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Practical aspects and clinical value of t(14;18) monitoring in peripheral blood of the follicular lymphoma patients

Časopis lékařů českých, 2007, Vol.146 (4), p.374-81; discussion 381-2

2007

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The molecular genetic assessment of prognostic factors in carcioma of the prostate: a pilot study

Ceskoslovenské patologie, 2006-07, Vol.42 (3), p.130-132

2006

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Invasive ductal carcinoma of the breast: study of the number of copies of the CCND1 gene and chromosome 11 using fluorescence in situ hybridization (FISH) in comparison with expression of cyclin D1 protein and estrogen receptors (ER alpha) with immunohistochemical detection

Časopis lékařů českých, 2002-11, Vol.141 (22), p.708

2002

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Lenalidomide treatment in myelodysplastic syndrome with 5q deletion--Czech MDS group experience

Vnitřní lékar̆stvĭ, 2015-12, Vol.61 (12), p.1028-1033

2015

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Chromosome banding analysis of peripheral blood lymphocytes stimulated with IL2 and CpG oligonucleotide DSP30 in patients with chronic lymphocytic leukemia

Klinická onkologie, 2013, Vol.26 (4), p.263-270

2013

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Molecular cytogenetic analysis of chromosomal aberrations in cells of low grade gliomas and its contribution for tumour classification

Klinická onkologie, 2014, Vol.27 (3), p.183-191

2014

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Importance of chromosomal changes correlated to prognostic factors in ovarian and cervical malignant tumors

Ceská gynekologie, 2008-04, Vol.73 (2), p.79

2008

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Chromosome instability syndromes

Časopis lékařů českých, 2002, Vol.141 (1), p.16

2002

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Increased risk of malignancies in heterozygotes in families of patients with Nijmegen breakage syndrome

Časopis lékařů českých, 2006, Vol.145 (2), p.138-143

2006

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The interphase fluorescence in situ hybridization (I-FISH) technique in patients with chronic lymphatic leukemia (CLL)

Časopis lékařů českých, 2000-06, Vol.139 (11), p.334

2000

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Molecular cytogenetic diagnosis of Klinefelter's syndrome in men more frequently detects sex chromosome mosaicism than classical cytogenetic methods

Časopis lékařů českých, 1999-04, Vol.138 (8), p.235

1999

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Long-term results of the UHKT-911 study of adult patients under 65 years of age with de novo acute myeloid leukemias without favorable karyotypes

Vnitřní lékar̆stvĭ, 2003-03, Vol.49 (3), p.174

2003

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Lymphocyte immunophenotyping and cytogenetics for more precise prognosis in patients with type B chronic lymphatic leukemia

Časopis lékařů českých, 2003-02, Vol.142 (2), p.106

2003

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Methods in molecular cytogenetics for determination of prognostically important chromosome changes in patients with chronic lymphatic leukemias

Časopis lékařů českých, 2000-09, Vol.139 (18), p.564

2000

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Prognostic significance of cytogenetic changes in patients with acute myeloid leukemia (AML). (Analysis of results in 105 patients treated at the Hemato-oncology Clinic of the University Hospital in Olomouc from 1997 to 2000

Vnitřní lékar̆stvĭ, 2001-09, Vol.47 Suppl 1, p.8

2001

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New findings in the genetics of Alzheimer-type dementia

Časopis lékařů českých, 1988-02, Vol.127 (7), p.204

Topinková, E

1988

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The fragile X chromosome syndrome

Československá pediatrie, 1987-11, Vol.42 (11), p.650

1987

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Cytogenetic findings in patients with primary myelodysplastic syndrome and their prognostic significance. (Analysis of results in 65 patients)

Vnitřní lékar̆stvĭ, 1994-09, Vol.40 (9), p.577

1994

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Cytogenetic study in multiple myeloma. I. Chromosome findings in 56 patients

Vnitřní lékar̆stvĭ, 1990-11, Vol.36 (11), p.1072

1990

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Molecular genetic diagnosis of autosomal dominant polycystic kidney disease

Sbornik lekarsky, 2002, Vol.103 (4), p.435

2002

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Results of the cytogenetic examination of 54 patients with polycythemia vera

Vnitřní lékar̆stvĭ, 1988-04, Vol.34 (4), p.322

1988

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Acute Ph1 positive lymphatic leukemia in adults

Vnitřní lékar̆stvĭ, 1987-09, Vol.33 (9), p.760

1987

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Bone marrow chromosomes in 172 patients with chronic myeloid leukemia

Vnitřní lékar̆stvĭ, 1988-07, Vol.34 (7), p.694

1988

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Cytogenetic study in multiple myeloma. II. Clinical significance of chromosomal changes

Vnitřní lékar̆stvĭ, 1990-11, Vol.36 (11), p.1081

1990

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Chromosome findings in the myelodysplastic syndrome

Vnitřní lékar̆stvĭ, 1986-03, Vol.32 (3), p.216

1986

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Practical aspects and clinical value of t(14;18) monitoring in peripheral blood of the follicular lymphoma patients

The molecular genetic assessment of prognostic factors in carcioma of the prostate: a pilot study

Invasive ductal carcinoma of the breast: study of the number of copies of the CCND1 gene and chromosome 11 using fluorescence in situ hybridization (FISH) in comparison with expression of cyclin D1 protein and estrogen receptors (ER alpha) with immunohistochemical detection

Lenalidomide treatment in myelodysplastic syndrome with 5q deletion--Czech MDS group experience

Chromosome banding analysis of peripheral blood lymphocytes stimulated with IL2 and CpG oligonucleotide DSP30 in patients with chronic lymphocytic leukemia

Molecular cytogenetic analysis of chromosomal aberrations in cells of low grade gliomas and its contribution for tumour classification

Importance of chromosomal changes correlated to prognostic factors in ovarian and cervical malignant tumors

Chromosome instability syndromes

Increased risk of malignancies in heterozygotes in families of patients with Nijmegen breakage syndrome

The interphase fluorescence in situ hybridization (I-FISH) technique in patients with chronic lymphatic leukemia (CLL)

Molecular cytogenetic diagnosis of Klinefelter's syndrome in men more frequently detects sex chromosome mosaicism than classical cytogenetic methods

Long-term results of the UHKT-911 study of adult patients under 65 years of age with de novo acute myeloid leukemias without favorable karyotypes

Lymphocyte immunophenotyping and cytogenetics for more precise prognosis in patients with type B chronic lymphatic leukemia

Methods in molecular cytogenetics for determination of prognostically important chromosome changes in patients with chronic lymphatic leukemias

Prognostic significance of cytogenetic changes in patients with acute myeloid leukemia (AML). (Analysis of results in 105 patients treated at the Hemato-oncology Clinic of the University Hospital in Olomouc from 1997 to 2000

New findings in the genetics of Alzheimer-type dementia

The fragile X chromosome syndrome

Cytogenetic findings in patients with primary myelodysplastic syndrome and their prognostic significance. (Analysis of results in 65 patients)

Cytogenetic study in multiple myeloma. I. Chromosome findings in 56 patients

Molecular genetic diagnosis of autosomal dominant polycystic kidney disease

Results of the cytogenetic examination of 54 patients with polycythemia vera

Acute Ph1 positive lymphatic leukemia in adults

Bone marrow chromosomes in 172 patients with chronic myeloid leukemia

Cytogenetic study in multiple myeloma. II. Clinical significance of chromosomal changes

Chromosome findings in the myelodysplastic syndrome

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