SVIBOR - Papers quoted in CC - project code: 3-01-086

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Papers quoted in Current Contents on project 3-01-086


Quoted papers: 4
Other papers: 69
Total: 73


Title: HETEROCHROMATIC VARIABILITY IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA

Authors:
Petković, Iskra (36570)
Nakić, Melita (74392)
Konja, Josip (76313)
Journal: Cancer Genetics Cytogenetics
ISSN: 0165-4608
Volume: 54
Year: 1991
Pages: from 67 to 69
Number of references: 13
Language: engleski
Summary: An analysis of the C-segment variability of chromosomes 1,9, i 16was carried out in 38 children with ALL, and 90 control subjects.When studying location variants, no differences were foundbetween group of patients and the normal controls. A largerquantity of structural heterochromatin was, however, observed onchromosomes 1,9, and 16, and a higher frequency of homologouschromosomes heteromorphism in children with ALL when comparedwith the control group.
Keywords: Acute Lymphoblastic Leukemia, C-segment of chromosomes 1,9,16, Variability of chromosomes

Title: CYTOGENETIC ANALYSIS IN CHILDREN WITH ACUTE NONLYMPHOCYTIC LEUKEMIA

Authors:
Petković, Iskra (36570)
Konja, Josip (76313)
Nakić, Melita (74392)
Journal: Cancer Genetics Cytogenetics
ISSN: 0165-4608
Volume: 58
Year: 1992
Pages: from 155 to 159
Number of references: 25
Language: engleski
Summary: In this work we present the results of cytogenetic analysis ofthe malignant cells in 27 children with acute nonlymphocyticleukemia (ANLL). The aim of our investigations was to determinethe frequency and types of chromosome aberations in ourpopulation of children with ANLL. Successful cytogenetic analysiswas carried out in 24 (89%) patients. Aberrant karyotypes ofmalignant cells were established in 58% of the cases. The mostfrequent chromosomal abnormality was t(8;21), identified in 5(20.8%) patients i.e., 4 of 10 M2-ANLL. Aberration frequency ofchromosome 11 was 16.6% and was identified in 3 of 8 M5-ANLL.Trisomy 8 and monosomy 7 were identified in one patient each withM3 and M2-ANLL, respectively, del (13), a rare chromosomeaberration in hemoblastosis, was found in a child with M1 t(8;21)and the loss of chromosome Y. Translocation t(1;11;21) with breakin regions 1q23, 11q22, is unusual and was identified in a boywith M2-ANLL; it can be considered as a variant form of thet(8;21).
Keywords: Cytogenetic analysis, chromosome, acute myeloid leukemia

Title: CHROMOSOMAL ANALYSIS OF TWO NEUROBLASTOMA

Authors:
Petković, Iskra (36570)
Nakić, Melita (74392)
Čepulić, Mladen (110195)
Konja, Josip (76313)
Journal: Cancer Genetics Cytogenetics
ISSN: 0165-4608
Volume: 65
Year: 1993
Pages: from 167 to 169
Number of references: 9
Language: engleski
Summary: We report the results of cytogenetic analysis in two childrenwith neuroblastoma. The analysis was performed on slides obtainedfrom a 24-hour bone marrow (BM) culture or by a direct method ofthe primary tumor tissue. The structural and numeric karyotypeaberrations were established, including structural aberrations ofchromosome 1. The finding of i(1q) and t(1;5) (p22;q13) is ofinterest because these chromosome aberations are rare in thistype of disease.
Keywords: Neuroblastoma, Crkomosome analysis

Title: UMBILICAL CORD BLOOD TRANSPLANTATION IN A PATIENT WITH PHILADELPHIA CHROMOSOME-POSITIVE CHRONIC MYELOID LEUKEMIA

Authors:
Bogdanić, Vinko
Nemet, Davor
Kaštelan, Andrija
Latin, Vera
Petrovečki, Mladen
Brkljačić - Šurlaković, Ljerka
Konja, Josip (76313)
Journal: TRANSPLANTATION
Number: 3
ISSN: 0041-1337
Volume: 56
Year: 1993
Pages: from 477 to 479
Number of references: 14
Language: engleski
Summary: Human umbilical cord blood contains haematopoieticstem/progenitor cells and is sufficient to induce haematopoieticreconstitution. In this case report, we present a 28-month oldgirl with chronic myelogenous Ph+ leukaemia who received HLAidentical cord blood graft. At birth, lo6 ml cord blood wascollected and frozen in 10% DMSO at -196 C. The patient receiveda total body irradiation (12 Gy in three daily fraction) andcyclophosphamide (120 mg/kg) followed by cord blood infusion. Atotal of 8.3 x 10 6/ml nucleated and 0.8 x 10 9/kg wastransplanted. Cyclosporin was used as a GVHD prophylaxis.Engraftment was documented on day 18 without any symptoms ofacute GVHD.Tus these results suggest that umbilical-cord blood isa sufficient source of cells for haematologic reconstitution.
Keywords: Umbilical cord blood transplantation, chronic myeloid leukemia


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