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Diagnosis of tuberous sclerosis complex focusing on prenatal period

Ceská gynekologie, 2016-04, Vol.81 (2), p.147

2016

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Leiomyomas of the uterine body: Molecular-genetical aspects of formation and development

Ceská gynekologie, 2016-01, Vol.81 (1), p.48

2016

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Gene mutations connected to Waldenstöm macroglobulinemia

Vnitřní lékar̆stvĭ, 2016-01, Vol.62 (1), p.40-43

2016

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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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News in diagnostics and therapy of multiple endocrine neoplasia type 1

Vnitřní lékar̆stvĭ, 2015-10, Vol.61 (10), p.896-899

Starý, Karel

2015

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First experiences with preimplantation genetic screening of chromosomal aberrations using oligonucleotide-based array comparative genomic hybridization

Časopis lékařů českých, 2015, Vol.154 (3), p.127

2015

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Mutagenic effect of advanced paternal age in neurocardiofaciocutaneous syndrome

Časopis lékařů českých, 2014, Vol.153 (5), p.242

2014

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Detection of chromosome changes by CGH, array-CGH and SNP array techniques in tumours

Ceskoslovenské patologie, 2014-01, Vol.50 (1), p.25-29

2014

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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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Rapid detection of the most common chromosomal aneuploidies in the second-trimester amniotic fluid using QF-PCR

Ceská gynekologie, 2013-08, Vol.78 (4), p.373

2013

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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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Extracellular chromosome 21--derived microRNAs in maternal circulation: evaluation of their diagnostic potential for screening of Down syndrome

Ceská gynekologie, 2012-10, Vol.77 (5), p.395

2012

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Chromosomal integration of the sixth human herpes virus (HHV-6)

Epidemiologie, mikrobiologie, imunologie, 2012-09, Vol.61 (3), p.58

2012

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Summary of recommendations for the diagnosis and therapy of BCR/ABL-negative myeloproliferation of the Czech Working Group for Ph-negative myeloproliferative disease (CZEMP) of the Czech Hematologic Society CLS JEP

Vnitřní lékar̆stvĭ, 2012-02, Vol.58 (2), p.163-168

2012

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Genetic factors in etiology of uterine fibroids

Ceská gynekologie, 2012-02, Vol.77 (1), p.58

2012

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Molecular basis of Waldenström macroglobulinemia

Klinická onkologie, 2012, Vol.25 (6), p.413-420

2012

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Histological diagnosis of Ph-negative myeloproliferative neoplasia. An overview

Ceskoslovenské patologie, 2011-07, Vol.47 (3), p.84-93

Campr, V

2011

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Analysis of cell free fetal DNA fragmentation rate in pregnant women during the course of gravidit

Ceská gynekologie, 2010-08, Vol.75 (4), p.312

2010

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Clinical relevance of chromosomal aberrations in bone and soft tissue tumors in children and young adults

Klinická onkologie, 2009, Vol.22 (2), p.58-66

2009

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Commentary on development of the prognostic factors concept in chronic lymphocytic leukaemia: the route from prognostic factors to therapy response predictors

Klinická onkologie, 2009, Vol.22 (6), p.254-263

2009

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Dilemma of the results interpretation of molecular genetic analysis with a focus on CFTR gene mutations in men with reproductive disorders and in gamete donors

Ceská gynekologie, 2008-12, Vol.73 (6), p.323

Hrdlicka, I

2008

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Noninvasive fetal sex detection from maternal plasma in pregnant women

Ceská gynekologie, 2008-06, Vol.73 (3), p.150

2008

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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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Molecular genetics of myocardial infarction

Vnitřní lékar̆stvĭ, 2007-04, Vol.53 (4), p.348-353

2007

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Quality of life in the patients with disorders of sexual development and with Y chromosome in karyotype

Časopis lékařů českých, 2007, Vol.146 (3), p.215-217

Lisá, L

2007

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Diagnosis of tuberous sclerosis complex focusing on prenatal period

Leiomyomas of the uterine body: Molecular-genetical aspects of formation and development

Gene mutations connected to Waldenstöm macroglobulinemia

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

News in diagnostics and therapy of multiple endocrine neoplasia type 1

First experiences with preimplantation genetic screening of chromosomal aberrations using oligonucleotide-based array comparative genomic hybridization

Mutagenic effect of advanced paternal age in neurocardiofaciocutaneous syndrome

Detection of chromosome changes by CGH, array-CGH and SNP array techniques in tumours

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

Rapid detection of the most common chromosomal aneuploidies in the second-trimester amniotic fluid using QF-PCR

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

Extracellular chromosome 21--derived microRNAs in maternal circulation: evaluation of their diagnostic potential for screening of Down syndrome

Chromosomal integration of the sixth human herpes virus (HHV-6)

Summary of recommendations for the diagnosis and therapy of BCR/ABL-negative myeloproliferation of the Czech Working Group for Ph-negative myeloproliferative disease (CZEMP) of the Czech Hematologic Society CLS JEP

Genetic factors in etiology of uterine fibroids

Molecular basis of Waldenström macroglobulinemia

Histological diagnosis of Ph-negative myeloproliferative neoplasia. An overview

Analysis of cell free fetal DNA fragmentation rate in pregnant women during the course of gravidit

Clinical relevance of chromosomal aberrations in bone and soft tissue tumors in children and young adults

Commentary on development of the prognostic factors concept in chronic lymphocytic leukaemia: the route from prognostic factors to therapy response predictors

Dilemma of the results interpretation of molecular genetic analysis with a focus on CFTR gene mutations in men with reproductive disorders and in gamete donors

Noninvasive fetal sex detection from maternal plasma in pregnant women

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

Molecular genetics of myocardial infarction

Quality of life in the patients with disorders of sexual development and with Y chromosome in karyotype

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