These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
123 related articles for article (PubMed ID: 224637)
1. Fingerprint inclusions and circular structures in the muscle. Report of a case. Matsubara S; Mair WG Acta Neuropathol; 1979 Jul; 47(2):161-2. PubMed ID: 224637 [TBL] [Abstract][Full Text] [Related]
5. Pleomorphic mitochondrial and different filamentous inclusions in inflammatory myopathies associated with mtDNA deletions. Molnar M; Schröder JM Acta Neuropathol; 1998 Jul; 96(1):41-51. PubMed ID: 9678512 [TBL] [Abstract][Full Text] [Related]
6. A case of nemaline myopathy with ophthalmoplegia and mitochondrial abnormalities. Fukunaga H; Osame M; Igata A J Neurol Sci; 1980 May; 46(2):169-77. PubMed ID: 6247453 [TBL] [Abstract][Full Text] [Related]
7. Inclusion body myositis. Tomé FM; Fardeau M; Lebon P; Chevallay M Acta Neuropathol Suppl; 1981; 7():287-91. PubMed ID: 6261517 [TBL] [Abstract][Full Text] [Related]
8. The occurrence of paracrystalline mitochondrial inclusions in normal human skeletal muscle. Hammersen F; Gidlöf A; Larsson J; Lewis DH Acta Neuropathol; 1980; 49(1):35-41. PubMed ID: 6243837 [TBL] [Abstract][Full Text] [Related]
9. Clinically unsuspected inclusion body myositis. Purvis J; Fam AG; Lewis A J Rheumatol; 1991 Feb; 18(2):289-92. PubMed ID: 1850803 [TBL] [Abstract][Full Text] [Related]
10. Myopathy with mitochondrial inclusion bodies: histological and metabolic studies. Sulaiman WR; Doyle D; Johnson RH; Jennett S J Neurol Neurosurg Psychiatry; 1974 Nov; 37(11):1236-46. PubMed ID: 4376164 [TBL] [Abstract][Full Text] [Related]
11. Centronuclear myopathy with unusual mitochondrial abnormalities. Canal N; Comi GC; Comola M; Testa D; Mora M; Cornelio F Clin Neuropathol; 1985; 4(1):23-7. PubMed ID: 2983917 [TBL] [Abstract][Full Text] [Related]
14. Mitochondrial paracrystalline inclusions in the peroneus brevis muscle of patients with peripheral neuropathy. Marbini A; Gemignani F; Bragaglia MM; Govoni E Clin Neuropathol; 1987; 6(1):38-42. PubMed ID: 3032487 [TBL] [Abstract][Full Text] [Related]
15. Familial inclusion body myositis among Kurdish-Iranian Jews. Massa R; Weller B; Karpati G; Shoubridge E; Carpenter S Arch Neurol; 1991 May; 48(5):519-22. PubMed ID: 1850594 [TBL] [Abstract][Full Text] [Related]
16. Oculopharyngeal muscular dystrophy. A case with abnormal mitochondria and "fingerprint" inclusions. Julien J; Vital C; Vallat JM; Vallat M; Le Blanc M J Neurol Sci; 1974 Feb; 21(2):165-9. PubMed ID: 4374513 [No Abstract] [Full Text] [Related]
17. A qualitative and quantitative study of the ultrastructure of regenerating muscle fibres in Duchenne muscular dystrophy and polymyositis. Watkins SC; Cullen MJ J Neurol Sci; 1987 Dec; 82(1-3):181-92. PubMed ID: 3440865 [TBL] [Abstract][Full Text] [Related]
18. Neuropathy and mitochondrial myopathy. Peyronnard JM; Charron L; Bellavance A; Marchand L Ann Neurol; 1980 Mar; 7(3):262-8. PubMed ID: 6252825 [TBL] [Abstract][Full Text] [Related]
19. Inclusion body myositis with abundant ring fibers. Del Bigio MR; Jay V Acta Neuropathol; 1992; 85(1):105-10. PubMed ID: 1337419 [TBL] [Abstract][Full Text] [Related]
20. Nemaline myopathy and a mitochondrial neuromuscular disorder in one family. Shapira YA; Yarom R; Blank A Neuropediatrics; 1981 May; 12(2):152-65. PubMed ID: 6267500 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]