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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1989 1
1994 1
1995 1
1998 5
1999 1
2000 2
2001 3
2003 2
2004 1
2006 3
2007 3
2009 2
2010 3
2011 2
2012 3
2013 1
2014 3
2015 2
2016 1
2017 1
2018 4
2019 4
2020 3
2021 2
2022 1
2023 0

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49 results

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Page 1
From a branchial fistula to a branchiootorenal syndrome: a case report and review of the literature.
Senel E, Kocak H, Akbiyik F, Saylam G, Gulleroglu BN, Senel S. Senel E, et al. J Pediatr Surg. 2009 Mar;44(3):623-5. doi: 10.1016/j.jpedsurg.2008.10.034. J Pediatr Surg. 2009. PMID: 19302870 Review.
Branchial abnormalities constitute 32% to 45% of all neck pathologies in children. They may be a part of branchiootorenal (BOR) syndrome, which is characterized by branchial arch anomalies, preauricular pits, hearing impairment, and renal malformations. ...Ho …
Branchial abnormalities constitute 32% to 45% of all neck pathologies in children. They may be a part of branchiootorenal (BOR) sy
Cochlear implantation in Branchiootorenal syndrome - case report and review of the literature.
Tian L, West N, Cayé-Thomasen P. Tian L, et al. Cochlear Implants Int. 2022 Jan;23(1):52-57. doi: 10.1080/14670100.2021.1973209. Epub 2021 Sep 9. Cochlear Implants Int. 2022. PMID: 34498539 Review.
INTRODUCTION: Branchiootorenal syndrome (BOR) manifests with branchial fistulae, otological anomalies and renal dysplasia. ...
INTRODUCTION: Branchiootorenal syndrome (BOR) manifests with branchial fistulae, otological anomalies and renal dysplas …
Branchio-oto-renal syndrome.
Kochhar A, Fischer SM, Kimberling WJ, Smith RJ. Kochhar A, et al. Am J Med Genet A. 2007 Jul 15;143A(14):1671-8. doi: 10.1002/ajmg.a.31561. Am J Med Genet A. 2007. PMID: 17238186 Review.
Branchio-oto-renal syndrome, a phenotype consisting of hearing loss, auricular malformations, branchial arch remnants, and renal anomalies is now recognized as one of the more common forms of autosomal dominant syndromic hearing impairment. ...H
Branchio-oto-renal syndrome, a phenotype consisting of hearing loss, auricular malformations, branchial arch rem
Branchio-oto-renal syndrome.
Rodríguez Soriano J. Rodríguez Soriano J. J Nephrol. 2003 Jul-Aug;16(4):603-5. J Nephrol. 2003. PMID: 14696767 Review.
Branchio-oto-renal (BOR) syndrome is an autosomal dominant disorder characterized by the association of branchial cysts or fistulae, external ear malformation and/or preauricular pits, hearing loss and renal anomalies. Mutations in the EYA1 gene
Branchio-oto-renal (BOR) syndrome is an autosomal dominant disorder characterized by the association of branchia
Branchio-oto-renal syndrome.
Smith RJ, Schwartz C. Smith RJ, et al. J Commun Disord. 1998 Sep-Oct;31(5):411-20; quiz 421. doi: 10.1016/s0021-9924(98)00013-6. J Commun Disord. 1998. PMID: 9777487 Review.
Branchio-oto-renal (BOR) syndrome is an autosomal dominant disorder with branchial, otologic, and renal manifestations. The branchial manifestations usually are inconsequential, however the hearing impairment and renal malformations can b
Branchio-oto-renal (BOR) syndrome is an autosomal dominant disorder with branchial, otologic, and renal m
Imaging Findings in Syndromes with Temporal Bone Abnormalities.
Ginat DT. Ginat DT. Neuroimaging Clin N Am. 2019 Feb;29(1):117-128. doi: 10.1016/j.nic.2018.08.004. Epub 2018 Oct 29. Neuroimaging Clin N Am. 2019. PMID: 30466636 Review.
This article reviews the imaging features of selected congenital syndromes with temporal bone abnormalities, including Treacher Collins syndrome, oculo-auriculo-vertebral dysplasia spectrum, Klippel-Feil syndrome, branchio-oto-renal syndrome
This article reviews the imaging features of selected congenital syndromes with temporal bone abnormalities, including Treacher Collins s
Microtia and Related Facial Anomalies.
Hartzell LD, Chinnadurai S. Hartzell LD, et al. Clin Perinatol. 2018 Dec;45(4):679-697. doi: 10.1016/j.clp.2018.07.007. Epub 2018 Sep 18. Clin Perinatol. 2018. PMID: 30396412 Review.
Infants may be born with external ear deformities or malformations that can present a diagnostic clue to an affiliated syndrome while also presenting the possibility of surgical intervention. ...
Infants may be born with external ear deformities or malformations that can present a diagnostic clue to an affiliated syndrome while …
Kidney-ear axis.
Abbasi AH, Ramadan R, Hoffman A, Abassi Z. Abbasi AH, et al. Isr Med Assoc J. 2007 Nov;9(11):814-8. Isr Med Assoc J. 2007. PMID: 18085042 Free article. Review. No abstract available.
[Congenital anomalies of the external ear].
Wernheden E, Krogerus C, Andersen PS, Hesselfeldt-Nielsen J. Wernheden E, et al. Ugeskr Laeger. 2019 Nov 25;181(48):V05190300. Ugeskr Laeger. 2019. PMID: 31791458 Free article. Review. Danish.
Attentiveness to other malformations in newborns with ear anomalies is important, as they often appear as part of syndromes such as Goldenhar syndrome, Treacher Collins syndrome and branchio-oto-renal syndrome. ...
Attentiveness to other malformations in newborns with ear anomalies is important, as they often appear as part of syndromes such as Goldenha …
Branchio-oto-renal syndrome: comprehensive review based on nationwide surveillance in Japan.
Morisada N, Nozu K, Iijima K. Morisada N, et al. Pediatr Int. 2014 Jun;56(3):309-14. doi: 10.1111/ped.12357. Pediatr Int. 2014. PMID: 24730701 Review.
Branchio-oto-renal (BOR) syndrome is an autosomal dominant disorder characterized by branchiogenic malformation, hearing loss and renal anomalies. The prevalence of BOR syndrome is 1/40,000 in Western countries, and nationwide surv
Branchio-oto-renal (BOR) syndrome is an autosomal dominant disorder characterized by branchiogenic malformation,
49 results