These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

321 related articles for article (PubMed ID: 27460667)

  • 1. 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; 118(6):888-894. PubMed ID: 27460667
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in children.
    Yang Z; McMahon CJ; Smith LR; Bersola J; Adesina AM; Breinholt JP; Kearney DL; Dreyer WJ; Denfield SW; Price JF; Grenier M; Kertesz NJ; Clunie SK; Fernbach SD; Southern JF; Berger S; Towbin JA; Bowles KR; Bowles NE
    Circulation; 2005 Sep; 112(11):1612-7. PubMed ID: 16144992
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 62(1):77-80. PubMed ID: 29753918
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Early onset of cardiomyopathy and intellectual disability in a girl with Danon disease associated with a de novo novel mutation of the LAMP2 gene.
    Sugie K; Yoshizawa H; Onoue K; Nakanishi Y; Eura N; Ogawa M; Nakano T; Sakaguchi Y; Hayashi YK; Kishimoto T; Shima M; Saito Y; Nishino I; Ueno S
    Neuropathology; 2016 Dec; 36(6):561-565. PubMed ID: 27145725
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 25(6):493-501. PubMed ID: 25900304
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Generalized lysosome-associated membrane protein-2 defect explains multisystem clinical involvement and allows leukocyte diagnostic screening in Danon disease.
    Fanin M; Nascimbeni AC; Fulizio L; Spinazzi M; Melacini P; Angelini C
    Am J Pathol; 2006 Apr; 168(4):1309-20. PubMed ID: 16565504
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 25(5):423-31. PubMed ID: 27497751
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Danon disease: focusing on heart.
    Cheng Z; Fang Q
    J Hum Genet; 2012 Jul; 57(7):407-10. PubMed ID: 22695892
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Danon disease: a focus on processing of the novel LAMP2 mutation and comments on the beneficial use of peripheral white blood cells in the diagnosis of LAMP2 deficiency.
    Majer F; Vlaskova H; Krol L; Kalina T; Kubanek M; Stolnaya L; Dvorakova L; Elleder M; Sikora J
    Gene; 2012 May; 498(2):183-95. PubMed ID: 22365987
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Malignant cardiac phenotypic expression of Danon disease (LAMP2 cardiomyopathy).
    Samad F; Jain R; Jan MF; Sulemanjee NZ; Menaria P; Kalvin L; Bush M; Jahangir A; Khandheria BK; Tajik AJ
    Int J Cardiol; 2017 Oct; 245():201-206. PubMed ID: 28874292
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification and functional analysis of a novel de novo missense mutation located in the initiation codon of LAMP2 associated with early onset female Danon disease.
    Wang Y; Bai M; Zhang P; Peng Y; Chen Z; He Z; Xu J; Zhu Y; Yan D; Wang R; Zhang Z
    Mol Genet Genomic Med; 2023 Sep; 11(9):e2216. PubMed ID: 37288668
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel LAMP2 p.G93R mutation associated with mild Danon disease presenting with familial hypertrophic cardiomyopathy.
    Xu J; Wang L; Liu X; Dai Q
    Mol Genet Genomic Med; 2019 Oct; 7(10):e00941. PubMed ID: 31464081
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical Findings and Prognosis of Danon Disease. An Analysis of the Spanish Multicenter Danon Registry.
    López-Sainz Á; Salazar-Mendiguchía J; García-Álvarez A; Campuzano Larrea O; López-Garrido MÁ; García-Guereta L; Fuentes Cañamero ME; Climent Payá V; Peña-Peña ML; Zorio-Grima E; Jordá-Burgos P; Díez-López C; Brugada R; García-Pinilla JM; García-Pavía P
    Rev Esp Cardiol (Engl Ed); 2019 Jun; 72(6):479-486. PubMed ID: 30108015
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 73(2):376-80. PubMed ID: 19057086
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Danon disease presenting with early onset of hypertrophic cardiomyopathy and peripheral pigmentary retinal dystrophy in a female with a
    Meinert M; Englund E; Hedberg-Oldfors C; Oldfors A; Kornhall B; Lundin C; Wittström E
    Ophthalmic Genet; 2019 Jun; 40(3):227-236. PubMed ID: 31264915
    [No Abstract]   [Full Text] [Related]  

  • 17. Clinical utility of genetic testing in the early diagnosis of Danon disease mimicking hypertrophic cardiomyopathy: a case report.
    Novelli V; Bisignani A; Pelargonio G; Primiano G; Narducci ML; Palmieri V; Tiziano FD; Zeppilli P; Servidei S; Crea F; Genuardi M
    BMC Cardiovasc Disord; 2020 Apr; 20(1):156. PubMed ID: 32248794
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 16(1):39. PubMed ID: 33933120
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.