Results 41 to 50 of about 25,027 (259)

FGF23 and its role in X-linked hypophosphatemia-related morbidity

open access: yesOrphanet Journal of Rare Diseases, 2019
BackgroundX-linked hypophosphatemia (XLH) is an inherited disease of phosphate metabolism in which inactivating mutations of the Phosphate Regulating Endopeptidase Homolog, X-Linked (PHEX) gene lead to local and systemic effects including impaired growth,
S. Beck-Nielsen   +9 more
semanticscholar   +1 more source

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

Hypophosphatemia [PDF]

open access: yesJournal of the American Society of Nephrology, 2007
Current evidence regarding the clinical consequences of hypophosphatemia is not straightforward. Given the potentially different implications of hypophosphatemia among various patient groups, this commentary touches on patients with low serum phosphate after acute hospitalization, those with chronic ambulatory hypophosphatemia, and those with ...
David W. Mozingo, Arthur D. Mason,
openaire   +3 more sources

The Factors That Cause Hypophosphatemia in Patients Receivig Clinical Nutrition Treatment

open access: yesTürk Yoğun Bakim Derneği Dergisi, 2022
Objective:One of the most important issues to be considered in patients who are started on nutritional therapy is refeeding syndrome (RS), which can occur within the first four days. Hypophosphatemia (serum phosphorus level
Kezban Akçay   +3 more
doaj   +1 more source

Novel PHEX gene locus‐specific database: Comprehensive characterization of vast number of variants associated with X‐linked hypophosphatemia (XLH)

open access: yesHuman Mutation, 2021
X‐linked hypophosphatemia (XLH), the most common form of hereditary hypophosphatemia, is caused by disrupting variants in the PHEX gene, located on the X chromosome. XLH is inherited in an X‐linked pattern with complete penetrance observed for both males
Soodabeh Sarafrazi   +15 more
semanticscholar   +1 more source

Diagnosis and management of X-linked hypophosphatemia in children and adolescent in the Gulf Cooperation Council countries

open access: yesArchives of Osteoporosis, 2021
Introduction X-linked hypophosphatemia (XLH) is a rare inherited cause of hypophosphatemic rickets and osteomalacia. It is caused by mutations in the phosphate-regulating endopeptidase homolog, X-linked (PHEX). This results in increased plasma fibroblast
Fahad Al Juraibah   +12 more
semanticscholar   +1 more source

Hypophosphatemia in cancer patients

open access: yesClinical Kidney Journal, 2021
Dysregulation of phosphorus homeostasis resulting in hypophosphatemia is common in cancer patients and can result in serious complications and impact outcomes.
S. Adhikari   +3 more
semanticscholar   +1 more source

Hypophosphatemia after Right Hepatectomy for Living Donor Liver Transplantation

open access: yesCanadian Journal of Gastroenterology, 2004
Hypophosphatemia has been described in patients undergoing right hepatectomy for liver cancer and in living donors for liver transplantation who also received total parenteral nutrition.
Kelly W Burak   +6 more
doaj   +1 more source

Incidence of complications in 25 adult patients with X-linked hypophosphatemia.

open access: yesJournal of Clinical Endocrinology and Metabolism, 2021
CONTEXT Adults with X-linked hypophosphatemia (XLH) present complications other than osteomalacia. OBJECTIVE To describe the incidence and severity of comorbidities in adults with XLH. DESIGN Observational retrospective study.
H. Kato   +8 more
semanticscholar   +1 more source

Home - About - Disclaimer - Privacy