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2. External ear anomalies and hearing impairment in Noonan Syndrome. van Trier DC; van Nierop J; Draaisma JMT; van der Burgt I; Kunst H; Croonen EA; Admiraal RJC Int J Pediatr Otorhinolaryngol; 2015 Jun; 79(6):874-878. PubMed ID: 25862627 [TBL] [Abstract][Full Text] [Related]
3. Noonan Syndrome: An Underestimated Cause of Severe to Profound Sensorineural Hearing Impairment. Which Clues to Suspect the Diagnosis? Ziegler A; Loundon N; Jonard L; Cavé H; Baujat G; Gherbi S; Couloigner V; Marlin S Otol Neurotol; 2017 Sep; 38(8):1081-1084. PubMed ID: 28742629 [TBL] [Abstract][Full Text] [Related]
4. Sensorineural hearing loss in patients with typical retinitis pigmentosa. McDonald JM; Newsome DA; Rintelmann WF Am J Ophthalmol; 1988 Feb; 105(2):125-31. PubMed ID: 3341428 [TBL] [Abstract][Full Text] [Related]
5. Familial sensorineural hearing loss: a correlative study of audiologic, radiographic, and vestibular findings. Chan KH; Eelkema EA; Furman JM; Kamerer DB Ann Otol Rhinol Laryngol; 1991 Aug; 100(8):620-5. PubMed ID: 1872511 [TBL] [Abstract][Full Text] [Related]
6. Audiological findings in Noonan syndrome. Tokgoz-Yilmaz S; Turkyilmaz MD; Cengiz FB; Sjöstrand AP; Kose SK; Tekin M Int J Pediatr Otorhinolaryngol; 2016 Oct; 89():50-4. PubMed ID: 27619028 [TBL] [Abstract][Full Text] [Related]
7. CHARGE syndrome: a window of opportunity for audiologic intervention. Edwards BM; Kileny PR; Van Riper LA Pediatrics; 2002 Jul; 110(1 Pt 1):119-26. PubMed ID: 12093956 [TBL] [Abstract][Full Text] [Related]
8. [Familial hyperthyroidism and cochlear hearing loss syndrome with manifestation at a young age]. Stolbová D; Mozný J; Límanová Z; Macurová H Cesk Otolaryngol; 1983 Feb; 32(1):34-9. PubMed ID: 6839374 [No Abstract] [Full Text] [Related]
9. Cryopyrin-associated periodic syndromes: otolaryngologic and audiologic manifestations. Ahmadi N; Brewer CC; Zalewski C; King KA; Butman JA; Plass N; Henderson C; Goldbach-Mansky R; Kim HJ Otolaryngol Head Neck Surg; 2011 Aug; 145(2):295-302. PubMed ID: 21493283 [TBL] [Abstract][Full Text] [Related]
10. [Audiologic analysis of a family with nonsyndromic genetic progressive sensorineural hearing loss]. Ni D; Dan H; Mo J Zhonghua Er Bi Yan Hou Ke Za Zhi; 1999 Apr; 34(2):77-80. PubMed ID: 12764852 [TBL] [Abstract][Full Text] [Related]
11. Early-onset sensorineural hearing loss in a child with Turner syndrome. Roush J; Davenport ML; Carlson-Smith C J Am Acad Audiol; 2000 Sep; 11(8):446-53. PubMed ID: 11012240 [TBL] [Abstract][Full Text] [Related]
12. Detection of normal-hearing carriers of the gene for the autosomal dominant progressive sensorineural hearing loss. Stolbová D; Valvoda M Acta Otolaryngol; 1985; 99(5-6):509-15. PubMed ID: 4024898 [TBL] [Abstract][Full Text] [Related]
14. [Audiologic features of mitochondrial DNA A3243G mutation and its correlation with mutation rate]. Xue JF; Chen L; Ma YN; Zhao DH; Duan JB; Wang ZX; Qi Y; Liu YH Zhonghua Yi Xue Za Zhi; 2012 Oct; 92(40):2830-4. PubMed ID: 23290211 [TBL] [Abstract][Full Text] [Related]
15. Neurofibromatosis/Noonan phenotype: a variable feature of type 1 neurofibromatosis. Colley A; Donnai D; Evans DG Clin Genet; 1996 Feb; 49(2):59-64. PubMed ID: 8740913 [TBL] [Abstract][Full Text] [Related]
16. Audiologic and impedancemetric findings within thalassaemic patients. Onerci M; Aslan S; Gümrük F; Aksoy S; Belgin E; Ozçelik T; Altay C Int J Pediatr Otorhinolaryngol; 1994 Jan; 28(2-3):167-72. PubMed ID: 8157415 [TBL] [Abstract][Full Text] [Related]
17. Audiologic aspects of the search for DFNA20: a gene causing late-onset, progressive, sensorineural hearing loss. Elfenbein JL; Fisher RA; Wei S; Morell RJ; Stewart C; Friedman TB; Friderici K Ear Hear; 2001 Aug; 22(4):279-88. PubMed ID: 11527035 [TBL] [Abstract][Full Text] [Related]
18. Molecular genetic advances in semicircular canal abnormalities and sensorineural hearing loss: a report of 16 cases. Yu KK; Mukherji S; Carrasco V; Pillsbury HC; Shores CG Otolaryngol Head Neck Surg; 2003 Dec; 129(6):637-46. PubMed ID: 14663429 [TBL] [Abstract][Full Text] [Related]
19. Idiopathic sensorineural hearing loss in the only hearing ear. Berrettini S; De Vito A; Bruschini L; Fortunato S; Forli F Acta Otorhinolaryngol Ital; 2016 Apr; 36(2):119-26. PubMed ID: 27196076 [TBL] [Abstract][Full Text] [Related]