Výsledky vyhledávání - "Timmermans, Inge"

Mutation analysis of the SCN5A gene in 147 Brugada syndrome probands

Autor: Daneels, Dorien, Peeters, Uschi, Brugada, Pedro, Bonduelle, Mary-Louise, Raimondi, Daniele, Tanyalcin, Ibrahim, Peirsman, Liszl, Timmermans, Inge, Pappaert, Gudrun, Van Malderen, Sophie, Biervliet, Martine, Verdonck, Daisy, Van Dooren, Sonia

Brugada syndrome (BrS) is a cardiac channelopathy manifesting in apparently structural normal hearts and inherited as an autosomal dominant trait with incomplete penetrance and variable expression. The clinical diagnosis is based on documented ventri

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3848::a3159b3c43a9e94138cc33c31de285be
https://biblio.vub.ac.be/vubir/mutation-analysis-of-the-scn5a-gene-in-147-brugada-syndrome-probands(0ae7ff22-e77f-4aad-844c-74bae819a36a).html

Zobrazit plný text záznamu

Mutation Analysis of the SCN5A Gene in 122 Brugada Syndrome Probands

Autor: Daneels, Dorien, Peeters, Uschi, Brugada, Pedro, Bonduelle, Mary-Louise, Gazzo, A., Raimondi, Daniele, Peirsman, Liszl, Timmermans, Inge, Pappaert, Gudrun, Van Malderen, Sophie, Biervliet, Martine, Verdonck, Daisy, Van Dooren, Sonia

Brugada syndrome (BrS) is a cardiac channelopathy manifesting in structural normal hearts and inherited as an autosomal dominant trait with incomplete penetrance and variable expression. The clinical diagnosis is based on the appearance of a type 2 S

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3848::88a7f319c2cc55b8ab3118783f2f392f
https://biblio.vub.ac.be/vubir/mutation-analysis-of-the-scn5a-gene-in-122-brugada-syndrome-probands(10156555-eaa9-401d-b74d-f9e73d5114a8).html

Zobrazit plný text záznamu

Genotype-phenotype discrepancies in Brugada syndrome

Autor: Van Dooren, Sonia, Brugada, Pedro, Daneels, Dorien, Peeters, Uschi, Peirsman, Liszl, Timmermans, Inge, Kindermans, Kiliana, Biervliet, Martine, Pappaert, Gudrun, Bonduelle, Mary-Louise

Brugada syndrome is one of common inheritable arrhythmogenic disorders in apparently structurally normal hearts, inherited as an autosomal dominant trait with incomplete penetrance and variable expression. Clinical diagnosis is based on documented ve

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3848::1212ef6cd0e9fdd65cfd17f8c12fe176
https://biblio.vub.ac.be/vubir/genotypephenotype-discrepancies-in-brugada-syndrome(77006b5a-0cb6-4fc0-ab0c-59ed73652015).html

Zobrazit plný text záznamu

AmplideX FMR1 PCR kit as a substitute for the Southern blot technique to detect large CGG repeats in FMR1 gene

Autor: Bessems, Sophie, Timmermans, Inge, Vercammen, M., Van Der Wilt, Linda, Endels, Kristof, Stouffs, Katrien, Caljon, Ben, Lissens, Willy, Bonduelle, Mary-Louise, Seneca, Sara

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3848::f119110de29ebe14013289d730878c4e
https://biblio.vub.ac.be/vubir/amplidex-fmr1-pcr-kit-as-a-substitute-for-the-southern-blot-technique-to-detect-large-cgg-repeats-in-fmr1-gene(8511a5b2-1709-4299-ab0a-a99ec703431e).html

Zobrazit plný text záznamu

Genotype-phenotype discrepancies in Brugada syndrome

Autor: Van Dooren, Sonia, Brugada, Pedro, Daneels, Dorien, Peeters, Uschi, Peirsman, Liszl, Timmermans, Inge, Pappaert, Gudrun, Bonduelle, Mary-Louise

Brugada syndrome (BrS) is one of common inheritable arrhythmogenic disorders in apparently structurally normal hearts, inherited as an autosomal dominant trait with incomplete penetrance and variable expression. Clinical diagnosis is based on documen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3848::8232dcdf52c335f1776231750cbff1ba
https://biblio.vub.ac.be/vubir/genotypephenotype-discrepancies-in-brugada-syndrome(b14b5057-fab7-4d1a-a744-3412d1e07a70).html

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání