The Turkish Journal of Pediatrics
Smilar Issues: 14 Record Found
Persistent elevated serum levels of intact parathyroid hormone after reoperation for primary hyperparathyroidism and after pamidronate therapy Abstract Similar Articles Mail to Editor Use of bisphosphonates for resistant hypercalcemia in children with acute lymphoblastic leukemia: report of two cases and review of the literature Abstract Similar Articles Mail to Editor Prediction of premature atherosclerosis by endothelial dysfunction and increased Iintima-media thickness in glycogen storage disease types Ia and III Abstract Similar Articles Mail to Editor The rapid correction of hypercalcemia at presentation of acute lymphoblastic leukemia using high-dose methylprednisolone Abstract Similar Articles Mail to Editor A novel mutation of the GLUT2 gene in a Turkish patient with Fanconi-Bickel syndrome Abstract Similar Articles Mail to Editor Hypercalcemia in Glycogen Storage Disease Type I Patients of Turkish Origin Abstract Similar Articles Mail to Editor Vitamin D Intoxication Abstract Similar Articles Mail to Editor Nephrocalcinosis as a Complication of Subcutaneous Fat Necrosis of the Newborn Abstract Similar Articles Mail to Editor Evaluation of central nervous system in patients with glycogen storage disease type 1a Abstract Similar Articles Mail to Editor Cholestasis and hypercalcemia secondary to panhypopituitarism in a newborn Abstract Similar Articles Mail to Editor A Fanconi-Bickel syndrome patient with a novel mutation and accompanying situs inversus totalis Abstract Similar Articles Mail to Editor Squamous cell carcinoma associated with Xeroderma pigmentosum: an unusual presentation with a tremendously huge mass over the face and paraneoplastic hypercalcemia-hyperleukocytosis Abstract Similar Articles Mail to Editor Acute renal failure due to severe hypercalcemia and nephrocalcinosis treated with two doses of pamidronate in an infant with Williams-Beuren syndrome Abstract Similar Articles Mail to Editor Glycogen storage disease type 0 due to a novel frameshift mutation in glycogen synthase 2 (GYS2) gene in a child presenting with fasting hypoglycemia and postprandial hyperglycemia Abstract Similar Articles Mail to Editor
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