Tadej Pajic
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Explore the profile of Tadej Pajic including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
60
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0
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Recent Articles
1.
Drofenik A, Blinc A, Bozic Mijovski M, Pajic T, Vrtovec M, Sever M
Radiol Oncol
. 2024 Oct;
58(4):565-572.
PMID: 39361963
Background: V617F () mutation is associated with clonal hemopoiesis in myeloproliferative neoplasms as well as with faster progression of cardiovascular diseases. Little is known about the relationship between allele burden...
2.
Anzej Doma S, Kraljic N, Kristan A, Debeljak N, Maver A, Pajic T, et al.
Front Med (Lausanne)
. 2024 Sep;
11:1440712.
PMID: 39309680
Background: Congenital erythrocytosis (CE) is increasingly recognized as the cause of erythrocytosis in patients in whom polycythemia vera and secondary acquired causes have been excluded. The aim of our study...
3.
Pajic T
Methods Mol Biol
. 2023 May;
2663:233-251.
PMID: 37204714
Laboratory testing for Factor V Leiden and Prothrombin G20210A genetic variants permits defining the increased relative risk for venous thromboembolism in selected patients. Laboratory DNA testing for these variants may...
4.
Belcic Mikic T, Vratanar B, Pajic T, Anzej Doma S, Debeljak N, Zupan I, et al.
J Clin Med
. 2021 Dec;
10(24).
PMID: 34945099
, and mutations define clonal thrombocytosis in about 90% of patients with sustained isolated thrombocytosis. In the remainder of patients (triple-negative patients) diagnosing clonal thrombocytosis is especially difficult due to...
5.
Kristan A, Pajic T, Maver A, Rezen T, Kunej T, Kolic R, et al.
Front Genet
. 2021 Aug;
12:689868.
PMID: 34349782
An erythrocytosis is present when the red blood cell mass is increased, demonstrated as elevated hemoglobin and hematocrit in the laboratory evaluation. Congenital predispositions for erythrocytosis are rare, with germline...
6.
Belcic Mikic T, Pajic T, Zver S, Sever M
Int J Mol Sci
. 2021 Apr;
22(7).
PMID: 33806036
mutations are a revolutionary discovery and represent an important hallmark of myeloproliferative neoplasms (MPN), especially essential thrombocythemia and primary myelofibrosis. To date, several mutations were identified, with only frameshift mutations...
7.
Kristan A, Gaspersic J, Rezen T, Kunej T, Kolic R, Vuga A, et al.
J Clin Lab Anal
. 2021 Feb;
35(4):e23715.
PMID: 33534944
Background: Erythrocytosis is a condition with an excessive number of erythrocytes, accompanied by an elevated haemoglobin and/or haematocrit value. Congenital erythrocytosis has a diverse genetic background with several genes involved...
8.
Pajic T, Belcic Mikic T, Podgornik H, Klun J, Sucurovic S, Zver S, et al.
J Vis Exp
. 2020 Sep;
(162).
PMID: 32925885
High resolution melting analysis (HRM) is a powerful method for genotyping and genetic variation scanning. Most HRM applications depend on saturating DNA dyes that detect sequence differences, and heteroduplexes that...
9.
Anzej Doma S, Skerget M, Pajic T, Sever M
Ann Hematol
. 2020 Jan;
99(3):519-525.
PMID: 31970449
One hundred and eight consecutive acute myeloid leukemia (AML) patients aged 60 or less treated with two different induction regimens were retrospectively analyzed. Induction regimen for the first 50 consecutive...
10.
Belcic Mikic T, Pajic T, Sever M
Sci Rep
. 2019 Dec;
9(1):19838.
PMID: 31882869
Suspicion of myeloproliferative neoplasms (MPNs) and especially essential thrombocythemia (ET) in primary care is often based solely on blood counts, with patients referred to a haematologist without a thorough evaluation....