Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

OBJECTIVE: Hypophosphatemic rickets (HR) is a rare renal phosphate-wasting disorder, which is usually X-linked and is commonly caused by PHEX mutations. The treatment and follow-up of HR is challenging due to imperfect treatment options. METHODS: Here we present nationwide initial and follow-up data...

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Bibliografiset tiedot
Julkaisussa:J Clin Res Pediatr Endocrinol
Päätekijät: Şıklar, Zeynep, Turan, Serap, Bereket, Abdullah, Baş, Firdevs, Güran, Tülay, Akberzade, Azad, Abacı, Ayhan, Demir, Korcan, Böber, Ece, Özbek, Mehmet Nuri, Kara, Cengiz, Poyrazoğlu, Şükran, Aydın, Murat, Kardelen, Aslı, Tarım, Ömer, Eren, Erdal, Hatipoğlu, Nihal, Büyükinan, Muammer, Akyürek, Nesibe, Çetinkaya, Semra, Bayramoğlu, Elvan, Selver Eklioğlu, Beray, Uçaktürk, Ahmet, Abalı, Saygın, Gökşen, Damla, Kor, Yılmaz, Ünal, Edip, Esen, İhsan, Yıldırım, Ruken, Akın, Onur, Çayır, Atilla, Dilek, Emine, Kırel, Birgül, Anık, Ahmet, Çatlı, Gönül, Berberoğlu, Merih
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Galenos Publishing 2020
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Original Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7291408/
https://ncbi.nlm.nih.gov/pubmed/31514490
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/jcrpe.galenos.2019.2019.0098
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