Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

162 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
In Vivo Mapping of Human Ventricular Fibrillation in Brugada Syndrome: The Role of Repolarization Heterogeneity.
Pannone L, Della Rocca DG, Vergara P, Sorgente A, Del Monte A, Vetta G, Cespon Fernandez M, Talevi G, Eltsov I, Calburean PA, Overeinder I, Bala G, Almorad A, Ströker E, Pappaert G, Sieira J, de Ravel T, Van Dooren S, Gharaviri A, La Meir M, Brugada P, Chierchia GB, Sarkozy A, de Asmundis C. Pannone L, et al. Among authors: de ravel t. Circ Arrhythm Electrophysiol. 2024 Dec;17(12):e013290. doi: 10.1161/CIRCEP.124.013290. Epub 2024 Dec 3. Circ Arrhythm Electrophysiol. 2024. PMID: 39624903
SCN5A mutation in Brugada syndrome is associated with substrate severity detected by electrocardiographic imaging and high-density electroanatomic mapping.
Pannone L, Monaco C, Sorgente A, Vergara P, Gauthey A, Calburean PA, Bisignani A, Paparella G, Ramak R, Overeinder I, Bala G, Almorad A, Ströker E, Pappaert G, Sieira J, Brugada P, Van Dooren S, de Ravel T, La Meir M, Chierchia GB, de Asmundis C. Pannone L, et al. Among authors: de asmundis c, de ravel t. Heart Rhythm. 2022 Jun;19(6):945-951. doi: 10.1016/j.hrthm.2022.01.034. Epub 2022 Feb 4. Heart Rhythm. 2022. PMID: 35124229
Genetic Testing in Brugada Syndrome: A 30-Year Experience.
Pannone L, Bisignani A, Osei R, Gauthey A, Sorgente A, Monaco C, Della Rocca DG, Del Monte A, Strazdas A, Mojica J, Al Housari M, Miraglia V, Mouram S, Vetta G, Paparella G, Ramak R, Overeinder I, Bala G, Almorad A, Ströker E, Pappaert G, Sieira J, de Ravel T, La Meir M, Sarkozy A, Brugada P, Chierchia GB, Van Dooren S, de Asmundis C. Pannone L, et al. Among authors: de ravel t. Circ Arrhythm Electrophysiol. 2024 Apr;17(4):e012374. doi: 10.1161/CIRCEP.123.012374. Epub 2024 Mar 1. Circ Arrhythm Electrophysiol. 2024. PMID: 38426305
Case report: Coexistence of myotonia congenita and Brugada syndrome in one family.
Cordenier A, Flamez A, de Ravel T, Gheldof A, Pannone L, De Asmundis C, Pappaert G, Bissay V. Cordenier A, et al. Among authors: de asmundis c, de ravel t. Front Neurol. 2022 Sep 23;13:1011956. doi: 10.3389/fneur.2022.1011956. eCollection 2022. Front Neurol. 2022. PMID: 36212636 Free PMC article.
Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome.
Beysen D, De Jaegere S, Amor D, Bouchard P, Christin-Maitre S, Fellous M, Touraine P, Grix AW, Hennekam R, Meire F, Oyen N, Wilson LC, Barel D, Clayton-Smith J, de Ravel T, Decock C, Delbeke P, Ensenauer R, Ebinger F, Gillessen-Kaesbach G, Hendriks Y, Kimonis V, Laframboise R, Laissue P, Leppig K, Leroy BP, Miller DT, Mowat D, Neumann L, Plomp A, Van Regemorter N, Wieczorek D, Veitia RA, De Paepe A, De Baere E. Beysen D, et al. Among authors: de jaegere s, de paepe a, de ravel t, de baere e. Hum Mutat. 2008 Nov;29(11):E205-19. doi: 10.1002/humu.20819. Hum Mutat. 2008. PMID: 18642388 Free article.
Tumor spectrum in children with Noonan syndrome and SOS1 or RAF1 mutations.
Denayer E, Devriendt K, de Ravel T, Van Buggenhout G, Smeets E, Francois I, Sznajer Y, Craen M, Leventopoulos G, Mutesa L, Vandecasseye W, Massa G, Kayserili H, Sciot R, Fryns JP, Legius E. Denayer E, et al. Among authors: de ravel t. Genes Chromosomes Cancer. 2010 Mar;49(3):242-52. doi: 10.1002/gcc.20735. Genes Chromosomes Cancer. 2010. PMID: 19953625
An augmented ABCA4 screen targeting noncoding regions reveals a deep intronic founder variant in Belgian Stargardt patients.
Bauwens M, De Zaeytijd J, Weisschuh N, Kohl S, Meire F, Dahan K, Depasse F, De Jaegere S, De Ravel T, De Rademaeker M, Loeys B, Coppieters F, Leroy BP, De Baere E. Bauwens M, et al. Among authors: de rademaeker m, de jaegere s, de ravel t, de baere e, de zaeytijd j. Hum Mutat. 2015 Jan;36(1):39-42. doi: 10.1002/humu.22716. Hum Mutat. 2015. PMID: 25346251
Genetic screening of LCA in Belgium: predominance of CEP290 and identification of potential modifier alleles in AHI1 of CEP290-related phenotypes.
Coppieters F, Casteels I, Meire F, De Jaegere S, Hooghe S, van Regemorter N, Van Esch H, Matuleviciene A, Nunes L, Meersschaut V, Walraedt S, Standaert L, Coucke P, Hoeben H, Kroes HY, Vande Walle J, de Ravel T, Leroy BP, De Baere E. Coppieters F, et al. Among authors: de jaegere s, de ravel t, de baere e. Hum Mutat. 2010 Oct;31(10):E1709-66. doi: 10.1002/humu.21336. Hum Mutat. 2010. PMID: 20683928 Free PMC article.
The ICF syndrome: new case and update.
De Ravel TJ, Deckers E, Alliet PL, Petit P, Fryns JP. De Ravel TJ, et al. Genet Couns. 2001;12(4):379-85. Genet Couns. 2001. PMID: 11837609 Review.
162 results