2 results match your criteria: "Department of Pediatric Endocrinology Hospital Dona Estefânia Lisboa Portugal.[Affiliation]"

The authors present a new association of two heterozygous TACR3 mutations (p.Arg230His and p.Trp275*) responsible for a clinical trait of normosmic congenital hypogonadotropic hypogonadism in a family.

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Introduction: In 2012, an international expert committee in diabetes wrote in favor of screening adult and paediatric patients for glucose intolerance and type 2 diabetes using glycated haemoglobin. The aim of this study was to evaluate glycated haemoglobin utility as a screening tool in a young obese mainly Caucasian population.

Material And Methods: Children [(n = 266), body mass index z-score 3.

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