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Items: 1 to 20 of 133

1.

Myopathy with tubulin-reactive crystalline inclusions.

Vu TH, Hays AP, Tanji K, Younger D, Gundersen GG, Eastwood A, Braun CW, DiMauro S, Bonilla E.

Neurology. 2001 Jul 10;57(1):149-52.

PMID:
11445649
2.

Myopathy with tubulin-reactive inclusions in two cats.

Shelton GD, Sturges BK, Lyons LA, Williams DC, Aleman M, Jiang Y, Mizisin AP.

Acta Neuropathol. 2007 Nov;114(5):537-42. Epub 2007 Mar 29.

PMID:
17393175
3.

Involvement of clusterin and the aggresome in abnormal protein deposits in myofibrillar myopathies and inclusion body myositis.

Ferrer I, Carmona M, Blanco R, Moreno D, Torrejón-Escribano B, Olivé M.

Brain Pathol. 2005 Apr;15(2):101-8.

PMID:
15912881
4.

Unfolded protein response and aggresome formation in hereditary reducing-body myopathy.

Liewluck T, Hayashi YK, Ohsawa M, Kurokawa R, Fujita M, Noguchi S, Nonaka I, Nishino I.

Muscle Nerve. 2007 Mar;35(3):322-6.

PMID:
17099882
5.

Development of polyglucosan inclusions in skeletal muscle.

Valentine BA, Cooper BJ.

Neuromuscul Disord. 2006 Oct;16(9-10):603-7. Epub 2006 Aug 21.

PMID:
16919952
6.

Study of some components of the cytoskeleton in muscular disorders with nonspecific cytoplasmic bodies.

Caron A, Gohel C, Mollaret K, Morello R, Chapon F.

Acta Neuropathol. 1999 Mar;97(3):267-74.

PMID:
10090674
7.

SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy.

Tomelleri G, Palmucci L, Tonin P, Mongini T, Marini M, L'erario R, Rizzuto N, Vattemi G.

Brain. 2006 Aug;129(Pt 8):2085-92. Epub 2006 May 19.

8.

Sarcoplasmic body myopathy--a rare hereditary myopathy with characteristic inclusions.

Engvall M, Ahlberg G, Hedberg B, Edström L, Ansved T.

Acta Neurol Scand. 2005 Oct;112(4):223-7.

PMID:
16146490
9.

Hyperthyroid myopathy with mitochondrial paracrystalline rectangular inclusions.

Lloreta J, Roquer J, Corominas JM, Serrano S.

Ultrastruct Pathol. 1996 Jan-Feb;20(1):61-65.

PMID:
8789211
10.

Expression of the intermediate filament protein synemin in myofibrillar myopathies and other muscle diseases.

Olivé M, Goldfarb L, Dagvadorj A, Sambuughin N, Paulin D, Li Z, Goudeau B, Vicart P, Ferrer I.

Acta Neuropathol. 2003 Jul;106(1):1-7. Epub 2003 Apr 1.

PMID:
12669240
11.

Characteristics of myosin in nemaline myopathy.

Sreter FA, Aström KE, Romanul FC, Young RR, Jones HR Jr.

J Neurol Sci. 1976 Jan;27(1):99-116.

PMID:
175135
12.

Congenital myopathies with inclusion bodies: a brief review.

Goebel HH.

Neuromuscul Disord. 1998 May;8(3-4):162-8. Review.

PMID:
9631396
13.

Polysaccharide storage myopathy--case report and literature review.

Miladi MI, Feki I, Choyakh F, Ben Hmida M, Zouari N, Mhiri C.

Clin Neuropathol. 2005 May-Jun;24(3):126-32. Review.

PMID:
15943164
14.

Episodic muscle pain, stiffness, and weakness associated with tubular aggregates and myoedema.

Mahjneh I, Lamminen A, Tuominen H.

Eur J Neurol. 2007 May;14(5):569-71.

PMID:
17437618
15.

[Crystalline bodies in the orbicular muscle sarcoplasm of the aged].

Radnot M.

Arch Ophtalmol Rev Gen Ophtalmol. 1974 May;34(5):431-6. French. No abstract available.

PMID:
4374912
16.

Desmin myopathy with cardiomyopathy.

Cameron CH, Mirakhur M, Allen IV.

Acta Neuropathol. 1995;89(6):560-6.

PMID:
7676812
17.

Hereditary distal myopathy with granulo-filamentous cytoplasmic inclusions containing desmin, dystrophin and vimentin.

Helliwell TR, Green AR, Green A, Edwards RH.

J Neurol Sci. 1994 Jul;124(2):174-87.

PMID:
7964869
18.

Desmin-related myopathy: report of a rare case.

Sridhar E, Sharma MC, Sarkar C, Singh S, Das T.

Neurol India. 2005 Jun;53(2):229-31.

19.

[Reducing body myopathy--a case report].

Kobayashi Y, Nihei K, Kuwajima K, Nonaka I.

Rinsho Shinkeigaku. 1992 Jan;32(1):62-7. Review. Japanese.

PMID:
1321016
20.

Hyaline body myopathy: adulthood manifestations.

Rafay MF, Halliday W, Bril V.

Can J Neurol Sci. 2005 May;32(2):253-6.

PMID:
16018165
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