Peripheral neuropathy associated with hereditary and sporadic inclusion body myositis: confirmation by electron microscopy and morphometry

[1]  C. Witt,et al.  Mapping of a candidate region for susceptibility to inclusion body myositis in the human major histocompatibility complex , 1999, Immunogenetics.

[2]  P. Barkhaus,et al.  Quantitative electrophysiologic studies in sporadic inclusion body myositis , 1999, Muscle & nerve.

[3]  Hagen H. Kitzler,et al.  Methionine homozygosity at prion gene codon 129 may predispose to sporadic inclusion-body myositis , 1999, The Lancet.

[4]  N. Darín,et al.  Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles , 1998, Annals of neurology.

[5]  A. Amato,et al.  Inclusion body myositis in twins , 1998, Neurology.

[6]  J. Schröder,et al.  Pleomorphic mitochondrial and different filamentous inclusions in inflammatory myopathies associated with mtDNA deletions , 1998, Acta Neuropathologica.

[7]  M. Dalakas,et al.  HLA allele distribution distinguishes sporadic inclusion body myositis from hereditary inclusion body myopathies , 1998, Journal of Neuroimmunology.

[8]  J. Schröder,et al.  Mitochondrial abnormalities and peripheral neuropathy in inflammatory myopathy, especially inclusion body myositis. , 1997 .

[9]  K. Shibata,et al.  Ocular manifestations in adult T-cell leukemia/lymphoma , 1997, Annals of Hematology.

[10]  M. Dalakas,et al.  An inflammatory, familial, inclusion body myositis with autoimmune features and a phenotype identical to sporadic inclusion body myositis. Studies in three families. , 1997, Brain : a journal of neurology.

[11]  J. Szabó,et al.  Epstein-Barr virus permissively infects human syncytiotrophoblasts in vitro and induces replication of human T cell leukemia-lymphoma virus type I in dually infected cells. , 1997, Virology.

[12]  M. Dalakas,et al.  Inclusion Body Myositis , 1997, Neurology.

[13]  J Miller,et al.  Inclusion body myositis in HIV-1 and HTLV-1 infected patients. , 1996, Brain : a journal of neurology.

[14]  S. Carpenter.  Inclusion Body Myositis, a Review , 1996, Journal of neuropathology and experimental neurology.

[15]  M. Dalakas,et al.  The spectrum of familial inclusion body myopathies in 13 families and a description of a quadriceps-sparing phenotype in non-Iranian Jews , 1996, Neurology.

[16]  J. Schröder,et al.  Developmental and pathological changes at the node and paranode in human sural nerves , 1996, Microscopy research and technique.

[17]  S. Dimauro,et al.  Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: A study of 56 patients , 1996, Annals of neurology.

[18]  D. Jewell,et al.  Contribution of genes of the major histocompatibility complex to susceptibility and disease phenotype in inflammatory bowel disease , 1996, The Lancet.

[19]  S. Dimauro,et al.  Inclusion body myositis and myopathies , 1995, Annals of neurology.

[20]  W. Engel,et al.  New advances in the understanding of sporadic inclusion‐body myositis and hereditary inclusion‐body myopathies , 1995, Current opinion in rheumatology.

[21]  J. Schröder,et al.  Increase of mitochondria in vasa nervorum of cases with mitochondrial myopathy, Kearns‐Sayre syndrome, progressive externaI ophthalmoplegia and MEWS * , 1995, Neuropathology and applied neurobiology.

[22]  E. Holme,et al.  Mitochondrial DNA Deletions in Muscle Fibers in Inclusion Body Myositis , 1995, Journal of neuropathology and experimental neurology.

[23]  F L Mastaglia,et al.  HLA associations with inclusion body myositis , 1994, Clinical and experimental immunology.

[24]  J. Schröder.  Neuropathy Associated with Mitochondrial Disorders , 1993, Brain pathology.

[25]  A. Hedström,et al.  Inclusion body myositis: peripheral nerve involvement Combined morphological and electrophysiological studies on peripheral nerves , 1990, Journal of the Neurological Sciences.

[26]  W J Litchy,et al.  Inclusion body myositis. Observations in 40 patients. , 1989, Brain : a journal of neurology.

[27]  R. Wortmann,et al.  Clinical heterogeneity and treatment response in inclusion body myositis. , 1989, Arthritis and rheumatism.

[28]  H. Mitsumoto,et al.  Inclusion body myositis presenting as treatment-resistant polymyositis. , 1987, Arthritis and rheumatism.

[29]  M. Danon,et al.  Inclusion Body Myositis Associated with Systemic Sarcoidosis , 1986, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

[30]  S. M. Chou,et al.  Inclusion body myositis: a chronic persistent mumps myositis? , 1986, Human pathology.

[31]  G. Gibson,et al.  Inclusion body myositis (IBM) , 1983, Neurology.

[32]  C. L. Jackson,et al.  Fine-structure mapping of the hereditary inclusion body myopathy locus. , 1999, Genomics.