Browsing by Author "Gökalp D."

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Adult langerhans cell histiocytosis: Differential diagnosis

Çil T.; Gökalp D.; Tuzcu A.; Işikdoğan A.; Bahçeci M. (Turkiye Klinikleri, 2007)

Langerhans cell histiocytosis is a group of idiopathic disorders characterized by the abnormal proliferation of specialized bone marrow-derived Langerhans cells. There are one to two cases per million population. Most ...
Assessment of thyroid function in children aged 1-13 years with beta-thalassemia major

Pirinççioğlu A.G.; Deniz T.; Gökalp D.; Beyazit N.; Haspolat K.; Söker M. (Brieflands, 2011)

Objective: Hypothyroidism usually appears in the second decade of life and is thought to be associated with iron overload in patients with thalassemia major. This study aimed to evaluate thyroid dysfunctions in patients ...
A case with lipoid proteinosis intersected with diabetes mellitus

Gökalp D.; Tuzcu A.; Bahçeci M.; Yildirim M.; Akdeniz S.; Özekinci S.; Urakçi Z. (Turkiye Klinikleri, 2009)

Lipoid proteinosis (LP) is a rare disorder inherited as an autosomal recessive trait. LP is characterized by deposition of hyaline-like material in the skin, mucous membranes, and other tissues. LP has been mapped to ...