-
1
-
-
0026027805
-
A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage
-
BECKMANN, J.S., RICHARD, I., HILLAIRE, D. et al.: A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage. Comptes Rendus de l'Académie des sciences (Paris), 312: 141-148, 1991.
-
(1991)
Comptes Rendus de l'Académie des Sciences (Paris)
, vol.312
, pp. 141-148
-
-
Beckmann, J.S.1
Richard, I.2
Hillaire, D.3
-
2
-
-
0020606260
-
Severe childhood muscular dystrophy affecing both sexes and frequent in Tunisia
-
BEN HAMIDA, M., FARDEAU, M. and ATTIA, N.: Severe childhood muscular dystrophy affecing both sexes and frequent in Tunisia. Muscle Nerve, 6: 496-480, 1983.
-
(1983)
Muscle Nerve
, vol.6
, pp. 496-1480
-
-
Ben Hamida, M.1
Fardeau, M.2
Attia, N.3
-
3
-
-
0017259099
-
Benign myopathy with autosomal dominant inheritance: A report of three pedigrees
-
BETHLEM, J. and VAN WIJNGAARDEN, G.: Benign myopathy with autosomal dominant inheritance: a report of three pedigrees. Brain, 99: 91-100, 1976.
-
(1976)
Brain
, vol.99
, pp. 91-100
-
-
Bethlem, J.1
Van Wijngaarden, G.2
-
4
-
-
0011290733
-
The limb-girdle syndrome
-
Vinken, P. J., Bruyn, G.W. (eds.), Amsterdam: North Holland
-
BRADLEY, W.G.: The limb-girdle syndrome. In: Vinken, P. J., Bruyn, G.W. (eds.), Handbook of clinical neurology. Vol. 40. Amsterdam: North Holland, 433-469, 1979.
-
(1979)
Handbook of Clinical Neurology.
, vol.40
, pp. 433-469
-
-
Bradley, W.G.1
-
5
-
-
10544221103
-
Electrodiagnostic features of Charcot-Marie-Tooth disease
-
CHRISTIE, B.G.B.: Electrodiagnostic features of Charcot-Marie-Tooth disease. Proc. Roy. Soc. Med., 54: 321-324, 1961.
-
(1961)
Proc. Roy. Soc. Med.
, vol.54
, pp. 321-324
-
-
Christie, B.G.B.1
-
6
-
-
0022497685
-
Adult onset autosomal dominant limb-girdle muscular dystrophy
-
CHUTKOW, J.G., HEFFNER, R.R., KRAMER, A.A. and EDWARDS, J.M.: Adult onset autosomal dominant limb-girdle muscular dystrophy. Ann. Neurol., 20: 240-248, 1986.
-
(1986)
Ann. Neurol.
, vol.20
, pp. 240-248
-
-
Chutkow, J.G.1
Heffner, R.R.2
Kramer, A.A.3
Edwards, J.M.4
-
7
-
-
0015788562
-
Histopathologie des unités motrices dans les maladies neuromusculaires
-
COERS, C. and TELERMAN-TOPPET, N.: Histopathologie des unités motrices dans les maladies neuromusculaires. Ann. Anatol. Pathol., 18: 235-250, 1973.
-
(1973)
Ann. Anatol. Pathol.
, vol.18
, pp. 235-250
-
-
Coers, C.1
Telerman-Toppet, N.2
-
8
-
-
0019188802
-
Clinical features and classification of the muscular dystrophies
-
GARDNER-MEDWIN, D.: Clinical features and classification of the muscular dystrophies. Br. Med. Bull., 36: 109, 1980.
-
(1980)
Br. Med. Bull.
, vol.36
, pp. 109
-
-
Gardner-Medwin, D.1
-
9
-
-
0023856168
-
Clinical and genetic investigation in autosomal dominant limb-girdle dystrophy
-
GILCHRIST, J.M., PERICAK-VANCE, M. A., SILVERMAN, L. and ROSES, A.D.: Clinical and genetic investigation in autosomal dominant limb-girdle dystrophy. Neurology, 38: 5-9, 1988.
-
(1988)
Neurology
, vol.38
, pp. 5-9
-
-
Gilchrist, J.M.1
Pericak-Vance, M.A.2
Silverman, L.3
Roses, A.D.4
-
10
-
-
0026764256
-
Dystrophinopathy in isolated cases of myopathy in females
-
HOFFMAN, E. P., ARAHTA, K., MINETTI, C. et al.: Dystrophinopathy in isolated cases of myopathy in females. Neurology, 42: 967-975, 1992.
-
(1992)
Neurology
, vol.42
, pp. 967-975
-
-
Hoffman, E.P.1
Arahta, K.2
Minetti, C.3
-
11
-
-
0017569986
-
Chronic-spinal muscular atrophy simulating facioscapulohumeral type and limb-girdle type of muscular dystrophy
-
KAZAKOV, V.M., KOVALENKO, T.M., SKOROMETZ, A.A. and MIKHAILOV, E.P.: Chronic-spinal muscular atrophy simulating facioscapulohumeral type and limb-girdle type of muscular dystrophy. Eur. Neurol., 16: 90-98, 1977.
-
(1977)
Eur. Neurol.
, vol.16
, pp. 90-98
-
-
Kazakov, V.M.1
Kovalenko, T.M.2
Skorometz, A.A.3
Mikhailov, E.P.4
-
12
-
-
0000089061
-
Heredofamilial proximal spinal muscular atrophy simulating muscular dystrophy
-
KUGELBERG, E. and WELANDER, L.: Heredofamilial proximal spinal muscular atrophy simulating muscular dystrophy. Arch. Neurol. Psychiat. (Chic.), 75: 500-509, 1956.
-
(1956)
Arch. Neurol. Psychiat. (Chic.)
, vol.75
, pp. 500-509
-
-
Kugelberg, E.1
Welander, L.2
-
13
-
-
0027102414
-
A large inbred Palestinian family with two forms of muscular dystrophy
-
MAHJNEH, I., VANELLI, G., BUSHBY, K. and MARCONI, G.: A large inbred Palestinian family with two forms of muscular dystrophy. Neuromusc. Dis., 2: 277-283, 1992.
-
(1992)
Neuromusc. Dis.
, vol.2
, pp. 277-283
-
-
Mahjneh, I.1
Vanelli, G.2
Bushby, K.3
Marconi, G.4
-
14
-
-
0025876630
-
Limb-girdle muscular dystrophy with autosomal dominant inheritance
-
MARCONI, G.P., PIZZI, A., ARIMONDI, C.G. and VANELLI, B.: Limb-girdle muscular dystrophy with autosomal dominant inheritance. Acta Neurol. Scand., 38: 234-238, 1991.
-
(1991)
Acta Neurol. Scand.
, vol.38
, pp. 234-238
-
-
Marconi, G.P.1
Pizzi, A.2
Arimondi, C.G.3
Vanelli, B.4
-
15
-
-
0014598411
-
Chronic spinal muscular atrophy in adults. Part 1. The Kugelberg-Welander syndrome
-
MEADOWS, J.C., MARSDEN, C.D. and HARRIMAN, D.G.F.: Chronic spinal muscular atrophy in adults. Part 1. The Kugelberg-Welander syndrome. J. Neurol. Sci., 9: 527-550, 1969.
-
(1969)
J. Neurol. Sci.
, vol.9
, pp. 527-550
-
-
Meadows, J.C.1
Marsden, C.D.2
Harriman, D.G.F.3
-
16
-
-
0015762845
-
Hereditary quadriceps myopathy
-
MICHAEL, L., ESPIR, E. and MATTHEWS, W. B.: Hereditary quadriceps myopathy. J. Neurol. Neurosurg. Psychiat., 36: 1041-1045, 1973.
-
(1973)
J. Neurol. Neurosurg. Psychiat.
, vol.36
, pp. 1041-1045
-
-
Michael, L.1
Espir, E.2
Matthews, W.B.3
-
17
-
-
17644431425
-
Progressive muskeldystrophie, VIII Haufigkeit, Klinik und Genetik der Typen I und II
-
MOSER VON, H., WIESMANN, U., RICHTERICH, R. and ROSSI, E.: Progressive muskeldystrophie, VIII Haufigkeit, Klinik und Genetik der Typen I und II. Schweis. Med. Wochenschr., 96: 169-205, 1966.
-
(1966)
Schweis. Med. Wochenschr.
, vol.96
, pp. 169-205
-
-
Von Moser, H.1
Wiesmann, U.2
Richterich, R.3
Rossi, E.4
-
18
-
-
0024510023
-
Distinction of Becker from limb-girdle muscular dystrophy by means of dystrophin DNA probes
-
NORMAN, A., THOMAS, N., COACKLEY, J. and HARPER, P.: Distinction of Becker from limb-girdle muscular dystrophy by means of dystrophin DNA probes. Lancet, I: 466-468, 1989.
-
(1989)
Lancet
, vol.1
, pp. 466-468
-
-
Norman, A.1
Thomas, N.2
Coackley, J.3
Harper, P.4
-
19
-
-
0025753198
-
Limb-girdle syndrome: A genetic study of 22 large Brazilian families comparison with X-linked Duchenne and Becker dystrophies
-
PASSOS-BUENO, M.R., VAINZOF, M., PAVANELLO, R. C., PAVANELLO-FILHO, I., LIMA, M. and SATS, M.: Limb-girdle syndrome: a genetic study of 22 large Brazilian families comparison with X-linked Duchenne and Becker dystrophies. J. Neurol. Sci., 103: 65-75, 1991.
-
(1991)
J. Neurol. Sci.
, vol.103
, pp. 65-75
-
-
Passos-Bueno, M.R.1
Vainzof, M.2
Pavanello, R.C.3
Pavanello-Filho, I.4
Lima, M.5
Sats, M.6
-
20
-
-
0026356242
-
Benign muscular dystrophy with autosomal dominant inheritance
-
SOMER, H., LAULAMAA, V., PALJARVI, L. et al.: Benign muscular dystrophy with autosomal dominant inheritance. Neuromusc. Dis., 1: 267-274, 1991.
-
(1991)
Neuromusc. Dis.
, vol.1
, pp. 267-274
-
-
Somer, H.1
Laulamaa, V.2
Paljarvi, L.3
-
21
-
-
0020519420
-
Quadriceps myopathy: A variant of the limb-girdle dystrophy syndrome
-
SWASH, M. and HEATHFIELD, K. W. G.: Quadriceps myopathy: a variant of the limb-girdle dystrophy syndrome. J. Neurol. Neurosurg. Psychiat., 46: 355-357, 1983.
-
(1983)
J. Neurol. Neurosurg. Psychiat.
, vol.46
, pp. 355-357
-
-
Swash, M.1
Heathfield, K.W.G.2
-
22
-
-
0021702696
-
Clinical study of proximal spinal muscular atrophy. Report on 89 cases
-
TONALI, P., SERVIDEI, S., UNCINI, A., RESTUCCIA, D. and GALLUZZI, G.: Clinical study of proximal spinal muscular atrophy. Report on 89 cases. Ital. J. NeuroL Sci., 5: 423-432, 1984.
-
(1984)
Ital. J. NeuroL Sci.
, vol.5
, pp. 423-432
-
-
Tonali, P.1
Servidei, S.2
Uncini, A.3
Restuccia, D.4
Galluzzi, G.5
-
23
-
-
0000042975
-
On classification, natural history and treatment of the myopathies
-
WALTON, J.N. and NATTRASS, F.J.: On classification, natural history and treatment of the myopathies. Brain, 77: 169, 1954.
-
(1954)
Brain
, vol.77
, pp. 169
-
-
Walton, J.N.1
Nattrass, F.J.2
-
24
-
-
10544227162
-
Two cases of myopathy limited to the quadriceps
-
WALTON, J.N.: Two cases of myopathy limited to the quadriceps. J. Neurol. Neurosurg. Psychiat., 19: 106-108, 1956.
-
(1956)
J. Neurol. Neurosurg. Psychiat.
, vol.19
, pp. 106-108
-
-
Walton, J.N.1
-
25
-
-
0344222928
-
Heriditary proximal spinal muscular atrophy - A clinical entity simulating muscular dystrophy
-
WOHLFART, G., FEX, G. and ELIASSON, S.: Heriditary proximal spinal muscular atrophy - a clinical entity simulating muscular dystrophy. Acta Psychiat. Scand., 30: 395-406, 1955.
-
(1955)
Acta Psychiat. Scand.
, vol.30
, pp. 395-406
-
-
Wohlfart, G.1
Fex, G.2
Eliasson, S.3
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