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Hydrops fetalis and failure of hematopoietic stem cell transplantation – A long route to the diagnosis of SPTA1-associated hereditary spherocytosis

Blood cells, molecules, & diseases, 2022-07, Vol.95, p.102664-102664, Article 102664

2022

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Effect of CALR and JAK2 mutations on the clinical and hematological phenotypes of the disease in patients with myelofibrosis - long-term experience from a single center

Neoplasma, 2018, Vol.65 (2), p.296

2018

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P1564: FAMILIAL ERYTHROCYTOSES IN THE CZECH REPUBLIC ‐ GENETIC CHARACTERIZATION AND HEPCIDIN REGULATION

HemaSphere, 2022-06, Vol.6 (Suppl), p.1445-1446

2022

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Thrombin Generation Testing in Patients with Myelofibrosis

Clinical laboratory (Heidelberg), 2018-01, Vol.64 (9), p.1373

2018

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Flow cytometric monitoring of the in vitro inhibition of the phosphorylation of CRKL and of SRC family kinases in patients with chronic myelogenous leukemia treated with tyrosine kinase inhibitors

International journal of laboratory hematology, 2015-02, Vol.37 (1), p.e11-e15

2015

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FcγRIIIA receptor genotype does not influence an outcome in patients with follicular lymphoma treated with risk-adapted immunochemotherapy

Neoplasma, 2011, Vol.58 (3), p.263

2011

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High Incidence of Unbalanced Chromosomal Changes in Mantle Cell Lymphoma Detected by Comparative Genomic Hybridization

Leukemia & lymphoma, 2004-09, Vol.45 (9), p.1835-1846

2004

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Operational cures after interferon-alpha in patients with chronic myeloid leukemia in Central and Northern Moravia

Journal of interferon & cytokine research, 2012-05, Vol.32 (5), p.230

2012

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Non-anemic homozygous β° thalassemia in an African-American family : Association of high fetal hemoglobin levels with β thalassemia alleles

American journal of hematology, 2001-09, Vol.68 (1), p.43-50

2001

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Cryptic MLL-AF10 fusion caused by insertion of duplicated 5′ part of MLL into 10p12 in acute leukemia: a case report

Cancer genetics and cytogenetics, 2005-10, Vol.162 (2), p.179-182

2005

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Principle and importance of using the array CGH in hematooncology

Časopis lékařů českých, 2006, Vol.145 (1), p.9-13

2006

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Hemoglobin Sydney--alpha beta 2 67 (E11) Val-Ala and hemoglobin Olomouc alpha 2 beta 2 86 (F 2) Ala-Asp in Czech families. DNA sequence analysis for a more accurate diagnosis of hemoglobinopathies

Vnitřní lékar̆stvĭ, 1998-06, Vol.44 (6), p.347

1998

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New beta0-thalassaemic insertion mutation (CD 7/8, +G) in a Slovak family, associated with the Mediterranean haplotype IX

Vnitřní lékar̆stvĭ, 1999-03, Vol.45 (3), p.151

1999

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Hemoglobin Haná or alpha 2 beta 2 63 (E7) His-Asn: a new unstable hemoglobin variant with a paradoxically different clinical manifestations in smokers and non-smokers in the same family

Vnitřní lékar̆stvĭ, 1997-05, Vol.43 (5), p.267

1997

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Unstable Santa Ana hemoglobin or alpha 2 beta 2 88 (F4) Leu-Pro detected in a Slovak girl

Vnitřní lékar̆stvĭ, 1996-04, Vol.42 (4), p.258

1996

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198The choice of conditioning regimen regarding the host T-cell levels seems to be an effective way how to achieve the donor cells engraftment including effective tumour control and reduce the toxicity of some non-myeloablative allogeneic stem cell transplantations in lymphomas

Biology of blood and marrow transplantation, 2003-02, Vol.9 (2), p.122-123

2003

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Hydrops fetalis and failure of hematopoietic stem cell transplantation – A long route to the diagnosis of SPTA1-associated hereditary spherocytosis

Effect of CALR and JAK2 mutations on the clinical and hematological phenotypes of the disease in patients with myelofibrosis - long-term experience from a single center

P1564: FAMILIAL ERYTHROCYTOSES IN THE CZECH REPUBLIC ‐ GENETIC CHARACTERIZATION AND HEPCIDIN REGULATION

Thrombin Generation Testing in Patients with Myelofibrosis

Flow cytometric monitoring of the in vitro inhibition of the phosphorylation of CRKL and of SRC family kinases in patients with chronic myelogenous leukemia treated with tyrosine kinase inhibitors

FcγRIIIA receptor genotype does not influence an outcome in patients with follicular lymphoma treated with risk-adapted immunochemotherapy

High Incidence of Unbalanced Chromosomal Changes in Mantle Cell Lymphoma Detected by Comparative Genomic Hybridization

Operational cures after interferon-alpha in patients with chronic myeloid leukemia in Central and Northern Moravia

Non-anemic homozygous β° thalassemia in an African-American family : Association of high fetal hemoglobin levels with β thalassemia alleles

Cryptic MLL-AF10 fusion caused by insertion of duplicated 5′ part of MLL into 10p12 in acute leukemia: a case report

Principle and importance of using the array CGH in hematooncology

Hemoglobin Sydney--alpha beta 2 67 (E11) Val-Ala and hemoglobin Olomouc alpha 2 beta 2 86 (F 2) Ala-Asp in Czech families. DNA sequence analysis for a more accurate diagnosis of hemoglobinopathies

New beta0-thalassaemic insertion mutation (CD 7/8, +G) in a Slovak family, associated with the Mediterranean haplotype IX

Hemoglobin Haná or alpha 2 beta 2 63 (E7) His-Asn: a new unstable hemoglobin variant with a paradoxically different clinical manifestations in smokers and non-smokers in the same family

Unstable Santa Ana hemoglobin or alpha 2 beta 2 88 (F4) Leu-Pro detected in a Slovak girl

198The choice of conditioning regimen regarding the host T-cell levels seems to be an effective way how to achieve the donor cells engraftment including effective tumour control and reduce the toxicity of some non-myeloablative allogeneic stem cell transplantations in lymphomas

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