267 related articles for article (PubMed ID: 29753918)
1. 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]
2. 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]
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. 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]
5. 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]
6. 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]
7. Danon disease presenting with dilated cardiomyopathy and a complex phenotype.
Taylor MRG; Ku L; Slavov D; Cavanaugh J; Boucek M; Zhu X; Graw S; Carniel E; Barnes C; Quan D; Prall R; Lovell MA; Mierau G; Ruegg P; Mandava N; Bristow MR; Towbin JA; Mestroni L;
J Hum Genet; 2007; 52(10):830-835. PubMed ID: 17899313
[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. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. 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]
15. 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]
16. A case report of delayed diagnosis of danon disease: Caused by a newly recognized mutation in the lysosome-associated membrane protein-2 gene.
Zhang Y; Ren H; Zhou S
Medicine (Baltimore); 2020 Oct; 99(40):e22640. PubMed ID: 33019488
[TBL] [Abstract][Full Text] [Related]
17. Heart transplantation in Danon disease: Long term single centre experience and review of the literature.
Di Nora C; Miani D; D'Elia AV; Poli S; Iascone M; Nucifora G; Finato N; Sponga S; Proclemer A; Livi U
Eur J Med Genet; 2020 Feb; 63(2):103645. PubMed ID: 30959184
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. 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]
[Next] [New Search]