Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Melita Nakić"'
Autor:
Gordana Jakovljević, Božo Krušlin, Srđan Rogošić, Ika Kardum-Skelin, Melita Nakić, Sanja Mrsić-Davidović, Renata Zadro
Publikováno v:
Pediatric Blood & Cancer. 54:606-609
We report a 2-year-old female with a subcutaneous tumor who was initially misdiagnosed as suffering from Ewing sarcoma with a positive EWSR1 rearrangement and EWS/FLI1 transcript. After finding lymphoblasts in peripheral blood, the diagnosis of acute
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61f06bca79b0be5b6becc75bf82bf6f0
https://doi.org/10.1002/pbc.22365
https://doi.org/10.1002/pbc.22365
Publikováno v:
Cancer Genetics and Cytogenetics. 88:57-65
This paper presents the results of cytogenetic analysis in 55 children with acute lymphatic leukemia (ALL). Acquired chromosome aberrations were identified in 35 (63.6%) children. Difference in frequency of clonal aberrations depending on age of pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c1da7fbd89d8fcdeaa1472ebd88c226
https://doi.org/10.1016/0165-4608(95)00293-6
https://doi.org/10.1016/0165-4608(95)00293-6
Autor:
Gordana Jakovljević, Ika Kardum-Skelin, Srđan Rogošić, Srđana Čulić, Jasminka Stepan, Alenka Gagro, Ivančica Škarić, Lili Mikecin, Aleksandra Bonevski, Ingeborg Barišić, Melita Nakić
Publikováno v:
Collegium antropologicum
Volume 34
Issue 2
Volume 34
Issue 2
Familial hemophagocytic lymphohistiocytosis (FLH) is an autosomal recessively inherited multisystem disease. This defect in cellular cytotoxicity is a life threatening condition characterized by fever, rash, splenomegaly, cytopenias and neurologic ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::6506e6e93a3d264b66208e6867878636
https://pubmed.ncbi.nlm.nih.gov/20698142
https://pubmed.ncbi.nlm.nih.gov/20698142
Publikováno v:
Collegium antropologicum
Volume 34
Issue 1
Volume 34
Issue 1
Juvenile myelomonocytic leukemia (JMML) is a rare clonal myeloproliferative disorder affecting young children. The natural course of JMML is rapidly fatal with 80% of patients surviving less than three years. Allogeneic hematopoietic stem cell transp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::c7710ab3eb94bfaae6e326627fefcedc
https://hrcak.srce.hr/51273
https://hrcak.srce.hr/51273
Autor:
Melita Nakić, Vlasta Duranovic, Vlatka Mejaški-Bošnjak, Lucija Lujić, J. Lenicek Krleza, Renata Zadro, D. Coen Herak
Pediatric stroke is significantly less common than stroke in adults, but represents a major challenge to public health authorities. The aim of this retrospective study was to identify the total and annual number of children younger than 18 years with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4f228c5d81e25e2a5518f5753120ac1
https://www.bib.irb.hr/427412
https://www.bib.irb.hr/427412
We present a 6-year-old girl with acute myeloid leukemia (AML)-M5, normal karyotype at the time of diagnosis, and t(1 ; 3)(p36 ; q21) at relapse. The t(1 ; 3)(p36 ; q21) is a rare but recurrent chromosomal aberration in human malignancies that it is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::012781e0a1965d7789501b1cde70f80d
https://www.bib.irb.hr/390854
https://www.bib.irb.hr/390854
Publikováno v:
Cancer Genetics and Cytogenetics. 65:167-169
We report the results of cytogenetic analysis in two children with neuroblastoma. The analysis was performed on slides obtained from a 24-hour bone marrow (BM) culture or by a direct method of the primary tumor tissue. The structural and numeric kary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2120eb6daab909508c6d4eb99016acc7
https://doi.org/10.1016/0165-4608(93)90228-e
https://doi.org/10.1016/0165-4608(93)90228-e
Autor:
Melita Nakić, Vesna Žižić
Publikováno v:
Medicus
Volume 10
Issue 2_Maligni tumori
Volume 10
Issue 2_Maligni tumori
Članak daje pregled mogućnosti citodijagnostike i tumorskih biljega u ranom otkrivanju i dijagnosticiranju malignih bolesti, posebno u djece, te prognostičko značenje u terapijskom praćenju bolesnika. Obrađene su citodijagnostičke metode uz su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______951::66f7a9b15a5c7f1fc005f9844253c019
https://hrcak.srce.hr/19343
https://hrcak.srce.hr/19343
Publikováno v:
Cancer Genetics and Cytogenetics. 54:67-69
An analysis of the C-segment variability of chromosomes 1, 9, and 16 was carried out in 38 children with ALL, and 90 control subjects. When studying location variants, no differences were found between group of patients and the normal controls. A lar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d855aaf18b09ea058c74d8e5ae028462
https://doi.org/10.1016/0165-4608(91)90031-o
https://doi.org/10.1016/0165-4608(91)90031-o
Publikováno v:
Cancer genetics and cytogenetics. 76(2)
The results of a cytogenetic analysis in an embryonal rhabdomyosarcoma are presented. A tetraploid karyotype with double minute chromosomes (dmin) was identified using a direct method of tumor tissue treatment. In 5% of the examined cells, evidence o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e99867a4a1af8f4a44f0758b2377043f
https://pubmed.ncbi.nlm.nih.gov/7923061
https://pubmed.ncbi.nlm.nih.gov/7923061