Results 101 to 110 of about 2,726 (200)
A case of Gitelman syndrome with severe hyponatraemia and hypophosphataemia
, 2013 Gitelman syndrome (GS) is a renal tubular disorder of the thiazide-sensitive sodium chloride cotransporter, which is located in the distal tubule of the loop of Henle. We present a rare case of GS complicated by severe hyponatraemia and hypophosphataemia.
Yaqub, Sonia +3 more
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Myocardial damage due to hypokalaemia and hypophosphataemia.
, 1984 A case of severe hypokalaemia with stupor, skeletal muscle and heart muscle damage is reported. An initial infusion of glucose-insulin and potassium (GIK) produced a temporary clinical improvement with reduction of creatine kinase (CKMB) and elevation of
C. Scoppetta +5 more
core +1 more source
Limited evidence for monitoring and treatment of hypophosphataemia in critically ill patients
, 2015 Hypophosphataemia is a potentially hazardous metabolic disturbance which is common in critically ill patients. The condition is reported to be associated with severe complications and increased mortality.
Thormar, Katrin +3 more
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, 2016 Background Although associated with severe clinical complications, phosphate remains a neglected ion. Additionally, phosphate balance during continuous renal replacement therapy (CRRT) is complex and multifunctional.
Broman, Marcus +2 more
core +2 more sources
Tumor-induced phosphopenic osteomalacia: modern approaches to diagnostics and treatment
Современная ревматологияPhosphopenic osteomalacia (PPOM) is a rare variant of paraneoplastic syndrome caused by tumor synthesis of fibroblast growth factor 23 (FGF23). FGF23 secretion leads to a decrease in phosphate reabsorption and calcitriol levels, which leads to the ...
A. A. Kondrashov +4 more
doaj +1 more source
Ferric carboxymaltose-induced hypophosphataemia after kidney transplantation
, 2017 Background: Ferric carboxymaltose (FCM) can induce hypophosphataemia in the general population and patients with chronic kidney disease (CKD). Less is known about the effect of FCM in the kidney transplant population.
Hesselink, D. A. +13 more
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Pharmacological management of X‐linked hypophosphataemia
, 2018 The most common heritable disorder of renal phosphate wasting, X‐linked hypophosphataemia (XLH), was discovered to be caused by inactivating mutations in the phosphate regulating gene with homology to endopeptidases on the X‐chromosome (PHEX) gene in ...
Imel, Erik A. +3 more
core +1 more source
, 2017 Objective: To compare in two epochs of differing phosphate provision serum calcium, phosphate, potassium, and sodium concentrations and the frequency of abnormality of these electrolytes and of sepsis in preterm infants who received an optimised higher ...
Howe, Rosalind +15 more
core +1 more source
Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia [PDF]
, 2019 X-linked hypophosphataemia (XLH) is the most common cause of inherited phosphate wasting and is associated with severe complications such as rickets, lower limb deformities, pain, poor mineralization of the teeth and disproportionate short stature in ...
Schnabel, D +19 more
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