Search results

Records found: 4  
Your query: Author Sysno = "^sav_un_auth 0204508^"
  1. TitleA novel HNF4A pathogenic variant in a case of congenital hyperinsulinism with glycogenosis - like phenotype
    Author Škopková Martina SAVBIOMED - Biomedicínske centrum SAV
    Co-authors Staník Juraj SAVBIOMED - Biomedicínske centrum SAV
    Brennerová Katarína
    Daniš Daniel 1989 SAVBIOMED - Biomedicínske centrum SAV
    Rosoľanková Monika
    Salingova Anna
    Bzduch Vladimir
    Klimeš Iwar SAVBIOMED - Biomedicínske centrum SAV
    Gašperíková Daniela SAVBIOMED - Biomedicínske centrum SAV
    Action APVV-0107-12. Molekulárno-genetický výskum s farmakogenetickými konsekvenciami u detí s hyperinzulinemickými hypoglykémiami : 2013-2017 : BMC-ÚEE
    Source document ESHG 2017 : European Human Genetics Conference. P. P06.14B. - : ESHG European Society of Human Genetics, 2017 ; European Human Genetics Conference ESHG 2017
    CategoryGII - Other publications and documents which is not possible to categorize into classes/categories mentioned above
    Year2017
    article

    article

  2. TitleA novel HNF4A mutation c. 427-1G A causing congenital hyperinsulinism and glycogenosis - like phenotype
    Author Staník Juraj SAVBIOMED - Biomedicínske centrum SAV
    Co-authors Škopková Martina SAVBIOMED - Biomedicínske centrum SAV
    Brennerová Katarína
    Daniš Daniel 1989 SAVBIOMED - Biomedicínske centrum SAV
    Rosoľanková Monika
    Salingova Anna
    Bzduch Vladimir
    Klimeš Iwar SAVBIOMED - Biomedicínske centrum SAV
    Gašperíková Daniela SAVBIOMED - Biomedicínske centrum SAV
    Action APVV-0107-12. Molekulárno-genetický výskum s farmakogenetickými konsekvenciami u detí s hyperinzulinemickými hypoglykémiami : 2013-2017 : BMC-ÚEE
    Source document Genetics of diabetes and its role in precision medicine : 6th EASD - SGGD meeting. P. 120. - Leiden : Leiden University Medical Center, 2017 ; EASD - SGGD meeting Genetics of diabetes and its role in precision medicine
    CategoryGII - Other publications and documents which is not possible to categorize into classes/categories mentioned above
    Year2017
    article

    article

  3. TitleA novel HNF4A pathogenic variant in a case of congenital hyperinsulinism with glycogenosis - like phenotype
    Author Gašperíková Daniela SAVBIOMED - Biomedicínske centrum SAV
    Co-authors Škopková Martina SAVBIOMED - Biomedicínske centrum SAV
    Brennerová Katarína
    Daniš Daniel 1989 SAVBIOMED - Biomedicínske centrum SAV
    Rosoľanková Monika
    Salingova Anna
    Bzduch Vladimir
    Klimeš Iwar SAVBIOMED - Biomedicínske centrum SAV
    Staník Juraj SAVBIOMED - Biomedicínske centrum SAV
    Action APVV-0107-12. Molekulárno-genetický výskum s farmakogenetickými konsekvenciami u detí s hyperinzulinemickými hypoglykémiami : 2013-2017 : BMC-ÚEE
    Source document Genomics of rare disease : abstract book. P. 15. - Hinxton, 2017 ; Genomics of rare disease
    CategoryGII - Other publications and documents which is not possible to categorize into classes/categories mentioned above
    Year2017
    article

    article

  4. TitleCongenital hyperinsulinism and glycogenosis-like phenotype due to a novel HNF4A mutation
    Author Staník Juraj SAVBIOMED - Biomedicínske centrum SAV
    Co-authors Škopková Martina
    Brennerová Katarína
    Daniš Daniel 1989 SAVBIOMED - Biomedicínske centrum SAV
    Rosoľanková Monika
    Salingova Anna
    Bzdúch Vladimír
    Klimeš Iwar SAVBIOMED - Biomedicínske centrum SAV
    Gašperíková Daniela SAVBIOMED - Biomedicínske centrum SAV
    Action APVV-0107-12. Molekulárno-genetický výskum s farmakogenetickými konsekvenciami u detí s hyperinzulinemickými hypoglykémiami : 2013-2017 : BMC-ÚEE
    Source document Diabetes Research and Clinical Practice. Vol. 126 (2017) p. 144-150
    CategoryADCA - Scientific papers in foreign journals registered in Current Contents Connect with IF (impacted)
    Category of document (from 2022)V3 - Vedecký výstup publikačnej činnosti z časopisu
    Type of documentčlánok
    Year2017
    DOI 10.1016/j.diabres.2017.02.014
    article

    article



  This site uses cookies to make them easier to browse. Learn more about how we use cookies.