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124 related items for PubMed ID: 39153757

  • 1. Diagnosis of dysferlinopathy masked by a superimposed hypothyroid myopathy.
    Benn KW, Bhalala OG, Day TJ, French CR.
    BMJ Case Rep; 2024 Aug 16; 17(8):. PubMed ID: 39153757
    [Abstract] [Full Text] [Related]

  • 2. ["Therapy-resistant polymyositis" - is the diagnosis correct?].
    Ceccon G, Lehmann HC, Neuen-Jacob E, Meng G, Fink GR, Wunderlich G.
    Z Rheumatol; 2017 Sep 16; 76(7):640-643. PubMed ID: 28523511
    [Abstract] [Full Text] [Related]

  • 3. Severe proximal myopathy secondary to Hashimoto's thyroiditis.
    Jervis W, Shah N, Mongolu SK, Sathyapalan T.
    BMJ Case Rep; 2019 Jul 27; 12(7):. PubMed ID: 31352397
    [Abstract] [Full Text] [Related]

  • 4. [Hypothyroidism with leading myopathy in a patient suffering from systemic lupus erythematosus and Hashimoto's thyroiditis].
    Judex A, Hartung W, Schölmerich J, Fleck M.
    Med Klin (Munich); 2008 Oct 15; 103(10):731-5. PubMed ID: 18936898
    [Abstract] [Full Text] [Related]

  • 5. Dysferlinopathy misdiagnosed with juvenile polymyositis in the pre-symptomatic stage of hyperCKemia: a case report and literature review.
    Contreras-Cubas C, Barajas-Olmos F, Frayre-Martínez MI, Siordia-Reyes G, Guízar-Sánchez CC, García-Ortiz H, Orozco L, Baca V.
    BMC Med Genomics; 2022 Jun 20; 15(1):139. PubMed ID: 35725460
    [Abstract] [Full Text] [Related]

  • 6. Asymptomatic sporadic dysferlinopathy presenting with elevation of serum creatine kinase. Typical distribution of muscle involvement shown by MRI but not by CT.
    Okahashi S, Ogawa G, Suzuki M, Ogata K, Nishino I, Kawai M.
    Intern Med; 2008 Jun 20; 47(4):305-7. PubMed ID: 18277035
    [Abstract] [Full Text] [Related]

  • 7. Heterogeneous characteristics of Korean patients with dysferlinopathy.
    Park HJ, Hong JM, Suh GI, Shin HY, Kim SM, Sunwoo IN, Suh BC, Choi YC.
    J Korean Med Sci; 2012 Apr 20; 27(4):423-9. PubMed ID: 22468107
    [Abstract] [Full Text] [Related]

  • 8. [Dysferlin expression in limb-girdle muscular dystrophy and Miyoshi myopathy: analysis of 45 cases].
    Ren SC, Yan CZ, Li MX, Liu SP, Wu JL, Zhao YY, Li W, Li DN.
    Zhonghua Yi Xue Za Zhi; 2007 Jun 05; 87(21):1486-90. PubMed ID: 17785089
    [Abstract] [Full Text] [Related]

  • 9. Limb-girdle muscular dystrophy type 2B misdiagnosed as polymyositis at the early stage: Case report and literature review.
    Xu C, Chen J, Zhang Y, Li J.
    Medicine (Baltimore); 2018 May 05; 97(21):e10539. PubMed ID: 29794729
    [Abstract] [Full Text] [Related]

  • 10. Dysferlinopathy: a clinical and histopathological study of 28 patients from India.
    Nalini A, Gayathri N.
    Neurol India; 2008 May 05; 56(3):379-85; discussion 386-7. PubMed ID: 18974568
    [Abstract] [Full Text] [Related]

  • 11. Hypothyroid myopathy with unusually high serum creatine kinase values.
    Finsterer J, Stöllberger C, Grossegger C, Kroiss A.
    Horm Res; 1999 May 05; 52(4):205-8. PubMed ID: 10725787
    [Abstract] [Full Text] [Related]

  • 12. Progress and challenges in diagnosis of dysferlinopathy.
    Fanin M, Angelini C.
    Muscle Nerve; 2016 Nov 05; 54(5):821-835. PubMed ID: 27501525
    [Abstract] [Full Text] [Related]

  • 13. Limb-Girdle Muscular Dystrophy 2B and Miyoshi Presentations of Dysferlinopathy.
    Patel NJ, Van Dyke KW, Espinoza LR.
    Am J Med Sci; 2017 May 05; 353(5):484-491. PubMed ID: 28502335
    [Abstract] [Full Text] [Related]

  • 14. Immunohistochemistry of sarcolemmal membrane-associated proteins in formalin-fixed and paraffin-embedded skeletal muscle tissue: a promising tool for the diagnostic evaluation of common muscular dystrophies.
    Suriyonplengsaeng C, Dejthevaporn C, Khongkhatithum C, Sanpapant S, Tubthong N, Pinpradap K, Srinark N, Waisayarat J.
    Diagn Pathol; 2017 Feb 20; 12(1):19. PubMed ID: 28219397
    [Abstract] [Full Text] [Related]

  • 15. Limb girdle muscular dystrophy type 2L presenting as necrotizing myopathy.
    Schneider I, Stoltenburg G, Deschauer M, Winterholler M, Hanisch F.
    Acta Myol; 2014 May 20; 33(1):19-21. PubMed ID: 24843231
    [Abstract] [Full Text] [Related]

  • 16. DYSF mutation analysis in a group of Chinese patients with dysferlinopathy.
    Zhao Z, Hu J, Sakiyama Y, Okamoto Y, Higuchi I, Li N, Shen H, Takashima H.
    Clin Neurol Neurosurg; 2013 Aug 20; 115(8):1234-7. PubMed ID: 23254335
    [Abstract] [Full Text] [Related]

  • 17. Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypes.
    Nguyen K, Bassez G, Krahn M, Bernard R, Laforêt P, Labelle V, Urtizberea JA, Figarella-Branger D, Romero N, Attarian S, Leturcq F, Pouget J, Lévy N, Eymard B.
    Arch Neurol; 2007 Aug 20; 64(8):1176-82. PubMed ID: 17698709
    [Abstract] [Full Text] [Related]

  • 18. [Progressive muscular weakness of lower limbs revealing a limb girdle muscular dystrophy].
    Saintmard G, Brands G, Debray FG, Lognard M.
    Rev Med Liege; 2017 Jul 20; 72(7-8):373-376. PubMed ID: 28795552
    [Abstract] [Full Text] [Related]

  • 19. Hypothyroid myopathy mimicking postpolio syndrome.
    Verma R, Lalla R, Sahu R.
    BMJ Case Rep; 2012 Aug 24; 2012():. PubMed ID: 22922922
    [Abstract] [Full Text] [Related]

  • 20. Hypothyroid myopathy with a strikingly elevated serum creatine kinase level.
    Scott KR, Simmons Z, Boyer PJ.
    Muscle Nerve; 2002 Jul 24; 26(1):141-4. PubMed ID: 12115960
    [Abstract] [Full Text] [Related]

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