Results 91 to 100 of about 2,726 (200)

Hypophosphataemia in infants with CHD treated with amino acid infant formula

open access: yes, 2018
ObjectiveGrowth among infants with CHD is poor, and is multifactorial with multiple contributing factors. Unexplained hypophosphataemia has been reported among infants and children with complex medical needs consuming amino acid infant formula as the ...
Bharucha, Tara   +4 more
core   +1 more source

Approach to hypophosphataemia in intensive care units - a nationwide survey

open access: yes, 2012
Evidence-based guidelines for monitoring of serum phosphate levels and for the treatment of hypophosphataemia in critically ill patients are lacking.
Spronk, P. E.   +5 more
core  

Ventricular bigeminy and trigeminy caused by hypophosphataemia during diabetic ketoacidosis treatment: a case report

open access: yesItalian Journal of Pediatrics, 2019
Background Hypophosphatemia has many causes, and is often encountered during DKA (Diabetic Ketoacidosis) treatment. However, it rarely requires clinical intervention.
Konrad Miszczuk   +5 more
doaj   +1 more source

Severe asymptomatic hypophosphataemia in a child with T-acute lymphoblastic leukaemia

open access: yes, 2017
Hypophosphataemia is a metabolic disorder that is commonly encountered in critically ill patients. Phosphate has many roles in physiological functions, thus the depletion of serum phosphate could lead to impairment in multiple organ systems, which ...
Mohd Nazirul Mubin bin Puteh Ahmad
core   +1 more source

Cytomorphology, osmotic fragility, glucose-6-phosphate dehydrogenase and oxidant/antioxidant status in postparturient haemoglobinuria in dairy cattle and buffaloes

open access: yesBulgarian Journal of Veterinary Medicine
The present study was carried out to elucidate the role of blood phosphorus (P), erythrocytic glucose-6-phosphate dehydrogenase (G6PD), glutathione peroxidase (GSH-Px), malonaldehyde (MDA), and nitric oxide (NO) on the integrity of the cell membranes of ...
A. I. Hassanin   +2 more
doaj   +1 more source

Rare genetic diseases of the bone tissue: the case of a family with osteogenesis imperfecta and X-linked hypophosphataemia

open access: yesОстеопороз и остеопатии, 2018
Osteogenesis imperfecta (OI) and X-linked hypophosphataemia (XLH) are rare genetic diseases, which lead to childhood-onset bone fragility, low-trauma fractures and limb deformities. OI occurs as a result of impaired type 1 collagen synthesis at different
Irina Yu. Popova   +5 more
doaj   +1 more source

Hypophosphataemia: a feature of malaria? [PDF]

open access: yesBMJ, 1987
Les taux seriques de phosphate sont souvent diminues dans le paludisme.
openaire   +2 more sources

Publication Only

open access: yes
HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Refeeding hypophosphataemia in a Malaysian intensive care unit: incidence, risk factors and outcomes [PDF]

open access: yes, 2015
Introduction: Refeeding syndrome is characterised by acute electrolyte derangement following the start of nutrition. Hypophosphataemia is the predominant feature of the electrolyte derangement, hence commonly used for its definition. We aim to assess the
Mat Nor, Mohd Basri   +4 more
core  

Lamivudine, Entecavir, or Tenofovir Treatment of Hepatitis B Infection: Effects on Calcium, Phosphate, FGF23 and Indicators of Bone Metabolism

open access: yesAnnals of Hepatology, 2017
Background. Patients with chronic hepatitis B virus (HBV) are often treated with nucleoside/nucleotide antiviral agents and metabolic bone toxicity is a possible concern.Objective. To determine the relationships between fibroblast growth factor 23 (FGF23)
Ramesh Saeedi   +11 more
doaj   +1 more source

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