Krstovski, N.

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  • Krstovski, N. (3)
Projects

Author's Bibliography

Targeted mutational profiling of childhood and adult acute lymphoblastic leukemia patients

Perić, Jelena; Karan-Đurašević, Teodora; Kostić, Tatjana ; Marjanović, Irena; Lazić, J.; Virijević, M.; Krstovski, N.; Dokmanović, Lidija; Tomin, D.; Vidović, A.; Suvajdžić-Vuković, Nada; Janić, D.; Pavlović, Sonja; Tošić, Nataša

(Ferrata Storti Foundation, Pavia, 2017)

TY  - CONF
AU  - Perić, Jelena
AU  - Karan-Đurašević, Teodora
AU  - Kostić, Tatjana 
AU  - Marjanović, Irena
AU  - Lazić, J.
AU  - Virijević, M.
AU  - Krstovski, N.
AU  - Dokmanović, Lidija
AU  - Tomin, D.
AU  - Vidović, A.
AU  - Suvajdžić-Vuković, Nada
AU  - Janić, D.
AU  - Pavlović, Sonja
AU  - Tošić, Nataša
PY  - 2017
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/1071
PB  - Ferrata Storti Foundation, Pavia
C3  - Haematologica-The Hematology Journal
T1  - Targeted mutational profiling of childhood and adult acute lymphoblastic leukemia patients
EP  - 653
SP  - 653
VL  - 102
UR  - https://hdl.handle.net/21.15107/rcub_imagine_1071
ER  - 
@conference{
author = "Perić, Jelena and Karan-Đurašević, Teodora and Kostić, Tatjana  and Marjanović, Irena and Lazić, J. and Virijević, M. and Krstovski, N. and Dokmanović, Lidija and Tomin, D. and Vidović, A. and Suvajdžić-Vuković, Nada and Janić, D. and Pavlović, Sonja and Tošić, Nataša",
year = "2017",
publisher = "Ferrata Storti Foundation, Pavia",
journal = "Haematologica-The Hematology Journal",
title = "Targeted mutational profiling of childhood and adult acute lymphoblastic leukemia patients",
pages = "653-653",
volume = "102",
url = "https://hdl.handle.net/21.15107/rcub_imagine_1071"
}
Perić, J., Karan-Đurašević, T., Kostić, T., Marjanović, I., Lazić, J., Virijević, M., Krstovski, N., Dokmanović, L., Tomin, D., Vidović, A., Suvajdžić-Vuković, N., Janić, D., Pavlović, S.,& Tošić, N.. (2017). Targeted mutational profiling of childhood and adult acute lymphoblastic leukemia patients. in Haematologica-The Hematology Journal
Ferrata Storti Foundation, Pavia., 102, 653-653.
https://hdl.handle.net/21.15107/rcub_imagine_1071
Perić J, Karan-Đurašević T, Kostić T, Marjanović I, Lazić J, Virijević M, Krstovski N, Dokmanović L, Tomin D, Vidović A, Suvajdžić-Vuković N, Janić D, Pavlović S, Tošić N. Targeted mutational profiling of childhood and adult acute lymphoblastic leukemia patients. in Haematologica-The Hematology Journal. 2017;102:653-653.
https://hdl.handle.net/21.15107/rcub_imagine_1071 .
Perić, Jelena, Karan-Đurašević, Teodora, Kostić, Tatjana , Marjanović, Irena, Lazić, J., Virijević, M., Krstovski, N., Dokmanović, Lidija, Tomin, D., Vidović, A., Suvajdžić-Vuković, Nada, Janić, D., Pavlović, Sonja, Tošić, Nataša, "Targeted mutational profiling of childhood and adult acute lymphoblastic leukemia patients" in Haematologica-The Hematology Journal, 102 (2017):653-653,
https://hdl.handle.net/21.15107/rcub_imagine_1071 .

Association between MTHFR, SLC19A1 and DHFR genetic polymorphisms and clinical and biochemical parameters of methotrexate induced toxicity in children with acute lymphoblastic leukaemia

Lazić, J.; Dokmanović, Lidija; Krstovski, N.; Pavlović, Sonja; Zukić, Branka; Kotur, Nikola; Milosević, G.; Janić, D.

(Elsevier Sci Ltd, Oxford, 2013)

TY  - CONF
AU  - Lazić, J.
AU  - Dokmanović, Lidija
AU  - Krstovski, N.
AU  - Pavlović, Sonja
AU  - Zukić, Branka
AU  - Kotur, Nikola
AU  - Milosević, G.
AU  - Janić, D.
PY  - 2013
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/693
PB  - Elsevier Sci Ltd, Oxford
C3  - European Journal of Cancer
T1  - Association between MTHFR, SLC19A1 and DHFR genetic polymorphisms and clinical and biochemical parameters of methotrexate induced toxicity in children with acute lymphoblastic leukaemia
EP  - S358
SP  - S358
VL  - 49
UR  - https://hdl.handle.net/21.15107/rcub_imagine_693
ER  - 
@conference{
author = "Lazić, J. and Dokmanović, Lidija and Krstovski, N. and Pavlović, Sonja and Zukić, Branka and Kotur, Nikola and Milosević, G. and Janić, D.",
year = "2013",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "European Journal of Cancer",
title = "Association between MTHFR, SLC19A1 and DHFR genetic polymorphisms and clinical and biochemical parameters of methotrexate induced toxicity in children with acute lymphoblastic leukaemia",
pages = "S358-S358",
volume = "49",
url = "https://hdl.handle.net/21.15107/rcub_imagine_693"
}
Lazić, J., Dokmanović, L., Krstovski, N., Pavlović, S., Zukić, B., Kotur, N., Milosević, G.,& Janić, D.. (2013). Association between MTHFR, SLC19A1 and DHFR genetic polymorphisms and clinical and biochemical parameters of methotrexate induced toxicity in children with acute lymphoblastic leukaemia. in European Journal of Cancer
Elsevier Sci Ltd, Oxford., 49, S358-S358.
https://hdl.handle.net/21.15107/rcub_imagine_693
Lazić J, Dokmanović L, Krstovski N, Pavlović S, Zukić B, Kotur N, Milosević G, Janić D. Association between MTHFR, SLC19A1 and DHFR genetic polymorphisms and clinical and biochemical parameters of methotrexate induced toxicity in children with acute lymphoblastic leukaemia. in European Journal of Cancer. 2013;49:S358-S358.
https://hdl.handle.net/21.15107/rcub_imagine_693 .
Lazić, J., Dokmanović, Lidija, Krstovski, N., Pavlović, Sonja, Zukić, Branka, Kotur, Nikola, Milosević, G., Janić, D., "Association between MTHFR, SLC19A1 and DHFR genetic polymorphisms and clinical and biochemical parameters of methotrexate induced toxicity in children with acute lymphoblastic leukaemia" in European Journal of Cancer, 49 (2013):S358-S358,
https://hdl.handle.net/21.15107/rcub_imagine_693 .

Clinical features of the most common fusion genes in childhood acute lymphoblastic leukemia

Lazić, J.; Tošić, Nataša; Dokmanović, Lidija; Krstovski, N.; Rodić, P.; Pavlović, Sonja; Janić, D.

(Humana Press Inc, Totowa, 2010)

TY  - JOUR
AU  - Lazić, J.
AU  - Tošić, Nataša
AU  - Dokmanović, Lidija
AU  - Krstovski, N.
AU  - Rodić, P.
AU  - Pavlović, Sonja
AU  - Janić, D.
PY  - 2010
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/423
AB  - Contemporary protocols ensure high-remission rate and long-term free survival in children with acute lymphoblastic leukemia (ALL), but small percentage of patients is still incurable. Molecular genetic methods helped to establish submicroscopic classification as well as minimal residual disease follow-up, considered to be responsible for relapse. Our study enrolled 70 pediatric patients with de novo ALL, analyzed using reverse transcriptase-polymerase chain reaction for the presence of four major risk-stratifying translocations (BCR/ABL, MLL/AF4, TEL/AML1, and E2A/PBX1). Bone marrow samples were collected at diagnosis, at the end of induction phase, and after intensive chemotherapy with the aim to establish the correlation between chromosomal aberration, clinical features, and treatment response. Presenting the results of this study, we offer another evidence of variable incidence and clinical characteristics of ALL subtypes.
PB  - Humana Press Inc, Totowa
T2  - Medical Oncology
T1  - Clinical features of the most common fusion genes in childhood acute lymphoblastic leukemia
EP  - 453
IS  - 2
SP  - 449
VL  - 27
DO  - 10.1007/s12032-009-9232-x
ER  - 
@article{
author = "Lazić, J. and Tošić, Nataša and Dokmanović, Lidija and Krstovski, N. and Rodić, P. and Pavlović, Sonja and Janić, D.",
year = "2010",
abstract = "Contemporary protocols ensure high-remission rate and long-term free survival in children with acute lymphoblastic leukemia (ALL), but small percentage of patients is still incurable. Molecular genetic methods helped to establish submicroscopic classification as well as minimal residual disease follow-up, considered to be responsible for relapse. Our study enrolled 70 pediatric patients with de novo ALL, analyzed using reverse transcriptase-polymerase chain reaction for the presence of four major risk-stratifying translocations (BCR/ABL, MLL/AF4, TEL/AML1, and E2A/PBX1). Bone marrow samples were collected at diagnosis, at the end of induction phase, and after intensive chemotherapy with the aim to establish the correlation between chromosomal aberration, clinical features, and treatment response. Presenting the results of this study, we offer another evidence of variable incidence and clinical characteristics of ALL subtypes.",
publisher = "Humana Press Inc, Totowa",
journal = "Medical Oncology",
title = "Clinical features of the most common fusion genes in childhood acute lymphoblastic leukemia",
pages = "453-449",
number = "2",
volume = "27",
doi = "10.1007/s12032-009-9232-x"
}
Lazić, J., Tošić, N., Dokmanović, L., Krstovski, N., Rodić, P., Pavlović, S.,& Janić, D.. (2010). Clinical features of the most common fusion genes in childhood acute lymphoblastic leukemia. in Medical Oncology
Humana Press Inc, Totowa., 27(2), 449-453.
https://doi.org/10.1007/s12032-009-9232-x
Lazić J, Tošić N, Dokmanović L, Krstovski N, Rodić P, Pavlović S, Janić D. Clinical features of the most common fusion genes in childhood acute lymphoblastic leukemia. in Medical Oncology. 2010;27(2):449-453.
doi:10.1007/s12032-009-9232-x .
Lazić, J., Tošić, Nataša, Dokmanović, Lidija, Krstovski, N., Rodić, P., Pavlović, Sonja, Janić, D., "Clinical features of the most common fusion genes in childhood acute lymphoblastic leukemia" in Medical Oncology, 27, no. 2 (2010):449-453,
https://doi.org/10.1007/s12032-009-9232-x . .
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