Results 1 to 10 of about 25,027 (259)

Body mass index and blood urea nitrogen to creatinine ratio predicts refeeding hypophosphatemia of anorexia nervosa patients with severe malnutrition [PDF]

open access: goldJournal of Eating Disorders, 2021
Aim To investigate development of refeeding hypophosphatemia during the refeeding period and the extent of the decrease in the serum phosphorus level among anorexia nervosa patients with severe malnutrition.
Michitaka Funayama   +5 more
doaj   +3 more sources

Burosumab and Dental Abscesses in Children With X‐Linked Hypophosphatemia

open access: goldJBMR Plus, 2022
X‐linked hypophosphatemia (XLH) is a rare genetic disorder that disrupts skeletal and dental mineralization. In addition to rickets in children, XLH patients also have frequent spontaneous dental abscesses that increase the risk of tooth loss and may ...
Margaux Gadion   +8 more
semanticscholar   +2 more sources

Hypophosphatemia Associated with Intravenous Iron Therapies for Iron Deficiency Anemia: A Systematic Literature Review

open access: yesTherapeutics and Clinical Risk Management, 2020
John A Glaspy,1 Michelle Z Lim-Watson,2 Michael A Libre,3 Swagata S Karkare,3 Nandini Hadker,3 Aleksandra Bajic-Lucas,2 William E Strauss,2 Naomi V Dahl2 1UCLA School of Medicine, Los Angeles, CA, USA; 2AMAG Pharmaceuticals, Inc., Waltham, MA, USA ...
Glaspy JA   +7 more
doaj   +2 more sources

Burosumab Therapy in Children with X-Linked Hypophosphatemia

open access: yesNew England Journal of Medicine, 2018
BACKGROUND X‐linked hypophosphatemia is characterized by increased secretion of fibroblast growth factor 23 (FGF‐23), which leads to hypophosphatemia and consequently rickets, osteomalacia, and skeletal deformities.
Thomas O Carpenter   +2 more
exaly   +2 more sources

A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Trial Evaluating the Efficacy of Burosumab, an Anti-FGF23 Antibody, in Adults With X-Linked Hypophosphatemia: Week 24 Primary Analysis

open access: yesJournal of Bone and Mineral Research, 2018
In X‐linked hypophosphatemia (XLH), inherited loss‐of‐function mutations in the PHEX gene cause excess circulating levels of fibroblast growth factor 23 (FGF23), leading to lifelong renal phosphate wasting and hypophosphatemia.
Karl L Insogna   +2 more
exaly   +2 more sources

The Lifelong Impact of X-Linked Hypophosphatemia: Results From a Burden of Disease Survey

open access: yesJournal of the Endocrine Society, 2019
Context X-linked hypophosphatemia (XLH) is characterized by excess fibroblast growth factor 23 (FGF23), hypophosphatemia, skeletal abnormalities, and growth impairment. We aimed to understand the burden of disease of XLH across the lifespan.
Alison Skrinar   +2 more
exaly   +2 more sources

Hypophosphatemia at Admission is Associated with Increased Mortality in COVID-19 Patients

open access: yesInternational Journal of General Medicine, 2021
Ruoran Wang,1,* Min He,1,2,* Yan Kang1,2 1Department of Critical Care Medicine, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan Province, People’s Republic of China; 2COVID19 Medical Team (Hubei) of West China Hospital, Sichuan ...
Wang R, He M, Kang Y
doaj   +2 more sources

Indications for the evaluation and supplementation of hypophosphatemia: an umbrella systematic review of reviews and guidelines [PDF]

open access: yesBMC Medicine
Background Hypophosphatemia, defined as low serum phosphate levels, is a frequent yet underrecognized condition associated with significant morbidity.
Seraina Netzer   +3 more
doaj   +2 more sources

Hypophosphatemia and Rhabdomyolysis [PDF]

open access: bronzeJournal of Clinical Investigation, 1978
Clinical observations suggest that overt rhabdomyolysis may occur if severe hypophosphatemia is superimposed upon a pre-existing subclinical myopathy. To examine this possibility, a subclinical muscle cell injury was induced in 23 dogs by feeding them a phosphorus- and calorie-deficient diet until they lost 30% of their original weight. To induce acute,
J P, Knochel   +5 more
openaire   +4 more sources

Approach to a Child with Hypophosphatemia [PDF]

open access: yesBiomolecules
Hypophosphatemia is a rare ion disorder in children, but it carries the risk of serious clinical sequelae in tissues and organs with high energy requirements, such as bone tissue.
Agnieszka Antonowicz   +3 more
doaj   +2 more sources

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