Yazar "Kara C." için listeleme
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A case report of xp21 contiguous gene syndrome: Adrenal hypoplasia congenita, glycerol kinase deficiency, and duchenne muscular dystrophy
Kara C.; Yılmaz G.C.; Bitkin E.Ç.; Aydın M. (Galenos Yayincilik,, 2016)Objective: X-linked adrenal hypoplasia congenita (AHC) is characterized by primary adrenal insufficiency caused by deletion or mutation of the DAX-1 gene and is frequently associated with hypogonadotropic hypogonadism. It ... -
Congenital goitrous hypothyroidism, deafness and iodide organification defect in four siblings: Pendred or pseudo-pendred syndrome?
Kara C.; Kiliç M.; Uçaktürk A.; Aydin M. (2010)Pendred syndrome (PDS) is an autosomal recessive disorder characterized by congenital deafness, goiter and iodide organification defect. Presence of inner ear malformations is essential for the clinical diagnosis. Most ... -
Effects of High-Dose Methotrexate Therapy on Glucose Metabolism in Childhood Acute Lymphoblastic Leukemia
Methotrexate (MTX) has been used in the treatment of childhood acute lymphoblastic leukemia (ALL) for over 40 years. A number of the acute toxicities are common with high dose methotrexate (HDMTX) infusion, including ... -
Herbal product use in patients with chronic kidney disease
OBJECTIVE: Recently, despite the developments in diagnosis and treatment of diseases, herbal product use in patients with chronic diseases has become more frequent. The aim of our study was to investigate the frequency of ... -
Plasma and urine osmolality in the differential diagnosis of syndromes of inappropriate ADH secretion and cerebral salt wasting
Kara C.; Uçaktürk A.; Günindi F.; Aydin M. (2010)To evaluate the usefulness of the measurements of plasma and urine osmolality to make a differential diagnosis in the early period of hyponatremia occurring children hospitalized due to cerebral damage. This study was ...