Umran Caliskan
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Explore the profile of Umran Caliskan including associated specialties, affiliations and a list of published articles.
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52
Citations
219
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Recent Articles
1.
Simsek A, Tokgoz H, Caliskan U
Turk J Pediatr
. 2025 Mar;
67(1):117-122.
PMID: 40084731
Background: Granulocytic sarcoma (GS), or myeloid sarcoma or chloroma, is a tumoral mass containing myeloblasts and immature granulocytes in an anatomic site other than the bone marrow. GS is very...
2.
Zulfikar B, Koc B, Sahin F, Sasmaz H, Kavakli K, Balkan C, et al.
Res Pract Thromb Haemost
. 2024 Nov;
8(7):102588.
PMID: 39582809
Background: Hemophilia B (HB), an X-linked recessive inherited bleeding disorder, exhibits a high prevalence among males. Objectives: To present the first national cohort of persons with HB to define the...
3.
Akyol S, Yilmaz E, Tokgoz H, Karaman K, Pekpak E, Ozcan A, et al.
Ann Hematol
. 2024 Nov;
104(1):123-130.
PMID: 39579250
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disease, with a high mortality if left untreated. In addition, the disease has unique diagnostic challenges. Therefore, despite the existing guidelines on management, current...
4.
Gok V, Leblebisatan G, Gurlek Gokcebay D, Guler S, Dogan M, Bozdogan S, et al.
Br J Haematol
. 2024 May;
205(1):236-242.
PMID: 38811201
Pyruvate kinase (PK) is a key enzyme of anaerobic glycolysis. The genetic heterogeneity of PK deficiency (PKD) is high, and over 400 unique variants have been identified. Twenty-nine patients who...
5.
Hangul M, Kose M, Pekcan S, Caliskan U, Tokgoz H, Tana Aslan A, et al.
Balkan Med J
. 2022 Sep;
39(5):366-373.
PMID: 36089832
Background: Pulmonary embolism is a clinical condition caused by the obstruction of the pulmonary artery and its branches with endogenous, exogenous embolism, or local thrombus formation. It is a rare...
6.
Karaman S, Kebudi R, Kizilocak H, Karakas Z, Demirag B, Evim M, et al.
J Pediatr Hematol Oncol
. 2022 Aug;
44(8):e1039-e1045.
PMID: 36036521
Background: Central nervous system fungal infections (CNSFI) are seen in patients with hematologic malignancies and have high morbidity and mortality. Because of their rarity, there is limited data on CNSFI...
7.
Kavakli K, Ozbek S, Antmen A, Sahin F, Aytac S, Kupesiz A, et al.
Turk J Haematol
. 2021 Jan;
38(2):101-110.
PMID: 33508912
Objective: This study aimed to observe the preventive effect of prophylactic treatment on joint health in people with hemophilia (PwH) and to investigate the importance of integration of ultrasonographic examination...
8.
Karapinar D, Patiroglu T, Metin A, Caliskan U, Celkan T, Yilmaz B, et al.
Pediatr Blood Cancer
. 2019 Jul;
66(10):e27923.
PMID: 31321910
Background: Severe congenital neutropenia is a rare disease, and autosomal dominantly inherited ELANE mutation is the most frequently observed genetic defect in the registries from North America and Western Europe....
9.
Belviranli S, Ozkagnici A, Tokgoz H, Bitirgen G, Caliskan U
Eur J Ophthalmol
. 2019 Jun;
31(2):NP106-NP108.
PMID: 31187640
Purpose: To describe a case of traumatic hyphema in a patient with severe hemophilia A. Case: We present a case of a 16-year-old boy with severe hemophilia A who presented...
10.
Gultekin N, Yilmaz F, Tokgoz H, Tarakci N, Caliskan U
Indian Pediatr
. 2019 Mar;
56(2):143-144.
PMID: 30819996
Introduction: Glanzmann thrombasthenia is a rare congenital platelet dysfunction. Case Characteristics: A 2-day-old male neonate delivered at 35 weeks' gestation was referred with extensive bruising and jaundice. His elder sibling...