Search Results - Laštůvková, Jana

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  1. 1
    Dimensions of liquidity and their factors in the Slovenian banking sector

    Dimensions of liquidity and their factors in the Slovenian banking sector by Lastuvkova, Jana

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  2. 2
    Czech family confirms the new 1p36.13‐1p36.12 microdeletion syndrome

    Czech family confirms the new 1p36.13‐1p36.12 microdeletion syndrome by Seeman, Pavel, Čejnová, Vlasta, Černá, Šárka, Rennerová, Ladislava, Trková, Marie, Kofer, Josef, Laštůvková, Jana

    Published in Clinical genetics
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  3. 3
    Spectrum and frequencies of non GJB2 gene mutations in Czech patients with early non‐syndromic hearing loss detected by gene panel NGS and whole‐exome sequencing

    Spectrum and frequencies of non GJB2 gene mutations in Czech patients with early non‐syndromic hearing loss detected by gene panel NGS and whole‐exome sequencing by Safka Brozkova, Dana, Poisson Marková, Simona, Mészárosová, Anna Uhrová, Jenčík, Ján, Čejnová, Vlasta, Čada, Zdeněk, Laštůvková, Jana, Rašková, Dagmar, Seeman, Pavel

    Published in Clinical genetics
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  4. 4
    Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene

    Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene by Čada, Zdeněk, Šafka Brožková, Dana, Balatková, Zuzana, Plevová, Pavlína, Rašková, Dagmar, Laštůvková, Jana, Černý, Rudolf, Bandúrová, Veronika, Koucký, Vladimír, Hrubá, Silvie, Komarc, Martin, Jenčík, Ján, Poisson Marková, Simona, Plzák, Jan, Kluh, Jan, Seeman, Pavel

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  5. 5
    The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes—A Comprehensive Study of the GJB2/DFNB1 Region

    The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes—A Comprehensive Study of the GJB2/DFNB1 Region by Safka Brozkova, Dana, Uhrova Meszarosova, Anna, Lassuthova, Petra, Varga, Lukáš, Staněk, David, Borecká, Silvia, Laštůvková, Jana, Čejnová, Vlasta, Rašková, Dagmar, Lhota, Filip, Gašperíková, Daniela, Seeman, Pavel

    Published in Genes
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  6. 6
    DFNB35 due to a novel mutation in the ESRRB gene in a Czech consanguineous family

    DFNB35 due to a novel mutation in the ESRRB gene in a Czech consanguineous family by Šafka Brožková, Dana, Laštůvková, Jana, Machalová, Eliška, Lisoňová, Jana, Trková, Marie, Seeman, Pavel

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  7. 7
    Is the exchange rate a factor of bank liquidity changes? Study of the Czech Republic

    Is the exchange rate a factor of bank liquidity changes? Study of the Czech Republic by Kasparovska, Vlasta, Lastvkova, Jana, Stelec, Lubos

    Published in Society and economy
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  8. 8
    An Evaluation of the Readiness for the Implementation of the IFRS 13 Standard and its Impacts on the Financial Reporting of the Banks

    An Evaluation of the Readiness for the Implementation of the IFRS 13 Standard and its Impacts on the Financial Reporting of the Banks by Kašparovská, Vlasta, Gláserová, Jana, Laštůvková, Jana

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  9. 9
    Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant

    Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethn... by Safka Brozkova, Dana, Varga, Lukas, Uhrova Meszarosova, Anna, Slobodova, Zuzana, Skopkova, Martina, Soltysova, Andrea, Ficek, Andrej, Jencik, Jan, Lastuvkova, Jana, Gasperikova, Daniela, Seeman, Pavel

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  10. 10
    Fatal neonatal nephrocutaneous syndrome in 18 Roma children with EGFR deficiency

    Fatal neonatal nephrocutaneous syndrome in 18 Roma children with EGFR deficiency by Mazurova, Stella, Tesarova, Marketa, Zeman, Jiri, Stranecky, Viktor, Hansikova, Hana, Baxova, Alica, Giertlova, Maria, Lastuvkova, Jana, Chovanova, Vanda, Rusnakova, Simona, Knapkova, Maria, Minarik, Gabriel, Honzik, Tomas, Magner, Martin

    Published in Journal of dermatology
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  11. 11
    A founder COL4A4 pathogenic variant resulting in autosomal recessive Alport syndrome accounts for most genetic kidney failure in Romani people

    A founder COL4A4 pathogenic variant resulting in autosomal recessive Alport syndrome accounts for most genetic kidney failure in Romani people by Plevova, Pavlina, Indrakova, Jana, Savige, Judy, Kuhnova, Petra, Tvrda, Petra, Cerna, Dita, Hilscherova, Sarka, Kudrejova, Monika, Polendova, Daniela, Jaklova, Radka, Langova, Martina, Jahnova, Helena, Lastuvkova, Jana, Dusek, Jiri, Gut, Josef, Vlckova, Marketa, Solarova, Pavla, Kreckova, Gabriela, Kantorova, Eva, Soukalova, Jana, Slavkovsky, Rastislav, Zapletalova, Jana, Tichy, Tomas, Thomasova, Dana

    Published in Frontiers in medicine
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  12. 12
    Variant c.2158-2AG in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant

    Variant c.2158-2AG in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethni... by Safka Brozkova, Dana, Varga, Lukas, Uhrova Meszarosova, Anna, Slobodova, Zuzana, Skopkova, Martina, Soltysova, Andrea, Ficek, Andrej, Jencik, Jan, Lastuvkova, Jana, Gasperikova, Daniela, Seeman, Pavel

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  13. 13
    Autosomal recessive hereditary spastic paraplegia type SPG35 due to a novel variant in the FA2H gene in a Czech patient

    Autosomal recessive hereditary spastic paraplegia type SPG35 due to a novel variant in the FA2H gene in a Czech patient by Uhrova Meszarosova, Anna, Safka Brozkova, Dana, Vyhnalek, Martin, Mazanec, Radim, Lastuvkova, Jana, Trkova, Marie, Bittoova, Martina, Soldatova, Inna, Seeman, Pavel

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