-
1
-
-
76949122075
-
Myopathia distalis tarda hereditaria
-
WELANDER L. Myopathia distalis tarda hereditaria. Acta Med Scand 1951;141(Suppl. 265):1-124.
-
(1951)
Acta Med Scand
, vol.141
, Issue.265 SUPPL.
, pp. 1-124
-
-
Welander, L.1
-
2
-
-
0036315171
-
Welander distal myopathy outside the Swedish population: Phenotype and genotype
-
VON TELL D, SOMER H, UDD B, EDSTROM L, BORG K, AHLBERG G. Welander distal myopathy outside the Swedish population: phenotype and genotype. Neuromuscul Disord 2002;12:544-7.
-
(2002)
Neuromuscul Disord
, vol.12
, pp. 544-547
-
-
Von Tell, D.1
Somer, H.2
Udd, B.3
Edstrom, L.4
Borg, K.5
Ahlberg, G.6
-
3
-
-
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
-
4
-
-
0031979926
-
Assignment of the tibial muscular dystrophy (TMD) locus to chromosome 2q31
-
HARAVUORI H, MÄKELÄ-BENGS P, UDD B et al. Assignment of the tibial muscular dystrophy (TMD) locus to chromosome 2q31. Am J Hum Genet 1998;62:620-6.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 620-626
-
-
Haravuori, H.1
Mäkelä-Bengs, P.2
Udd, B.3
-
5
-
-
0032880011
-
Genetic linkage of Welander distal myopathy to chromosome 2p13
-
ÅHLBERG G, VON TELL D, BORG K et al. Genetic linkage of Welander distal myopathy to chromosome 2p13. Ann Neurol 1999;46:399-404.
-
(1999)
Ann Neurol
, vol.46
, pp. 399-404
-
-
Åhlberg, G.1
Von Tell, D.2
Borg, K.3
-
6
-
-
0036723943
-
Tibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titin
-
HACKMAN P, VIHOLA A, HARAVUORI H et al. Tibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titin. Am J Hum Genet 2002;71:492-500.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 492-500
-
-
Hackman, P.1
Vihola, A.2
Haravuori, H.3
-
7
-
-
10144255830
-
Limb-girdle muscular dystrophy: A follow up study of 79 patients
-
MAHJNEH I, BUSHBY K, PIZZI A, BASHIR R, MARCONI G. limb-girdle muscular dystrophy: a follow up study of 79 patients. Acta Neurol Scand 1996;94:177-89.
-
(1996)
Acta Neurol Scand
, vol.94
, pp. 177-189
-
-
Mahjneh, I.1
Bushby, K.2
Pizzi, A.3
Bashir, R.4
Marconi, G.5
-
8
-
-
0026350030
-
Imaging methods reveal unexpected patchy lesions in late onset distal myopathy
-
UDD B, LAMMINEN A, SOMER H. Imaging methods reveal unexpected patchy lesions in late onset distal myopathy. Neuromusc Disord 1991;1:271-80.
-
(1991)
Neuromusc Disord
, vol.1
, pp. 271-280
-
-
Udd, B.1
Lamminen, A.2
Somer, H.3
-
9
-
-
0026439379
-
Imaging techniques in myotonic dystrophy: A comparative study of ultrasound, computed tomography and magnetic resonance imaging of skeletal muscles
-
SCHEDEL H, REMERS CD, NÄGELE M, WITT TN, PONGRATZ DE, VOGL T. Imaging techniques in myotonic dystrophy: a comparative study of ultrasound, computed tomography and magnetic resonance imaging of skeletal muscles. Eur J Radiol 1992;15:230-8.
-
(1992)
Eur J Radiol
, vol.15
, pp. 230-238
-
-
Schedel, H.1
Remers, C.D.2
Nägele, M.3
Witt, T.N.4
Pongratz, D.E.5
Vogl, T.6
-
10
-
-
0034846609
-
Muscle computed tomography in peripheral neuropathies
-
MARCONI G., MAHJNEH I, PIZZI A. Muscle computed tomography in peripheral neuropathies. Acta Neurol Scand 2001;104:156-61.
-
(2001)
Acta Neurol Scand
, vol.104
, pp. 156-161
-
-
Marconi, G.1
Mahjneh, I.2
Pizzi, A.3
-
12
-
-
0025241450
-
Magnetic resonance imaging of primary skeletal muscle diseases: Patterns of distribution and severity of involvement
-
LAMMINEN AE: Magnetic resonance imaging of primary skeletal muscle diseases: patterns of distribution and severity of involvement. Br J Radiol 1990;63:946-50.
-
(1990)
Br J Radiol
, vol.63
, pp. 946-950
-
-
Lamminen, A.E.1
-
13
-
-
0008263932
-
Histopathological basis of muscle imaging
-
Fleckenstein JL, Crues JV, Reimers CD, eds. New York: Springer-Verlag
-
REIMERS CD, FISHER P, PONGRATZ DE. Histopathological basis of muscle imaging. In: Fleckenstein JL, Crues JV, Reimers CD, eds. Muscle imaging in health and disease. New York: Springer-Verlag, 1996;183-91.
-
(1996)
Muscle Imaging in Health and Disease
, pp. 183-191
-
-
Reimers, C.D.1
Fisher, P.2
Pongratz, D.E.3
-
14
-
-
0027972476
-
Distribution of muscle degeneration in Welander distal myopathy - A magnetic resonance and muscle biopsy study
-
ÅHLBERG G, JAKOBSSON F, FRANSSON A, MORITZ Å, BORG K, EDSTRÖM L. Distribution of muscle degeneration in Welander distal myopathy - a magnetic resonance and muscle biopsy study. Neuromusc Disord 1994;4:55-62.
-
(1994)
Neuromusc Disord
, vol.4
, pp. 55-62
-
-
Åhlberg, G.1
Jakobsson, F.2
Fransson, A.3
Moritz, Å.4
Borg, K.5
Edström, L.6
-
15
-
-
0030968884
-
Sarcopenia: Origins and relevance
-
ROSENBERG IH: Sarcopenia: origins and relevance. J Nutr 1997;127:990S.
-
(1997)
J Nutr
, vol.127
-
-
Rosenberg, I.H.1
-
16
-
-
0021320516
-
"Rimmed vacuole myopathy" sparing the quadriceps: A unique disorder in Iranian Jews
-
ARGOV A, 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, A.1
Yarom, R.2
-
17
-
-
0036203649
-
Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy
-
MERCURI E, COUNSELL S, ALLSOP J et al. Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy. Neuropediatrics 2002;33:10-14.
-
(2002)
Neuropediatrics
, vol.33
, pp. 10-14
-
-
Mercuri, E.1
Counsell, S.2
Allsop, J.3
-
18
-
-
0019189310
-
Studies of muscular performance in normal and dystrophic subjects
-
EDWARDS RHT. Studies of muscular performance in normal and dystrophic subjects. Br Med Bull 1980;36:159-64.
-
(1980)
Br Med Bull
, vol.36
, pp. 159-164
-
-
Edwards, R.H.T.1
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