43 results on '"Ozono, Keiichi"'
Search Results
2. A family with brachydactyly mental retardation syndrome with a missense variant in HDAC4
3. Inconvenience and adaptation in Japanese adult achondroplasia and hypochondroplasia: A cross-sectional study
4. A novel COL1A1 deletion/insertion pathogenic variant in a patient with osteogenesis imperfecta
5. Two girls with a neonatal screening-negative 21-hydroxylase deficiency requiring treatment with hydrocortisone for virilization in late childhood
6. Clinical Practice Guidelines for Hypophosphatasia*
7. Pediatric drug development in Japan: Current issues and perspectives
8. A nationwide questionnaire survey targeting Japanese pediatric endocrinologists regarding transitional care in childhood, adolescent, and young adult cancer survivors
9. Clinical Practice Guidelines for Achondroplasia*
10. Metreleptin treatment for congenital generalized lipodystrophy type 4 (CGL4): a case report
11. Responses to the Letter to the Editor “Does growth-hormone treatment affect patients with and without a mitochondrial disorder differentially ?” (Vol. 27, No. 2, p. 107–108, 2018)
12. Endocrinological and phenotype evaluation in a patient with acrodysostosis
13. Relationship between dose of antithyroid drugs and adverse events in pediatric patients with Graves’ disease
14. Incidence of diabetes mellitus and neoplasia in Japanese short-statured children treated with growth hormone in the Genetics and Neuroendocrinology of Short Stature International Study (GeNeSIS)
15. Childbirth and fertility preservation in childhood and adolescent cancer patients: a second national survey of Japanese pediatric endocrinologists
16. Hormonal and Genetical Assessment of a Japanese Girl with Weaver Syndrome
17. Three novel mutations of the MCT8 (SLC16A2) gene: individual and temporal variations of endocrinological and radiological features
18. Current concepts in perinatal mineral metabolism
19. Longitudinal observation of serum anti-Müllerian hormone in three girls after cancer treatment
20. Gonadal function, fertility, and reproductive medicine in childhood and adolescent cancer patients: a national survey of Japanese pediatric endocrinologists
21. Pheochromocytoma complicated by cyanotic congenital heart disease: a case report
22. Treatment situation of male hypogonadotropic hypogonadism in pediatrics and proposal of testosterone and gonadotropins replacement therapy protocols
23. Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan
24. Effect of Growth Hormone Treatment on Quality of Life in Japanese Children with Growth Hormone Deficiency: An Analysis from a Prospective Observational Study
25. Therapeutic Use of Oral Sodium Phosphate (Phosribbon® Combination Granules) in Hereditary Hypophosphatemic Rickets
26. Therapeutic Efficacy and Safety of GH in Japanese Children with Down Syndrome Short Stature Accompanied by GH Deficiency
27. Treatment of Hypophosphatemic Rickets with Phosphate and Active Vitamin D in Japan: A Questionnaire-based Survey
28. Favorable Impact of Growth Hormone Treatment on Cholesterol Levels in Turner Syndrome
29. A Male Patient with Humoral Hypercalcemia of Malignancy (HHM) with Leukocytosis Caused by Cutaneous Squamous Cell Carcinoma Resulting from Recessive Dystrophic Epidermolysis Bullosa
30. Elevated Bone Turnover in an Infantile Patient with Mucolipidosis II; No Association with Hyperparathyroidism
31. Wnt Signaling in Bone
32. Clinical Characteristics of Perinatal Lethal Hypophosphatasia: A Report of 6 Cases
33. A Japanese Male Patient with Fibular Aplasia, Tibial Campomelia and Oligodactyly': An Additional Case Report
34. A Case of Primary Hyperparathyroidism in Childhood Found by a Chance Hematuria
35. A Case of Persistent Hyperinsulinemic Hypoglycemia of Infancy Successfully Managed with Subcutaneous Octreotide Injection and Nocturnal Intravenous Glucose Supply
36. Molecular Bases of Diseases Characterized by Hypophosphatemia and Phosphaturia: New Understanding
37. A Spectrum of Clinical Presentations in Seven Japanese Patients with Vitamin D Deficiency
38. Beneficial Effect of Oral Bisphosphonate Treatment on Bone Loss Induced by Chronic Administration of Furosemide without Alteration of Its Administration and Urinary Calcium Loss
39. G-protein Stimulatory .ALPHA. Subunit is Involved in Osteogenic Activity in Osteoblastic Cell Line SaOS-2 Cells
40. A Case with Marshall-Smith Syndrome without Life-threatening Complications
41. Longitudinal Observation of a Patient with Leri-Weill Dyschondrosteosis and SHOX Haploinsufficiency
42. Delayed Bone Age Observed in Fetuses with Symmetrical Intrauterine Growth Retardation Assessed by the Ossification of Selected Bones
43. A Case of Vitamin D Dependency Type I
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