-
1
-
-
0028951204
-
Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14
-
Bejaoui K, Hirabayashi K, Hentati F, et al. Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14. Neurology 1995:45:768-72.
-
(1995)
Neurology
, vol.45
, pp. 768-772
-
-
Bejaoui, K.1
Hirabayashi, K.2
Hentati, F.3
-
2
-
-
0028813434
-
Autosomal dominant distal myopathy: Linkage to chromosome 14
-
Laing NG, Laing BA, Meredith C, et al. Autosomal dominant distal myopathy: linkage to chromosome 14. Am J Hum Genet 1995:56:422-7.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 422-427
-
-
Laing, N.G.1
Laing, B.A.2
Meredith, C.3
-
3
-
-
0029011231
-
Distal myopathies. 25th ENMC International workshop
-
18-20 November 1994, Naarden, The Netherlands
-
Somer H. Distal myopathies. 25th ENMC International workshop. 18-20 November 1994, Naarden, The Netherlands. Neuromusc Disord 1995:5:249-52.
-
(1995)
Neuromusc Disord
, vol.5
, pp. 249-252
-
-
Somer, H.1
-
4
-
-
0003132648
-
Myopathia distalis tarda hereditaria
-
Welander L. Myopathia distalis tarda hereditaria. Acta Med Scand 1951:141:1-124.
-
(1951)
Acta Med Scand
, vol.141
, pp. 1-124
-
-
Welander, L.1
-
5
-
-
0018594106
-
Motor neuron firing range, axonal conduction velocity, and muscle fibre histochemistry in neuromuscular diseases
-
Borg J, Grimby L, Hannerz J. Motor neuron firing range, axonal conduction velocity, and muscle fibre histochemistry in neuromuscular diseases. Muscle Nerve 1979:2:423-30.
-
(1979)
Muscle Nerve
, vol.2
, pp. 423-430
-
-
Borg, J.1
Grimby, L.2
Hannerz, J.3
-
6
-
-
0014485677
-
Signs of neuropathy in distal hereditary myopathy (Welander)
-
Stålberg E, Ekstedt J. Signs of neuropathy in distal hereditary myopathy (Welander). Electroenceph clin Neurophysiol 1969:26:343.
-
(1969)
Electroenceph Clin Neurophysiol
, vol.26
, pp. 343
-
-
Stålberg, E.1
Ekstedt, J.2
-
7
-
-
0016763981
-
Histochemical and histopathological changes in skeletal muscles in late-onset hereditary myopathy (Welander)
-
Edström L. Histochemical and histopathological changes in skeletal muscles in late-onset hereditary myopathy (Welander). J Neurol Sci 1975:26:147-57.
-
(1975)
J Neurol Sci
, vol.26
, pp. 147-157
-
-
Edström, L.1
-
8
-
-
0025770238
-
Welander's distal myopathy: Clinical, neurophysiological and muscle biopsy observations in young and middle-aged adults with early symptoms
-
Borg K, Åhlberg G, Borg J, Edström L. Welander's distal myopathy: clinical, neurophysiological and muscle biopsy observations in young and middle-aged adults with early symptoms. J Neurol Neurosurg Psychiat 1991:54:494-8.
-
(1991)
J Neurol Neurosurg Psychiat
, vol.54
, pp. 494-498
-
-
Borg, K.1
Åhlberg, G.2
Borg, J.3
Edström, L.4
-
9
-
-
0024582686
-
Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reation
-
Weber JL, May PE. Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reation. Am J Hum Genet 1989:44:388-96.
-
(1989)
Am J Hum Genet
, vol.44
, pp. 388-396
-
-
Weber, J.L.1
May, P.E.2
-
10
-
-
0000926583
-
Nonradioactive multiplex procedure for genotyping of microsatellite markers
-
Vignal A, Gyapay G, Hazan J, et al. Nonradioactive multiplex procedure for genotyping of microsatellite markers. Methods Mol Genet 1993:211-21.
-
(1993)
Methods Mol Genet
, pp. 211-221
-
-
Vignal, A.1
Gyapay, G.2
Hazan, J.3
-
11
-
-
0026446099
-
A second generation linkage map of the human genome
-
Weissenbach J, Gyapay G, Dib C, et al. A second generation linkage map of the human genome. Nature 1992:359:794-801.
-
(1992)
Nature
, vol.359
, pp. 794-801
-
-
Weissenbach, J.1
Gyapay, G.2
Dib, C.3
-
13
-
-
0023205323
-
Exclusion mapping
-
Edwards JH. Exclusion mapping. J Med Genet 1987:24:539-43.
-
(1987)
J Med Genet
, vol.24
, pp. 539-543
-
-
Edwards, J.H.1
-
15
-
-
0022634885
-
Autosomal recessive distal muscular dystrophy as anew type of progressive muscular dystrophy: Seven cases in eight families, including an autopsied case
-
Miyoshi K, Kawai H, Iwasa M, Kuska K, Nishino H. Autosomal recessive distal muscular dystrophy as anew type of progressive muscular dystrophy: seven cases in eight families, including an autopsied case. Brain 1986:109:31-54.
-
(1986)
Brain
, vol.109
, pp. 31-54
-
-
Miyoshi, K.1
Kawai, H.2
Iwasa, M.3
Kuska, K.4
Nishino, H.5
-
16
-
-
0019481203
-
Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation
-
Nonaka I, Sunohara N, Ishiura S, Satoyosi E. Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation. J Neurol Sci 1981:51:141-55.
-
(1981)
J Neurol Sci
, vol.51
, pp. 141-155
-
-
Nonaka, I.1
Sunohara, N.2
Ishiura, S.3
Satoyosi, E.4
-
17
-
-
0027278526
-
Tibial muscular dystrophy. Late adult onset distal myopathy in 66 Finnish patients
-
Udd B, Partanen J, Halonen P, et al. Tibial muscular dystrophy. Late adult onset distal myopathy in 66 Finnish patients. Arch Neurol 1993:50:604-8.
-
(1993)
Arch Neurol
, vol.50
, pp. 604-608
-
-
Udd, B.1
Partanen, J.2
Halonen, P.3
-
18
-
-
0007478851
-
Molecular pathology
-
Bios Scientific Publishers
-
Strachan T, Read AP. Molecular pathology. In: Human Molecular Genetics. Bios Scientific Publishers, 1996:401-26.
-
(1996)
Human Molecular Genetics
, pp. 401-426
-
-
Strachan, T.1
Read, A.P.2
-
19
-
-
0026741581
-
Dinucleotide repeat polymorphism at the SCN4A locus suggest allelic heterogeneity of hyperkalemic periodic paralysis and paramyotonia congenita
-
D. M-Y
-
McClatchey I, Trofatter J, D. M-Y, et al. Dinucleotide repeat polymorphism at the SCN4A locus suggest allelic heterogeneity of hyperkalemic periodic paralysis and paramyotonia congenita. Am J Hum Genet 1992:50:896-901.
-
(1992)
Am J Hum Genet
, vol.50
, pp. 896-901
-
-
McClatchey, I.1
Trofatter, J.2
-
20
-
-
0028326542
-
A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p
-
Bashir R, Strachan T, Keers S, et al. A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p. Hum Mol Genet 1994:3:455-7.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 455-457
-
-
Bashir, R.1
Strachan, T.2
Keers, S.3
-
21
-
-
0026690760
-
Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: Linkage of an autosomal form to chromosome 5q
-
Speer MC, Yamaoka LH, Gilchrist JH, et al. Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal form to chromosome 5q. Am J Hum Genet 1992:50:1211-7.
-
(1992)
Am J Hum Genet
, vol.50
, pp. 1211-1217
-
-
Speer, M.C.1
Yamaoka, L.H.2
Gilchrist, J.H.3
-
22
-
-
84965220279
-
A lecture on myopathy and a distal form
-
Gowers WR. A lecture on myopathy and a distal form. Br Med J 1902:2:89-92.
-
(1902)
Br Med J
, vol.2
, pp. 89-92
-
-
Gowers, W.R.1
-
23
-
-
0023832568
-
Molecular cloning and chromosomal localization of a grene coding for human cardiac myosin heavy chain
-
Matsuoka R, Chambers A, Kimura M, et al. Molecular cloning and chromosomal localization of a grene coding for human cardiac myosin heavy chain. Am J Med Genet 1989:29:369-76.
-
(1989)
Am J Med Genet
, vol.29
, pp. 369-376
-
-
Matsuoka, R.1
Chambers, A.2
Kimura, M.3
-
24
-
-
0023197380
-
Two different forms of beta myosin heavy chain are expressed in human striated muscle
-
Jandreski MA, Sole MJ, Liew C-C. Two different forms of beta myosin heavy chain are expressed in human striated muscle. Hum Genet 1987:77:127-31.
-
(1987)
Hum Genet
, vol.77
, pp. 127-131
-
-
Jandreski, M.A.1
Sole, M.J.2
Liew, C.-C.3
|