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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Detaylı Bibliyografya
Yayımlandı:J Clin Res Pediatr Endocrinol
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Galenos Publishing 2020
Konular:
Original Article
Online Erişim: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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