135 related articles for article (PubMed ID: 38372174)
1. Dilated Cardiomyopathy With Concomitant Salt-Losing Renal Tubulopathy Caused by Heterozygous
de Frutos F; Diez-Lopez C; García-Romero E; Gondra L; Madariaga L; Ariceta G; García-Castaño A; Melilli E; Herrador L; Triguero-Llonch L; Gran F; Rosenfeld L; Llatjos R; Comin-Colet J; González-Costello J
Circ Genom Precis Med; 2024 Apr; 17(2):e004336. PubMed ID: 38372174
[No Abstract] [Full Text] [Related]
2. mTOR-Activating Mutations in
Schlingmann KP; Jouret F; Shen K; Nigam A; Arjona FJ; Dafinger C; Houillier P; Jones DP; Kleinerüschkamp F; Oh J; Godefroid N; Eltan M; Güran T; Burtey S; Parotte MC; König J; Braun A; Bos C; Ibars Serra M; Rehmann H; Zwartkruis FJT; Renkema KY; Klingel K; Schulze-Bahr E; Schermer B; Bergmann C; Altmüller J; Thiele H; Beck BB; Dahan K; Sabatini D; Liebau MC; Vargas-Poussou R; Knoers NVAM; Konrad M; de Baaij JHF
J Am Soc Nephrol; 2021 Nov; 32(11):2885-2899. PubMed ID: 34607910
[TBL] [Abstract][Full Text] [Related]
3. A novel de novo CASZ1 heterozygous frameshift variant causes dilated cardiomyopathy and left ventricular noncompaction cardiomyopathy.
Guo J; Li Z; Hao C; Guo R; Hu X; Qian S; Zeng J; Gao H; Li W
Mol Genet Genomic Med; 2019 Aug; 7(8):e828. PubMed ID: 31268246
[TBL] [Abstract][Full Text] [Related]
4. Cardiac α-Actin (ACTC1) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated Cardiomyopathy.
Frank D; Yusuf Rangrez A; Friedrich C; Dittmann S; Stallmeyer B; Yadav P; Bernt A; Schulze-Bahr E; Borlepawar A; Zimmermann WH; Peischard S; Seebohm G; Linke WA; Baba HA; Krüger M; Unger A; Usinger P; Frey N; Schulze-Bahr E
Circ Genom Precis Med; 2019 Aug; 12(8):e002491. PubMed ID: 31430208
[TBL] [Abstract][Full Text] [Related]
5. A PLN nonsense variant causes severe dilated cardiomyopathy in a novel autosomal recessive inheritance mode.
Li Z; Chen P; Xu J; Yu B; Li X; Wang DW; Wang DW
Int J Cardiol; 2019 Mar; 279():122-125. PubMed ID: 30638982
[TBL] [Abstract][Full Text] [Related]
6. The CnB1 p.D102A variant is linked to dilated cardiomyopathy via impaired Calcineurin activity.
Jinqiang Zhuang MD; Ruijun Yuan MD; Yizeng MD; Congliang Miao MD; Dandan Zhou MD; Anli Na MD; Xinying Yang MD; Hui Xu MD; Hong J
J Mol Cell Cardiol; 2020 Nov; 148():15-24. PubMed ID: 32882262
[TBL] [Abstract][Full Text] [Related]
7. Compound heterozygous RMND1 gene variants associated with chronic kidney disease, dilated cardiomyopathy and neurological involvement: a case report.
Gupta A; Colmenero I; Ragge NK; Blakely EL; He L; McFarland R; Taylor RW; Vogt J; Milford DV
BMC Res Notes; 2016 Jun; 9():325. PubMed ID: 27350610
[TBL] [Abstract][Full Text] [Related]
8. Implications of Genetic Testing in Dilated Cardiomyopathy.
Verdonschot JAJ; Hazebroek MR; Krapels IPC; Henkens MTHM; Raafs A; Wang P; Merken JJ; Claes GRF; Vanhoutte EK; van den Wijngaard A; Heymans SRB; Brunner HG
Circ Genom Precis Med; 2020 Oct; 13(5):476-487. PubMed ID: 32880476
[TBL] [Abstract][Full Text] [Related]
9. Novel Genetic Variants in BAG3 and TNNT2 in a Swedish Family with a History of Dilated Cardiomyopathy and Sudden Cardiac Death.
Fernlund E; Österberg AW; Kuchinskaya E; Gustafsson M; Jansson K; Gunnarsson C
Pediatr Cardiol; 2017 Aug; 38(6):1262-1268. PubMed ID: 28669108
[TBL] [Abstract][Full Text] [Related]
10. TFEB Overexpression, Not mTOR Inhibition, Ameliorates RagC
Kim M; Lu L; Dvornikov AV; Ma X; Ding Y; Zhu P; Olson TM; Lin X; Xu X
Int J Mol Sci; 2021 May; 22(11):. PubMed ID: 34071043
[TBL] [Abstract][Full Text] [Related]
11. [Dilated cardiomyopathy caused by p.E446K mutation in SCN5A gene].
Zakliaz'minskaia EV; Chapurnykh AV; Voronina TS; Van EIu; Shestak AG; Saber S; Dzemeshkevich SL
Kardiologiia; 2014; 54(3):92-6. PubMed ID: 25102755
[TBL] [Abstract][Full Text] [Related]
12. An LMNA synonymous variant associated with severe dilated cardiomyopathy: Case report.
Gao S; Mumme-Monheit A; Chen SN; Spector EB; Slavov D; Baralle FE; Bristow MR; Mestroni L; Taylor MRG;
Am J Med Genet A; 2022 Feb; 188(2):600-605. PubMed ID: 34652067
[TBL] [Abstract][Full Text] [Related]
13. Familial dilated cardiomyopathy caused by a novel variant in the Lamin A/C gene: a case report.
Huang J; Wan Q; Zou Y; Wang L; Pan Y
BMC Cardiovasc Disord; 2020 Sep; 20(1):423. PubMed ID: 32962641
[TBL] [Abstract][Full Text] [Related]
14. A frameshift deletion mutation in the cardiac myosin-binding protein C gene associated with dilated phase of hypertrophic cardiomyopathy and dilated cardiomyopathy.
Hitomi N; Kubo T; Kitaoka H; Hirota T; Hamada T; Hoshikawa E; Hayato K; Okawa M; Kimura A; Doi YL
J Cardiol; 2010 Sep; 56(2):189-96. PubMed ID: 20605413
[TBL] [Abstract][Full Text] [Related]
15. [RF ablation of longstanding persistent atrial fibrillation in patient with familial dilated cardiomyopathy].
Derejko P; Zakrzewska J; Szumowski Ł; Szufladowicz E; Bodalski R; Michałek P; Walczak E; Bilińska ZT; Walczak F
Kardiol Pol; 2008 Jan; 66(1):109-13. PubMed ID: 18266197
[TBL] [Abstract][Full Text] [Related]
16. Familial dilated cardiomyopathy.
Dubrey S; Cha K
Am Heart J; 1995 Dec; 130(6):1313-4. PubMed ID: 7484798
[No Abstract] [Full Text] [Related]
17. [Research progress on the expression of the
Lin X
Zhongguo Dang Dai Er Ke Za Zhi; 2023 Oct; 25(10):1084-1088. PubMed ID: 37905768
[TBL] [Abstract][Full Text] [Related]
18. Lamin A/C deficiency as a cause of familial dilated cardiomyopathy.
Malhotra R; Mason PK
Curr Opin Cardiol; 2009 May; 24(3):203-8. PubMed ID: 19384091
[TBL] [Abstract][Full Text] [Related]
19. Familial dilated cardiomyopathy and spontaneous ventricular arrhythmias.
Jordaens L; de Pauw M; Caes F
Am J Cardiol; 1996 Sep; 78(5A):102-4. PubMed ID: 8820844
[TBL] [Abstract][Full Text] [Related]
20. [Reversible dilated cardiomyopathy and hyperthyroidism].
Rodríguez Blanco VM; Barriales Alvarez V; Segovia Martínez E; Morís de la Tassa C; Barriales Villa R; Cortina Llosa A
Rev Esp Cardiol; 1996 Oct; 49(10):770-2. PubMed ID: 9036481
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]