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Autoimmune hypoparathyroidism in a 12-year-old girl with McKusick cartilage hair hypoplasia
Pediatric Nephrology, 08/11/09
Bacchetta J et al. – The authors report on a 12–year–old girl with a new mutation of the RMRP gene and a severe multisystemic CHH (hematological and pulmonary lesions, severe immune deficiency, arthritis, pancreatic insufficiency, malabsorption, chronic diarrhea) receiving parenteral nutrition who presented with acute symptomatic hypocalcemia and hypercalciuria associated with the presence of autoantibodies directed against the calcium–sensor receptor
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Revised American Thyroid Association Management Guidelines for Patients with Thyroid Nodules and Differentiated Thyroid Cancer
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Thyroid lymphoma and airway obstruction – is there a rationale for surgical management?
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Radioactive iodine for hyperthyroidism in children and adolescents: referral rate and response to treatment
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