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 *

161 related articles for article (PubMed ID: 33505424)

  • 1. Case Report: Identification of Mutations in
    Zhang L; Yang F; Chen M; Zhou M; Qian T; Mujtaba MO; Mohammed AH; Yin J; Cheng X; Chen J; Qin Y; Yang S
    Front Genet; 2020; 11():589838. PubMed ID: 33505424
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. LAMP2 exon-copy number variations in Danon disease heterozygote female probands: Infrequent or underdetected?
    Majer F; Piherova L; Reboun M; Stara V; Pelak O; Norambuena P; Stranecky V; Krebsova A; Vlaskova H; Dvorakova L; Kmoch S; Kalina T; Kubanek M; Sikora J
    Am J Med Genet A; 2018 Nov; 176(11):2430-2434. PubMed ID: 30194816
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. New deletion in
    Sivitskaya L; Vaikhanskaya T; Danilenko N; Liaudanski A; Davydenko O; Zhelev N
    Folia Med (Plovdiv); 2022 Oct; 64(5):853-862. PubMed ID: 36876541
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial X-linked cardiomyopathy (Danon disease): diagnostic confirmation by mutation analysis of the LAMP2gene.
    Balmer C; Ballhausen D; Bosshard NU; Steinmann B; Boltshauser E; Bauersfeld U; Superti-Furga A
    Eur J Pediatr; 2005 Aug; 164(8):509-14. PubMed ID: 15889279
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

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

  • 13. 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]  

  • 14. Danon disease is an underdiagnosed cause of advanced heart failure in young female patients: a LAMP2 flow cytometric study.
    Gurka J; Piherova L; Majer F; Chaloupka A; Zakova D; Pelak O; Krebsova A; Peichl P; Krejci J; Freiberger T; Melenovsky V; Kautzner J; Kalina T; Sikora J; Kubanek M
    ESC Heart Fail; 2020 Oct; 7(5):2534-2543. PubMed ID: 32657043
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Case Report: A Novel
    Li Z; Ma F; Li R; Xiao Z; Zeng H; Wang DW
    Front Cardiovasc Med; 2021; 8():763240. PubMed ID: 34901223
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Danon Disease Due to a Novel LAMP2 Microduplication.
    Lines MA; Hewson S; Halliday W; Sabatini PJ; Stockley T; Dipchand AI; Bowdin S; Siriwardena K
    JIMD Rep; 2014; 14():11-6. PubMed ID: 24222494
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 90(4):366-71. PubMed ID: 26748608
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Danon Disease: Entire
    Shalata A; Bar-Shai M; Hadid Y; Mahroum M; Mintz H; Shalata ZE; Radzishevsky E; Genizi J; Lorber A; Ben-Yosef T; Yaniv L
    Genes (Basel); 2023 Jul; 14(8):. PubMed ID: 37628591
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Danon disease for the cardiologist: case report and review of the literature.
    D'souza RS; Mestroni L; Taylor MRG
    J Community Hosp Intern Med Perspect; 2017 Mar; 7(2):107-114. PubMed ID: 28638575
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.