Zobrazeno 1 - 10
of 632
pro vyhledávání: '"Hypophosphataemia"'
Autor:
Enrique Casado, Carlos Gómez-Alonso, Guillem Pintos-Morell, Rosa Bou-Torrent, Ana Coral Barreda-Bonis, José Vicente Torregrosa, José Jesús Broseta-Monzó, Pedro Arango-Sancho, Sara Chocrón-de-Benzaquen, Yoko Olmedilla-Ishishi, Begoña Soler-López
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-15 (2023)
Abstract Background There are currently no models for the transition of patients with metabolic bone diseases (MBDs) from paediatric to adult care. The aim of this project was to analyse information on the experience of physicians in the transition o
Externí odkaz:
https://doaj.org/article/25428c7cb49d4af693e09da1738c21c1
Publikováno v:
ESC Heart Failure, Vol 10, Iss 2, Pp 1294-1304 (2023)
Abstract Aims Iron deficiency is a common finding among patients with heart failure (HF) and is associated with adverse outcomes, including decreased quality of life, increased risk of hospitalization, and decreased survival. Intravenous ferric carbo
Externí odkaz:
https://doaj.org/article/9c503788dd1847b79fbd01eb5d2d8a2e
Autor:
Sophie Cole, Maria T. Sanchez-Santos, Spyros Kolovos, Muhammad Kassim Javaid, Rafael Pinedo-Villanueva
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-18 (2023)
Abstract Background X-linked hypophosphataemia (XLH) is a rare genetic condition passed on through the X chromosome which causes multiple symptoms including weakened teeth, bones, and muscles. Due to the rarity of the condition, little is known about
Externí odkaz:
https://doaj.org/article/f116b59a3522438fb9c9cca67a3181f0
Publikováno v:
JCRPE, Vol 14, Iss 3, Pp 344-349 (2022)
X-linked hypophosphatemia (XLH) is a rare genetic disorder with X-linked dominant inheritance. Mutations in the PHEX gene increase fibroblast growth factor 23 (FGF23) concentrations, causing loss of phosphorus at the proximal tubule. Most pediatric p
Externí odkaz:
https://doaj.org/article/774c4533a810405a8d13d5638b4bbf50
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/b78393f2c69246a196fe2d04d51f67de
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-9 (2021)
Abstract Background The mechanism by which hypophosphataemia develops following kidney transplantation remains debated, and limited research is available regarding risk factors. This study aimed to assess the association between recipient and donor v
Externí odkaz:
https://doaj.org/article/4bc01c47b8b0497baf9b331911962578
Autor:
Carlos Javier Parramón-Teixidó, Laura Gómez-Ganda, Beatriz García-Palop, Marcos Linés-Palazón, Albert Blanco-Grau, José Bruno Montoro-Ronsano, Susana Clemente-Bautista
Publikováno v:
Anales de Pediatría, Vol 95, Iss 3, Pp 139-146 (2021)
Resumen: Introducción: La nutrición parenteral agresiva con aportes energéticos y proteicos altos se utiliza para mejorar el crecimiento y el neurodesarrollo en recién nacidos prematuros de muy bajo peso. No obstante, hallazgos recientes sugieren
Externí odkaz:
https://doaj.org/article/34143c8523444ef4b0cb560ab4af6a43
Akademický článek
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Akademický článek
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Autor:
Xenophon Kassianides, Sunil Bhandari
Publikováno v:
Drugs in Context, Vol 10, Pp 1-29 (2021)
Third-generation intravenous (i.v.) iron preparations are safe and efficacious and are increasingly used in the treatment of iron-deficiency anaemia. Hypophosphataemia is emerging as an established side-effect following the administration of certain
Externí odkaz:
https://doaj.org/article/9578cb19a77c42c0b0af98ce38d088a1