دورية أكاديمية
Proteinuria and progressive kidney failure due to an inborn error of metabolism: Questions
| العنوان: | Proteinuria and progressive kidney failure due to an inborn error of metabolism: Questions |
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| المؤلفون: | Ünal Uzun, Özlem, Cengiz, Nurcan, Çavdarlı, Büşra, Bayrakçı, Umut, Kiremitçi, Saba, Küçükçongar Yavaş, Aynur |
| المساهمون: | MÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, orcid:0000-0002-4977-8310, Cengiz, Nurcan |
| بيانات النشر: | SpringerLink |
| سنة النشر: | 2021 |
| مصطلحات موضوعية: | Child, Inborn error of metabolism, Anemia, Proteinuria, Dysostosis multiplex, Kidney disease, Cherry-red spot |
| الوصف: | A 6-year-old patient was admitted to our clinic with a suspected diagnosis of an inborn error of metabolism (IEM). He was born at term with a birth weight of 3620 g with an uneventful delivery. He was the first child of nonconsanguineous Turkish parents, and his sibling was healthy. |
| نوع الوثيقة: | article in journal/newspaper |
| وصف الملف: | application/pdf |
| اللغة: | English |
| تدمد: | 0931-041X 1432-198X |
| العلاقة: | Pediatric Nephrology; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; Uzun, Ö.Ü., Cengiz, N., Çavdarlı, B. et al. Proteinuria and progressive kidney failure due to an inborn error of metabolism: Questions. Pediatr Nephrol (2021). https://doi.org/10.1007/s00467-020-04891-yTest; https://hdl.handle.net/20.500.12809/8933Test; https://doi.org/10.1007/s00467-020-04891-yTest |
| DOI: | 10.1007/s00467-020-04891-y |
| الإتاحة: | https://doi.org/20.500.12809/8933Test https://doi.org/10.1007/s00467-020-04891-yTest https://hdl.handle.net/20.500.12809/8933Test |
| حقوق: | info:eu-repo/semantics/openAccess |
| رقم الانضمام: | edsbas.F20906AE |
| قاعدة البيانات: | BASE |
| تدمد: | 0931041X 1432198X |
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| DOI: | 10.1007/s00467-020-04891-y |