Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Eda Didem Kurt Sukur"'
Autor:
Ayca Burcu Kahraman, Bekir Karakaya, Yılmaz Yıldız, Saygin Kamaci, Selman Kesici, Pelin Ozlem Simsek-Kiper, Eda Didem Kurt-Sukur, Benan Bayrakcı, Goknur Haliloglu
Publikováno v:
Neuromuscular Disorders. 32:931-934
Autor:
Eda Didem Kurt-Sukur, Eileen Brennan, Meryl Davis, Colin Forman, George Hamilton, Nicos Kessaris, Stephen D. Marks, Clare A. McLaren, Kishore Minhas, Premal A. Patel, Derek J. Roebuck, Jelena Stojanovic, Sam Stuart, Kjell Tullus
Publikováno v:
European Journal of Pediatrics. 181:3367-3375
Renovascular hypertension in most cases requires endovascular treatment and/or surgery. This is technically much more difficult in small children and there is very limited published knowledge in this age group. We here present treatment and outcome o
Autor:
Demet Baltu, Eda Didem Kurt Sukur, Ersin Gumus, Tugba Tastemel Ozturk, Yasin Maruf Ergen, Duygu Demirtas, Bora Gülhan, Fatih Ozaltin, Diclehan Orhan, Hasan Özen, Ali Düzova
Publikováno v:
Pediatric Nephrology.
Autor:
Demet Baltu, Eda Didem Kurt Sukur, Ersin Gumus, Tugba Tastemel Ozturk, Yasin Maruf Ergen, Duygu Demirtas, Bora Gülhan, Fatih Ozaltin, Diclehan Orhan, Hasan Özen, Ali Düzova
Publikováno v:
Pediatric Nephrology.
Publikováno v:
Pediatric allergy, immunology, and pulmonology. 24(3)
Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disease characterized by recurrent bacterial and fungal infections and is due to impaired function of superoxide-producing nicotinamide adenine dinucleotide phosphate oxidase. Pat
Publikováno v:
Pediatric Nephrology (Berlin, Germany)
Background Knowledge on normal progress and treatment of Henoch-Schönlein purpura nephritis (HSPN) is limited. This study reviews outcome, clinical, pathological, and therapeutic factors affecting the prognosis of HSPN patients. Methods Forty-nine c
Autor:
Manish D. Sinha, Maria Stack, Maduri Raja, Eda Didem Kurt-Sukur, Barbara Ruggiero, Dean Wallace, Kjell Tullus, Louise Oni, Caroline A. Jones, Catherine Quinlan, Jenna F. Gritzfeld
Publikováno v:
RHEUMATOLOGY
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0d96f5184dfd2fce42e9e7df394d889
Autor:
Gülen Eda Utine, Yasemin Alanay, Pelin Ozlem Simsek-Kiper, Koray Boduroğlu, Eda Didem Kurt-Sukur
Publikováno v:
American Journal of Medical Genetics Part A. 167:2065-2074
This study shares data on 417 patients with genetic disorders of skeleton including 10 fetal autopsies encountered in a 5-year period at a tertiary university hospital in Ankara, Turkey. We included patients with osteochondrodysplasias, excluding ove