-
1
-
-
0022510445
-
Mononuclear cells in myopathies: Quantitation of functionally distinct subsets, recognition of antigen-specific cell-mediated cytotoxicity in some diseases, and implications for the pathogenesis of the different inflammatory myopathies
-
Engel AG, Arahata K: Mononuclear cells in myopathies: quantitation of functionally distinct subsets, recognition of antigen-specific cell-mediated cytotoxicity in some diseases, and implications for the pathogenesis of the different inflammatory myopathies. Hum Pathol 1986, 17:704-721.
-
(1986)
Hum Pathol
, vol.17
, pp. 704-721
-
-
Engel, A.G.1
Arahata, K.2
-
2
-
-
0026429550
-
Polymyositis, dermatomyositis and inclusion-body myositis
-
Dalakas MC: Polymyositis, dermatomyositis and inclusion-body myositis. N Engl J Med 1991, 325:1487-1498.
-
(1991)
N Engl J Med
, vol.325
, pp. 1487-1498
-
-
Dalakas, M.C.1
-
3
-
-
0742321934
-
Proposed pathogenetic cascade of inclusion-body myositis: Importance of amyloid-beta, misfolded proteins, predisposing genes, and aging
-
Askanas V, Engel WK: Proposed pathogenetic cascade of inclusion-body myositis: importance of amyloid-beta, misfolded proteins, predisposing genes, and aging. Curr Opin Rheumatol 2003, 15:737-744. This is a detailed review of what is currently known of the pathogenesis of IBM.
-
(2003)
Curr Opin Rheumatol
, vol.15
, pp. 737-744
-
-
Askanas, V.1
Engel, W.K.2
-
4
-
-
0141651951
-
Polymyositis and dermatomyositis
-
Dalakas MC, Hohlfeld R: Polymyositis and dermatomyositis. Lancet 2003, 362:971-982.
-
(2003)
Lancet
, vol.362
, pp. 971-982
-
-
Dalakas, M.C.1
Hohlfeld, R.2
-
5
-
-
0038015907
-
Diagnosis and treatment of inflammatory muscle diseases
-
Hilton-Jones D: Diagnosis and treatment of inflammatory muscle diseases. J Neurol Neurosurg Psychiatry 2003, 74(suppl 2):ii25-ii31.
-
(2003)
J Neurol Neurosurg Psychiatry
, vol.74
, Issue.2 SUPPL.
-
-
Hilton-Jones, D.1
-
6
-
-
0037381381
-
Inflammatory myopathies: Clinical, diagnostic and therapeutic aspects
-
Mastaglia FL, Garlepp MJ, Phillips BA, et al.: Inflammatory myopathies: clinical, diagnostic and therapeutic aspects. Muscle Nerve 2003, 27:407-425. A highly comprehensive recent review of the idiopathic inflammatory myopathies.
-
(2003)
Muscle Nerve
, vol.27
, pp. 407-425
-
-
Mastaglia, F.L.1
Garlepp, M.J.2
Phillips, B.A.3
-
7
-
-
10744229686
-
Polymyositis: An over-diagnosed entity
-
van der Meulen MF, Bronner IM, Hoogendijk JE, et al.: Polymyositis: an over-diagnosed entity. Neurology 2003, 61:316-321. A detailed clinicopathologic study of the subclassification of inflammatory myopathy by Bohan and Peter and more recent histopathologic criteria are reported.
-
(2003)
Neurology
, vol.61
, pp. 316-321
-
-
Van Der Meulen, M.F.1
Bronner, I.M.2
Hoogendijk, J.E.3
-
8
-
-
0016850495
-
Polymyositis and dermatomyositis (first of two parts)
-
Bohan A, Peter JB: Polymyositis and dermatomyositis (first of two parts). N Engl J Med 1975, 292:344-347.
-
(1975)
N Engl J Med
, vol.292
, pp. 344-347
-
-
Bohan, A.1
Peter, J.B.2
-
9
-
-
0017640201
-
Computer-assisted analysis of 153 patients with polymyositis and dermatomyositis
-
Baltimore
-
Bohan A, Peter JB, Bowman RL, et al.: Computer-assisted analysis of 153 patients with polymyositis and dermatomyositis. Medicine (Baltimore) 1977, 56:255-286.
-
(1977)
Medicine
, vol.56
, pp. 255-286
-
-
Bohan, A.1
Peter, J.B.2
Bowman, R.L.3
-
10
-
-
0036866028
-
Idiopathic inflammatory myopathies: Epidemiology, classification, and diagnostic criteria
-
Mastaglia FL, Phillips BA: Idiopathic inflammatory myopathies: epidemiology, classification, and diagnostic criteria. Rheum Dis Clin North Am 2002, 28:723-741.
-
(2002)
Rheum Dis Clin North Am
, vol.28
, pp. 723-741
-
-
Mastaglia, F.L.1
Phillips, B.A.2
-
11
-
-
0027403228
-
Adult idiopathic polymyositis without elevation of creatine kinase. Case report and review of the literature
-
Gran JT, Myklebust G, Johansen S: Adult idiopathic polymyositis without elevation of creatine kinase. Case report and review of the literature. Scand J Rheumatol 1993, 22:94-98.
-
(1993)
Scand J Rheumatol
, vol.22
, pp. 94-98
-
-
Gran, J.T.1
Myklebust, G.2
Johansen, S.3
-
12
-
-
0028817374
-
Laboratory evaluation of the inflammatory myopathies
-
Rider LG, Miller FW: Laboratory evaluation of the inflammatory myopathies. Clin Diagn Lab Immunol 1995, 2:1-9.
-
(1995)
Clin Diagn Lab Immunol
, vol.2
, pp. 1-9
-
-
Rider, L.G.1
Miller, F.W.2
-
13
-
-
0035043073
-
Anti-Jo-1 positive inclusion body myositis with a marked and sustained clinical improvement after oral prednisone
-
Hengstman GJ, Ter Laak HJ, van Engelen BG, et al.: Anti-Jo-1 positive inclusion body myositis with a marked and sustained clinical improvement after oral prednisone. J Neurol Neurosurg Psychiatry 2001, 70:706.
-
(2001)
J Neurol Neurosurg Psychiatry
, vol.70
, pp. 706
-
-
Hengstman, G.J.1
Ter Laak, H.J.2
Van Engelen, B.G.3
-
15
-
-
0036709575
-
A case of limb-girdle muscular dystrophy with serum anti-nuclear antibody which led to a mistaken diagnosis of polymyositis
-
Funauchi M, Nozaki Y, Yoo BS, et al.: A case of limb-girdle muscular dystrophy with serum anti-nuclear antibody which led to a mistaken diagnosis of polymyositis. Clin Exp Rheumatol 2002, 20:707-708.
-
(2002)
Clin Exp Rheumatol
, vol.20
, pp. 707-708
-
-
Funauchi, M.1
Nozaki, Y.2
Yoo, B.S.3
-
16
-
-
0034881381
-
Inclusion body myositis mimicking motor neuron disease
-
Dabby R, Lange DJ, Trojaborg W, et al.: Inclusion body myositis mimicking motor neuron disease. Arch Neurol 2001, 58:1253-1256.
-
(2001)
Arch Neurol
, vol.58
, pp. 1253-1256
-
-
Dabby, R.1
Lange, D.J.2
Trojaborg, W.3
-
17
-
-
0036866049
-
Muscle biopsy findings in inflammatory myopathies
-
Dalakas MC: Muscle biopsy findings in inflammatory myopathies. Rheum Dis Clin North Am 2002, 28:779-798.
-
(2002)
Rheum Dis Clin North Am
, vol.28
, pp. 779-798
-
-
Dalakas, M.C.1
-
18
-
-
0028807858
-
Analysis of cytokine expression in muscle in inflammatory myopathies, Duchenne dystrophy, and non-weak controls
-
Lundberg I, Brengman JM, Engel AG: Analysis of cytokine expression in muscle in inflammatory myopathies, Duchenne dystrophy, and non-weak controls. J Neuroimmunol 1995, 63:9-16.
-
(1995)
J Neuroimmunol
, vol.63
, pp. 9-16
-
-
Lundberg, I.1
Brengman, J.M.2
Engel, A.G.3
-
19
-
-
0028961960
-
Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): Immunocytochemical and genetic analyses
-
Arahata K, Ishihara T, Fukunaga H, et al.: Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analyses. Muscle Nerve 1995, 2:356-366.
-
(1995)
Muscle Nerve
, vol.2
, pp. 356-366
-
-
Arahata, K.1
Ishihara, T.2
Fukunaga, H.3
-
21
-
-
10544230641
-
Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy
-
Pegoraro E, Mancias P, Swerdlow SH, et al.: Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy. Ann Neurol 1996, 40:782-791.
-
(1996)
Ann Neurol
, vol.40
, pp. 782-791
-
-
Pegoraro, E.1
Mancias, P.2
Swerdlow, S.H.3
-
22
-
-
0031005529
-
Pulsed intravenous methylprednisolone therapy for inflammatory myopathies: Evaluation of the effect by comparing two consecutive biopsies from the same muscle
-
Matsubara S, Hirai S, Sawa Y: Pulsed intravenous methylprednisolone therapy for inflammatory myopathies: evaluation of the effect by comparing two consecutive biopsies from the same muscle. J Neuroimmunol 1997, 76:75-80.
-
(1997)
J Neuroimmunol
, vol.76
, pp. 75-80
-
-
Matsubara, S.1
Hirai, S.2
Sawa, Y.3
-
24
-
-
10744220559
-
Class I MHC detection as a diagnostic tool in noninformative muscle biopsies of patients suffering from dermatomyositis (DM)
-
Civatte M, Schleinitz N, Krammer P, et al.: Class I MHC detection as a diagnostic tool in noninformative muscle biopsies of patients suffering from dermatomyositis (DM). Neuropathol Appl Neurobiol 2003, 29:546-552.
-
(2003)
Neuropathol Appl Neurobiol
, vol.29
, pp. 546-552
-
-
Civatte, M.1
Schleinitz, N.2
Krammer, P.3
-
25
-
-
12144287801
-
Muscle inflammation and MHC class I up-regulation in muscular dystrophy with lack of dysferlin: An immunopathological study
-
Confalonieri P, Oliva L, Andreetta F, et al.: Muscle inflammation and MHC class I up-regulation in muscular dystrophy with lack of dysferlin: an immunopathological study. J Neuroimmunol 2003, 142:130-136. This is an interesting pathologic study comparing biopsy findings in dysferlinopathy with those seen in PM.
-
(2003)
J Neuroimmunol
, vol.142
, pp. 130-136
-
-
Confalonieri, P.1
Oliva, L.2
Andreetta, F.3
-
26
-
-
0011261078
-
Conditional up-regulation of MHC class I in skeletal muscle leads to self-sustaining autoimmune myositis and myositis-specific autoantibodies
-
Nagaraju K, Raben N, Loeffler L, et al.: Conditional up-regulation of MHC class I in skeletal muscle leads to self-sustaining autoimmune myositis and myositis-specific autoantibodies. Proc Natl Acad Sci U S A 2000, 97:9209-9214.
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 9209-9214
-
-
Nagaraju, K.1
Raben, N.2
Loeffler, L.3
-
27
-
-
0028835527
-
Diagnostic criteria for the limb-girdle muscular dystrophies: Report of the ENMC Consortium on limb-girdle dystrophies
-
Bushby KM: Diagnostic criteria for the limb-girdle muscular dystrophies: report of the ENMC Consortium on limb-girdle dystrophies. Neuromuscul Disord 1995, 5:71-74.
-
(1995)
Neuromuscul Disord
, vol.5
, pp. 71-74
-
-
Bushby, K.M.1
-
28
-
-
1042268038
-
The congenital and limb-girdle muscular dystrophies: Sharpening the focus, blurring the boundaries
-
Kirschner J, Bonnemann CG: The congenital and limb-girdle muscular dystrophies: sharpening the focus, blurring the boundaries. Arch Neurol 2004, 61:189-199. This is a good general summary of the clinical and molecular aspects of congenital muscular dystrophies and LGMD.
-
(2004)
Arch Neurol
, vol.61
, pp. 189-199
-
-
Kirschner, J.1
Bonnemann, C.G.2
-
29
-
-
0042071489
-
The 10 autosomal recessive limb-girdle muscular dystrophies
-
Zatz M, de Paula F, Starling A, et al.: The 10 autosomal recessive limb-girdle muscular dystrophies. Neuromuscul Disord 2003, 13:532-544. This is a detailed review of the clinical and molecular aspects of the recessive LGMDs.
-
(2003)
Neuromuscul Disord
, vol.13
, pp. 532-544
-
-
Zatz, M.1
De Paula, F.2
Starling, A.3
-
30
-
-
0036866960
-
Clarifying the boundaries between the inflammatory and dystrophic myopathies: Insights from molecular diagnostics and microarrays
-
Hoffman EP, Rao D, Pachman LM: Clarifying the boundaries between the inflammatory and dystrophic myopathies: insights from molecular diagnostics and microarrays. Rheum Dis Clin North Am 2002, 28:743-757.
-
(2002)
Rheum Dis Clin North Am
, vol.28
, pp. 743-757
-
-
Hoffman, E.P.1
Rao, D.2
Pachman, L.M.3
-
31
-
-
0029996165
-
Limb girdle muscular dystrophy: A radiologic and manometric study of the pharynx and esophagus
-
Stubgen JP: Limb girdle muscular dystrophy: a radiologic and manometric study of the pharynx and esophagus. Dysphagia 1996, 11:25-29.
-
(1996)
Dysphagia
, vol.11
, pp. 25-29
-
-
Stubgen, J.P.1
-
32
-
-
0037738510
-
Defective membrane repair in dysferlin-deficient muscular dystrophy
-
Bansal D, Miyake K, Vogel SS, et al.: Defective membrane repair in dysferlin-deficient muscular dystrophy. Nature 2003, 423:168-172. This excellent study sheds light on the biologic role of dysferlin in calcium-dependent membrane fusion and repair.
-
(2003)
Nature
, vol.423
, pp. 168-172
-
-
Bansal, D.1
Miyake, K.2
Vogel, S.S.3
-
33
-
-
0037151075
-
Calcium-sensitive phospholipid binding properties of normal and mutant ferlin C2 domains
-
Davis DB, Doherty KR, Delmonte AJ, et al.: Calcium-sensitive phospholipid binding properties of normal and mutant ferlin C2 domains. J Biol Chem 2002, 277:22883-22888.
-
(2002)
J Biol Chem
, vol.277
, pp. 22883-22888
-
-
Davis, D.B.1
Doherty, K.R.2
Delmonte, A.J.3
-
34
-
-
0036022277
-
Clinical heterogeneity in dysferlinopathy
-
Ueyama H, Kumamoto T, Horinouchi H, et al.: Clinical heterogeneity in dysferlinopathy. Intern Med 2002, 41:532-536.
-
(2002)
Intern Med
, vol.41
, pp. 532-536
-
-
Ueyama, H.1
Kumamoto, T.2
Horinouchi, H.3
-
35
-
-
0034719093
-
Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathy
-
Illarioshkin SN, Ivanova-Smolenskaya IA, Greenberg CR, et al.: Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathy. Neurology 2000, 55:1931-1933.
-
(2000)
Neurology
, vol.55
, pp. 1931-1933
-
-
Illarioshkin, S.N.1
Ivanova-Smolenskaya, I.A.2
Greenberg, C.R.3
-
36
-
-
0034709195
-
Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation
-
McNally EM, Ly CT, Rosenmann H, et al.: Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation. Am J Med Genet 2000, 91:305-312.
-
(2000)
Am J Med Genet
, vol.91
, pp. 305-312
-
-
McNally, E.M.1
Ly, C.T.2
Rosenmann, H.3
-
37
-
-
0032884692
-
Prominent inflammatory changes on muscle biopsy in patients with Miyoshi myopathy
-
Rowin J, Meriggioli MN, Cochran EJ, et al.: Prominent inflammatory changes on muscle biopsy in patients with Miyoshi myopathy. Neuromuscul Disord 1999, 9:417-420.
-
(1999)
Neuromuscul Disord
, vol.9
, pp. 417-420
-
-
Rowin, J.1
Meriggioli, M.N.2
Cochran, E.J.3
-
39
-
-
0032850960
-
Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B
-
Bittner RE, Anderson LV, Burkhardt E, et al.: Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B. Nat Genet 1999, 23:141-142.
-
(1999)
Nat Genet
, vol.23
, pp. 141-142
-
-
Bittner, R.E.1
Anderson, L.V.2
Burkhardt, E.3
-
40
-
-
0344420060
-
Dystrophin and mutations: One gene, several proteins, multiple phenotypes
-
Muntoni F, Torelli S, Ferlini A: Dystrophin and mutations: one gene, several proteins, multiple phenotypes. Lancet Neurol 2003, 2:731-740. This is an excellent review of the molecular genetics and associated phenotypes of the dystrophinopathies.
-
(2003)
Lancet Neurol
, vol.2
, pp. 731-740
-
-
Muntoni, F.1
Torelli, S.2
Ferlini, A.3
-
41
-
-
0035295673
-
Pharmacologic and genetic therapy for childhood muscular dystrophies
-
Escolar DM, Scacheri CG: Pharmacologic and genetic therapy for childhood muscular dystrophies. Curr Neurol Neurosci Rep 2001, 1:168-174.
-
(2001)
Curr Neurol Neurosci Rep
, vol.1
, pp. 168-174
-
-
Escolar, D.M.1
Scacheri, C.G.2
-
42
-
-
0028904169
-
Genetic and biochemical normalization in female carriers of Duchenne muscular dystrophy: Evidence for failure of dystrophin production in dystrophin-competent myonuclei
-
Pegoraro E, Schimke RN, Garcia C, et al.: Genetic and biochemical normalization in female carriers of Duchenne muscular dystrophy: evidence for failure of dystrophin production in dystrophin-competent myonuclei. Neurology 1995, 45:677-690.
-
(1995)
Neurology
, vol.45
, pp. 677-690
-
-
Pegoraro, E.1
Schimke, R.N.2
Garcia, C.3
-
43
-
-
0033583984
-
Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in the Netherlands: A cohort study
-
Hoogerwaard EM, Bakker E, Ippel PF, et al.: Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in The Netherlands: a cohort study. Lancet 1999, 353:2116-2119.
-
(1999)
Lancet
, vol.353
, pp. 2116-2119
-
-
Hoogerwaard, E.M.1
Bakker, E.2
Ippel, P.F.3
-
44
-
-
1642377315
-
Molecular basis of facioscapulohumeral muscular dystrophy
-
Tupler R, Gabellini D: Molecular basis of facioscapulohumeral muscular dystrophy. Cell Mol Life Sci 2004, 61:557-566.
-
(2004)
Cell Mol Life Sci
, vol.61
, pp. 557-566
-
-
Tupler, R.1
Gabellini, D.2
-
45
-
-
0036327398
-
A nonischemic forearm exercise test for McArdle disease
-
Kazemi-Esfarjani P, Skomorowska E, Jensen TD, et al.: A nonischemic forearm exercise test for McArdle disease. Ann Neurol 2002, 52:153-159.
-
(2002)
Ann Neurol
, vol.52
, pp. 153-159
-
-
Kazemi-Esfarjani, P.1
Skomorowska, E.2
Jensen, T.D.3
-
46
-
-
0028321739
-
Late-onset muscular weakness in phosphofructokinase deficiency due to exon 5/iniron 5 junction poini mutation: A unique disorder or the natural course of this glycolytic disorder?
-
Argov Z, Barash V, Soffer D, et al.: Late-onset muscular weakness in phosphofructokinase deficiency due to exon 5/iniron 5 junction poini mutation: a unique disorder or the natural course of this glycolytic disorder? Neurology 1994, 44:1097-1100.
-
(1994)
Neurology
, vol.44
, pp. 1097-1100
-
-
Argov, Z.1
Barash, V.2
Soffer, D.3
-
47
-
-
0029974752
-
Late-onset muscle weakness in partial phosphofructokinase deficiency: A unique myopathy with vacuoles, abnormal mitochondria, and absence of the common exon 5/intron 5 junction point mutation
-
Sivakumar K, Vasconcelos O, Goldfarb L, et al.: Late-onset muscle weakness in partial phosphofructokinase deficiency: a unique myopathy with vacuoles, abnormal mitochondria, and absence of the common exon 5/intron 5 junction point mutation. Neurology 1996, 46:1337-1342.
-
(1996)
Neurology
, vol.46
, pp. 1337-1342
-
-
Sivakumar, K.1
Vasconcelos, O.2
Goldfarb, L.3
-
48
-
-
0033541105
-
A diagnostic protocol for adult-onset glycogen storage disease type II
-
Ausems MG, Lochman P, van Diggelen OP, et al.: A diagnostic protocol for adult-onset glycogen storage disease type II. Neurology 1999, 52:851-853.
-
(1999)
Neurology
, vol.52
, pp. 851-853
-
-
Ausems, M.G.1
Lochman, P.2
Van Diggelen, O.P.3
-
49
-
-
0027300620
-
Respiratory insufficiency in adult-type acid maltase deficiency
-
Moufarrej NA, Bertorini TE: Respiratory insufficiency in adult-type acid maltase deficiency. South Med J 1993, 86:560-567.
-
(1993)
South Med J
, vol.86
, pp. 560-567
-
-
Moufarrej, N.A.1
Bertorini, T.E.2
-
50
-
-
0029965060
-
A mild adult myopathic variant of type IV glycogenosis
-
Bornemann A, Besser R, Shin YS, et al.: A mild adult myopathic variant of type IV glycogenosis. Neuromuscul Disord 1996, 6:95-99.
-
(1996)
Neuromuscul Disord
, vol.6
, pp. 95-99
-
-
Bornemann, A.1
Besser, R.2
Shin, Y.S.3
-
51
-
-
0041307111
-
Primary carnitine deficiency in a male adult
-
Karmaniolas K, Ioannidis P, Liatis S, et al.: Primary carnitine deficiency in a male adult. J Med 2002, 33:105-110.
-
(2002)
J Med
, vol.33
, pp. 105-110
-
-
Karmaniolas, K.1
Ioannidis, P.2
Liatis, S.3
-
53
-
-
1542328875
-
The diagnosis of mitochondrial muscle disease
-
Taylor RW, Schaefer AM, Barron MJ, et al.: The diagnosis of mitochondrial muscle disease. Neuromuscul Disord 2004, 14:237-245. This review provides a useful diagnostic approach to mitochondrial myopathy.
-
(2004)
Neuromuscul Disord
, vol.14
, pp. 237-245
-
-
Taylor, R.W.1
Schaefer, A.M.2
Barron, M.J.3
-
54
-
-
0036154682
-
Neuromuscular manifestations of endocrine disorders
-
Alshekhlee A, Kaminski HJ, Ruff RL: Neuromuscular manifestations of endocrine disorders. Neurol Clin 2002, 20:35-58, v-vi
-
(2002)
Neurol Clin
, vol.20
, pp. 35-58
-
-
Alshekhlee, A.1
Kaminski, H.J.2
Ruff, R.L.3
-
55
-
-
0036225048
-
Polymyositis-like syndrome in hypothyroidism: Review of cases reported over the past twenty-five years
-
Madariaga MG: Polymyositis-like syndrome in hypothyroidism: review of cases reported over the past twenty-five years. Thyroid 2002, 12:331-336.
-
(2002)
Thyroid
, vol.12
, pp. 331-336
-
-
Madariaga, M.G.1
-
56
-
-
0037058765
-
Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy
-
Nishino I, Noguchi S, Murayama K, et al.: Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy. Neurology 2002, 59:1689-1693.
-
(2002)
Neurology
, vol.59
, pp. 1689-1693
-
-
Nishino, I.1
Noguchi, S.2
Murayama, K.3
-
57
-
-
0041624026
-
GNE mutations causing distal myopathy with rimmed vacuoles with inflammation
-
Yabe I, Higashi T, Kikuchi S, et al.: GNE mutations causing distal myopathy with rimmed vacuoles with inflammation. Neurology 2003, 61:384-386. This case report demonstrates that patients with hereditary IBM may have inflammation on biopsy.
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(2003)
Neurology
, vol.61
, pp. 384-386
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Yabe, I.1
Higashi, T.2
Kikuchi, S.3
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58
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10744233770
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Coexistence of X-linked recessive Emery-Dreifuss muscular dystrophy with inclusion body myositis-like morphology
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Berl
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Fidzianska A, Rowinska-Marcinska K, Hausmanowa-Petrusewicz I: Coexistence of X-linked recessive Emery-Dreifuss muscular dystrophy with inclusion body myositis-like morphology. Acta Neuropathol (Berl) 2004, 107:197-203.
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(2004)
Acta Neuropathol
, vol.107
, pp. 197-203
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Fidzianska, A.1
Rowinska-Marcinska, K.2
Hausmanowa-Petrusewicz, I.3
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