A. Ariza, Jaume Coll, M. Fernández-Figueras, M.Dolores Lopez, J. Maté, Olga García, A. Fernández‐Vasalo, J. Navas‐Palacios (1995)
Desmin myopathy: a multisystem disorder involving skeletal, cardiac, and smooth muscle.Human pathology, 26 9
Weimer (1995)
Manufacturers' Specifications & Reference Synopsis (MSRS) Catalog
Fukuhara (1977)
Core/targetoid fibres and multiple cytoplasmic bodies in organophosphate neuropathyActa Neuropathol (Berlin), 40
J. Bleecker, A. Engel, Birgit Ertl (1996)
Myofibrillar Myopathy with Abnormal Foci of Desmin Positivity. II. Immunocytochemical Analysis Reveals Accumulation of Multiple Other ProteinsJournal of Neuropathology and Experimental Neurology, 55
Clark (1978)
Autosomal dominant myofibrillar inclusion body myopathy: clinical histologic, histochemical and ultrastructural characteristics (abstr)Neurology, 28
H. Goebel, J. Muller, H. Gillen, A. Merritt (1978)
Autosomal dominant “spheroid body myopathy”Muscle & Nerve, 1
H. Goebel (1995)
Desmin‐related neuromuscular disordersMuscle & Nerve, 18
Hans Goebel, T. Voit, I. Warlo, K. Jacobs, U. Johannsen, Müller Cr (1994)
Immunohistologic and electron microscopic abnormalities of desmin and dystrophin in familial cardiomyopathy and myopathy.Revue neurologique, 150 6-7
Lydie Rappaport, F. Contard, Jane-Lyse Samuel, Claude Delcayre, F. Marotte, Fernando Tomé, Michel Fardeau (1988)
Storage of phosphorylated desmin in a familial myopathyFEBS Letters, 231
T. Bertorini, B. Adornato, J. Kučera (1978)
Benign focal amyotrophy.Archives of neurology, 43 5
Emery (1997)
Diagnostic Criteria for Neuromuscular Disorders
Fardeau (1978)
Une nouvelle affection musculaire familale définie par l'accumulation intra-sarcoplasmique d'un matériel granulofilamentaire dense en microscopie électroniqueRev Neurol (Paris), 134
Bertini (1991)
Neuromyopathy and restrictive cardiomyopathy with accumulation of intermediate filaments: a clinical, morphological and biochemical studyActa Neuropathol (Berlin), 81
Birgit Ertl, J. Bleecker, A. Engel (1994)
Similarities and differences between target formations and the ledions in desmin storage myopathyNeurology, 44
A. Caron, F. Chapon, C. Berthelin, F. Viader, B. Lechevalier (1993)
Inclusions in familial cytoplasmic body myopathy are stained by anti-dystrophin antibodiesNeuromuscular Disorders, 3
J. Vajsar, L. Becker, R. Freedom, E. Murphy (1993)
Familial desminopathy: myopathy with accumulation of desmin-type intermediate filaments.Journal of Neurology, Neurosurgery & Psychiatry, 56
J. Bleecker, A. Engel (1994)
Expression of CD45 isoforms on T cells in inflammatory myopathiesBrain Pathology, 4
H. Goebel, M. Fardeau (1995)
Desmin in myology 24th European Neuromuscular Center-sponsored workshop held 5–6 November 1993, Naarden, The NetherlandsNeuromuscular Disorders, 5
F. Muntoni, G. Catani, A. Mateddu, M. Rimoldi, T. Congiu, G. Faa, M. Marrosu, C. Cianchetti, M. Porcu (1994)
Familial cardiomyopathy, mental retardation and myopathy associated with desmin-type intermediate filamentsNeuromuscular Disorders, 4
T. Helliwell, Alexander Green, Alexander Green, R. Edwards (1994)
Hereditary distal myopathy with granulo-filamentous cytoplasmic inclusions containing desmin, dystrophin and vimentinJournal of the Neurological Sciences, 124
Bertini (1994)
Reducing body myopathy and desmin storage in skeletal muscle: morphological and biochemical findingsActa Neuropathol (Berlin), 87
A. Prelle, Maurizio Moggio, Giacomo Comi, A. Gallanti, N. Checcarelli, N. Bresolin, P. Ciscato, F. Fortunato, G. Scarlato (1992)
Congenital myopathy associated with abnormal accumulation of desmin and dystrophinNeuromuscular Disorders, 2
L. Halbig, H. Goebel, H. Hopf, R. Moll (1991)
Spheroid-cytoplasmic complexes in a congenital myopathy.Revue neurologique, 147 4
Osborn (1983)
The cytoplasmic bodies in a congenital myopathy can be stained with antibodies to desmin, the muscle specific intermediate filament proteinActa Neuropathol (Berlin), 62
Navarro (1994)
Desmin myopathy. Report of two cases with different clinical phenotype and review of the literature (abstr)Clin Neuropathol, 13
J. Thiery (1967)
Mise en evidence des polysaccharides sur coupes fines en microscopie electroniqueJournal of Microscopy, 6
L. Edström, L. Thornell, A. Eriksson (1980)
A new type of hereditary distal myopathy with characteristic sarcoplasmic bodies and intermediate (skeletin) filamentsJournal of the Neurological Sciences, 47
S. Horowitz, H. Schmalbruch (1994)
Autosomal dominant distal myopathy with desmin storage: A clinicopathologic and electrophysiologic study of a large kinshipMuscle & Nerve, 17
M. Sabatelli, E. Bertini, E. Ricci, G. Salviati, S. Magi, M. Papacci, P. Tonali (1992)
Peripheral neuropathy with giant axons and cardiomyopathy associated with desmin type intermediate filaments in skeletal muscleJournal of the Neurological Sciences, 109
A. Fidziańska, H. Goebel, M. Osborn, H. Lenard, G. Osse, U. Langenbeck (1983)
Mallory body‐like inclusions in a hereditary congenital neuromuscular diseaseMuscle & Nerve, 6
A. Fidziańska, B. Ryniewicz, M. Barcikowska, H. Goebel (1995)
A new familial congenital myopathy in children with desmin and dystrophin reacting plaquesJournal of the Neurological Sciences, 131
F. Chapon, F. Viader, M. Fardeau, F. Tomé, N. Daluzeau, C. Berthelin, J. Thenint, B. Lechevalier (1989)
[Familial myopathy with "cytoplasmic body" (or "spheroid") type inclusions, disclosed by respiratory insufficiency].Revue neurologique, 145 6-7
Neuromuscular Disorders – Pubmed
Published: Feb 27, 1997
Access the full text.
Sign up today, get DeepDyve free for 14 days.