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International Journal of Pediatric Otorhinolaryngology, ISSN 0165-5876, 10/2019, Volume 125, pp. 92 - 97
The aim of the study was to clarify differences in the prevalence and features of bony malformations in inner ear between congenital unilateral sensorineural... 
Congenital abnormalities | Infants | Etiology | Unilateral hearing loss | Bilateral hearing loss | Inner ear | Index Medicus
Journal Article
Otolaryngology - Head and Neck Surgery (Japan), ISSN 0914-3491, 10/2018, Volume 90, Issue 11, pp. 948 - 952
Journal Article
Japanese Journal of Allergology, ISSN 0021-4884, 2016, Volume 65, Issue 8, pp. 990 - 993
Journal Article
Practica Oto-Rhino-Laryngologica, ISSN 0032-6313, 2017, Volume 110, Issue 6, pp. 391 - 396
Journal Article
Journal of Otolaryngology of Japan, ISSN 0030-6622, 2016, Volume 119, Issue 1, pp. 46 - 55
Journal Article
Japanese Journal of Allergology, ISSN 0021-4884, 2015, Volume 64, Issue 7, pp. 942 - 951
Journal Article
Arerugi = [Allergy], ISSN 0021-4884, 07/2015, Volume 64, Issue 7, p. 942
It is difficult to know how the children with Japanese cedar pollinosis (JCP) recognize their own symptoms and quality of life (QOL). In addition, the... 
Cryptomeria - immunology | Rhinitis, Allergic, Seasonal - physiopathology | Parents - psychology | Grandparents - psychology | Humans | Adolescent | Quality of Life | Female | Male | Surveys and Questionnaires | Child
Journal Article
Journal Article
Journal Article
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 09/2017, Volume 12, Issue 1, pp. 157 - 157
Background: To date, 102 genes have been reported as responsible for non-syndromic hearing loss, some of which are associated with specific audiogram features.... 
DFNA8/12 | DFNB21 | Mid-frequency hearing loss | TECTA | MEDICINE, RESEARCH & EXPERIMENTAL | DOMAIN | TECTORIAL MEMBRANE | PHENOTYPES | LOCUS | IMPAIRMENT | GENETICS & HEREDITY | DEAFNESS | ZP3 | Mitochondrial DNA | Genetic aspects | Research | Gene mutations | Health aspects | Hearing loss | Exons | Genes | Genomes | Hearing impairment | Inner ear | Proteins | Genotype & phenotype | Hearing | Molecular modelling | Mutation | Protein structure | Index Medicus
Journal Article
Clinical and Experimental Nephrology, ISSN 1342-1751, 2/2019, Volume 23, Issue 2, pp. 207 - 214
Journal Article