Search Results - "Izakova, S"

P445: CRYPTIC TRANSLOCATION T(5;11)(Q35;P15) RESULTING IN NUP98::NSD1 GENE FUSION IN ADULTS WITH DE NOVO ACUTE MYELOID LEUKEMIA (AML) by Ransdorfova, S., Markova, J., Valerianova, M., Brezinova, J., Onderkova, M., Mendlikova, I., Lizcova, L., Pavlistova, L., Svobodova, K., Izakova, S., Jonasova, A., Salek, C., Racil, Z., Zemanova, Z.

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Cytogenetic Clonal Evolution in Myelodysplastic Syndromes (MDS) with Isolated Del(5Q) by Zemanova, Z, Michalova, K, Brezinova, J, Svobodova, K, Lhotska, H, Sarova, I, Lizcova, L, Izakova, S, Ransdorfova, S, Pavlistova, L, Berkova, A, Skipalova, K, Belickova, M, Siskova, M, Neuwirtova, R, Cermak, J, Stopka, T, Jonasova, A

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170 MECHANISM OF FORMATION OF COMPLEX CHROMOSOMAL ABERRATIONS IN PATIENTS WITH MYELODYSPLASTIC SYNDROMES (MDS): CLONAL EVOLUTION OR CHROMOTHRIPSIS? by Zemanova, Z, Michalova, K, Brezinova, J, Lhotska, H, Svobodova, K, Sarova, I, Lizcova, L, Izakova, S, Ransdorfova, S, Krejcik, Z, Belickova, M, Siskova, M, Jonasova, A, Neuwirtova, R, Cermak, J

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264 Genomic imbalances in 73 patients with MDS and complex karyotypes by Zemanova, Z, Bystricka, D, Brezinova, J, Lizcova, L, Izakova, S, Sarova, I, Dostalova-Merkerova, M, Siskova, M, Jonasova, A, Neuwirtova, R, Cerna, O, Zmolikova, J, Cermak, J, Michalova, K

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Telomere length, molecular cytogenetic findings, and immunophenotypic features in previously untreated patients with B-chronic lymphocytic leukemia by Brezinova, J, Berkova, A, Vcelikova, S, Zemanova, Z, Izakova, S, Sarova, I, Cechova, H, Tajtlova, J, Grosova, L, Lizcova, L, Malinova, E, Zemanova, M, Cmunt, E, Karban, J, Trneny, M, Schwarz, J, Michalova, K

“…Telomere length was evaluated by terminal repeat fragment method in 66 previously untreated patients with B-chronic lymphocytic leukemia (B-CLL) to ascertain…”
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Topic: AS04-MDS Biology and Pathogenesis/AS04d-Somatic mutations by Zemanova, Z., Brezinova, J., Svobodova, K., Lhotska, H., Aghova, T., Vidlakova, D., Izakova, S., Lizcova, L., Ransdorfova, S., Mendlikova, I., Pavlistova, L., Belickova, M., Vesela, J., Siskova, M., Neuwirtova, R., Cermak, J., Stopka, T., Jonasova, A.

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P22 - Topic: AS04-MDS Biology and Pathogenesis/AS04d-Somatic mutations: THE DEL(5Q) SIZE IN MDS IS CORRELATED TO KARYOTYPE COMPLEXITY AND FREQUENCY OF TP53 MUTATIONS by Zemanova, Z., Brezinova, J., Svobodova, K., Lhotska, H., Aghova, T., Vidlakova, D., Izakova, S., Lizcova, L., Ransdorfova, S., Mendlikova, I., Pavlistova, L., Belickova, M., Vesela, J., Siskova, M., Neuwirtova, R., Cermak, J., Stopka, T., Jonasova, A.

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PB1710 ACUTE MYELOID LEUKEMIA WITH A RARE CRYPTIC T(8;16)(P11;P13) TRANSLOCATION AND MYST3/CREBBP FUSION by Brezinova, J., Ransdorfova, S., Valerianova, M., Onderkova, M., Izakova, S., Zemanova, Z., Markova, J., Vitek, A.

“…Background: The translocation t(8;16)(p11;p13) is a very rare cytogenetic finding in pediatric and adult de novo and therapy‐related acute myeloid leukemia…”
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90 - Cytogenetic Clonal Evolution in Myelodysplastic Syndromes (MDS) with Isolated Del(5Q) by Zemanova, Z., Michalova, K., Brezinova, J., Svobodova, K., Lhotska, H., Sarova, I., Lizcova, L., Izakova, S., Ransdorfova, S., Pavlistova, L., Berkova, A., Skipalova, K., Belickova, M., Siskova, M., Neuwirtova, R., Cermak, J., Stopka, T., Jonasova, A.

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The assessment of array comparative genomic hybridization in complex karyotype analyses by Bystřická, D, Zemanová, Z, Březinová, J, Gančarčíková, M, Grosová, L, Sárová, I, Izáková, S, Berková, A, Michalová, K

“…Molecular-cytogenetic methods were used to analyse and specify complex genome rearrangements in malignant cells. Twelve samples of bone marrow cells were…”
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PS1330 VARIABILITY IN THE EXTENT OF DEL(5Q) AND ITS CLINICAL IMPLICATION IN MYELODYSPLASTIC SYNDROMES (MDS) by Zemanova, Z., Brezinova, J., Michalova, K., Svobodova, K., Lhotska, H., Vesela, D., Izakova, S., Sarova, I., Lizcova, L., Ransdorfova, S., Pavlistova, L., Belickova, M., Vesela, J., Siskova, M., Neuwirtova, R., Cermak, J., Stopka, T., Jonasova, A.

“…Background: The interstitial deletion of the long arm of chromosome 5—del(5q)—is the most common cytogenetic abnormality in MDS occurring either as a sole…”
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