Found: 9
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Successful cochlear implantation in prelingual profound deafness resulting from the common 233delC mutation of the GJB2 gene in the Japanese.
- Published in:
- 2002
- By:
- Publication type:
- journal article
Successful Cochlear Implantation in Prelingual Profound Deafness Resulting From the Common 233delC Mutation of the GJB2 Gene in the Japanese.
- Published in:
- Laryngoscope, 2002, v. 112, n. 2, p. 255, doi. 10.1097/00005537-200202000-00011
- By:
- Publication type:
- Article
Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east Asians.
- Published in:
- Human Genetics, 2003, v. 114, n. 1, p. 44, doi. 10.1007/s00439-003-1018-1
- By:
- Publication type:
- Article
ALLERGIC FUNGAL RHINOSINUSITIS IN JAPAN: A CLINICAL ANALYSIS OF 8 CASES FROM OUR INSTITUTE AND A REVIEW OF 29 CASES REPORTED NATIONWIDE.
- Published in:
- Rhinology Supplement, 2018, v. 56, p. 513
- By:
- Publication type:
- Article
A wearable soft robot for movement assistance on eyelid closure.
- Published in:
- ROBOMECH Journal, 2018, v. 5, n. 1, p. 1, doi. 10.1186/s40648-018-0126-6
- By:
- Publication type:
- Article
Acoustic Breathiness Index for the Japanese-Speaking Population: Validation Study and Exploration of Affecting Factors.
- Published in:
- Journal of Speech, Language & Hearing Research, 2019, v. 62, n. 8, p. 2617, doi. 10.1044/2019_JSLHR-S-19-0077
- By:
- Publication type:
- Article
Ménière's Disease Is Associated with Single Nucleotide Polymorphisms in the Human Potassium Channel Genes, KCNE1 and KCNE3.
- Published in:
- ORL, 2005, v. 67, n. 5, p. 289, doi. 10.1159/000089410
- By:
- Publication type:
- Article
Ramsay Hunt Syndrome in a Patient with Rheumatoid Arthritis after Treatment with Infliximab.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
Ramsay Hunt Syndrome in a Patient with Rheumatoid Arthritis after Treatment with Infliximab.
- Published in:
- Case Reports in Cardiology, 2014, p. 1, doi. 10.1155/2014/897647
- By:
- Publication type:
- Article