-
1
-
-
0029011231
-
Distal myopathies
-
Workshop report from 25th ENMC International Workshop, 18-20 November 1994, Naarden, the Netherlands
-
[1] Somer H. Distal myopathies. Workshop report from 25th ENMC International Workshop, 18-20 November 1994, Naarden, the Netherlands. Neuromusc Disord 1995;5:249-252.
-
(1995)
Neuromusc Disord
, vol.5
, pp. 249-252
-
-
Somer, H.1
-
2
-
-
0003132648
-
Myopathia distalis tarda hereditaria
-
[2] 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
-
4
-
-
0027278526
-
Tibial muscular dystrophy. Late adult-onset distal myopathy in 66 Finnish patients
-
[4] Udd B, Partanen J, Halonen P, et al. Tibial muscular dystrophy. Late adult-onset distal myopathy in 66 Finnish patients. Arch Neurol 1993;50:604-608.
-
(1993)
Arch Neurol
, vol.50
, pp. 604-608
-
-
Udd, B.1
Partanen, J.2
Halonen, P.3
-
5
-
-
0022634885
-
Autosomal recessive distal muscular dystrophy as a new type of progressive muscular dystrophy: Seventeen cases in eight families including an autopsied case
-
[5] Miyoshi K, Kawai H, Iwasa M, Kusaka K, Nishino H. Autosomal recessive distal muscular dystrophy as a new type of progressive muscular dystrophy: seventeen 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
Kusaka, K.4
Nishino, H.5
-
6
-
-
0019481203
-
Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation
-
[6] Nonaka I, Sunohara N, Ishiura S, Satayoshi E. Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation. J Neurol Sci 1981;51:141-155.
-
(1981)
J Neurol Sci
, vol.51
, pp. 141-155
-
-
Nonaka, I.1
Sunohara, N.2
Ishiura, S.3
Satayoshi, E.4
-
7
-
-
0000114741
-
Distal myopathies
-
Engel AG, Franzini-Armstrong C, editors. New York: McGraw-Hill
-
[7] Griggs RC, Markesbery WR. Distal myopathies. In: Engel AG, Franzini-Armstrong C, editors. Myology, second ed, New York: McGraw-Hill, 1994:1246-1257.
-
(1994)
Myology, Second Ed
, pp. 1246-1257
-
-
Griggs, R.C.1
Markesbery, W.R.2
-
8
-
-
0028951204
-
Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14
-
[8] Bejaoui K, Hirabayashi K, Hentati F, et al. Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14. Neurology 1995;45:768-772.
-
(1995)
Neurology
, vol.45
, pp. 768-772
-
-
Bejaoui, K.1
Hirabayashi, K.2
Hentati, F.3
-
9
-
-
0028326542
-
A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p
-
[9] 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;3:455-457.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 455-457
-
-
Bashir, R.1
Strachan, T.2
Keers, S.3
-
10
-
-
0021320516
-
'Rimmed vacuole myopathy' sparing the quadriceps: A unique disorder in Iranian Jews
-
[10] Argov Z, Yarom R. 'Rimmed vacuole myopathy' sparing the quadriceps: a unique disorder in Iranian Jews. J Neurol Sci 1984;64:33-43.
-
(1984)
J Neurol Sci
, vol.64
, pp. 33-43
-
-
Argov, Z.1
Yarom, R.2
-
11
-
-
0030933296
-
Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9
-
[11] Ikeuchi T, Asaka T, Saito M, et al. Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9. Ann Neurol 1997;41:432-437.
-
(1997)
Ann Neurol
, vol.41
, pp. 432-437
-
-
Ikeuchi, T.1
Asaka, T.2
Saito, M.3
-
12
-
-
0030063986
-
Hereditary inclusion body myopathy maps to chromosome 9p1-q1
-
[12] Mitrani-Rosenbaum S, Argov Z, Blumenfeld A, et al. Hereditary inclusion body myopathy maps to chromosome 9p1-q1. Hum Mol Genet 1996;5:159-163.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 159-163
-
-
Mitrani-Rosenbaum, S.1
Argov, Z.2
Blumenfeld, A.3
-
14
-
-
0017687587
-
Distal myopathy: Electron microscopic and histochemical studies
-
[14] Markesbery WR, Griggs RC, Herr B. Distal myopathy: electron microscopic and histochemical studies. Neurology 1977;27:727-735.
-
(1977)
Neurology
, vol.27
, pp. 727-735
-
-
Markesbery, W.R.1
Griggs, R.C.2
Herr, B.3
-
15
-
-
0028787389
-
Inclusion body myositis and myopathies
-
[15] Griggs RC, Askanas V, DiMauro S, et al. Inclusion body myositis and myopathies. Ann Neurol 1995;38:705-713.
-
(1995)
Ann Neurol
, vol.38
, pp. 705-713
-
-
Griggs, R.C.1
Askanas, V.2
Dimauro, S.3
-
16
-
-
0008139317
-
Inclusion body myopathies
-
Askanas V, Serratrice G, Engel WK, editors. Cambridge University Press (in press)
-
[16] Fardeau M, Tome FMS. Inclusion body myopathies. In: Askanas V, Serratrice G, Engel WK, editors. Inclusion body myositis and myopathies, Cambridge University Press (in press).
-
Inclusion Body Myositis and Myopathies
-
-
Fardeau, M.1
Tome, F.M.S.2
-
17
-
-
0010309911
-
Hereditary neuromuscular disorder with inclusion body myositis-like filamentous inclusions: Clinical, pathological and tissue culture
-
[17] Fardeau M, Askanas V, Tomé FMS, Engel KW, Alvarez RB, Chevallay M. Hereditary neuromuscular disorder with inclusion body myositis-like filamentous inclusions: clinical, pathological and tissue culture. Neurology 1990;40(Suppl 1):120.
-
(1990)
Neurology
, vol.40
, Issue.SUPPL. 1
, pp. 120
-
-
Fardeau, M.1
Askanas, V.2
Tomé, F.M.S.3
Engel, K.W.4
Alvarez, R.B.5
Chevallay, M.6
-
18
-
-
0025874939
-
Familial inclusion body myositis among Kurdish-Iranian Jews
-
[18] Massa R, Weller B, Karpati G, Shoubridge E, Carpenter S. Familial inclusion body myositis among Kurdish-Iranian Jews. Arch Neurol 1991;48:519-522.
-
(1991)
Arch Neurol
, vol.48
, pp. 519-522
-
-
Massa, R.1
Weller, B.2
Karpati, G.3
Shoubridge, E.4
Carpenter, S.5
-
19
-
-
0000780231
-
'Familial inclusion body myositis' sparing the quadriceps with asymptomatic leukoencephalopathy in a Tunisian kindred
-
[19] Hentati F, Ben Hamida C, Tomé F, Oueslati S, Fardeau M, Ben Hamida M. 'Familial inclusion body myositis' sparing the quadriceps with asymptomatic leukoencephalopathy in a Tunisian kindred. Neurology 1991;41(Suppl 1):422.
-
(1991)
Neurology
, vol.41
, Issue.SUPPL. 1
, pp. 422
-
-
Hentati, F.1
Ben Hamida, C.2
Tomé, F.3
Oueslati, S.4
Fardeau, M.5
Ben Hamida, M.6
-
21
-
-
0026609582
-
Familial inclusion body myositis: Evidence for autosomal dominant inheritance
-
[21] Neville HE, Baumbach LL, Ringel SP, et al. Familial inclusion body myositis: evidence for autosomal dominant inheritance. Neurology 1992;42:897-902.
-
(1992)
Neurology
, vol.42
, pp. 897-902
-
-
Neville, H.E.1
Baumbach, L.L.2
Ringel, S.P.3
-
22
-
-
0029826654
-
The spectrum of familial inclusion body myopathies in 13 families and a description of a quadriceps sparing phenotype in non-Iranian Jews
-
[22] Sivakumar K, Dalakas MC. The spectrum of familial inclusion body myopathies in 13 families and a description of a quadriceps sparing phenotype in non-Iranian Jews. Neurology 1996;47:977-984.
-
(1996)
Neurology
, vol.47
, pp. 977-984
-
-
Sivakumar, K.1
Dalakas, M.C.2
-
23
-
-
0031979926
-
Assignment of the tibial muscular dystrophy locus to chromosome 2q31
-
[23] Haravuori H, Mäkelä-Bengs P, Udd B, et al. Assignment of the tibial muscular dystrophy locus to chromosome 2q31. Am J Hum Genet 1998;62:620-626.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 620-626
-
-
Haravuori, H.1
Mäkelä-Bengs, P.2
Udd, B.3
|