スポンサーリンク
Department of Otolaryngology, Hamamatsu University School of Medicine | 論文
- Association of SLC26A4 muations with clinical features and thyroid function in deaf infants with enlarged vestibular aqueduct
- Clinical features of patients with GJB2 (connexin 26) mutations : severity of hearing loss is correlated with genotypes and protein expression patterns
- Petrous Bone Meningioma Originating from the Jugular Foramen : Case Report
- Smoking, Alcohol, Sleep and Risk of Idiopathic Sudden Deafness : A Case-Control Study Using Pooled Controls
- Solitary squamous cell papilloma of the lung in a 40-year-old woman with recurrent laryngeal papillomatosis
- Two Distinct Mechanisms Underlie the Stimulation of Neurotransmitter Release by Phorbol Esters in Clonal Rat pheochromocytoma PC12 Cell^1
- Central Positional Vertigo : Clinico-anatomic Study
- Olfactory neuroblastoma with epithelial and endocrine differentiation transformed into ganglioneuroma after chemoradiotherapy
- Phosphoglyceride crystal deposition disease
- Novel USH2A mutations in Japanese Usher syndrome type 2 patients : marked differences in the mutation spectrum between the Japanese and other populations
- Mutation analysis of the MYO7A and CDH23 genes in Japanese patients with Usher syndrome type 1
- Hair roots as an mRNA source for mutation analysis of Usher syndrome-causing genes