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Journal Abstract Search

453 related items for PubMed ID: 12507416

  • 1. Limb-girdle muscular dystrophy.
    Mathews KD, Moore SA.
    Curr Neurol Neurosci Rep; 2003 Jan; 3(1):78-85. PubMed ID: 12507416
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  • 3. Dysferlin protein analysis in limb-girdle muscular dystrophies.
    Vainzof M, Anderson LV, McNally EM, Davis DB, Faulkner G, Valle G, Moreira ES, Pavanello RC, Passos-Bueno MR, Zatz M.
    J Mol Neurosci; 2001 Aug; 17(1):71-80. PubMed ID: 11665864
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  • 4. The differential diagnosis of the human dystrophinopathies and related disorders.
    Kakulas BA.
    Curr Opin Neurol; 1996 Oct; 9(5):380-8. PubMed ID: 8894415
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  • 5. The muscular dystrophies.
    Bushby KM.
    Baillieres Clin Neurol; 1994 Aug; 3(2):407-30. PubMed ID: 7952855
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  • 7. [Dystrophin and dystrophin-associated proteins. Their evaluation at the neuromuscular pathology laboratory].
    Navarro C.
    Rev Neurol; 1994 Aug; 28(2):154-8. PubMed ID: 10101784
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  • 8. Reliability and accuracy of skeletal muscle imaging in limb-girdle muscular dystrophies.
    ten Dam L, van der Kooi AJ, van Wattingen M, de Haan RJ, de Visser M.
    Neurology; 2012 Oct 16; 79(16):1716-23. PubMed ID: 23035061
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  • 11. Limb girdle muscular dystrophy: reappraisal of a rejected entity.
    van der Kooi AJ, de Visser M, Barth PG.
    Clin Neurol Neurosurg; 1994 Aug 16; 96(3):209-18. PubMed ID: 7988088
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  • 12. Dystrophin assay in muscular dystrophies: an Indian experience.
    Jain S, Sarkar C, Dinda AK, Maheshwari MC.
    Natl Med J India; 1993 Aug 16; 6(6):259-62. PubMed ID: 7950930
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  • 13. The frequency of patients with dystrophin abnormalities in a limb-girdle patient population.
    Arikawa E, Hoffman EP, Kaido M, Nonaka I, Sugita H, Arahata K.
    Neurology; 1991 Sep 16; 41(9):1491-6. PubMed ID: 1842672
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  • 14. Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2).
    Duggan DJ, Manchester D, Stears KP, Mathews DJ, Hart C, Hoffman EP.
    Neurogenetics; 1997 May 16; 1(1):49-58. PubMed ID: 10735275
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  • 15. Sarcolemmal proteins and the spectrum of limb-girdle muscular dystrophies.
    Bönnemann CG, Finkel RS.
    Semin Pediatr Neurol; 2002 Jun 16; 9(2):81-99. PubMed ID: 12139001
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  • 16. [Current diagnosis in muscular dystrophies. New developments, methods of examination and case examples].
    Weilbach FX, Kress W, Strassburg HM, Müller CR, Gold R.
    Nervenarzt; 1999 Feb 16; 70(2):89-100. PubMed ID: 10098143
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  • 17. The clinical spectrum and genetic variability of limb-girdle muscular dystrophy in a cohort of Chinese patients.
    Wang L, Zhang VW, Li S, Li H, Sun Y, Li J, Zhu Y, He R, Lin J, Zhang C.
    Orphanet J Rare Dis; 2018 Aug 14; 13(1):133. PubMed ID: 30107846
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  • 18. Genetics and muscle pathology in the diagnosis of muscular dystrophies: An update.
    Narasimhaiah D, Uppin MS, Ranganath P.
    Indian J Pathol Microbiol; 2022 May 14; 65(Supplement):S259-S270. PubMed ID: 35562158
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  • 19. [Muscular dystrophies detected by immunophenotyping and genotype analysis (mRNA and DNA)].
    Lukás Z, Vojtísková M, Fajkusová L, Bednarík J, Kadanka Z, Hájek J, Hermanová M, Vohánka S, Vytopil M.
    Cesk Patol; 2001 Nov 14; 37(4):137-45. PubMed ID: 11813630
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  • 20. Calpain 3 gene mutations: genetic and clinico-pathologic findings in limb-girdle muscular dystrophy.
    Chae J, Minami N, Jin Y, Nakagawa M, Murayama K, Igarashi F, Nonaka I.
    Neuromuscul Disord; 2001 Sep 14; 11(6-7):547-55. PubMed ID: 11525884
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