-
1
-
-
0026705376
-
Oculopharyngeal muscular dystrophy and mitochondrial abnormalities
-
ARENAS J., HUERTAS R.A., CAMPOS Y, CABELLO A., GUTIERREZ E. (1992). Oculopharyngeal muscular dystrophy and mitochondrial abnormalities. Muscle & Nerve. 14 : 1055.
-
(1992)
Muscle & Nerve
, vol.14
, pp. 1055
-
-
Arenas, J.1
Huertas, R.A.2
Campos, Y.3
Cabello, A.4
Gutierrez, E.5
-
3
-
-
0028915818
-
The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac a and ß myosin heavy chain genes on chromosome 14q11.2-q13
-
BHAIS B., XIE Y.G., SANSON M. et al. (1995). The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac a and ß myosin heavy chain genes on chromosome 14q11.2-q13. Hum Mol Genet, 4 : 429-434.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 429-434
-
-
Bhais, B.1
Xie, Y.G.2
Sanson, M.3
-
4
-
-
0019723012
-
La myopathie oculo-pharyngée (A propos d'une observation familiale)
-
COUTURIER J.C., CARRIER H., BRUNON A.M., DAVIDAS J.L., BADY B. (1981). La myopathie oculo-pharyngée (A propos d'une observation familiale). Lyon Med, 245 : 109-113.
-
(1981)
Lyon Med
, vol.245
, pp. 109-113
-
-
Couturier, J.C.1
Carrier, H.2
Brunon, A.M.3
Davidas, J.L.4
Bady, B.5
-
5
-
-
0025861703
-
Un cas de myopathie mitochondriale dans une famille de myopathie oculopharyngée
-
GOAS J.Y., LEROY J.P., MOCOUARD Y., ROUHART F. (1991). Un cas de myopathie mitochondriale dans une famille de myopathie oculopharyngée. Rev Neurol, 147 : 536-437.
-
(1991)
Rev Neurol
, vol.147
, pp. 536-1437
-
-
Goas, J.Y.1
Leroy, J.P.2
Mocouard, Y.3
Rouhart, F.4
-
6
-
-
0015968932
-
Oculopharyngeal muscular dystrophy : A case with abnormal mitochondria and « fringerprint » inclusions
-
JULIEN J., VITAL C., VALLAT M. (1974). Oculopharyngeal muscular dystrophy : a case with abnormal mitochondria and « fringerprint » inclusions. J Neurol Sci, 21 : 165-169.
-
(1974)
J Neurol Sci
, vol.21
, pp. 165-169
-
-
Julien, J.1
Vital, C.2
Vallat, M.3
-
7
-
-
0020661249
-
Chronic progressive external ophtalmoplegia (CPEO) : Clinical, morphological, and biochemical studies
-
MITSUMOTO H., APRILLE J.R., WRAY S.H., NEMNI R., BRADLEY W.G. (1983). Chronic progressive external ophtalmoplegia (CPEO) : clinical, morphological, and biochemical studies. Neurology, 33 : 452-461.
-
(1983)
Neurology
, vol.33
, pp. 452-461
-
-
Mitsumoto, H.1
Aprille, J.R.2
Wray, S.H.3
Nemni, R.4
Bradley, W.G.5
-
8
-
-
0026670288
-
Mitochondrial abnormalities in oculopharyngeal muscular dystrophy
-
MITSUMOTO H., BRADLEY W.G. (1992). Mitochondrial abnormalities in oculopharyngeal muscular dystrophy. Muscle & Nerve, 15 : 1210.
-
(1992)
Muscle & Nerve
, vol.15
, pp. 1210
-
-
Mitsumoto, H.1
Bradley, W.G.2
-
9
-
-
0025866434
-
Mitochondrial abnormalities in oculopharyngeal dystrophy
-
PAUZNER R., BLATT I., MOUALLEM M. (1991). Mitochondrial abnormalities in oculopharyngeal dystrophy. Muscle & Nerve, 14 : 947-952.
-
(1991)
Muscle & Nerve
, vol.14
, pp. 947-952
-
-
Pauzner, R.1
Blatt, I.2
Mouallem, M.3
-
10
-
-
0022552155
-
Oculopharyngeal muscular dystrophy : Recent ultrastructural evidence for mitochondrial abnormalities
-
PRATT M. R, MEYEHS P.K. (1986). Oculopharyngeal muscular dystrophy : Recent ultrastructural evidence for mitochondrial abnormalities. Laryngoscope, 96 : 368-367.
-
(1986)
Laryngoscope
, vol.96
, pp. 368-1367
-
-
Pratt, M.R.1
Meyehs, P.K.2
-
11
-
-
0025873627
-
Clinical syndromes associated with ragged red fibers
-
ROWLAND L.P., BLAKE D.M., HIRANO M., DI MAURO S., SCHON E.A., HAYS A.P., DEVIVO D.C. (1991). Clinical syndromes associated with ragged red fibers. Rev Neurol, 147 : 6-7.
-
(1991)
Rev Neurol
, vol.147
, pp. 6-7
-
-
Rowland, L.P.1
Blake, D.M.2
Hirano, M.3
Di Mauro, S.4
Schon, E.A.5
Hays, A.P.6
Devivo, D.C.7
-
12
-
-
0028987692
-
Oculopharyngeal muscular dystrophy : Clinical and morphological follow-up study reveals mitochonctrial alterations and unique nudear inclusions in a severe autosomal recessive type
-
SCHRODER J.M., KRABBE B., WEIS J. (1995). Oculopharyngeal muscular dystrophy : clinical and morphological follow-up study reveals mitochonctrial alterations and unique nudear inclusions in a severe autosomal recessive type. Neuropathol Appl Neurobiol, 21 : 68-73.
-
(1995)
Neuropathol Appl Neurobiol
, vol.21
, pp. 68-73
-
-
Schroder, J.M.1
Krabbe, B.2
Weis, J.3
-
13
-
-
0023247410
-
Myopathies oculaires : Étude nosologique de 49 cas
-
SERRATRICE G., PELLISSIER J.F. (1987). Myopathies oculaires : étude nosologique de 49 cas. Presse Med, 16 : 1969-1974.
-
(1987)
Presse Med
, vol.16
, pp. 1969-1974
-
-
Serratrice, G.1
Pellissier, J.F.2
-
14
-
-
84939092946
-
Progressive vagus-glossopharyngeal paralysis with ptosis : Contribution to group of family diseases
-
TAYLOR E.W. (1915). Progressive vagus-glossopharyngeal paralysis with ptosis : contribution to group of family diseases. J Neurol Ment Dis, 42 : 129-139.
-
(1915)
J Neurol Ment Dis
, vol.42
, pp. 129-139
-
-
Taylor, E.W.1
-
15
-
-
0018865908
-
Nuclear inclusions in oculopharyngeal dystrophy
-
TOMÉ F.M.S., FARDEAU M. (1980). Nuclear inclusions in oculopharyngeal dystrophy. Acta Neuropath, 49 : 85-87.
-
(1980)
Acta Neuropath
, vol.49
, pp. 85-87
-
-
Tomé, F.M.S.1
Fardeau, M.2
-
16
-
-
0002827582
-
Oculopharyngeal muscular dystrophy
-
Engel A.G., Franzini-Armstrong C., (eds), New York, Mc Graw-Hill Book Compagny, ch 45
-
8 ed., Engel A.G., Franzini-Armstrong C., (eds), New York, Mc Graw-Hill Book Compagny, vol. 2, ch 45, 1223-1235. Presse Med, 16 : 1969-1974.
-
(1994)
8 Ed.
, vol.2
, pp. 1223-1235
-
-
Tomé, F.M.S.1
Fardeau, M.2
-
17
-
-
8544227086
-
-
8 ed., Engel A.G., Franzini-Armstrong C., (eds), New York, Mc Graw-Hill Book Compagny, vol. 2, ch 45, 1223-1235. Presse Med, 16 : 1969-1974.
-
Presse Med
, vol.16
, pp. 1969-1974
-
-
-
18
-
-
0024580556
-
Decline in skeletal muscle mitochondrial respiratory chain function : Possible factor in aging
-
TROUNCE I., BYRNE E., MARZUKI S. (1989). Decline in skeletal muscle mitochondrial respiratory chain function : possible factor in aging. Lancet, 1 : 637-639.
-
(1989)
Lancet
, vol.1
, pp. 637-639
-
-
Trounce, I.1
Byrne, E.2
Marzuki, S.3
-
19
-
-
0000232611
-
Oculopharyngeal muscular dystrophy : A familial disease of late life characterized by dysphagia and progressive ptosis of eyelids
-
VICTOR H., HAYES R., ADAMS R.D. (1962). Oculopharyngeal muscular dystrophy : a familial disease of late life characterized by dysphagia and progressive ptosis of eyelids. N Engl J Med, 207 : 1267-1272.
-
(1962)
N Engl J Med
, vol.207
, pp. 1267-1272
-
-
Victor, H.1
Hayes, R.2
Adams, R.D.3
-
20
-
-
0029982255
-
Mitochondrial abnormalities in oculopharyngeal muscular dystrophy
-
WONG K.T., DICK D., ANDERSON J.R. (1996). Mitochondrial abnormalities in oculopharyngeal muscular dystrophy. Neuromusc Disord, 6 : 163-166.
-
(1996)
Neuromusc Disord
, vol.6
, pp. 163-166
-
-
Wong, K.T.1
Dick, D.2
Anderson, J.R.3
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