Ajlan Tukun
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Explore the profile of Ajlan Tukun including associated specialties, affiliations and a list of published articles.
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Articles
52
Citations
399
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0
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Recent Articles
1.
Kilavuz S, Basaranoglu M, Epcacan S, Bako D, Ozer A, Donmez Y, et al.
Metab Brain Dis
. 2022 Mar;
37(4):1283-1287.
PMID: 35254599
Gaucher disease type 2 is the most progressive and the rarest form of Gaucher disease, defined as the acute neuronopathic type. We presented two GD2 patients who died before three...
2.
Uner M, Saglam A, Tukun A, Aydin B, Akyol A, Uner A
Pediatr Dev Pathol
. 2022 Mar;
25(3):339-344.
PMID: 35227120
Constitutional mismatch repair deficiency (CMMRD) syndrome is characterized by biallelic mutations in a mismatch repair gene and is associated with development of childhood cancers and symptoms resembling neurofibromatosis type 1,...
3.
Yetim E, Topcuoglu M, Yurur Kutlay N, Tukun A, Oguz K, Arsava E
Sci Rep
. 2021 May;
11(1):10967.
PMID: 34040069
The chronological age of a person is a key determinant of etiology and prognosis in the setting of ischemic stroke. Telomere length, an indicator of biological aging, progressively shortens with...
4.
Hazan F, Gursoy S, Unalp A, Yilmaz U, Demirag B, Aydin Koker S, et al.
Neurol Sci
. 2021 Jan;
42(5):2045-2057.
PMID: 33443663
Neurofibromatosis type 1 (NF1) is caused by mutations in the NF1 gene. This retrospective study aims to evaluate the clinical manifestations and brain magnetic resonance images (MRI) analysis in 60...
5.
Korucu B, Tukun A, Helvaci O, Yeter H, Gonen S, Guz G, et al.
Turk J Med Sci
. 2020 Dec;
51(2):802-812.
PMID: 33306336
Background/aim: Bone disease is one of the most prominent complications after kidney transplantation. Bone diseases include osteoporosis, persistent secondary hyperparathyroidism, and avascular necrosis (AVN). We investigated the relationship between the...
6.
Gursoy S, Hazan F, Kaderli B, Mese T, Tukun A
J Clin Pediatr Dent
. 2020 Nov;
44(4):262-267.
PMID: 33167018
Objective: To evaluate orodental, facial, clinical and molecular characteristics of the patients with Noonan Syndrome (NS). Study Design: The orodental, clinical and molecular characteristics of 29 mutation-positive patients with NS...
7.
Cevik B, Mance-Calisir O, Atbasoglu E, Saka M, Alptekin K, Ucok A, et al.
J Psychiatr Res
. 2019 Feb;
111:169-185.
PMID: 30776705
Compared to the general population, individuals diagnosed with Schizophrenia (SCZ) experience a higher frequency and an earlier onset of chronic medical disorders, resulting in a reduction in life expectancy by...
8.
Eren-Keles E, Karabulut H, Cakmakli H, Adakli B, Kose S, Ugur-Dincaslan H, et al.
Genet Test Mol Biomarkers
. 2018 Nov;
22(12):680-685.
PMID: 30489176
Survivin is involved in the inhibition of apoptosis and the regulation of cell division. In addition to wild-type survivin (survivin-wt), at least four splice variants with differential functions (ΔEx3 and...
9.
Cihan M, Karabulut H, Yurur Kutlay N, Ruhi H, Tukun A, Olcay L
Turk J Haematol
. 2017 Feb;
34(2):151-158.
PMID: 28179212
Objective: Glucocorticoids (GCs) are the key drugs for the treatment of pediatric acute lymphoblastic leukemia (ALL). Herein, investigation of the relationship between the N363S and BclI polymorphisms of the GC...
10.
Altiner S, Karabulut H, Yararbas K, Tukun A, Collet C, Kocaay P, et al.
Clin Dysmorphol
. 2016 Nov;
26(3):175-178.
PMID: 27870659
No abstract available.