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Journal Abstract Search

220 related items for PubMed ID: 27179547

  • 1. Identification of Two Novel LAMP2 Gene Mutations in Danon Disease.
    Csányi B, Popoiu A, Hategan L, Hegedűs Z, Nagy V, Rácz K, Hőgye M, Sághy L, Iványi B, Csanády M, Forster T, Sepp R.
    Can J Cardiol; 2016 Nov; 32(11):1355.e23-1355.e30. PubMed ID: 27179547
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  • 3. Danon disease due to a novel splice mutation in the LAMP2 gene.
    Nadeau A, Therrien C, Karpati G, Sinnreich M.
    Muscle Nerve; 2008 Mar; 37(3):338-42. PubMed ID: 18004770
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  • 6. 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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  • 7. A new phenotype of severe dilated cardiomyopathy associated with a mutation in the LAMP2 gene previously known to cause hypertrophic cardiomyopathy in the context of Danon disease.
    Gourzi P, Pantou MP, Gkouziouta A, Kaklamanis L, Tsiapras D, Zygouri C, Constantoulakis P, Adamopoulos S, Degiannis D.
    Eur J Med Genet; 2019 Jan 01; 62(1):77-80. PubMed ID: 29753918
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  • 9. Early onset cardiomyopathy in females with Danon disease.
    Hedberg Oldfors C, Máthé G, Thomson K, Tulinius M, Karason K, Östman-Smith I, Oldfors A.
    Neuromuscul Disord; 2015 Jun 01; 25(6):493-501. PubMed ID: 25900304
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  • 10. LAMP2 Cardiomyopathy: Consequences of Impaired Autophagy in the Heart.
    Alcalai R, Arad M, Wakimoto H, Yadin D, Gorham J, Wang L, Burns E, Maron BJ, Roberts WC, Konno T, Conner DA, Perez-Atayde AR, Seidman JG, Seidman CE.
    J Am Heart Assoc; 2021 Sep 07; 10(17):e018829. PubMed ID: 34459252
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  • 11. Danon disease as a cause of concentric left ventricular hypertrophy in patients who underwent endomyocardial biopsy.
    Cheng Z, Cui Q, Tian Z, Xie H, Chen L, Fang L, Zhu K, Fang Q.
    Eur Heart J; 2012 Mar 07; 33(5):649-56. PubMed ID: 22108829
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  • 12. A novel LAMP2 mutation associated with severe cardiac hypertrophy and microvascular remodeling in a female with Danon disease: a case report and literature review.
    Bottillo I, Giordano C, Cerbelli B, D'Angelantonio D, Lipari M, Polidori T, Majore S, Bertini E, D'Amico A, Giannarelli D, De Bernardo C, Masuelli L, Musumeci F, Avella A, Re F, Zachara E, d'Amati G, Grammatico P.
    Cardiovasc Pathol; 2016 Mar 07; 25(5):423-31. PubMed ID: 27497751
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  • 13. 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 Mar 07; 31(4):224-31. PubMed ID: 22541782
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  • 19. The c.65-2A>G splice site mutation is associated with a mild phenotype in Danon disease due to the transcription of normal LAMP2 mRNA.
    Cetin H, Wöhrer A, Rittelmeyer I, Gencik M, Zulehner G, Zimprich F, Ströbel T, Zimprich A.
    Clin Genet; 2016 Oct 07; 90(4):366-71. PubMed ID: 26748608
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