181 related articles for article (PubMed ID: 10800587)
1. [Hereditary inclusion-body myopathy].
Kucharz EJ
Przegl Lek; 1999; 56(11):735-8. PubMed ID: 10800587
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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; 44(2):242-8. PubMed ID: 9708547
[TBL] [Abstract][Full Text] [Related]
5. [Inclusion body myositis and neuromuscular diseases with rimmed vacuoles].
Figarella-Branger D; Pellissier JF; Pouget J; Calore EE; Azulay JP; Desnuelle C; Serratrice G
Rev Neurol (Paris); 1992; 148(4):281-90. PubMed ID: 1332175
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1.
Argov Z; Tiram E; Eisenberg I; Sadeh M; Seidman CE; Seidman JG; Karpati G; Mitrani-Rosenbaum S
Ann Neurol; 1997 Apr; 41(4):548-51. PubMed ID: 9124813
[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. Novel missense mutation and large deletion of GNE gene in autosomal-recessive inclusion-body myopathy.
Del Bo R; Baron P; Prelle A; Serafini M; Moggio M; Fonzo AD; Castagni M; Bresolin N; Comi GP
Muscle Nerve; 2003 Jul; 28(1):113-7. PubMed ID: 12811782
[TBL] [Abstract][Full Text] [Related]
11. The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy.
Eisenberg I; Avidan N; Potikha T; Hochner H; Chen M; Olender T; Barash M; Shemesh M; Sadeh M; Grabov-Nardini G; Shmilevich I; Friedmann A; Karpati G; Bradley WG; Baumbach L; Lancet D; Asher EB; Beckmann JS; Argov Z; Mitrani-Rosenbaum S
Nat Genet; 2001 Sep; 29(1):83-7. PubMed ID: 11528398
[TBL] [Abstract][Full Text] [Related]
12. Inclusion body myositis.
Chou SM
Baillieres Clin Neurol; 1993 Nov; 2(3):557-77. PubMed ID: 8156143
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. 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]
15. Coexistence of X-linked recessive Emery-Dreifuss muscular dystrophy with inclusion body myositis-like morphology.
Fidziańska A; Rowińska-Marcińska K; Hausmanowa-Petrusewicz I
Acta Neuropathol; 2004 Mar; 107(3):197-203. PubMed ID: 14712398
[TBL] [Abstract][Full Text] [Related]
16. Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle.
Broccolini A; Gidaro T; De Cristofaro R; Morosetti R; Gliubizzi C; Ricci E; Tonali PA; Mirabella M
J Neurochem; 2008 May; 105(3):971-81. PubMed ID: 18182043
[TBL] [Abstract][Full Text] [Related]
17. Inclusion body myositis: an underdiagnosed myopathy of older people.
Munshi SK; Thanvi B; Jonnalagadda SJ; Da Forno P; Patel A; Sharma S
Age Ageing; 2006 Jan; 35(1):91-4. PubMed ID: 16364943
[TBL] [Abstract][Full Text] [Related]
18. [Inclusion body myositis (IBM) -- a review].
Czaplinski A; Renaud S; Fuhr P
Praxis (Bern 1994); 2003 Apr; 92(14):649-54. PubMed ID: 12723314
[TBL] [Abstract][Full Text] [Related]
19. 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
[TBL] [Abstract][Full Text] [Related]
20. [Inclusion body myositis associated with sacroidosis: a report of 3 cases].
Bouillot S; Coquet M; Ferrer X; Lagueny A; Leroy JP; Vital C
Ann Pathol; 2001 Aug; 21(4):334-6. PubMed ID: 11685131
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
