スポンサーリンク
Department Of Pediatrics Minoh City Hospital | 論文
- Marked Hypercalcemia in a Patient with Hypocalciuric Hypercalcemia without a Mutation in the Calcium-Sensing Receptor Gene
- Hereditary hypophosphatemic rickets with hypercalciuria : a study for the phosphate transporter gene type IIc and osteoblastic function
- Molecular Bases of Diseases Characterized by Hypophosphatemia and Phosphaturia : New Understanding
- Beneficial Effect of Oral Bisphosphonate Treatment on Bone Loss Induced by Chronic Administration of Furosemide without Alteration of Its Administration and Urinary Calcium Loss
- A Spectrum of Clinical Presentations in Seven Japanese Patients with Vitamin D Deficiency
- Treatment with recombinant IL-2 for recurrent respiratory infection in a case of cartilage-hair hypoplasia with autoimmune hemolytic anemia
- Alendronate and pharmacological doses of 1α OHD_3 therapy in a patient with McCune-Albright syndrome and accompanying hypophosphatemia
- A patient with Shiga toxin-associated hemolytic uremic syndrome who developed hyperkalemia in the recovery period
- Hypophosphatemic rickets accompanying McCune-Albright syndrome : evidence that a humoral factor causes hypophosphatemia
- Blunted effect of parathyroid hormone on adenosine 3',5'-cyclic monophosphate production is derived from ATP depletion in proximal convoluted tubules of hypophosphatemic mice
- The role of IGF-I in phosphate therapy for the short stature of patients with hypophosphatemic vitamin D-resistant rickets
- Solvent Extraction of Trivalent Rare Earth Metal Ions with Carboxylate Derivatives of Calixarenes
- Wnt signaling in bone metabolism
- A patient with membranoproliferative glomerulonephritis diagnosed by the third biopsy via endocapillary proliferative glomerulonephritis and focal membranoproliferative glomerulonephritis
- A Case of Primary Hyperparathyroidism in Childhood Found by a Chance Hematuria
- Hyperintensity of Posterior Pituitary on MR T1WI in a Boy with Central Diabetes Insipidus Caused by Missense Mutation of Neurophysin II Gene
- Clinical approach to clarifying the mechanism of abnormal bone metabolism in McCune-Albright syndrome
- Thick Target Yields of Characteristic X-Rays by p, d, ^3He^+ and ^4He^+ Bombardments
- 病原性大腸菌O157による完全型HUSで認められた神経合併症のリスク因子
- Rickets in Infancy and Childhood