Murat Özcan
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Murat Özcan has a total of 18 co-authors. Here are the top co-authors by number of shared publications:
Serdar Ümit Sarıcı
2 shared publicationsAli Bay
Gaziantep University, Faculty of Medicine, Department of Pediatrics, Division of Pediatric Hematology, Gaziantep, Turkey
1 shared publicationDemet Altun
1 shared publicationElif Habibe Aktekin
Gaziantep University, Faculty of Medicine, Department of Pediatrics, Division of Pediatric Hematology, Gaziantep, Turkey
1 shared publication- Fahriye Eksi
Department of Medical Microbiology, Faculty of Medicine, Gaziantep University, Gaziantep, Turkey
1 shared publication Fatma Begüm Tokatlıoğlu Özcan
1 shared publication
Latest Publications
- 4 May 2018
- Published by Caleo in Turkish Archives of Pediatrics
- Vol. 53 (1) , 45-47
Kala-Azar and leukemia: A rare association
Visceral leishmaniasis is an infectious disease that infects and multiplies in macrophages of the liver, spleen, and bone marrow. The most common clinical features are fever, splenomegaly, and anemia. Anemia, leucopenia, and thrombocytopenia are the main hematologic abnormalities commonly seen in visceral leishmaniasis. These findings can be seen in several types of hematologic disorders. The findings are similar to most hematologic disorders and so may make diagnosis problematic. It is difficult to confirm when it is seen except in epidemiologic areas. It can be fatal if it is not treated and appropriate treatment can be lifesaving. In this article a 12 year-old male patient who was followed-up with diagnosis of acute lymphoblastic leukemia and received maintenance therapy while being under remission after BFM-ALL-2000 treatment protocol and diagnosed with hemophagocytic lymphohistiocytosis due to Kala-azar during this period was presented.
- 4 May 2018
- Published by Caleo in Turkish Archives of Pediatrics
- Vol. 53 (1) , 45-47
Kala-Azar and leukemia: A rare association
Visceral leishmaniasis is an infectious disease that infects and multiplies in macrophages of the liver, spleen, and bone marrow. The most common clinical features are fever, splenomegaly, and anemia. Anemia, leucopenia, and thrombocytopenia are the main hematologic abnormalities commonly seen in visceral leishmaniasis. These findings can be seen in several types of hematologic disorders. The findings are similar to most hematologic disorders and so may make diagnosis problematic. It is difficult to confirm when it is seen except in epidemiologic areas. It can be fatal if it is not treated and appropriate treatment can be lifesaving. In this article a 12 year-old male patient who was followed-up with diagnosis of acute lymphoblastic leukemia and received maintenance therapy while being under remission after BFM-ALL-2000 treatment protocol and diagnosed with hemophagocytic lymphohistiocytosis due to Kala-azar during this period was presented.
- Open Access
- 1 January 2018
- Published by Cukurova Medical Journal in Cukurova Medical Journal
- Vol. 43 (2) , 493-494
Congenital giant melanocytic nevi in newborn
- 1 January 2018
- Published by Cukurova Medical Journal in Cukurova Medical Journal
- Vol. 43 (2) , 493-494
Open AccessCongenital giant melanocytic nevi in newborn
- 11 October 2017
- Published by Caleo in Turkish Archives of Pediatrics
- Vol. 52 (3) , 162-164
Hyperbilirubinemia due to minor blood group (anti-E) incompatibility in a newborn: a case report
In addition to Rh and ABO incompatibilities subgroup incompatibilities may rarely play a role among the causes of hemolytic anemia and indirect hyperbilirubinemia in newborns. The most common minor blood group antigens that cause blood incompatibility between the mother and baby are C, c, E, e, Kell, Duffy, Diego, Kidd and MNSs antigens. In this article, a newborn in whom hyperbilirubinemia due to anti-E minor blood group incompatibility developed and was treated with phototherapy succesfully is presented and minor blood group incompatibilities due to anti-E are reviewed.
- 11 October 2017
- Published by Caleo in Turkish Archives of Pediatrics
- Vol. 52 (3) , 162-164
Hyperbilirubinemia due to minor blood group (anti-E) incompatibility in a newborn: a case report
In addition to Rh and ABO incompatibilities subgroup incompatibilities may rarely play a role among the causes of hemolytic anemia and indirect hyperbilirubinemia in newborns. The most common minor blood group antigens that cause blood incompatibility between the mother and baby are C, c, E, e, Kell, Duffy, Diego, Kidd and MNSs antigens. In this article, a newborn in whom hyperbilirubinemia due to anti-E minor blood group incompatibility developed and was treated with phototherapy succesfully is presented and minor blood group incompatibilities due to anti-E are reviewed.
- Open Access
- 30 September 2017
- Published by Cukurova Medical Journal in Cukurova Medical Journal
- Vol. 42 (3) , 600-601
Kayısı çekirdeğine bağlı akut siyanür zehirlenmesi
Tr en Kayısı çekirdeğine bağlı akut siyanür zehirlenmesi
- 30 September 2017
- Published by Cukurova Medical Journal in Cukurova Medical Journal
- Vol. 42 (3) , 600-601
Open AccessKayısı çekirdeğine bağlı akut siyanür zehirlenmesi
Tr en Kayısı çekirdeğine bağlı akut siyanür zehirlenmesi
- 1 January 2016
- Published by Galenos Yayinevi in Journal of Dr Behcet Uz Children s Hospital
Human metapneumovirus pneumonia: Case report
- 1 January 2016
- Published by Galenos Yayinevi in Journal of Dr Behcet Uz Children s Hospital
Human metapneumovirus pneumonia: Case report