioro, eds. (Philadelphie: FA Davis Company)
    • MITSUMOTO H, CHAD DA, PIORO EP. (1998a). Clinical features: signs and symptoms. In Amyotrophic Lateral Sclerosis, H. Mitsumoto, D.A. Chad, and E. P. Pioro, eds. (Philadelphie: FA Davis Company), pp. 47-64.
    • (1998) Amyotrophic Lateral Sclerosis , pp. 47-64
    • Mitsumoto, H.1    Chad, D.A.2    Pioro, E.P.3
  • 30
    • 33749683788 scopus 로고    scopus 로고
    • Familial ALS
    • H. Mitsumoto, D.A. Chad, and E.P. Pioro, eds. (Philadelphie: FA Davis Company)
    • MITSUMOTO H, CHAD DA, PIORO EP. (1998b). Familial ALS. In Amyotrophic Lateral Sclerosis, H. Mitsumoto, D.A. Chad, and E.P. Pioro, eds. (Philadelphie: FA Davis Company), pp. 164-176.
    • (1998) Amyotrophic Lateral Sclerosis , pp. 164-176
    • Mitsumoto, H.1    Chad, D.A.2    Pioro, E.P.3
  • 31
    • 15044363922 scopus 로고    scopus 로고
    • History, terminology and classification of ALS
    • H. Mitsumoto, D. A. Chad, and E. P. Pioro, eds. (Philadelphia: FA Davis Company)
    • MITSUMOTO H, CHAD DA, PIORO EP. (1998c). History, terminology and classification of ALS. In Amyotrophic lateral sclerosis, H. Mitsumoto, D. A. Chad, and E. P. Pioro, eds. (Philadelphia: FA Davis Company), pp. 3-17.
    • (1998) Amyotrophic Lateral Sclerosis , pp. 3-17
    • Mitsumoto, H.1    Chad, D.A.2    Pioro, E.P.3
  • 33
    • 0030751103 scopus 로고    scopus 로고
    • Étude clinique des formes familiales de sclérose latérale amyotrophique. Revue de la littérature
    • MOULARD B, CAMU W, MALAFOSSE A, BILLIARD M, BALDY-MOULINIER M. (1997). Étude clinique des formes familiales de sclérose latérale amyotrophique. Revue de la littérature. Rev Neurol (Paris), 153: 314-324.
    • (1997) Rev Neurol (Paris) , vol.153 , pp. 314-324
    • Moulard, B.1    Camu, W.2    Malafosse, A.3    Billiard, M.4    Baldy-Moulinier, M.5
  • 34
    • 0022443737 scopus 로고
    • Familial adult motor neuron disease: Amyotrophic lateral sclerosis
    • MULDER DW, KURLAND LT, OFFORD KP, BEARD CM. (1986). Familial adult motor neuron disease: amyotrophic lateral sclerosis. Neurology, 36: 511-517.
    • (1986) Neurology , vol.36 , pp. 511-517
    • Mulder, D.W.1    Kurland, L.T.2    Offord, K.P.3    Beard, C.M.4
  • 37
    • 0017330502 scopus 로고
    • Studies on epidemiological, clinical, and etiological aspects of ALS disease in Sardinia, Southern Italy
    • ROSATI G, PINNA L, GRANIERI E, AIELLO I, TOLA R, AGNETTI V, PIRISI A et al. (1977). Studies on epidemiological, clinical, and etiological aspects of ALS disease in Sardinia, Southern Italy. Acta Neurol Scand, 55: 231-244.
    • (1977) Acta Neurol Scand , vol.55 , pp. 231-244
    • Rosati, G.1    Pinna, L.2    Granieri, E.3    Aiello, I.4    Tola, R.5    Agnetti, V.6    Pirisi, A.7
  • 38
    • 0017867105 scopus 로고
    • Amyotrophic lateral sclerosis. Clinical features and prognosis
    • ROSEN AD. (1978). Amyotrophic lateral sclerosis. Clinical features and prognosis. Arch Neurol, 35: 638-642.
    • (1978) Arch Neurol , vol.35 , pp. 638-642
    • Rosen, A.D.1
  • 39
    • 0024589232 scopus 로고
    • Immunocytochemical characterization of neurofibrillary tangles in amyotrophic lateral sclerosis and parkinsonism-dementia of Guam
    • SHANKAR SK, YANAGIHARA R, GARRUTO RM, GRUNDKE-IQBAL I, KOSIK KS, GAJDUSEK DC. (1989). Immunocytochemical characterization of neurofibrillary tangles in amyotrophic lateral sclerosis and parkinsonism-dementia of Guam. Ann Neurol, 25: 146-151.
    • (1989) Ann Neurol , vol.25 , pp. 146-151
    • Shankar, S.K.1    Yanagihara, R.2    Garruto, R.M.3    Grundke-Iqbal, I.4    Kosik, K.S.5    Gajdusek, D.C.6
  • 41
    • 12044249765 scopus 로고
    • Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity
    • SIDDIQUE T, FIGLEWICZ DA, PERICAK-VANCE MA, HAINES JL, ROULEAU G, JEFFERS AJ, SAPP P et al. (1991). Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity. N Engl J Med, 324: 1381-1384.
    • (1991) N Engl J Med , vol.324 , pp. 1381-1384
    • Siddique, T.1    Figlewicz, D.A.2    Pericak-Vance, M.A.3    Haines, J.L.4    Rouleau, G.5    Jeffers, A.J.6    Sapp, P.7
  • 42
    • 0029447638 scopus 로고
    • The diagnosis of amyotrophic lateral sclerosis. A discussion
    • SWASH M. (1995). The diagnosis of amyotrophic lateral sclerosis. A discussion. Adv Neurol, 68: 157-160.
    • (1995) Adv Neurol , vol.68 , pp. 157-160
    • Swash, M.1
  • 45
    • 0033905620 scopus 로고    scopus 로고
    • Clinical features of amyotrophic lateral sclerosis according to the El Escorial and Airlie House diagnostic criteria: A population-based study
    • TRAYNOR BJ, CODD MB, CORR B, FORDE C, FROST E, HARDIMAN OM. (2000). Clinical features of amyotrophic lateral sclerosis according to the El Escorial and Airlie House diagnostic criteria: A population-based study. Arch Neurol, 57: 1171-1176.
    • (2000) Arch Neurol , vol.57 , pp. 1171-1176
    • Traynor, B.J.1    Codd, M.B.2    Corr, B.3    Forde, C.4    Frost, E.5    Hardiman, O.M.6
  • 46
    • 0025843663 scopus 로고
    • Epidemiology of amyotrophic lateral sclerosis in Hordaland county, western Norway
    • TYSNES OB, VOLLSET SE, AARLI JA. (1991). Epidemiology of amyotrophic lateral sclerosis in Hordaland county, western Norway. Acta Neurol Scand, 83: 280-285.
    • (1991) Acta Neurol Scand , vol.83 , pp. 280-285
    • Tysnes, O.B.1    Vollset, S.E.2    Aarli, J.A.3
  • 47
    • 0034961192 scopus 로고    scopus 로고
    • Atypical motor neuron disease and related motor syndromes
    • VERMA A, BRADLEY WG. (2001). Atypical motor neuron disease and related motor syndromes. Semin Neurol, 21: 177-187.
    • (2001) Semin Neurol , vol.21 , pp. 177-187
    • Verma, A.1    Bradley, W.G.2
  • 49
    • 0023759628 scopus 로고
    • Familial motor neuron disease: Differing penetrance in large pedigrees
    • WILLIAMS DB, FLOATE DA, LEICESTER J. (1988). Familial motor neuron disease: differing penetrance in large pedigrees. J Neurol Sci, 86: 215-230.
    • (1988) J Neurol Sci , vol.86 , pp. 215-230
    • Williams, D.B.1    Floate, D.A.2    Leicester, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.