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Dive into the research topics where Vladimíra Vallová is active.

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Featured researches published by Vladimíra Vallová.


European Oncology and Haematology | 2012

Initial Experience with Determination of hTERC and MYCC Amplification in Cervical Intraepithelial Neoplasia and Cervical Carcinoma in the Czech Republic

Lucie Mouková; Vladimíra Vallová; Iva Slámová; Miroslava Kiššová; Petr Kuglík

Tumors are frequently characterized by series of cytogenetic abnormalities. Amplifications of hTERC (3q26) and MYCC (8q24) genes have been associated with cervical intraepithelial neoplasia (CIN) and carcinoma of uterine cervix. The results of genetic analysis could select patients with high risk of progression from CIN to carcinoma. In this study, chromosomal abnormalities in cytology specimens of cervical carcinoma or CIN of 26 patients were analyzed using new developed triple-colour HPV-FISH assay. HPV infection was proven in 85 % (22/26) of patients. Amplification of hTERC and MYCC gene was found in 46 % (12/26) and 62 % (16/26) of patients, respectively. Based on these results we were able to divide patients into high-risk, medium-risk and low-risk group. We confirmed that HPV-FISH assay can be used as an effective diagnostic procedure to identify patients carrying highly risking HPV infection and chromosomal aberrations associated with this malignancy. Patients of the high-risk group would benefit from intensive dispensarisation and aggressive therapy in the future. Tumors are frequently characterized by series of cytogenetic abnormalities. Amplifications of hTERC (3q26) and MYCC (8q24) genes have been associated with cervical intraepithelial neoplasia (CIN) and carcinoma of uterine cervix. The results of genetic analysis could select patients with high risk of progression from CIN to carcinoma. In this study, chromosomal abnormalities in cytology specimens of cervical carcinoma or CIN of 26 patients were analyzed using new developed triple-colour HPV-FISH assay. HPV infection was proven in 85 % (22/26) of patients. Amplification of hTERC and MYCC gene was found in 46 % (12/26) and 62 % (16/26) of patients, respectively. Based on these results we were able to divide patients into high-risk, medium-risk and low-risk group. We confirmed that HPV-FISH assay can be used as an effective diagnostic procedure to identify patients carrying highly risking HPV infection and chromosomal aberrations associated with this malignancy. Patients of the high-risk group would benefit from intensive dispensarisation and aggressive therapy in the future.


Molecular Cytogenetics | 2015

A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms

Eva Hladílková; Tuva Barøy; Madeleine Fannemel; Vladimíra Vallová; Doriana Misceo; Vesna Bryn; Iva Slámová; Šárka Prášilová; Petr Kuglík; Eirik Frengen


International Journal of Clinical and Experimental Pathology | 2014

Genome-wide screening of DNA copy number alterations in cervical carcinoma patients with CGH+SNP microarrays and HPV-FISH

Petr Kuglík; Jan Smetana; Vladimíra Vallová; Lucie Mouková; Kateřina Kašíková; Michaela Cvanová; Lucie Brožová


Archive | 2007

Comparison of prognostic impact of chromosome 1q21 gain in patients with multiple myeloma treated by Velcade, thalidomide and any conventional therapy

Pavel Němec; Henrieta Grešliková; Romana Zaoralová; Hana Filková; Vladimíra Vallová; Renata Kupská; Jana Smejkalová; Alexandra Oltová; Petr Kuglík; Roman Hájek


Neoplasma | 2016

Detection of oncogenic mutations in cervical carcinoma using method "High Resolution Melting" (HRM).

Markéta Wayhelová; Aneta Mikulášová; Jan Smetana; Vladimíra Vallová; Dita Matuchová; Hana Filková; Lucie Mouková; Petr Kuglík


Časopis lékařů českých | 2015

První zkušenosti s preimplantačním genetickým screeningem chromozomových abnormalit pomocí komparativní genomové hybridizace na oligonukleotidových DNA mikročipech

Petr Kuglík; Jan Smetana; Darja Němcová; Vladimíra Vallová; Aneta Mikulášová; Renata Gaillyová; Vít Hubinka; Marek Koudelka


Praktická gynekologie | 2013

Molekulární cytogenetika v diagnostice genetických abnormalit u karcinomu děložního hrdla

Petr Kuglík; Anna Laštůvková; Vladimíra Vallová; Kateřina Kašíková; Lucie Mouková


Archive | 2013

První zkušenosti s metodou aCGH u 19 jedinců s monoklonální gamapatií nejasného významu

Aneta Mikulášová; Vladimíra Vallová; Jan Smetana; Henrieta Grešliková; Renata Kupská; Lucie Říhová; Anna Potáčová; Viera Sandecká; Luděk Pour; Petr Kuglík; Roman Hájek


Klinická onkologie | 2013

Cytogenetické vyšetření lymfocytů periferní krve po stimulaciIL 2 a CpG oligonukleotidem DSP30 u pacientů s chronickoulymfocytární leukemiíridization and conventional cytogeneticsafter stimulation with CpG oligonucleotides and interleukin-2:A prospective analysis.

Kristina Štěpanovská; Gabriela Vaňková; Veronika Némethová; Lenka Tomášiková; Petra Šmuhařová; Eva Divíšková; Vladimíra Vallová; Petr Kuglík; Karla Plevová; Alexandra Oltová; Michael Doubek; Šárka Pospíšilová; Jiří Mayer


Blood | 2013

Genome Wide Profiling Of Chromosomal Abnormalities In 37 Patients With Monoclonal Gammopathy Of Undetermined Significance (MGUS)

Vladimíra Vallová; Jan Smetana; Henrieta Grešliková; Renata Kupská; Michaela Purgertova; Lucie Rihova; Viera Sandecká; Ludek Pour; Miroslav Penka; Petr Kuglík; Roman Hájek

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