Baris Malbora
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Explore the profile of Baris Malbora including associated specialties, affiliations and a list of published articles.
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59
Citations
288
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Recent Articles
1.
Eker I, Cevik Ozdemir H, Yilmaz F, Yesilipek A, Kupesiz A, Uygun V, et al.
Turk J Haematol
. 2025 Jan;
42(1):47-55.
PMID: 39846291
Objective: Preimplantation genetic diagnosis (PGD) with human leukocyte antigen (HLA) typing represents a significant advancement in treating inherited hematological disorders, particularly thalassemia major. This technology enables the birth of healthy...
2.
Bozkurt C, Hazar V, Malbora B, Kupesiz A, Aygunes U, Fisgin T, et al.
Pediatr Transplant
. 2024 Apr;
28(3):e14758.
PMID: 38659218
Background: Data on the risk factors and outcomes for pediatric patients with SARS-CoV-2 infection (COVID-19) following hematopoietic stem cell transplantation (HSCT) are limited. Objectives: The study aimed to analyze the...
3.
Malbora B, Sarbay H, Dogusan Z, Atay A
Pediatr Transplant
. 2023 Dec;
28(1):e14648.
PMID: 38063291
Background: The aim of this study was to assess the impact of serum panel reactive antibodies (PRA) on the outcomes of allogeneic hematopoietic stem cell transplantation (HSCT) in pediatric thalassemia...
4.
Kuptanon C, Morimoto M, Nicoli E, Stephen J, Yarnell D, Dorward H, et al.
Front Genet
. 2023 Mar;
14:1072784.
PMID: 36968585
Chediak-Higashi syndrome (CHS) is rare autosomal recessive disorder caused by bi-allelic variants in the Lysosomal Trafficking Regulator () gene. Diagnosis is established by the detection of pathogenic variants in in...
5.
Ozalp Gerceker G, Yildirim B, Aricioglu Sulun A, Bektas M, Hekimci Ozdemir H, Malbora B
Eur J Oncol Nurs
. 2022 Oct;
61:102206.
PMID: 36240681
Purpose: This observational study carried out to determine the incidence of poor nutritional status and symptom burden in children undergoing chemotherapy treatment. Methods: The research data collected from 187 children...
6.
Yesilipek M, Uygun V, Kupesiz A, Karasu G, Ozturk G, Ertem M, et al.
Bone Marrow Transplant
. 2022 Feb;
57(5):760-767.
PMID: 35210564
We report the national data on the outcomes of hematopoietic stem cell transplantation (HSCT) for thalassemia major (TM) patients in Turkey on behalf of the Turkish Pediatric Stem Cell Transplantation...
7.
Tufekci O, Ozdemir H, Malbora B, Ozbek N, Yarali N, Erdem A, et al.
J Pediatr Hematol Oncol
. 2021 Oct;
44(1):e223-e226.
PMID: 34669357
Hepatitis-associated aplastic anemia (HAA) is a form of acquired aplastic anemia (AA) in which bone marrow failure develops after an acute attack of hepatitis. Bone marrow failure leading to AA...
8.
Celiksoy M, Koker M, Gezdirici A, Ozsoy S, Malbora B, Gungor S
Immunol Res
. 2021 Aug;
69(5):461-466.
PMID: 34333755
Leukocyte adhesion deficiency is an autosomal recessive primary immunodeficiency that has been divided into three types: LAD1 (beta-2 integrin (CD18) family deficiency/defect), LAD2 (absence of fucosylated carbonhydrate ligands for selectins)...
9.
Guipponi M, Masclaux F, Sloan-Bena F, Di Sanza C, Ozbek N, Peyvandi F, et al.
Haematologica
. 2021 Jul;
107(5):1064-1071.
PMID: 34196169
Congenital afibrinogenemia is the most severe congenital fibrinogen disorder, characterized by undetectable fibrinogen in circulation. Causative mutations can be divided into two main classes: null mutations with no protein production...
10.
Sarbay H, Hagverdiyeva S, Turkkan E, Akcay S, Atay A, Malbora B
Int Ophthalmol
. 2021 May;
41(7):2533-2538.
PMID: 33956257
Purpose: Different and various system complications and late effects may occur after hematopoietic stem cell transplantation (HSCT). It was aimed to obtain information about the frequency of ophthalmologic complications and...