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1. Practical guide for the diagnosis and management of primary ciliary dyskinesia

2. Prevalence and causes of chronic cough in Japan

6. Two Pediatric Cases of Primary Ciliary Dyskinesia Caused by Loss‐of‐Function Variants in Oral‐Facial‐Digital Syndrome Gene, OFD1.

10. Prediction of Cochlear Implant Effectiveness With Surface-Based Morphometry

18. Congenital Cytomegalovirus Infection and Maternal Primary Cytomegalovirus Infection in Universal Newborn Hearing Screening Referral Patients: A Prospective Cohort Study

22. Differences in hearing levels between siblings with hearing loss caused by GJB2 mutations

26. A High Risk of Missing Congenital Cytomegalovirus-Associated Hearing Loss through Newborn Hearing Screening in Japan

31. Differences in hearing levels between siblings with hearing loss caused by GJB2 mutations

32. Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans

39. Additional file 6: of Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss

40. Additional file 7: of Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss

41. Additional file 1: of Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss

42. Vocal Hygiene Education Program Reduces Surgical Interventions for Benign Vocal Fold Lesions: A Randomized Controlled Trial

43. Sensitization to secretoglobin and lipocalins in a group of young children with risk of developing respiratory allergy

49. アレルギー性鼻炎を合併した小児急性鼻副鼻腔炎の治療

50. Recent advances in primary ciliary dyskinesia

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