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 *

223 related articles for article (PubMed ID: 36007715)

  • 1. Natural History of MYH7-Related Dilated Cardiomyopathy.
    de Frutos F; Ochoa JP; Navarro-Peñalver M; Baas A; Bjerre JV; Zorio E; Méndez I; Lorca R; Verdonschot JAJ; García-Granja PE; Bilinska Z; Fatkin D; Fuentes-Cañamero ME; García-Pinilla JM; García-Álvarez MI; Girolami F; Barriales-Villa R; Díez-López C; Lopes LR; Wahbi K; García-Álvarez A; Rodríguez-Sánchez I; Rekondo-Olaetxea J; Rodríguez-Palomares JF; Gallego-Delgado M; Meder B; Kubanek M; Hansen FG; Restrepo-Córdoba MA; Palomino-Doza J; Ruiz-Guerrero L; Sarquella-Brugada G; Perez-Perez AJ; Bermúdez-Jiménez FJ; Ripoll-Vera T; Rasmussen TB; Jansen M; Sabater-Molina M; Elliot PM; Garcia-Pavia P;
    J Am Coll Cardiol; 2022 Oct; 80(15):1447-1461. PubMed ID: 36007715
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic basis of cardiomyopathy and the genotypes involved in prognosis and left ventricular reverse remodeling.
    Tobita T; Nomura S; Fujita T; Morita H; Asano Y; Onoue K; Ito M; Imai Y; Suzuki A; Ko T; Satoh M; Fujita K; Naito AT; Furutani Y; Toko H; Harada M; Amiya E; Hatano M; Takimoto E; Shiga T; Nakanishi T; Sakata Y; Ono M; Saito Y; Takashima S; Hagiwara N; Aburatani H; Komuro I
    Sci Rep; 2018 Jan; 8(1):1998. PubMed ID: 29386531
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study.
    Jansen M; de Brouwer R; Hassanzada F; Schoemaker AE; Schmidt AF; Kooijman-Reumerman MD; Bracun V; Slieker MG; Dooijes D; Vermeer AMC; Wilde AAM; Amin AS; Lekanne Deprez RH; Herkert JC; Christiaans I; de Boer RA; Jongbloed JDH; van Tintelen JP; Asselbergs FW; Baas AF
    JACC Heart Fail; 2024 Jan; 12(1):134-147. PubMed ID: 37565978
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the
    Akhtar MM; Lorenzini M; Cicerchia M; Ochoa JP; Hey TM; Sabater Molina M; Restrepo-Cordoba MA; Dal Ferro M; Stolfo D; Johnson R; Larrañaga-Moreira JM; Robles-Mezcua A; Rodriguez-Palomares JF; Casas G; Peña-Peña ML; Lopes LR; Gallego-Delgado M; Franaszczyk M; Laucey G; Rangel-Sousa D; Basurte M; Palomino-Doza J; Villacorta E; Bilinska Z; Limeres Freire J; Garcia Pinilla JM; Barriales-Villa R; Fatkin D; Sinagra G; Garcia-Pavia P; Gimeno JR; Mogensen J; Monserrat L; Elliott PM
    Circ Heart Fail; 2020 Oct; 13(10):e006832. PubMed ID: 32964742
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy.
    Merlo M; Sinagra G; Carniel E; Slavov D; Zhu X; Barbati G; Spezzacatene A; Ramani F; Salcedo E; Di Lenarda A; Mestroni L; Taylor MR;
    Clin Transl Sci; 2013 Dec; 6(6):424-8. PubMed ID: 24119082
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Association of Genetic Variants With Outcomes in Patients With Nonischemic Dilated Cardiomyopathy.
    Escobar-Lopez L; Ochoa JP; Mirelis JG; Espinosa MÁ; Navarro M; Gallego-Delgado M; Barriales-Villa R; Robles-Mezcua A; Basurte-Elorz MT; Gutiérrez García-Moreno L; Climent V; Jiménez-Jaimez J; Mogollón-Jiménez MV; Lopez J; Peña-Peña ML; García-Álvarez A; Brion M; Ripoll-Vera T; Palomino-Doza J; Tirón C; Idiazabal U; Brögger MN; García-Hernández S; Restrepo-Córdoba MA; Gonzalez-Lopez E; Méndez I; Sabater M; Villacorta E; Larrañaga-Moreira JM; Abecia A; Fernández AI; García-Pinilla JM; Rodríguez-Palomares JF; Gimeno-Blanes JR; Bayes-Genis A; Lara-Pezzi E; Domínguez F; Garcia-Pavia P
    J Am Coll Cardiol; 2021 Oct; 78(17):1682-1699. PubMed ID: 34674813
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations.
    Domínguez F; Cuenca S; Bilińska Z; Toro R; Villard E; Barriales-Villa R; Ochoa JP; Asselbergs F; Sammani A; Franaszczyk M; Akhtar M; Coronado-Albi MJ; Rangel-Sousa D; Rodriguez-Palomares JF; Jiménez-Jáimez J; Garcia-Pinilla JM; Ripoll-Vera T; Mogollón-Jiménez MV; Fontalba-Romero A; Garcia-Medina D; Palomino-Doza J; de Gonzalo-Calvo D; Cicerchia M; Salazar-Mendiguchia J; Salas C; Pankuweit S; Hey TM; Mogensen J; Barton PJ; Charron P; Elliott P; Garcia-Pavia P;
    J Am Coll Cardiol; 2018 Nov; 72(20):2471-2481. PubMed ID: 30442290
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genotype-phenotype associations in dilated cardiomyopathy: meta-analysis on more than 8000 individuals.
    Kayvanpour E; Sedaghat-Hamedani F; Amr A; Lai A; Haas J; Holzer DB; Frese KS; Keller A; Jensen K; Katus HA; Meder B
    Clin Res Cardiol; 2017 Feb; 106(2):127-139. PubMed ID: 27576561
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dilated cardiomyopathy caused by truncating titin variants: long-term outcomes, arrhythmias, response to treatment and sex differences.
    Vissing CR; Rasmussen TB; Dybro AM; Olesen MS; Pedersen LN; Jensen M; Bundgaard H; Christensen AH
    J Med Genet; 2021 Dec; 58(12):832-841. PubMed ID: 33106378
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Digenic Inheritance of LAMA4 and MYH7 Mutations in Patient with Infantile Dilated Cardiomyopathy.
    Abdallah AM; Carlus SJ; Al-Mazroea AH; Alluqmani M; Almohammadi Y; Bhuiyan ZA; Al-Harbi KM
    Medicina (Kaunas); 2019 Jan; 55(1):. PubMed ID: 30650640
    [No Abstract]   [Full Text] [Related]  

  • 11. Clinical Phenotype and Genotype Associations With Improvement in Left Ventricular Function in Dilated Cardiomyopathy.
    Verdonschot JAJ; Hazebroek MR; Wang P; Sanders-van Wijk S; Merken JJ; Adriaansen YA; van den Wijngaard A; Krapels IPC; Brunner-La Rocca HP; Brunner HG; Heymans SRB
    Circ Heart Fail; 2018 Nov; 11(11):e005220. PubMed ID: 30571196
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Digenic inheritance of mutations in the cardiac troponin (TNNT2) and cardiac beta myosin heavy chain (MYH7) as the cause of severe dilated cardiomyopathy.
    Petropoulou E; Soltani M; Firoozabadi AD; Namayandeh SM; Crockford J; Maroofian R; Jamshidi Y
    Eur J Med Genet; 2017 Sep; 60(9):485-488. PubMed ID: 28642161
    [TBL] [Abstract][Full Text] [Related]  

  • 13. MYH7 variants cause complex congenital heart disease.
    Ritter A; Leonard J; Gray C; Izumi K; Levinson K; Nair DR; O'Connor M; Rossano J; Shankar V; Chowns J; Marzolf A; Owens A; Ahrens-Nicklas RC
    Am J Med Genet A; 2022 Sep; 188(9):2772-2776. PubMed ID: 35491958
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cardiac Phenotypes, Genetics, and Risks in Familial Noncompaction Cardiomyopathy.
    van Waning JI; Caliskan K; Michels M; Schinkel AFL; Hirsch A; Dalinghaus M; Hoedemaekers YM; Wessels MW; IJpma AS; Hofstra RMW; van Slegtenhorst MA; Majoor-Krakauer D
    J Am Coll Cardiol; 2019 Apr; 73(13):1601-1611. PubMed ID: 30947911
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genotype phenotype correlations of cardiac beta-myosin heavy chain mutations in Indian patients with hypertrophic and dilated cardiomyopathy.
    Rai TS; Ahmad S; Bahl A; Ahuja M; Ahluwalia TS; Singh B; Talwar KK; Khullar M
    Mol Cell Biochem; 2009 Jan; 321(1-2):189-96. PubMed ID: 18953637
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathy.
    Jansweijer JA; Nieuwhof K; Russo F; Hoorntje ET; Jongbloed JD; Lekanne Deprez RH; Postma AV; Bronk M; van Rijsingen IA; de Haij S; Biagini E; van Haelst PL; van Wijngaarden J; van den Berg MP; Wilde AA; Mannens MM; de Boer RA; van Spaendonck-Zwarts KY; van Tintelen JP; Pinto YM
    Eur J Heart Fail; 2017 Apr; 19(4):512-521. PubMed ID: 27813223
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic mutations and mechanisms in dilated cardiomyopathy.
    McNally EM; Golbus JR; Puckelwartz MJ
    J Clin Invest; 2013 Jan; 123(1):19-26. PubMed ID: 23281406
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genomic study of dilated cardiomyopathy in a group of Mexican patients using site-directed next generation sequencing.
    Carnevale A; Rosas-Madrigal S; Rosendo-Gutiérrez R; López-Mora E; Romero-Hidalgo S; Avila-Vazzini N; Jacobo-Albavera L; Domínguez-Pérez M; Vargas-Alarcón G; Pérez-Villatoro F; Navarrete-Martínez JI; Villarreal-Molina MT
    Mol Genet Genomic Med; 2020 Nov; 8(11):e1504. PubMed ID: 32969603
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Lack of Phenotypic Differences by Cardiovascular Magnetic Resonance Imaging in MYH7 (β-Myosin Heavy Chain)- Versus MYBPC3 (Myosin-Binding Protein C)-Related Hypertrophic Cardiomyopathy.
    Weissler-Snir A; Hindieh W; Gruner C; Fourey D; Appelbaum E; Rowin E; Care M; Lesser JR; Haas TS; Udelson JE; Manning WJ; Olivotto I; Tomberli B; Maron BJ; Maron MS; Crean AM; Rakowski H; Chan RH
    Circ Cardiovasc Imaging; 2017 Feb; 10(2):. PubMed ID: 28193612
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype.
    Kolokotronis K; Kühnisch J; Klopocki E; Dartsch J; Rost S; Huculak C; Mearini G; Störk S; Carrier L; Klaassen S; Gerull B
    Hum Mutat; 2019 Aug; 40(8):1101-1114. PubMed ID: 30924982
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.