about
Disruption of teashirt zinc finger homeobox 1 is associated with congenital aural atresia in humansA New Flap Technique for Reconstruction of Microtia and Congenital Aural Atresia.Cochlear Implantation in Extraordinary Cases.Causation of permanent unilateral and mild bilateral hearing loss in childrenOtologic and audiology aspects of microtia repair.Reconstruction of middle ear malformations.Reconstructive methods in hearing disorders - surgical methods.Optical and tomographic imaging of a middle ear malformation in the bullfrog (Rana catesbeiana).Advances in congenital aural atresia surgery: effects on outcome.Video Nasoendoscopic-Assisted Transoral Adenoidectomy with the PEAK PlasmaBlade: A Preliminary Report of a Case Series.Diagnosis and management strategies in congenital atresia of the external auditory canal. Study Group on Otological Malformations and Hearing Impairment.Congenital auditory meatal atresia: a numerical review.External and middle ear diseases: radiological diagnosis based on clinical signs and symptoms.Vibrant soundbridge in aural atresia: does severity matter?Long-term stent use can prevent postoperative canal stenosis in patients with congenital aural atresia.Classification and diagnosis of ear malformations.Anatomic Variants on Computed Tomography in Congenital Aural Atresia and Stenosis.Ear surgery in Treacher Collins syndrome.Bone conduction hearing in congenital aural atresia.Disregard of cholesteatoma in congenital aural stenosis.Two-stage aural atresia and stenosis surgery with the use of synthetic skin substitute.Otologic characteristics of individuals with deletions of distal 18q.Continuity of the incudostapedial joint: a novel prognostic factor in postoperative hearing outcomes in congenital aural atresia.Middle ear abnormalities in Van Maldergem syndrome.Facial nerve course in congenital aural atresia--identified by preoperative CT scanning and surgical findings.Evaluation of recovery from transient facial palsy following canalplasty and tympanoplasty for the treatment of congenital aural atresia.Narrowing critical regions and determining penetrance for selected 18q- phenotypes.
P2860
Q24630412-089DE1E8-6ED9-4D90-A675-56DC42CE4D63Q30368667-14238EAA-D7CF-44DF-B8C3-5939A38F65DDQ30407062-74240829-A3A2-422B-9887-CD79A8BB0FD7Q30425019-37D9D02E-9B8D-4836-84D3-4BFA6E825242Q30461998-A38BE742-1EE3-45F6-A1F4-0F7C776E6496Q30473000-52D4DDCE-69F9-4D57-95DC-9E1EBABB9187Q30473035-E87EB5A8-E3C9-4D6C-92B9-8E6E6178422BQ30503038-C18C0BEA-7B23-4DAD-ABC9-1B1BB786455CQ31111855-E0500AED-6D52-47F3-8DDD-5132B2CC48E9Q33552167-5072A3D2-2F2D-4056-92D1-D5E3D4169FDBQ33965181-B0DD08FC-EDF4-4A03-B7DA-E73F9D7F24FEQ37243888-184CCF56-91EF-4AF7-822A-752CC3F4CA65Q38018547-F1469A55-700D-4157-9EF3-9ADCB71B8246Q38137017-B64E8FCD-DFB7-4953-AEA4-6025F37DC01AQ38469338-8B5B2CA3-84B8-4109-AAB6-582260C63F5DQ38800939-A5217C95-B6A3-4A30-9335-20C694CBF030Q40257502-4E441B8E-0FCD-4032-BE92-ADD101E62EF9Q40577863-61328F06-EB0E-4E9C-8509-14971608A7E5Q40703015-4AC2C52D-7484-45FF-95D4-619B26FB0329Q43733074-8B03FEB3-DF6C-4634-B44B-A28A801A5727Q47214986-8156A8F8-630A-4C95-BB90-52E659A11075Q50355015-24BBED5B-157F-4A63-80A3-3DB73EED9496Q50434837-5A5EEEE7-B30C-43A8-B27B-8BC453193F60Q52118832-2EAEC8B2-2284-4E78-AEA0-F553B9DD2D71Q53405302-850A1A9D-ABFA-485A-A509-136DA2464451Q53514449-E640A6B8-5F24-4488-8981-CD9598429D4CQ54040009-5E3E3030-D8C9-4468-8B11-7C773FF67C6B
P2860
description
1989 nî lūn-bûn
@nan
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
1989年论文
@zh
1989年论文
@zh-cn
name
Congenital aural atresia.
@en
Congenital aural atresia.
@nl
type
label
Congenital aural atresia.
@en
Congenital aural atresia.
@nl
prefLabel
Congenital aural atresia.
@en
Congenital aural atresia.
@nl
P1433
P1476
Congenital aural atresia.
@en
P2093
Schuknecht HF
P304
P356
10.1288/00005537-198909000-00004
P407
P577
1989-09-01T00:00:00Z