DeGroote School of Medicine, McMaster University, Hamilton, ON N2G 1C5, Canada; mmsportdoc{at}mcmaster.ca In 2014, the IOC published a consensus statement entitled ‘Beyond the Female Athlete Triad: ...

6 Institute of Systems, Molecular and Integrative Biology, University of Liverpool and Department of Gastroenterology, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK Iron ...

For patients with heart failure and reduced or mildly reduced left ventricular ejection fraction, iron deficiency is common and associated with more severe symptoms, worse quality of life and an ...

Background Intravenous iron therapy with ferric derisomaltose (FDI) has been shown to improve outcomes in patients with heart failure with reduced ejection fraction (HFrEF) and iron deficiency.

Correspondence to Tomás P Carroll, Alpha-1 Foundation Ireland, Royal College of Surgeons in Ireland, Dublin, Ireland; tcarroll{at}rcsi.ie The ZZ genotype of alpha-1 antitrypsin deficiency (AATD) is ...

† Department of Biological Sciences, St. Mary’s University, San Antonio, Texas 78228, United States ‡ Department of Biochemistry and Biophysics, Texas A&M University, College Station, Texas 77840, ...

† Department of Chemistry, Purdue University, 560 Oval Drive, West Lafayette, Indiana 47907, United States ‡ Department of Molecular Biophysics and Biochemistry, Yale University, 266 Whitney Avenue, ...

Objective To estimate the magnitude and the determinants of iron deficiency among adolescents aged 10–19 years in the State of Qatar ... 10 The non-nutritional factors include increased body ...

All providers who responded to the study survey reported screening for iron deficiency, but only 70% did so routinely and there was significant variation in treatment. Iron deficiency (ID) represents ...

Phenylalanine hydroxylase (PAH) is the enzyme which converts phenylalanine into tyrosine. In case of its deficiency, hyperphenylalaninemia is observed, which leads to phenylketonuria (PKU), a ...

Mutations which can be considered severe are IVS10nt-11, P281L, L311P ... and phenylalanine tolerance in phenylalanine hydroxylase deficiency. Eur J Pediatr 1996;155(suppl 1):6–10.

Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21OHD) is a complex endocrine disorder characterized by ... This results in disturbances in the regulation of hemostasis, ...