Detalhe da pesquisa
1.
Role of TBX20 Truncating Variants in Dilated Cardiomyopathy and Left Ventricular Noncompaction.
Circ Genom Precis Med
; 17(2): e004404, 2024 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-38353104
2.
Genotype-phenotype correlations in hypertrophic cardiomyopathy: a multicenter study in Portugal and Spain of the TPM1 p.Arg21Leu variant.
Rev Esp Cardiol (Engl Ed)
; 75(3): 242-250, 2022 Mar.
Artigo
Inglês, Espanhol
| MEDLINE | ID: mdl-33642254
3.
The p.(Cys150Tyr) variant in CSRP3 is associated with late-onset hypertrophic cardiomyopathy in heterozygous individuals.
Eur J Med Genet
; 63(12): 104079, 2020 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-33035702
4.
Mutations in TRIM63 cause an autosomal-recessive form of hypertrophic cardiomyopathy.
Heart
; 106(17): 1342-1348, 2020 09.
Artigo
Inglês
| MEDLINE | ID: mdl-32451364
5.
Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy.
J Am Coll Cardiol
; 72(20): 2457-2467, 2018 11 13.
Artigo
Inglês
| MEDLINE | ID: mdl-30442288
6.
Cardiac-only Timothy Syndrome (COTS): Peripartum Cardiomyopathy and Long QT Syndrome.
Rev Esp Cardiol (Engl Ed)
; 72(10): 876-878, 2019 Oct.
Artigo
Inglês, Espanhol
| MEDLINE | ID: mdl-31097345
7.
Síndrome de Timothy exclusivamente cardiaco (COTS): miocardiopatía periparto y QT largo / Cardiac-only Timothy syndrome (COTS): peripartum cardiomyopathy and Long QT syndrome
Rev. esp. cardiol. (Ed. impr.)
; 72(10): 876-878, oct. 2019. ilus
Artigo
Espanhol
| IBECS (Espanha) | ID: ibc-189334
8.
Abordaje de las cardiopatías familiares desde la Medicina genómica / Approach to familial heart diseases from Genomic Medicine
Rev. colomb. cardiol
; 25(4): 264-276, jul.-ago. 2018. tab, graf
Artigo
Espanhol
| LILACS, COLNAL | ID: biblio-985469