431 related articles for article (PubMed ID: 15769920)
1. Familial inflammatory inclusion body myositis.
Ranque-Francois B; Maisonobe T; Dion E; Piette JC; Chauveheid MP; Amoura Z; Papo T
Ann Rheum Dis; 2005 Apr; 64(4):634-7. PubMed ID: 15769920
[TBL] [Abstract][Full Text] [Related]
2. 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; 19(1):13-20. PubMed ID: 10774946
[TBL] [Abstract][Full Text] [Related]
3. Correlation of muscle biopsy, clinical course, and outcome in PM and sporadic IBM.
Chahin N; Engel AG
Neurology; 2008 Feb; 70(6):418-24. PubMed ID: 17881720
[TBL] [Abstract][Full Text] [Related]
4. An inflammatory, familial, inclusion body myositis with autoimmune features and a phenotype identical to sporadic inclusion body myositis. Studies in three families.
Sivakumar K; Semino-Mora C; Dalakas MC
Brain; 1997 Apr; 120 ( Pt 4)():653-61. PubMed ID: 9153127
[TBL] [Abstract][Full Text] [Related]
5. 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; 152(4):889-95. PubMed ID: 9546349
[TBL] [Abstract][Full Text] [Related]
6. Analysis of HLA class I and II alleles in sporadic inclusion-body myositis.
Lampe JB; Gossrau G; Kempe A; Füssel M; Schwurack K; Schröder R; Krause S; Kohnen R; Walter MC; Reichmann H; Lochmüller H
J Neurol; 2003 Nov; 250(11):1313-7. PubMed ID: 14648147
[TBL] [Abstract][Full Text] [Related]
7. Inclusion body myopathy associated with motor neuron syndrome: three case reports.
Cafforio G; Pistolesi S; D'Avino C; Galluzzi F; Patricelli A; Solito B; Fontanini G; Siciliano G
Clin Neuropathol; 2005; 24(1):36-41. PubMed ID: 15696783
[TBL] [Abstract][Full Text] [Related]
8. [Histological data in inflammatory myositis].
Mikol J; Polivka M
Ann Med Interne (Paris); 2001 Nov; 152(7):465-79. PubMed ID: 11965088
[TBL] [Abstract][Full Text] [Related]
9. Clinical and muscle magnetic resonance imaging study of an Italian family with autosomal dominant inclusion body myopathy not linked to known genetic loci.
Rodolico C; Toscano A; Patitucci A; Muglia M; Gaeta M; D'Arrigo G; Migliorato A; Messina S; Quattrone A; Messina C; Vita G
Neurol Sci; 2005 Dec; 26(5):303-9. PubMed ID: 16388363
[TBL] [Abstract][Full Text] [Related]
10. [Diagnostic muscle MRI abnormality in a patient with inclusion body myositis].
Ono K; Takizawa Y; Komai K; Nitta E; Takamori M
Rinsho Shinkeigaku; 1998 May; 38(5):468-70. PubMed ID: 9805998
[TBL] [Abstract][Full Text] [Related]
11. Tau aggregates are abnormally phosphorylated in inclusion body myositis and have an immunoelectrophoretic profile distinct from other tauopathies.
Maurage CA; Bussière T; Sergeant N; Ghesteem A; Figarella-Branger D; Ruchoux MM; Pellissier JF; Delacourte A
Neuropathol Appl Neurobiol; 2004 Dec; 30(6):624-34. PubMed ID: 15541003
[TBL] [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; 40(6):864-72. PubMed ID: 9007091
[TBL] [Abstract][Full Text] [Related]
13. Familial inclusion body myositis in a mother and son with different ancestral MHC haplotypes.
Mastaglia F; Price P; Walters S; Fabian V; Miller J; Zilko P
Neuromuscul Disord; 2006 Nov; 16(11):754-8. PubMed ID: 16934978
[TBL] [Abstract][Full Text] [Related]
14. Magnetic resonance imaging criteria for distinguishing between inclusion body myositis and polymyositis.
Dion E; Cherin P; Payan C; Fournet JC; Papo T; Maisonobe T; Auberton E; Chosidow O; Godeau P; Piette JC; Herson S; Grenier P
J Rheumatol; 2002 Sep; 29(9):1897-906. PubMed ID: 12233884
[TBL] [Abstract][Full Text] [Related]
15. [Inclusion body myositis associated with chronic thyroiditis, Sjögren's syndrome and autoimmune cholangitis].
Hama K; Miwa H; Nishino I; Nonaka I; Kondo T
No To Shinkei; 2004 Jun; 56(6):503-7. PubMed ID: 15328839
[TBL] [Abstract][Full Text] [Related]
16. Magnetic resonance imaging of skeletal muscles in sporadic inclusion body myositis.
Cox FM; Reijnierse M; van Rijswijk CS; Wintzen AR; Verschuuren JJ; Badrising UA
Rheumatology (Oxford); 2011 Jun; 50(6):1153-61. PubMed ID: 21288962
[TBL] [Abstract][Full Text] [Related]
17. Clinical, serologic, and immunogenetic features of familial idiopathic inflammatory myopathy.
Rider LG; Gurley RC; Pandey JP; Garcia de la Torre I; Kalovidouris AE; O'Hanlon TP; Love LA; Hennekam RC; Baumbach LL; Neville HE; Garcia CA; Klingman J; Gibbs M; Weisman MH; Targoff IN; Miller FW
Arthritis Rheum; 1998 Apr; 41(4):710-9. PubMed ID: 9550481
[TBL] [Abstract][Full Text] [Related]
18. Rimmed vacuoles with beta-amyloid and tau protein deposits in the muscle of children with hereditary myopathy.
Fidziańska A; Glinka Z
Acta Neuropathol; 2006 Aug; 112(2):185-93. PubMed ID: 16788822
[TBL] [Abstract][Full Text] [Related]
19. Messenger RNA degradation may be inhibited in sporadic inclusion body myositis.
Nakano S; Shinde A; Ito H; Ito H; Kusaka H
Neurology; 2005 Aug; 65(3):420-5. PubMed ID: 16087907
[TBL] [Abstract][Full Text] [Related]
20. Proteomic analysis of inclusion body myositis.
Li J; Yin C; Okamoto H; Jaffe H; Oldfield EH; Zhuang Z; Vortmeyer AO; Rushing EJ
J Neuropathol Exp Neurol; 2006 Aug; 65(8):826-33. PubMed ID: 16896316
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
