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195 related items for PubMed ID: 11043436
1. Conductive hearing loss and multiple pre- and supra-auricular skin defects: a variant example of the Branchio-Oculo-Facial syndrome. Vantrappen G, Feenstra L, Fryns JP. Genet Couns; 2000; 11(3):273-6. PubMed ID: 11043436 [Abstract] [Full Text] [Related]
2. Branchio-oculo-facial syndrome. Raveh E, Papsin BC, Forte V. Int J Pediatr Otorhinolaryngol; 2000 Jun 30; 53(2):149-56. PubMed ID: 10906521 [Abstract] [Full Text] [Related]
3. Clinical presentation and the presence of hearing impairment in branchio-oculo-facial syndrome: a new mutation in the TFAP2A gene. Thomeer HG, Crins TT, Kamsteeg EJ, Buijsman W, Cruysberg JR, Knoers NV, Cremers CW. Ann Otol Rhinol Laryngol; 2010 Dec 30; 119(12):806-14. PubMed ID: 21250552 [Abstract] [Full Text] [Related]
4. [A nineteen year observation of a boy with branchio-oto-renal syndrome and chronic renal failure]. Sikora P, Zajaczkowska M, Katska E, Niedzielska G. Pol Merkur Lekarski; 2001 Apr 30; 10(58):291-3. PubMed ID: 11434182 [Abstract] [Full Text] [Related]
5. Treatment of otorhinolaryngological manifestations of three rare genetic syndromes: Branchio-Oculo-Facial (BOF), Ectrodactyly Ectodermal dysplasia Clefting (EEC) and focal dermal hypoplasia (Goltz syndrome). Skarzynski H, Podskarbi-Fayette R. Int J Pediatr Otorhinolaryngol; 2009 Jan 30; 73(1):143-51. PubMed ID: 19012972 [Abstract] [Full Text] [Related]
6. A different type of branchial fistula as part of a branchiootorenal syndrome. Can IH, Doğan S, Dönmez M, Doğan M, Samim EE. J Pediatr Surg; 2012 Feb 30; 47(2):404-7. PubMed ID: 22325402 [Abstract] [Full Text] [Related]
7. Branchio-oculo-facial syndrome with the atresia of external ear. Ozturk O, Tokmak A, Demirci L, Silan F, Guclu E. Int J Pediatr Otorhinolaryngol; 2005 Nov 30; 69(11):1575-8. PubMed ID: 15936829 [Abstract] [Full Text] [Related]
8. Further delineation of the branchio-oculo-facial syndrome. Lin AE, Gorlin RJ, Lurie IW, Brunner HG, van der Burgt I, Naumchik IV, Rumyantseva NV, Stengel-Rutkowski S, Rosenbaum K, Meinecke P. Am J Med Genet; 1995 Mar 13; 56(1):42-59. PubMed ID: 7747785 [Abstract] [Full Text] [Related]
9. Fully implantable hearing device as a new treatment of conductive hearing loss in Franceschetti syndrome. Tringali S, Pergola N, Ferber-Viart C, Truy E, Berger P, Dubreuil C. Int J Pediatr Otorhinolaryngol; 2008 Apr 13; 72(4):513-7. PubMed ID: 18261808 [Abstract] [Full Text] [Related]
10. Branchio-oculo-facial syndrome with bilateral linear scars of the neck. El Darouti MA, Marzouk SA, Azzam OA, Nada HR, Sobhi RM, El Nabarawi I. Int J Dermatol; 2005 Aug 13; 44(8):674-6. PubMed ID: 16101871 [Abstract] [Full Text] [Related]
11. Branchio-Oto-renal syndrome: a report on nine family groups. Bellini C, Piaggio G, Massocco D, Perfumo F, Bertini, Gusmano R, Serra G. Am J Kidney Dis; 2001 Mar 13; 37(3):505-9. PubMed ID: 11228174 [Abstract] [Full Text] [Related]
19. Branchio-oculo-facial syndrome and branchio-otic/branchio-oto-renal syndromes are distinct entities. Trummer T, Müller D, Schulze A, Vogel W, Just W. J Med Genet; 2002 Jan 13; 39(1):71-3. PubMed ID: 11826031 [No Abstract] [Full Text] [Related]
20. Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome. Lin AE, Semina EV, Daack-Hirsch S, Roeder ER, Curry CJ, Rosenbaum K, Weaver DD, Murray JC. Am J Med Genet; 2000 Apr 24; 91(5):387-90. PubMed ID: 10767004 [Abstract] [Full Text] [Related] Page: [Next] [New Search]