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PUBMED FOR HANDHELDS

Journal Abstract Search


167 related items for PubMed ID: 12775505

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  • 23. Mechanisms underlying intranuclear rod formation.
    Domazetovska A, Ilkovski B, Cooper ST, Ghoddusi M, Hardeman EC, Minamide LS, Gunning PW, Bamburg JR, North KN.
    Brain; 2007 Dec; 130(Pt 12):3275-84. PubMed ID: 17928315
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  • 24. [Nemaline congenital myopathy:clinical features and histopathological findings in nine patients].
    Botelho CH, Carod-Artal FJ, Kalil RK.
    Rev Neurol; 2007 Dec; 32(4):309-14. PubMed ID: 11333383
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  • 27. Rod distribution and muscle fiber type modification in the progression of nemaline myopathy.
    Gurgel-Giannetti J, Reed UC, Marie SK, Zanoteli E, Fireman MA, Oliveira AS, Werneck LC, Beggs AH, Zatz M, Vainzof M.
    J Child Neurol; 2003 Mar; 18(3):235-40. PubMed ID: 12731651
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  • 29. Adult nemaline myopathy with trabecular muscle fibers.
    Irodenko VS, Lee HS, de Armond SJ, Layzer RB.
    Muscle Nerve; 2009 Jun; 39(6):871-5. PubMed ID: 19229965
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  • 31. Congenital Nemaline Myopathy: The Value of Magnetic Resonance Imaging of Muscle.
    Ennis J, Dyment DA, Michaud J, McMillan HJ.
    Can J Neurol Sci; 2015 Sep; 42(5):338-40. PubMed ID: 26348902
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  • 32. Cullin-3 dependent deregulation of ACTN1 represents a new pathogenic mechanism in nemaline myopathy.
    Blondelle J, Tallapaka K, Seto JT, Ghassemian M, Clark M, Laitila JM, Bournazos A, Singer JD, Lange S.
    JCI Insight; 2019 Apr 16; 5(10):. PubMed ID: 30990797
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  • 33. Autosomal dominant nemaline myopathy: a new phenotype unlinked to previously known genetic loci.
    Jeannet PY, Mittaz L, Dunand M, Lobrinus JA, Bonafe L, Kuntzer T.
    Neuromuscul Disord; 2007 Jan 16; 17(1):6-12. PubMed ID: 17157023
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  • 36. [Clinical, pathological and genetic studies of two cases of childhood-onset nemaline myopathy].
    Huang K, Luo YE, Li QX, Duan HQ, Bi FF, Yang H, Luo YB.
    Zhongguo Dang Dai Er Ke Za Zhi; 2018 Oct 16; 20(10):804-808. PubMed ID: 30369353
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  • 37. 68-year old man with progressive weakness and ventilator dependent respiratory failure: a case report of sporadic late onset nemaline myopathy.
    Kirupaharan P, Kramer D, Gandler A, Kenyon L, Summer R.
    BMC Pulm Med; 2022 Mar 19; 22(1):97. PubMed ID: 35305606
    [Abstract] [Full Text] [Related]

  • 38. Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases.
    Schnitzler LJ, Schreckenbach T, Nadaj-Pakleza A, Stenzel W, Rushing EJ, Van Damme P, Ferbert A, Petri S, Hartmann C, Bornemann A, Meisel A, Petersen JA, Tousseyn T, Thal DR, Reimann J, De Jonghe P, Martin JJ, Van den Bergh PY, Schulz JB, Weis J, Claeys KG.
    Orphanet J Rare Dis; 2017 May 11; 12(1):86. PubMed ID: 28490364
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