The Turkish Journal of Pediatrics
Smilar Issues: 12 Record Found
Role of scintigraphy in congenital thyroid anomalies
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Precocious Puberty in a Girl with Down Syndrome due to
Primary Hypothyroidism
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Pituitary hyperplasia mimicking pituitary macroadenoma in two
adolescent patients with long-standing primary hypothyroidism:
case reports and review of literature
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Severe Rhabdomyolysis and Acute Renal Failure in an Adolescent with Hypothyroidism
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Congenital Hypothyroidism Screening Program in Turkey: A Local Evaluation
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Rhabdomyolysis due to Isoniazid Poisoning Resulting from the Use of Intramuscular Pyridoxine
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Monitoring and Prognostic Evaluation of Patients with Congenital Hypothyroidism Treated in a Pediatric Endocrinology Unit
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The importance of isoenzymes in creatinine kinase elevations
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Novel Nonsense Mutation of GPC3 Gene in a Patient with Simpson-Golabi-Behmel Syndrome
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Primary trimethylaminuria (fish odor syndrome) and hypothyroidism in an adolescent
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Thirty years of the newborn screening program in Central Serbia: the missed cases of congenital hypothyroidism
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A neglected cause of recurrent rhabdomyolysis, LPIN1 gene defect: a rare case from Turkey
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