Zobrazeno 1 - 10
of 92
pro vyhledávání: '"Idiopathic hypercalcemia"'
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 146, Iss 1-2, Pp 77-80 (2018)
Introduction. Recently, inactivation mutations of CYP24A1, the gene encoding vitamin D 24-hydroxylase, were identified in hypercalciuric nephrolithiasis and nephrocalcinosis. Here, we describe а long-term follow-up of a patient with hypercalciuric n
Externí odkaz:
https://doaj.org/article/9300614d39fb456eb1310bda5e88d2f2
Autor:
Juan Víctor Ariel Franco, Albert Feliu, Albert Balaguer, Marta Roqué-Figuls, Joaquin Escribano, Natàlia Ferré, Ester Parada
Publikováno v:
Nefrología (English Edition). 42:506-518
Objective: To assess the effects of pharmacological interventions in patients with idiopathic hypercalciuria. Methods: We performed a search of multiple databases, trial registries, grey literature and conference proceedings up to October 2019. We in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28d039db0942b7c6b8fb2f9ab1218afd
https://doi.org/10.1016/j.nefroe.2021.04.014
https://doi.org/10.1016/j.nefroe.2021.04.014
Akademický článek
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Publikováno v:
J Clin Exp Hepatol
Hypercalcemia is a rare metabolic abnormality seen in patients with cirrhosis and is usually considered a paraneoplastic manifestation of hepatocellular carcinoma. Idiopathic hypercalcemia in cirrhosis is a diagnosis of exclusion, which is considered
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc8d14743c0546e88fa123f59fccc156
https://doi.org/10.1016/j.jceh.2020.05.004
https://doi.org/10.1016/j.jceh.2020.05.004
Publikováno v:
Journal of Veterinary Internal Medicine
A 12‐year‐old, neutered female, domestic medium hair cat was evaluated for a nonhealing, oral mucosal ulceration. The cat had a history of idiopathic hypercalcemia that had been treated with a bisphosphonate for 41 months. Oral examination identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::626ec093e4d554e4c68ee7409cef36cd
https://doi.org/10.1111/jvim.15409
https://doi.org/10.1111/jvim.15409
Publikováno v:
European journal of medical genetics. 63(12)
Vitamin D plays an important role in calcium homeostasis and bone mineralization. Inefficient inactivation of vitamin D leads to a condition called idiopathic infantile hypercalcemia (IIH). In the last decade mutations in CYP24A1, the gene responsibl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14d23b507aa8d1daca98914f69106822
https://pubmed.ncbi.nlm.nih.gov/33186763
https://pubmed.ncbi.nlm.nih.gov/33186763
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 146, Iss 1-2, Pp 77-80 (2018)
Introduction. Recently, inactivation mutations of CYP24A1, the gene encoding vitamin D 24-hydroxylase, were identified in hypercalciuric nephrolithiasis and nephrocalcinosis. Here, we describe а long-term follow-up of a patient with hypercalciuric n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b11e4e89c4feb1ea3c5fe52e447d29e4
http://www.doiserbia.nb.rs/img/doi/0370-8179/2018/0370-81791700095P.pdf
http://www.doiserbia.nb.rs/img/doi/0370-8179/2018/0370-81791700095P.pdf
Publikováno v:
International Journal of Surgery Case Reports
Highlights • Ectopic parathyroid adenomas are rare. • PA’s can cause idiopathic hypercalcemia. • VATS in the recommended treatment of choice.
Introduction The most common cause of chronic hypercalcemia is primary hyperparathyroidism (PHP
Introduction The most common cause of chronic hypercalcemia is primary hyperparathyroidism (PHP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d51fa8ef395149e5842adfe0076e4b66
https://doi.org/10.1016/j.ijscr.2017.08.056
https://doi.org/10.1016/j.ijscr.2017.08.056
Autor:
Agnieszka Janiec, Ewa Kowalska, Mieczysław Litwin, Paulina Halat, Rafał Rola, Elżbieta Ciara, Ewa Pronicka, Marek Wójcik, Paweł Płudowski, Aldona Wierzbicka, Łukasz Obrycki, Natalia Łaszcz, Janusz Książyk
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 208:105824
Infantile hypercalcemia (IH), is a rare disorder caused by CYP24A1 or SLC34A1 variants which lead to disturbed catabolism of 25(OH)D3 and 125(OH)2D3 or increased generation of 125(OH)2D3. Aim of study To assess the status of 2425(OH)2D3 and other mar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfd43c6e835dcfa3de03af9651a2c527
https://doi.org/10.1016/j.jsbmb.2021.105824
https://doi.org/10.1016/j.jsbmb.2021.105824
Akademický článek
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