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Toplam kayıt 5, listelenen: 1-5
The role of initial clinical and laboratory findings in infants with hyperthyrotropinemia to predict transient or permanent hypothyroidism.
(Galenos Yayınevi, 2013)
Objective: Studies on the clinical course of children with hyperthyrotropinemia are scarce. We aimed to evaluate the role of presentation findings in such infants to predict eventual outcome.
Methods: Files of infants ...
Fetal and neonatal endocrine disruptors.
(Galenos Yayınevi, 2012)
Endocrine disruptors are substances commonly encountered in every setting and condition in the modern world. It is virtually impossible to avoid the contact with these chemical compounds in our daily life. Molecules defined ...
Novel growth hormone-releasing hormone receptor gene mutations in Turkish children with isolated growth hormone deficiency.
(Galenos Yayınevi, 2014)
Objective: Isolated growth hormone deficiency (IGHD) is defined as a medical condition associated with growth failure due to insufficient production of GH or lack of GH action. Mutations in the gene encoding for GH-releasing ...
Fine-needle aspiration biopsy in the diagnosis and follow-up of thyroid nodules in childhood.
(Galenos Yayınevi, 2010)
Objective: To assess the role of fine-needle aspiration biopsy (FNAB) in the management of pediatric thyroid nodules.
Methods: Results of 30 FNABs performed in our clinic were retrospectively reviewed. Clinical and surgical ...
McCune-Albright syndrome mimicking malignancy: an endocrine disease from oncologist's perspective.
(Galenos Yayınevi, 2012)
Fibrous dysplasia (FD) is categorized as either monostotic or polyostotic and may occur as a component of McCune-Albright syndrome (MAS). Imaging findings can mimic neoplastic diseases. We present a case of MAS initially ...