Zobrazeno 1 - 5
of 5
pro vyhledávání: '"B L Loeys"'
Autor:
A Rossetti, R L H Spatjens, S Kammerer, J Stoks, R Firneburg, S R Seyen, A T J M Helderman-Van Den Enden, A A M Wilde, B L Loeys, J Saenen, J Heijman, P G A Volders
Publikováno v:
European Heart Journal. 43
Background Since the association of a chromosomal risk haplotype harboring dipeptidyl peptidase-like protein-6 (DPP6) to familial idiopathic ventricular fibrillation (iVF), a growing number of DPP6 missense variants has been reported in patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be54b254242f67cc3ceb190dd5233756
https://doi.org/10.1093/eurheartj/ehac544.2886
https://doi.org/10.1093/eurheartj/ehac544.2886
Autor:
I, Luyckx, D, Proost, J M H, Hendriks, J, Saenen, E M, Van Craenenbroeck, T, Vermeulen, N, Peeters, W, Wuyts, I, Rodrigus, A, Verstraeten, L, Van Laer, B L, Loeys
Publikováno v:
Clinical genetics. 92(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1e56749eda180b6076f47f27a3163e02
https://pubmed.ncbi.nlm.nih.gov/29537095
https://pubmed.ncbi.nlm.nih.gov/29537095
Publikováno v:
AJNR Am J Neuroradiol
BACKGROUND AND PURPOSE: Loeys-Dietz syndrome (LDS) is a recently described entity that has the triad of arterial tortuosity and aneurysms, hypertelorism, and bifid uvula or cleft palate. Its neuroradiologic manifestations have not been well delineate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f9bd90d30428793a44b195cd496eaed
https://doi.org/10.3174/ajnr.a1651
https://doi.org/10.3174/ajnr.a1651
Autor:
J B, Saenen, E M, Van Craenenbroeck, D, Proost, F, Marchau, L, Van Laer, C J, Vrints, B L, Loeys
Publikováno v:
Clinical Genetics.
Sudden cardiac death (SCD) has an enormous impact on those who are left behind, evoking strong feelings of anxiety and incomprehension because such a dramatic event was not anticipated. Moreover, over the last decade a prominent genetic contribution
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8626467a33a27dc40bc17694fb51210f
Publikováno v:
American journal of medical genetics. 84(1)
The Meier-Gorlin syndrome, first described by Meier and Rothschild [1959: Helv Paediatr Acta 14:213-216] and further delineated by Gorlin et al. [1975: A Selected Miscellany, p 39-50], is characterized by short stature, slender body build, craniofaci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6344f3cf497b761ac2f94e82ed60eb84
https://pubmed.ncbi.nlm.nih.gov/10213048
https://pubmed.ncbi.nlm.nih.gov/10213048