Özlem Ünal Uzun (Ozlem Unal)

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 7

Top Topics

Pulmonary Embolism

Magnetic Resonance

Acute Kidney Injury

Top Venues

Journal of pediatric endocrinology & metabolism : JPEM

Pediatric nephrology (Berlin, Germany)

Case reports in pediatrics

This page only lists publications with an associated author ORCID identifier.

Publications

Aynur Küçükçongar Yavaş, Ayşenur Engin Erdal, Ayşegül Neşe Çıtak Kurt, Tuba Kurt, İlknur Cankurt, Özlem Ünal Uzun
Difficult to think about but easy to treat: scurvy. Journal of pediatric endocrinology & metabolism : JPEM (2023)
Gülhan Karakaya Molla, Mehtap Kağnıcı, Ayla Günlemez, Yaşar Yeni, Özlem Ünal Uzun
Two cases of MEGDHEL syndrome diagnosed with hyperammonemia. Journal of pediatric endocrinology & metabolism : JPEM 36 (2) (2022)
Gülhan Karakaya Molla, Mehtap Kağnıcı, Ayla Günlemez, Yaşar Yeni, Özlem Ünal Uzun
Two cases of MEGDHEL syndrome diagnosed with hyperammonemia. Journal of pediatric endocrinology & metabolism : JPEM 36 (2) (2022)
Gülhan Karakaya Molla, Mehtap Kağnıcı, Ayla Günlemez, Yaşar Yeni, Özlem Ünal Uzun
Two cases of MEGDHEL syndrome diagnosed with hyperammonemia. Journal of pediatric endocrinology & metabolism : JPEM (2022)
Özlem Ünal Uzun, Nurcan Cengiz, Büşra Çavdarlı, Umut Bayrakçı, Saba Kiremitçi, Aynur Küçükçongar Yavaş
Proteinuria and progressive kidney failure due to an inborn error of metabolism: Questions. Pediatric nephrology (Berlin, Germany) 36 (7) (2021)
Özlem Ünal Uzun, Nurcan Cengiz, Büşra Çavdarlı, Umut Bayrakçı, Saba Kiremitçi, Aynur Küçükçongar Yavaş
Proteinuria and progressive kidney failure due to an inborn error of metabolism: Answers. Pediatric nephrology (Berlin, Germany) 36 (7) (2021)
Mehmet Gunduz, Özlem Ünal Uzun
Dysmorphic Facial Features and Other Clinical Characteristics in Two Patients with PEX1 Gene Mutations. Case reports in pediatrics 2016 (2016)