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10. Naxos disease in Saudi Arabia. Bukhari I; Juma'a N J Eur Acad Dermatol Venereol; 2004 Sep; 18(5):614-6. PubMed ID: 15324409 [TBL] [Abstract][Full Text] [Related]
11. Biventricular involvement in a Turkish boy with palmoplantar hyperkeratosis and curly hair, an unusual presentation of Naxos-Carvajal syndrome. Kilic T; Babaoglu K; Aygün F; Vural A; Ural D; Agacdiken A; Anik Y; Komsuoglu B Int J Cardiol; 2007 Feb; 115(3):e122-5. PubMed ID: 17125858 [TBL] [Abstract][Full Text] [Related]
12. Naxos disease: cardiocutaneous syndrome due to cell adhesion defect. Protonotarios N; Tsatsopoulou A Orphanet J Rare Dis; 2006 Mar; 1():4. PubMed ID: 16722579 [TBL] [Abstract][Full Text] [Related]
13. Arrhythmogenic dilated cardiomyopathy due to a novel mutation in the desmoplakin gene. Krishnamurthy S; Adhisivam B; Hamilton RM; Baskin B; Biswal N; Kumar M Indian J Pediatr; 2011 Jul; 78(7):866-9. PubMed ID: 21193976 [TBL] [Abstract][Full Text] [Related]
14. The twisting tale of woolly hair: a trait with many causes. Ramot Y; Zlotogorski A J Med Genet; 2015 Apr; 52(4):217-23. PubMed ID: 25561463 [TBL] [Abstract][Full Text] [Related]
16. Naxos disease and Carvajal variant. Salam AA; Remadevi KS; Kurup RP Indian Pediatr; 2013 Jun; 50(6):596-8. PubMed ID: 23942402 [TBL] [Abstract][Full Text] [Related]
17. Arrhythmogenic right ventricular cardiomyopathy (Naxos disease): report of a Turkish boy. Narin N; Akcakus M; Gunes T; Celiker A; Baykan A; Uzum K; Ferahbas A Pacing Clin Electrophysiol; 2003 Dec; 26(12):2326-9. PubMed ID: 14675023 [TBL] [Abstract][Full Text] [Related]
18. Case report of a Spanish patient with arrhythmogenic right ventricular cardiomyopathy and palmoplantar keratoderma without plakoglobin and desmoplakin gene modifications. Alonso-Orgaz S; Zamorano-León JJ; Fernandez-Arquero M; Villacastín J; Perez-Castellanos N; García-Torrent MJ; Macaya C; López Farré AJ Int J Cardiol; 2007 May; 118(2):275-7. PubMed ID: 17045679 [TBL] [Abstract][Full Text] [Related]
19. Novel founder mutation in French-Canadian families with Naxos disease. Marino TC; Maranda B; Leblanc J; Pratte A; Barabas M; Dupéré A; Lévesque S Clin Genet; 2017 Oct; 92(4):451-453. PubMed ID: 28098346 [No Abstract] [Full Text] [Related]