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Journal Abstract Search

484 related items for PubMed ID: 15694138

  • 1. Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contractures.
    Mercuri E, Bushby K, Ricci E, Birchall D, Pane M, Kinali M, Allsop J, Nigro V, Sáenz A, Nascimbeni A, Fulizio L, Angelini C, Muntoni F.
    Neuromuscul Disord; 2005 Feb; 15(2):164-71. PubMed ID: 15694138
    [Abstract] [Full Text] [Related]

  • 2. Limb-girdle muscular dystrophy type 2a with mutation in CAPN3: the first report in Taiwan.
    Wang CH, Liang WC, Minami N, Nishino I, Jong YJ.
    Pediatr Neonatol; 2015 Feb; 56(1):62-5. PubMed ID: 23597518
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  • 3. Protein and genetic diagnosis of limb girdle muscular dystrophy type 2A: The yield and the pitfalls.
    Fanin M, Angelini C.
    Muscle Nerve; 2015 Aug; 52(2):163-73. PubMed ID: 25900067
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  • 4. Analysis of the UK diagnostic strategy for limb girdle muscular dystrophy 2A.
    Groen EJ, Charlton R, Barresi R, Anderson LV, Eagle M, Hudson J, Koref MS, Straub V, Bushby KM.
    Brain; 2007 Dec; 130(Pt 12):3237-49. PubMed ID: 18055493
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  • 5. Muscle Magnetic Resonance Imaging in Patients with Various Clinical Subtypes of LMNA-Related Muscular Dystrophy.
    Lin HT, Liu X, Zhang W, Liu J, Zuo YH, Xiao JX, Zhu Y, Yuan Y, Wang ZX.
    Chin Med J (Engl); 2018 Jun 20; 131(12):1472-1479. PubMed ID: 29893365
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  • 6. Limb-girdle muscular dystrophy type 2A resulting from homozygous G2338C transversion mutation in the calpain-3 gene.
    Peddareddygari LR, Surgan V, Grewal RP.
    J Clin Neuromuscul Dis; 2010 Dec 20; 12(2):62-5. PubMed ID: 21386772
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  • 10. A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy.
    Vissing J, Barresi R, Witting N, Van Ghelue M, Gammelgaard L, Bindoff LA, Straub V, Lochmüller H, Hudson J, Wahl CM, Arnardottir S, Dahlbom K, Jonsrud C, Duno M.
    Brain; 2016 Aug 20; 139(Pt 8):2154-63. PubMed ID: 27259757
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  • 11. Muscle MRI findings in limb girdle muscular dystrophy type 2L.
    Sarkozy A, Deschauer M, Carlier RY, Schrank B, Seeger J, Walter MC, Schoser B, Reilich P, Leturq F, Radunovic A, Behin A, Laforet P, Eymard B, Schreiber H, Hicks D, Vaidya SS, Gläser D, Carlier PG, Bushby K, Lochmüller H, Straub V.
    Neuromuscul Disord; 2012 Oct 01; 22 Suppl 2():S122-9. PubMed ID: 22980763
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  • 12. Calpain 3 is important for muscle regeneration: evidence from patients with limb girdle muscular dystrophies.
    Hauerslev S, Sveen ML, Duno M, Angelini C, Vissing J, Krag TO.
    BMC Musculoskelet Disord; 2012 Mar 23; 13():43. PubMed ID: 22443334
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  • 14. Limb-girdle muscular dystrophy due to emerin gene mutations.
    Ura S, Hayashi YK, Goto K, Astejada MN, Murakami T, Nagato M, Ohta S, Daimon Y, Takekawa H, Hirata K, Nonaka I, Noguchi S, Nishino I.
    Arch Neurol; 2007 Jul 23; 64(7):1038-41. PubMed ID: 17620497
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  • 16. Muscle atrophy in Limb Girdle Muscular Dystrophy 2A: a morphometric and molecular study.
    Fanin M, Nascimbeni AC, Angelini C.
    Neuropathol Appl Neurobiol; 2013 Dec 23; 39(7):762-71. PubMed ID: 23414389
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  • 17. Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiency.
    Vattemi G, Neri M, Marini M, Gualandi F, Tonin P, Bertolasi L, Guglielmi V, Catalli C, Novelli G, Ferlini A, Tomelleri G.
    Neurologist; 2012 Sep 23; 18(5):306-9. PubMed ID: 22931740
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  • 19. The frequency of limb girdle muscular dystrophy 2A in northeastern Italy.
    Fanin M, Nascimbeni AC, Fulizio L, Angelini C.
    Neuromuscul Disord; 2005 Mar 23; 15(3):218-24. PubMed ID: 15725583
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  • 20. Entire CAPN3 gene deletion in a patient with limb-girdle muscular dystrophy type 2A.
    Jaka O, Azpitarte M, Paisán-Ruiz C, Zulaika M, Casas-Fraile L, Sanz R, Trevisiol N, Levy N, Bartoli M, Krahn M, López de Munain A, Sáenz A.
    Muscle Nerve; 2014 Sep 23; 50(3):448-53. PubMed ID: 24715573
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