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158 related items for PubMed ID: 23200905
1. Myopathy in a rhesus monkey with biopsy findings similar to human sporadic inclusion body myositis. Skuk D, Goulet M, Paradis M, Tremblay JP. Neuromuscul Disord; 2013 Feb; 23(2):155-9. PubMed ID: 23200905 [Abstract] [Full Text] [Related]
3. Inclusion body myositis associated with human T-lymphotropic virus-type I infection: eleven patients from an endemic area in Japan. Matsuura E, Umehara F, Nose H, Higuchi I, Matsuoka E, Izumi K, Kubota R, Saito M, Izumo S, Arimura K, Osame M. J Neuropathol Exp Neurol; 2008 Jan; 67(1):41-9. PubMed ID: 18091562 [Abstract] [Full Text] [Related]
4. Congenital myopathy with abundant ring fibres, rimmed vacuoles and inclusion body myositis-type inclusions. Fidziańska A, Kamińska A. Neuropediatrics; 2003 Feb; 34(1):40-4. PubMed ID: 12690567 [Abstract] [Full Text] [Related]
5. Muscle weakness correlates with muscle atrophy and precedes the development of inclusion body or rimmed vacuoles in the mouse model of DMRV/hIBM. Malicdan MC, Noguchi S, Hayashi YK, Nishino I. Physiol Genomics; 2008 Sep 17; 35(1):106-15. PubMed ID: 18628337 [Abstract] [Full Text] [Related]
9. Loss of TDP-43 function and rimmed vacuoles persist after T cell depletion in a xenograft model of sporadic inclusion body myositis. Britson KA, Ling JP, Braunstein KE, Montagne JM, Kastenschmidt JM, Wilson A, Ikenaga C, Tsao W, Pinal-Fernandez I, Russell KA, Reed N, Mozaffar T, Wagner KR, Ostrow LW, Corse AM, Mammen AL, Villalta SA, Larman HB, Wong PC, Lloyd TE. Sci Transl Med; 2022 Jan 19; 14(628):eabi9196. PubMed ID: 35044790 [Abstract] [Full Text] [Related]
10. [Inclusion body myositis: clinical and myopathological features]. Xie H, Wang L, Shen D. Zhonghua Nei Ke Za Zhi; 1997 Sep 19; 36(9):610-2. PubMed ID: 10436972 [Abstract] [Full Text] [Related]
11. Inclusion body myositis (IBM). Gayathri N, Anisya-Vasanth, Veerendra Kumar M, Das S, Santosh V, Yasha TC, Ramamohan Y, Taly AB, Gourie-Devi M, Shankar SK. Clin Neuropathol; 2000 Sep 19; 19(1):13-20. PubMed ID: 10774946 [Abstract] [Full Text] [Related]
12. Apolipoprotein E and apolipoprotein E messenger RNA in muscle of inclusion body myositis and myopathies. Mirabella M, Alvarez RB, Engel WK, Weisgraber KH, Askanas V. Ann Neurol; 1996 Dec 19; 40(6):864-72. PubMed ID: 9007091 [Abstract] [Full Text] [Related]
15. Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles. Darin N, Kyllerman M, Wahlström J, Martinsson T, Oldfors A. Ann Neurol; 1998 Aug 19; 44(2):242-8. PubMed ID: 9708547 [Abstract] [Full Text] [Related]
19. Light and electron microscopic immunolocalization of presenilin 1 in abnormal muscle fibers of patients with sporadic inclusion-body myositis and autosomal-recessive inclusion-body myopathy. Askanas V, Engel WK, Yang CC, Alvarez RB, Lee VM, Wisniewski T. Am J Pathol; 1998 Apr 19; 152(4):889-95. PubMed ID: 9546349 [Abstract] [Full Text] [Related]
20. Inclusion body myositis: atypical clinical presentations. Schlesinger I, Soffer D, Lossos A, Meiner Z, Argov Z. Eur Neurol; 1996 Apr 19; 36(2):89-93. PubMed ID: 8654492 [Abstract] [Full Text] [Related] Page: [Next] [New Search]