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PUBMED FOR HANDHELDS

Journal Abstract Search


241 related items for PubMed ID: 20173215

  • 1. LAMP2 microdeletions in patients with Danon disease.
    Yang Z, Funke BH, Cripe LH, Vick GW, Mancini-Dinardo D, Peña LS, Kanter RJ, Wong B, Westerfield BH, Varela JJ, Fan Y, Towbin JA, Vatta M.
    Circ Cardiovasc Genet; 2010 Apr; 3(2):129-37. PubMed ID: 20173215
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  • 3. Danon disease: case report and detection of new mutation.
    Regelsberger G, Höftberger R, Pickl WF, Zlabinger GJ, Körmöczi U, Salzer-Muhar U, Luckner D, Bodamer OA, Mayr JA, Muss WH, Budka H, Bernheimer H.
    J Inherit Metab Dis; 2009 Dec; 32 Suppl 1():S115-22. PubMed ID: 19588270
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  • 4. Danon disease caused by two novel mutations of the LAMP2 gene: implications for two ends of the clinical spectrum.
    Hong D, Shi Z, Wang Z, Yuan Y.
    Clin Neuropathol; 2012 Dec; 31(4):224-31. PubMed ID: 22541782
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  • 5. Identification of LAMP2 Mutations in Early-Onset Danon Disease With Hypertrophic Cardiomyopathy by Targeted Next-Generation Sequencing.
    Fu L, Luo S, Cai S, Hong W, Guo Y, Wu J, Liu T, Zhao C, Li F, Huang H, Huang M, Wang J.
    Am J Cardiol; 2016 Sep 15; 118(6):888-894. PubMed ID: 27460667
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  • 6. Identification of a novel LAMP2 mutation responsible for X-chromosomal dominant Danon disease.
    Horváth J, Ketelsen UP, Geibel-Zehender A, Boehm N, Olbrich H, Korinthenberg R, Omran H.
    Neuropediatrics; 2003 Jun 15; 34(5):270-3. PubMed ID: 14598234
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  • 10. Danon disease: focusing on heart.
    Cheng Z, Fang Q.
    J Hum Genet; 2012 Jul 15; 57(7):407-10. PubMed ID: 22695892
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  • 13. Danon disease: a case report and literature review.
    Xu J, Li Z, Liu Y, Zhang X, Niu F, Zheng H, Wang L, Kang L, Wang K, Xu B.
    Diagn Pathol; 2021 May 01; 16(1):39. PubMed ID: 33933120
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  • 14. Novel LAMP2 mutations in Chinese patients with Danon disease cause varying degrees of clinical severity.
    Luo SS, Xi JY, Cai S, Zhao CB, Lu JH, Zhu WH, Lin J, Qiao K, Wang Y, Ye ZR.
    Clin Neuropathol; 2014 May 01; 33(4):284-91. PubMed ID: 24691104
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  • 15. Novel LAMP-2 mutation in a family with Danon disease presenting with hypertrophic cardiomyopathy.
    Dougu N, Joho S, Shan L, Shida T, Matsuki A, Uese K, Hirono K, Ichida F, Tanaka K, Nishino I, Inoue H.
    Circ J; 2009 Feb 01; 73(2):376-80. PubMed ID: 19057086
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  • 19. New deletion in LAMP2 causing familial Danon disease. Effect of the X-chromosome inactivation.
    Sivitskaya L, Vaikhanskaya T, Danilenko N, Liaudanski A, Davydenko O, Zhelev N.
    Folia Med (Plovdiv); 2022 Oct 31; 64(5):853-862. PubMed ID: 36876541
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