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Pediatric Endocrine Case Reports I
SAT-081 Hidden in Plain Sight: Rethinking Our Approach to Allan-Herndon-Dudley Syndrome
Article
Year: 2020
Pages: 1
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SAT-077 Two Cases of Hypoparathyroidism Due to Activating Calcium Sensing Receptor Mutation
Article
Year: 2020
Pages: 1
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SAT-055 A De Novo 1p13.2 Deletion Related to Short Stature, Hypothyroidism and Mild Developmental Delay
Article
Year: 2020
Pages: 1
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SAT-063 Polymicrobial Suppurative Thyroiditis Masquerading as Thyroid Storm
Article
Year: 2020
Pages: 1
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SAT-059 Congenital Craniopharyngioma: A Rare and Challenging Disease
Article
Year: 2020
Pages: 1
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SAT-061 Severe Hypocalcemia in an Infant with Abnormal Microarray and Dysmorphic Features
Article
Year: 2020
Pages: 1
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SAT-054 Gigantism and Hypothalamic Obesity: Rare Endocrine Manifestations of Neurofibromatosis Type 1
Article
Year: 2020
Pages: 1
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SAT-057 A Novel IGSF1 Variant in a Boy with Central Hypothyroidism and Epiphyseal Dysplasia
Article
Year: 2020
Pages: 1
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SAT-060 Unusual Case of Short Stature and Poor Growth in Childhood
Article
Year: 2020
Pages: 1
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SAT-056 Autosomal Dominant Hypophosphatemic Rickets in Premature Twins Resolved with Iron Supplementation
Article
Year: 2020
Pages: 1
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SAT-074 A Rare Endocrine Cause of Pseudotumor Cerebri
Article
Year: 2020
Pages: 1
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SAT-071 Autoimmune Polyglandular Syndrome Type 1 with Common Variable Immunodeficiency
Article
Year: 2020
Pages: 1
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SAT-079 Is There an Association Between the Detection Method for Pediatric Thyroid Nodules and the Risk of Malignancy?
Article
Year: 2020
Pages: 1
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SAT-069 Advantages of Next Generation Sequencing (NGS) in Hypophosphatemic Disorders Diagnosis. First Case of SLC9A3R1 Gene Pathogenic Variant Detected in a Pediatric Patient
Article
Year: 2020
Pages: 1
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