229 results on '"Mizuno, Haruo"'
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2. The iodide transporter Slc26a7 impacts thyroid function more strongly than Slc26a4 in mice
3. Genotype-Phenotype Correlations in Thirty Japanese Patients with Congenital Hypothyroidism Attributable to TG Defects
4. Genotype–Phenotype Correlations in 30 Japanese Patients With Congenital Hypothyroidism Attributable to TG Defects.
5. A Case of Aseptic Meningitis Without Skin Rash Caused by Oka Varicella Vaccine
6. An infant with a heterozygous variant of ABCG5 presented with hypercholesterolemia only during breastfeeding
7. Congenital goitrous hypothyroidism is caused by dysfunction of the iodide transporter SLC26A7
8. Molecular and clinical features of KATP‐channel neonatal diabetes mellitus in Japan
9. Partial nephrogenic diabetes insipidus with a novel arginine vasopressin receptor 2 gene variant
10. A Case of Aseptic Meningitis Without Skin Rash Caused by Oka Varicella Vaccine
11. Regional Difference in Myelination in Monocarboxylate Transporter 8 Deficiency: Case Reports and Literature Review of Cases in Japan
12. Endothelin receptor antagonist attenuates inflammatory response and prolongs the survival time in a neonatal sepsis model
13. Japanese siblings with cartilage‐hair hypoplasia exhibiting different severity.
14. Clinical significance of heterozygous carriers associated with compensated hypothyroidism in R450H, a common inactivating mutation of the thyrotropin receptor gene in Japanese
15. Clinical characteristics of eight patients with congenital nephrogenic diabetes insipidus
16. Usefulness of insulin detemir in Japanese children with type 1 diabetes
17. Clinical and genetic investigation of 136 Japanese patients with congenital hypothyroidism
18. Clinical and genetic analyses of presumed shwachman-diamond syndrome in Japan
19. Elevation of serum creatine kinase in response to medical treatment of Gravesʼ disease in children
20. Multiple sclerosis with onset of cerebellar ataxia in an 18-month-old girl
21. Pregnancy outcome of Japanese patients with glucokinase–maturity‐onset diabetes of the young
22. Status and trends in the use of insulin analogs, insulin delivery systems and their association with glycemic control: comparison of the two consecutive recent cohorts of Japanese children and adolescents with type 1 diabetes mellitus
23. Enhanced signal transduction by a directly fused protein of interleukin-6 and its receptor
24. Incidence rate and characteristics of symptomatic vitamin D deficiency in children: a nationwide survey in Japan
25. Individual Clinically Diagnosed with CHARGE Syndrome but with a Mutation in KMT2D, a Gene Associated with Kabuki Syndrome: A Case Report
26. Molecular genetic and clinical delineation of 22 patients with congenital hypogonadotropic hypogonadism
27. Molecular and clinical features of KATP -channel neonatal diabetes mellitus in Japan
28. Transumbilical laparoendoscopic single-site gonadectomy for Turner's syndrome with Y-chromosome mosaicism
29. Clinical Features and Testicular Morphology in Patients with Kallmann Syndrome
30. Clinical features of late-onset circulatory dysfunction in premature infants
31. Functional ovarian cysts in a neonate with classical 21-hydroxylase deficiency: case report and review of the literature
32. Endothelin receptor antagonist attenuates oxidative stress in a neonatal sepsis piglet model
33. Edaravone, a Hydroxyl Radical Scavenger, Ameliorates the Severity of Pulmonary Hypertension in a Porcine Model of Neonatal Sepsis
34. Longitudinal Evaluation of Patients with a Homozygous R450H Mutation of the TSH Receptor Gene
35. Laparoscopic diagnosis and treatment of a phenotypic girl with mosaic 45,XO/46,X,idic(Y) mixed gonadal dysgenesis
36. Severity of Virilization of External Genitalia in Japanese Patients with Salt-wasting 21-hydroxylase Deficiency
37. Elevated Aldosterone in Amniotic Fluid and Maternal Blood Has Diagnostic Potential in Pregnancies Complicated with a Fetus of Bartter Syndrome
38. Possible Relationship between Elevated Plasma ACTH and Tall Stature in Familial Glucocorticoid Deficiency
39. 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)
40. Transient Hyper-17-OHPnemia Unrelated to Cross-Reactions with Residual Fetal Adrenal Cortex Products
41. Successful Treatment of Partial Nephrogenic Diabetes insipidus with Thiazide and Desmopressin
42. Interleukin-1β induces the expression of lipocortin 1 mRNA in cultured rat cortical astrocytes
43. Neurotrophic action of lipocortin 1 derived from astrocytes on cultured rat cortical neurons
44. Glucocorticoid induced the expression of mRNA and the secretion of lipocortin 1 in rat astrocytoma cells
45. Physicochemical Properties of Pork Meat during Salting Process.
46. Molecular Weight Determination of Agar by Sedimentation Equilibrium Measurements
47. The Emulsificating Ability of Oxidized Tapioka Starches with Sodium Hypochlorite.
48. Molecular Cloning and Structural Characterization of the Human Histidase Gene (HAL)
49. Trial Determination of the Ratio of Myosin and Actin in Raw Meat by Differential Scanning Calorimetry
50. Desalting and Water Restoration of Salted Jallyfish Rhizostomeae during Immersion in Water
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