T Celkan
Overview
Explore the profile of T Celkan including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
204
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0
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Recent Articles
1.
Tuysuz G, Yildiz I, Ozdemir N, Adaletli I, Kurugoglu S, Apak H, et al.
Mediterr J Hematol Infect Dis
. 2019 Jun;
11(1):e2019035.
PMID: 31205639
Objectives: To review a single center outcome of patients with Langerhans Cell Histiocytosis diagnosed at a tertiary referral hospital from Turkey.Methods: The files between 1989 and 2015 of 80 patients...
2.
Celkan T, Apak H, Yuksel L, Ercan G, Erener T, Diren S, et al.
Turk J Haematol
. 2016 Jun;
18(4):281-3.
PMID: 27264470
Gaucher-like cells (GLC) are sometimes indistinguishable from real Gaucher cells. GLC can be detected in various diseases. We present a 4.5 year old boy with massive cervical lympadenopathy and an...
3.
Celkan T, Apak H, Ozkan A, Aki H, Tasyurekli M, Yuksel L, et al.
Turk J Haematol
. 2016 Jun;
18(3):203-6.
PMID: 27264259
Unlabelled: A boy with no previous history of bleeding presented with ecchymoses and splenomegaly. He was followed up for thrombocytopenia and micromegakaryocytes for 20 months till clinically malignancy was diagnosed....
4.
Ng O, Erbilgin Y, Firtina S, Celkan T, Karakas Z, Aydogan G, et al.
Blood Cancer J
. 2014 Mar;
4:e192.
PMID: 24632884
WNT signaling has been implicated in the regulation of hematopoietic stem cells and plays an important role during T-cell development in thymus. Here we investigated WNT pathway activation in childhood...
5.
Tuysuz G, Ozdemir N, Sonmez E, Kannengiesser C, Celkan T
Genet Couns
. 2014 Feb;
24(4):393-7.
PMID: 24551982
Hereditary hyperferritinemia cataract syndrome (HHCS) is a rare disorder with an autosomal dominant trait. The disease is defined with early onset cataract and hyperferritinemia without iron overload. Here, we report...
6.
Peyvandi F, Palla R, Menegatti M, Siboni S, Halimeh S, Faeser B, et al.
J Thromb Haemost
. 2012 Feb;
10(4):615-21.
PMID: 22321862
Background: The European Network of Rare Bleeding Disorders (EN-RBD) was established to bridge the gap between knowledge and practise in the care of patients with RBDs. Objectives: To explore the...
7.
8.
Karaman S, Ercan O, Yildiz I, Bolayirli M, Celkan T, Apak H, et al.
J Pediatr Endocrinol Metab
. 2010 Sep;
23(7):669-74.
PMID: 20857839
Background: It is well known that survivors of acute lymphoblastic leukemia (ALL) show a tendency to become overweight. Cranial irradiation (CRT), is considered to be the primary risk factor for...
9.
Unuvar A, Kavakli K, Baytan B, Kazanci E, Sayli T, OREN H, et al.
Haemophilia
. 2007 Dec;
14(2):315-22.
PMID: 18081830
The development of an inhibitor against factor VIII (FVIII) is a serious complication in children with haemophilia A. Immune tolerance induction (ITI) therapy is generally considered to be the best...
10.
Berber E, Fidanci I, Un C, El-Maarri O, Aktuglu G, Gurgey A, et al.
Haemophilia
. 2006 Jul;
12(4):398-400.
PMID: 16834740
The most common cause for severe cases of hemophilia A is the homologous recombination involving intron 22 and related sequences outside the F8 gene. F8 coding regions of the gene...