-
1
-
-
0032033780
-
Restrictive cardiomyopathy, atrioventricular block and mild to subclinical myopathy in patients with desmin-immunoreactive material deposits
-
Arbustini E, Morbini P, Grasso E, et al. Restrictive cardiomyopathy, atrioventricular block and mild to subclinical myopathy in patients with desmin-immunoreactive material deposits. Jam Coll Cardiol 1998; 31: 645-53.
-
(1998)
Jam. Coll. Cardiol.
, vol.31
, pp. 645-653
-
-
Arbustini, E.1
Morbini, P.2
Grasso, E.3
-
2
-
-
0034836670
-
Combined cardiomyopathy and skeletal myopathy: Variant with atrial fibrillation and ventricular tachycardia
-
Vlay SC, Vlay LC, Coyle PK. Combined cardiomyopathy and skeletal myopathy: variant with atrial fibrillation and ventricular tachycardia. Pacing Clin Electrophysiol 2001; 24: 1389-97.
-
(2001)
Pacing Clin. Electrophysiol.
, vol.24
, pp. 1389-1397
-
-
Vlay, S.C.1
Vlay, L.C.2
Coyle, P.K.3
-
3
-
-
0028260022
-
Familial cardiac and skeletal myopathy associated with desmin accumulation
-
Porcu M, Muntoni F, Catani G, Mereu D. Familial cardiac and skeletal myopathy associated with desmin accumulation. Clin Cardiol 1994; 17:277-9.
-
(1994)
Clin. Cardiol.
, vol.17
, pp. 277-279
-
-
Porcu, M.1
Muntoni, F.2
Catani, G.3
Mereu, D.4
-
4
-
-
0031137226
-
Restrictive cardiomyopathy due to desmin accumulation in a family with evidence of autosomal dominant inheritance
-
Zachara E, Bertini E, Lioy E, Boldrini R, Prati PL, Bosman C. Restrictive cardiomyopathy due to desmin accumulation in a family with evidence of autosomal dominant inheritance. G Ital Cardiol 1997; 27: 436-42.
-
(1997)
G. Ital. Cardiol.
, vol.27
, pp. 436-442
-
-
Zachara, E.1
Bertini, E.2
Lioy, E.3
Boldrini, R.4
Prati, P.L.5
Bosman, C.6
-
5
-
-
0242361798
-
Myofibrillar myopathies
-
Olive-Plana M. Myofibrillar myopathies. Rev Neurol 2003; 37: 770-2.
-
(2003)
Rev. Neurol.
, vol.37
, pp. 770-772
-
-
Olive-Plana, M.1
-
6
-
-
0032701867
-
Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy linked to chromosome 10q
-
Melberg A, Oldfors A, Blomstrom-Lundqvist C, et al. Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy linked to chromosome 10q. Ann Neurol 1999; 46:684-92.
-
(1999)
Ann. Neurol.
, vol.46
, pp. 684-692
-
-
Melberg, A.1
Oldfors, A.2
Blomstrom-Lundqvist, C.3
-
7
-
-
0029133882
-
Desmin myopathy: A multisystem disorder involving skeletal, cardiac, and smooth muscle
-
Ariza A, Coll J, Fernandez-Figueras MT, et al. Desmin myopathy: a multisystem disorder involving skeletal, cardiac, and smooth muscle. Hum Pathol 1995; 26:1032-7.
-
(1995)
Hum. Pathol.
, vol.26
, pp. 1032-1037
-
-
Ariza, A.1
Coll, J.2
Fernandez-Figueras, M.T.3
-
8
-
-
0031879394
-
Desmin myopathy involving cardiac, skeletal and vascular smooth muscle: Report of a case with immunoelectron microscopy
-
Abraham SC, DeNofrio D, Loh E, Minda JM, Pieta GG, Reynolds C. Desmin myopathy involving cardiac, skeletal and vascular smooth muscle: report of a case with immunoelectron microscopy. Hum Pathol 1998;29:876-82.
-
(1998)
Hum. Pathol.
, vol.29
, pp. 876-882
-
-
Abraham, S.C.1
DeNofrio, D.2
Loh, E.3
Minda, J.M.4
Pieta, G.G.5
Reynolds, C.6
-
9
-
-
0029925575
-
Myofibrillar myopathy with abnormal foci of desmin positivity II. Immunocytochemical analysis
-
De Bleecker JL, Engel AG, Ertl BB. Myofibrillar myopathy with abnormal foci of desmin positivity II. immunocytochemical analysis. J Neuropathol Exp Neurol 1996; 55: 563-77.
-
(1996)
J. Neuropathol. Exp. Neurol.
, vol.55
, pp. 563-577
-
-
De Bleecker, J.L.1
Engel, A.G.2
Ertl, B.B.3
-
10
-
-
0036120620
-
Extensive induction of important mediators of fibrosis and dystrophic calcification in desmin-deficient cardiomyopathy
-
Mavroidis M, Capetanaki Y. Extensive induction of important mediators of fibrosis and dystrophic calcification in desmin-deficient cardiomyopathy. Am J Pathol 2002; 160: 943-52.
-
(2002)
Am. J. Pathol.
, vol.160
, pp. 943-952
-
-
Mavroidis, M.1
Capetanaki, Y.2
-
11
-
-
0031700768
-
The wide spectrum of myofibrillar myopathy suggests a multifactorial etiology and pathogenesis
-
Amato AA, Kagan CE, Jackson S, et al. The wide spectrum of myofibrillar myopathy suggests a multifactorial etiology and pathogenesis. Neurology 1998; 51:1646-55.
-
(1998)
Neurology
, vol.51
, pp. 1646-1655
-
-
Amato, A.A.1
Kagan, C.E.2
Jackson, S.3
-
12
-
-
0031214113
-
Null mutation in the desmin gene gives rise to a cardiomyopathy
-
Thornell LE, Carlsson L, Li Z, Mericskay M, Paulin D. Null mutation in the desmin gene gives rise to a cardiomyopathy. J Moll Cell Cardiol 1997; 29:2107-24.
-
(1997)
J. Mol. Cell Cardiol.
, vol.29
, pp. 2107-2124
-
-
Thornell, L.E.1
Carlsson, L.2
Li, Z.3
Mericskay, M.4
Paulin, D.5
-
13
-
-
0034673647
-
Desmin myopathy, A skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene
-
Dalakas MC, Park KY, Semino-Mora C, Lee SL, Sivakumar K, Goldfrab LG. Desmin myopathy, A skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene. N Engl J Med 2000; 342: 770-80.
-
(2000)
N. Engl. J. Med.
, vol.342
, pp. 770-780
-
-
Dalakas, M.C.1
Park, K.Y.2
Semino-Mora, C.3
Lee, S.L.4
Sivakumar, K.5
Goldfrab, L.G.6
-
14
-
-
0020522975
-
Mallory body-like inclusions in a hereditary congenital neuromuscular disease
-
Fidzianska A, Goebel HH, Osborn M, Lenard HG, Osse G, Langenbeck U. Mallory body-like inclusions in a hereditary congenital neuromuscular disease. Muscle Nerve 1983; 6:195-200.
-
(1983)
Muscle Nerve
, vol.6
, pp. 195-200
-
-
Fidzianska, A.1
Goebel, H.H.2
Osborn, M.3
Lenard, H.G.4
Osse, G.5
Langenbeck, U.6
-
15
-
-
0025857175
-
Neuromyopathy and restrictive cardiomyopathy with accumulation of intermediate filaments: A clinical, morphological and biochemical study
-
Bertini E, Bosman C, Ricci E. Neuromyopathy and restrictive cardiomyopathy with accumulation of intermediate filaments: a clinical, morphological and biochemical study. Acta Neuropathol 1991; 81:632-40.
-
(1991)
Acta Neuropathol.
, vol.81
, pp. 632-640
-
-
Bertini, E.1
Bosman, C.2
Ricci, E.3
-
16
-
-
0023618521
-
Subsarcolemmal vermiform deposits in skeletal muscle, associated with familial cardiomyopathy: Report of two cases of a new entity
-
Calderon A, Becker LE, Murphy EG. Subsarcolemmal vermiform deposits in skeletal muscle, associated with familial cardiomyopathy: report of two cases of a new entity. Pediatr Neurosci 1987; 13:108-12.
-
(1987)
Pediatr. Neurosci.
, vol.13
, pp. 108-112
-
-
Calderon, A.1
Becker, L.E.2
Murphy, E.G.3
-
17
-
-
0018653436
-
Myocardiopathie familiale. Etude de deux families avec biopsies myocardique et musculaire
-
Sacrez A, Porte A, Batzenschlager A, et al. Myocardiopathie familiale. Etude de deux families avec biopsies myocardique et musculaire. Arch Mal Coeur Vaiss 1979;72: 786-92.
-
(1979)
Arch. Mal. Coeur. Vaiss.
, vol.72
, pp. 786-792
-
-
Sacrez, A.1
Porte, A.2
Batzenschlager, A.3
-
18
-
-
0019501737
-
An unusual familial cardiomyopathy characterized by aberrant accumulations of desmin-type intermediate filaments
-
Stoeckel ME, Osborn M, Porte A, Sacrez A, Batzenschlager A, Weber K. An unusual familial cardiomyopathy characterized by aberrant accumulations of desmin-type intermediate filaments. Virchows Arch Pathol Anat 1981; 393: 53-60.
-
(1981)
Virchows Arch. Pathol. Anat.
, vol.393
, pp. 53-60
-
-
Stoeckel, M.E.1
Osborn, M.2
Porte, A.3
Sacrez, A.4
Batzenschlager, A.5
Weber, K.6
-
19
-
-
0018068469
-
Une nouvelle affection musculaire familiale, definie par le accumulation intra-sarcoplasmique de un materiel granulofilamentaire dense en microscopie electronique
-
Fardeau M, Godet-Guillain J, Tome FM et al. Une nouvelle affection musculaire familiale, definie par le accumulation intra-sarcoplasmique de un materiel granulofilamentaire dense en microscopie electronique. Rev Neurol 1978; 134: 411-25.
-
(1978)
Rev. Neurol.
, vol.134
, pp. 411-425
-
-
Fardeau, M.1
Godet-Guillain, J.2
Tome, F.M.3
-
20
-
-
0742305818
-
Myofibrillar myopathy: Clinical, morphological and genetic studies in 63 patients
-
Selcen D, Ohno K, Engel G. Myofibrillar myopathy: clinical, morphological and genetic studies in 63 patients. Brain 2004; 127: 439-51.
-
(2004)
Brain
, vol.127
, pp. 439-451
-
-
Selcen, D.1
Ohno, K.2
Engel, G.3
-
21
-
-
10644282203
-
Clinical and histologic studies of a Qatari family with myofibrillar myopathy
-
El-Menyar A, Al Suwaidi J, Bener A. Clinical and histologic studies of a Qatari family with myofibrillar myopathy. Saudi Medical Journal 2004; 25: 447-50.
-
(2004)
Saudi Medical Journal
, vol.25
, pp. 447-450
-
-
El-Menyar, A.1
Al Suwaidi, J.2
Bener, A.3
|