Ozlem Anlas
Overview
Explore the profile of Ozlem Anlas including associated specialties, affiliations and a list of published articles.
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Articles
12
Citations
14
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0
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Recent Articles
1.
Kamis S, Cil M, Yagci B, Anlas O
J Med Case Rep
. 2024 Nov;
18(1):562.
PMID: 39568018
Background: Diamond-Blackfan anemia is a rare congenital disorder characterized by erythroid hypoplasia and is associated with mutations in ribosomal protein genes. This case report describes a novel variant in the...
2.
Ozalp O, Anlas O
Indian J Hematol Blood Transfus
. 2024 May;
40(2):268-280.
PMID: 38708170
Hemoglobinopathies are the most common monogenic disorders in the world. Traditional diagnostic algorithms generated by conventional methods for thalassemia can be labor-intensive and time-consuming due to the complexities of the...
3.
Sanli Z, Anlas O
Mol Syndromol
. 2024 Apr;
15(2):89-95.
PMID: 38585552
Introduction: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common form of familial cerebral small vessel disease in adults and is caused by variants. Clinical...
4.
Kisla Ekinci R, Anlas O, Ozalp O
Arch Rheumatol
. 2023 Sep;
38(2):299-306.
PMID: 37680524
Objectives: This study aims to investigate a genetic panel in patients with periodic fever, aphthous stomatitis, pharyngitis, and adenitis (PFAPA) syndrome and examine its performance for an accurate differential diagnosis....
5.
Sarigecili E, Anlas O
Ann Indian Acad Neurol
. 2023 Aug;
26(3):290-293.
PMID: 37538433
No abstract available.
6.
Anlas O, Olmez A, Karaman B, Duzcan F, Yuksel S, Tumkaya F, et al.
Mol Syndromol
. 2023 Jun;
14(3):246-253.
PMID: 37323193
Introduction: Chromosomal abnormalities are mostly found in 0.5-0.8% of live-born infants with developmental and morphological defects. Paracentric inversions are structural intrachromosomal rearrangements resulting in a risk of chromosomally unbalanced gametes...
7.
Kisla Ekinci R, Ozalp O, Anlas O, Atmis B, Ata A, Balci S
Int J Rheum Dis
. 2023 Apr;
26(10):2064-2068.
PMID: 37088798
Multicentric carpotarsal osteolysis (MCTO) syndrome, is typically characterized by progressive bone resorption in especially carpal and tarsal bones, in addition to abnormal facial appearance and proteinuria. This disorder is caused...
8.
Boga Z, Anlas O, Acik V, Ozalp O, Gezercan Y
Turk Neurosurg
. 2023 Mar;
33(3):423-430.
PMID: 36951025
Aim: To elucidate the role of microRNAs (miRNAs) in the development of cerebral aneurysms. Material And Methods: This study compared the expression levels of miR-26a, miR-29a and miR-448-3p in 50...
9.
Kisla Ekinci R, Zararsiz A, Urel Demir G, Anlas O
Pediatr Allergy Immunol Pulmonol
. 2022 Sep;
35(3):129-132.
PMID: 36121781
Sideroblastic anemia with B cell immunodeficiency, periodic fevers, and developmental delay (SIFD) syndrome is caused by biallelic TRNT1 mutations. TRNT1 gene encodes a CCA-adding tRNA nucleotidyl transferase enzyme. Mutant TRNT1...
10.
Kisla Ekinci R, Anlas O, Ozalp O
Eur J Med Genet
. 2022 Jul;
65(8):104555.
PMID: 35777620
Deficiency of Adenosine deaminase 2 (DADA2) is a monogenic inflammatory disease, caused by mutations in ADA2 gene, which encodes an extracellular enzyme acting as a monocyte differentiation factor. DADA2 is...