Publications by authors named "H Kirmizibekmez"

Phytochemical investigations on the aerial parts of Hypericum cerastioides led to the isolation and identification of a novel normonoterpene (1) and a previously undescribed benzophenone glycoside (3) along with eleven known secondary metabolites (2, 4-13). Their structures were deduced based on extensive 1D and 2D NMR analyses as well as HRESIMS. Compound 1 is a rare type of normonoterpene derivative with eight carbon atoms.

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Objectives: Subclinical hypothyroidism (SH) is defined by normal free triiodothyronine (fT3) and free thyroxine (fT4) levels, elevated thyroid-stimulating hormone levels, and the absence of overt clinical signs of hypothyroidism. The natural course of SH is influenced by the underlying etiology. The purpose of this study was to evaluate the etiologic causes of SH.

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Objective: To determine inequalities in access to diabetes technologies and the effect of socioeconomic factors on families with children with type 1 diabetes.

Methods: In this multicenter cross-sectional study, parents of children with type 1 diabetes completed a questionnaire about household sociodemographic characteristics, latest HbA1c values, continuous glucose monitoring (CGM) and insulin pump use of children, the education and working status of parents. These characteristics were compared between technology use (only-CGM, only-pump, CGM+pump, no technology use).

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Objective: Central precocious puberty (CPP) is treated with long-acting gonadotropin releasing hormone (GnRH) analogues (GnRHa). Some adult patients undergoing GnRHa treatment experienced prolonged QT syndrome, which is associated with an increased risk of serious cardiac events, such as myocardial infarction, stroke, arrhythmias, and sudden cardiac death.

Methods: Seventy-four patients, aged between 5 and 11 years and diagnosed with CPP but with no other concomitant disease or medication use, underwent electrocardiogram (ECG) assessment.

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Article Synopsis
  • The study focuses on autosomal-recessive hypophosphataemic rickets type 2 (ARHR2), a rare disease linked to ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) deficiency, often seen in survivors of generalized arterial calcification of infancy (GACI).
  • Researchers analyzed clinical, biochemical, and genetic data from 18 patients across 9 medical centers, revealing common symptoms like limb deformities and short stature, with a mean age of diagnosis at around 4.2 years.
  • Findings suggest that ARHR2 typically appears later in life than GACI; understanding previous calcifications or related health issues can aid in diagnosing ARHR2 in patients treated for
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