Sudden hearing loss due to fibromuscular dysplasiaKUNSTMANN, E; EICKELMANN, A; SUDHOFF, H et al.Journal of laryngology and otology. 2009, Vol 123, Num 3, pp 359-362, issn 0022-2151, 4 p.Article

Remote tentorium meningioma causing sudden sensorineural deafiless. CommentaryDE RIDDER, Dirk; MENOVSKY, Tomas; VAN LAER, Carl et al.Surgical neurology. 2008, Vol 70, Num 3, pp 312-318, issn 0090-3019, 7 p.Article

Daughter and her mildly affected father with keipert syndromeDUMIC, Miroslav; KOKIC, Durda Dovzak; MATIC, Toni et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 22, pp 2488-2492, issn 1552-4825, 5 p.Article

Impact of prognostic factors on recovery from sudden hearing lossCEYLAN, A; CELENK, F; KEMALOGLU, Y. K et al.Journal of laryngology and otology. 2007, Vol 121, Num 11, pp 1035-1040, issn 0022-2151, 6 p.Article

Causes of childhood deafness in Pukhtoonkhwa Province of Pakistan and the role of consanguinitySAJJAD, M; KHATTAK, A. A; BUNN, J. E. G et al.Journal of laryngology and otology. 2008, Vol 122, Num 10, pp 1057-1063, issn 0022-2151, 7 p.Article

Craniofacial-deafness-hand syndrome revisitedSOMMER, Annemarie; BARTHOLOMEW, Dennis W.American journal of medical genetics. 2003, Vol 123A, Num 1, pp 91-94, issn 0148-7299, 4 p.Article

Alstrom syndrome : Progressive deafness and blindnessWELSH, Louis W.The Annals of otology, rhinology & laryngology. 2007, Vol 116, Num 4, pp 281-285, issn 0003-4894, 5 p.Article

Efficiency of Stenger test in confirming profound, unilateral pseudohypacusisDURMAZ, A; KARAHATAY, S; SATAR, B et al.Journal of laryngology and otology. 2009, Vol 123, Num 8, pp 840-844, issn 0022-2151, 5 p.Article

Hearing results following intratympanic gentamicin perfusion for Ménière's diseaseKYRODIMOS, E; AIDONIS, I; SISMANIS, A et al.Journal of laryngology and otology. 2009, Vol 123, Num 4, pp 379-382, issn 0022-2151, 4 p.Article

The Pakistan (Lahore) cochlear implant programme : issues relating to implantation in a developing countryKHAN, M. I. J; MUKHTAR, N; SAEED, S. R et al.Journal of laryngology and otology. 2007, Vol 121, Num 8, pp 745-750, issn 0022-2151, 6 p.Article

A novel missense mutation in the Connexin 26 gene associated with autosomal recessive sensorineural deafnessLESHINSKY-SILVER, E; BERMAN, Z; VINKLER, C et al.Hearing research. 2005, Vol 202, Num 1-2, pp 258-261, issn 0378-5955, 4 p.Article

A novel connexin 26 mutation associated with autosomal recessive sensorineural deafnessFREI, Klemens; LUCAS, Trevor; RAMSEBNER, Reinhard et al.Audiology & neuro-otology. 2004, Vol 9, Num 1, pp 47-50, issn 1420-3030, 4 p.Article

Initial outcomes from universal newborn hearing screening in AvonSIM, R. J; MATTHEW, S; FOLE, R. J et al.Journal of laryngology and otology. 2009, Vol 123, Num 9, pp 982-989, issn 0022-2151, 8 p.Article

Thiamine Responsive Megaloblastic Anemia SyndromeGANESH, Ramaswamy; VASANTHI, Thiruvengadam; GOWRISHANKAR, Kalpana et al.Indian journal of pediatrics. 2009, Vol 76, Num 3, pp 313-314, issn 0019-5456, 2 p.Article

Effects of open heart surgery on hearing thresholds measured by high frequency audiometryIRIZ, A; CAGLI, K; GOCER, C et al.Journal of laryngology and otology. 2008, Vol 122, Num 8, pp 795-798, issn 0022-2151, 4 p.Article

Superficial siderosis of the CNS : Report of three cases and review of the literatureMILIARAS, George; BOSTANTJOPOULOU, Sevasti; ARGYROPOULOU, Maria et al.Clinical neurology and neurosurgery. 2006, Vol 108, Num 5, pp 499-502, issn 0303-8467, 4 p.Article

Pontine Tegmental Cap Dysplasia: The Severe End of the Clinical SpectrumRAUSCHER, C; PORETTI, A; NEUHANN, T. M et al.Neuropediatrics. 2009, Vol 40, Num 1, pp 43-46, issn 0174-304X, 4 p.Article

Sensorineural deafness, abnormal genitalia, synostosis of metacarpals and metatarsals 4 and 5, and mental retardation : Description of a second patient and exclusion of HOXD13MENDIOROZ, Jacobo; FERNANDEZ-TORAL, Joaquin; SUAREZ, Etelvina et al.American journal of medical genetics. 2005, Vol 135A, Num 2, pp 211-213, issn 0148-7299, 3 p.Article

Bjornstad syndromeAGGARWAL, Deepa; SARDANA, Kabir; KUMAR, Praveen et al.Indian journal of pediatrics. 2004, Vol 71, Num 8, pp 759-761, issn 0019-5456, 3 p.Article

A maternal hereditary deafness pedigree of the A1555G mitochondrial mutation, causing aminoglycoside ototoxicity predispositionBAI, Y.-H; REN, C.-C; GONG, X.-R et al.Journal of laryngology and otology. 2008, Vol 122, Num 10, pp 1037-1041, issn 0022-2151, 5 p.Article

Screening for monogenetic del(GJB6-D13S1830) and digenic del(GJB6-D13S1830)/GJB2 patterns of inheritance in deaf individuals from Eastern AustriaFREI, Klemens; RAMSEBNER, Reinhard; LUCAS, Trevor et al.Hearing research. 2004, Vol 196, Num 1-2, pp 115-118, issn 0378-5955, 4 p.Article

Auditory cortical activation and speech perception in cochlear implant usersGREEN, K. M. J; JULYAN, P. J; HASTINGS, D. L et al.Journal of laryngology and otology. 2008, Vol 122, Num 3, pp 238-245, issn 0022-2151, 8 p.Article

Effect on hearing of ganciclovir therapy for asymptomatic congenital cytomegalovirus infection : four to 10 year follow upLACKNER, A; ACHAM, A; ALBORNO, T et al.Journal of laryngology and otology. 2009, Vol 123, Num 4, pp 391-396, issn 0022-2151, 6 p.Article

Bioinformatics analysis of candidate genes and mutations in a congenital sensorineural hearing loss pedigree : detection of 52 genes for the DFNA52 locusPAN QIONG; HU, Z; FENG, Y et al.Journal of laryngology and otology. 2008, Vol 122, Num 10, pp 1029-1036, issn 0022-2151, 8 p.Article

Faisalabad histiocytosis mimics rosai-dorfman disease : Brothers with lymphadenopathy, intrauterine fractures, short stature, and sensorineural deafnessROSSBACH, Hans-Christoph; DALENCE, Carlos; WYNN, Tung et al.Pediatric blood & cancer. 2006, Vol 47, Num 5, pp 629-632, issn 1545-5009, 4 p.Article