Oguz Soylemezoglu
Overview
Explore the profile of Oguz Soylemezoglu including associated specialties, affiliations and a list of published articles.
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125
Citations
855
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Recent Articles
1.
Yasar H, Leventoglu E, Buyukkaragoz B, Fidan K, Bakkaloglu S, Soylemezoglu O
Turk J Pediatr
. 2024 Nov;
66(5):649-657.
PMID: 39582457
Background: Dent's disease (DD) is a rare X-linked recessive tubulopathy characterized by low molecular weight proteinuria, hypercalciuria, nephrocalcinosis/nephrolithiasis and chronic kidney disease. With this manuscript, we reported three patients diagnosed...
2.
Celegen K, Gulhan B, Fidan K, Yuksel S, Yilmaz N, Yilmaz A, et al.
Clin Exp Nephrol
. 2024 Jul;
28(10):1038-1039.
PMID: 38970651
No abstract available.
3.
Celegen K, Gulhan B, Fidan K, Yuksel S, Yilmaz N, Yilmaz A, et al.
Clin Exp Nephrol
. 2024 May;
28(10):1027-1037.
PMID: 38704765
Background: Atypical hemolytic uremic syndrome (aHUS) is a rare, mostly complement-mediated thrombotic microangiopathy. The majority of patients are infants. In contrast to infantile-onset aHUS, the clinical and genetic characteristics of...
4.
Gulhan B, Ekici O, Dursun I, Goknar N, Yuksel S, Alaygut D, et al.
Clin Nephrol
. 2024 May;
102(2):79-88.
PMID: 38699986
Aims: Hepatocyte nuclear factor 1β () mutations are the most common monogenic cause of congenital anomalies of the kidney and urinary tract (CAKUT). We aimed to investigate clinical and genetic...
5.
Gulhan B, Ozaltin F, Fidan K, Ozcakar Z, Soylemezoglu O
Turk J Pediatr
. 2024 Mar;
66(1):1-16.
PMID: 38523374
Classical clinical triad of hemolytic uremic syndrome (HUS) is microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury associated with endothelial cell injury. Several situations, including infections, medications, malignancies, and transplantation...
6.
Leventoglu E, Ogut B, Gonul I, Fidan K, Soylemezoglu O
Klin Padiatr
. 2024 Feb;
236(5):301-302.
PMID: 38330998
Acute postinfectious glomerulonephritis (APIGN) is one of the most common causes of acute glomerulonephritis in children. It may lead to inflammation and proliferation of glomerular tissue through immunologic mechanisms (Balasubramanian...
7.
Huseynli B, Buyukkaragoz B, Leventoglu E, Fidan K, Bakkaloglu S, Ozturk A, et al.
Semin Dial
. 2024 Jan;
37(2):122-130.
PMID: 38228322
Spontaneous tendon or ligament ruptures are quite rare and mostly associated with chronic systemic diseases such as diabetes mellitus, systemic lupus erythematosus, rheumatoid arthritis, and chronic kidney disease (CKD). In...
8.
Grabitz C, Sugianto R, Doyon A, Azukaitis K, Anarat A, Bacchetta J, et al.
Transplantation
. 2024 Jan;
108(5):1212-1219.
PMID: 38227773
Background: Children requiring kidney replacement therapy experience high burden of cardiovascular (CV) disease leading to increased mortality. Intima-media thickness (IMT) indicating atherosclerosis is a validated surrogate marker for future CV...
9.
Sunar-Yayla E, Esmeray Senol P, Gezgin Yildirim D, Soylemezoglu O
Turk J Pediatr
. 2024 Jan;
65(6):973-979.
PMID: 38204312
Background: Familial Mediterranean fever (FMF) is the most common and autosomal recessive inherited autoinflammatory disease. The most common signs and symptoms are fever, abdominal pain, chest pain, and arthritis. The...
10.
Ozturk N, Kaya Z, Boyunaga O, Soylemezoglu O
CEN Case Rep
. 2024 Jan;
13(4):302-305.
PMID: 38189897
There is no information on renal vein thrombosis induced by COVID-19 infection in a neonate. Few cases of renal vein thrombosis caused by COVID-19 infection have been reported in predominantly...