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2. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

6. Neutralizing Type I Interferon Autoantibodies in Japanese Patients with Severe COVID-19

12. RMRP‐related short stature: A report of six additional Japanese individuals with cartilage hair hypoplasia and literature review

14. A MinION-based Long-Read Sequencing Application With One-Step PCR for the Genetic Diagnosis of 21-Hydroxylase Deficiency

17. Growth Hormone Injection Log Analysis with Electronic Injection Device for Qualifying Adherence to Low-Irritant Formulation and Exploring Influential Factors on Adherence

22. Phenotypic Variation in 46,XX Disorders of Sex Development due to the 4th Zinc Finger Domain Variant of WT1 : A Familial Case Report

25. International Consensus Guideline on Small for Gestational Age: Etiology and Management From Infancy to Early Adulthood

28. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

30. Clinical and Genetic Characterization of Patients with Artemis Deficiency in Japan

31. A visualization system for erectile vascular dynamics

33. The High Relevance of 21-Deoxycortisol, (Androstenedione + 17α-Hydroxyprogesterone)/Cortisol, and 11-Deoxycortisol/17α-Hydroxyprogesterone for Newborn Screening of 21-Hydroxylase Deficiency

40. The risk of COVID-19 death is much greater and age-dependent with type I IFN autoantibodies

43. Cover Image, Volume 38, Issue 1

44. Phenotypic Variation in 46,XX Disorders of Sex Development due to the Fourth Zinc Finger Domain Variant of WT1: A Familial Case Report.

45. Neutralizing Type I Interferon Autoantibodies in Japanese Patients With Severe COVID-19

46. Two ovarian candidate enhancers, identified by time series enhancer RNA analyses, harbor rare genetic variations identified in ovarian insufficiency

49. Clinical guidelines for the diagnosis and treatment of 21-hydroxylase deficiency (2021 revision)

50. Transcriptome Analysis of Umbilical Cord Mesenchymal Stem Cells Revealed Fetal Programming Due to Chorioamnionitis

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