10 results on '"Imamine, Hiroki"'
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2. Clinical significance of heterozygous carriers associated with compensated hypothyroidism in R450H, a common inactivating mutation of the thyrotropin receptor gene in Japanese
3. Clinical characteristics of eight patients with congenital nephrogenic diabetes insipidus
4. Longitudinal Evaluation of Patients with a Homozygous R450H Mutation of the TSH Receptor Gene
5. Severity of Virilization of External Genitalia in Japanese Patients with Salt-wasting 21-hydroxylase Deficiency
6. Possible Relationship between Elevated Plasma ACTH and Tall Stature in Familial Glucocorticoid Deficiency
7. Prevalence of SEN virus among children in Japan
8. A Case of a Preterm Infant with 21-Hydroxylase Deficiency: Implications of the Biochemical Diagnosis with Urinary Pregnanetriolone by Gas Chromatography/Mass Spectrometry in Selected Ion Monitoring (GCMS-SIM)
9. The Tei Index Permits Evaluation of Cardiopulmonary Function during Inhaled Nitric Oxide Therapy in the Hypoxic Newborn Piglet.
10. A Study of Circular Questions : Reappraisal from the Perspective of How They Are Received by Clients
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