Works by Schmidt, Magdalena


Results: 31
    1

    Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome.

    Published in:
    Nephrology Dialysis Transplantation, 2019, v. 34, n. 3, p. 485, doi. 10.1093/ndt/gfy028
    By:
    • Braun, Daniela A;
    • Warejko, Jillian K;
    • Ashraf, Shazia;
    • Tan, Weizhen;
    • Daga, Ankana;
    • Schneider, Ronen;
    • Hermle, Tobias;
    • Jobst-Schwan, Tilman;
    • Widmeier, Eugen;
    • Majmundar, Amar J;
    • Nakayama, Makiko;
    • Schapiro, David;
    • Rao, Jia;
    • Schmidt, Johanna Magdalena;
    • Hoogstraten, Charlotte A;
    • Hugo, Hannah;
    • Bakkaloglu, Sevcan A;
    • Kari, Jameela A;
    • Desoky, Sherif El;
    • Daouk, Ghaleb
    Publication type:
    Article
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    Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome.

    Published in:
    2018
    By:
    • Braun, Daniela A.;
    • Lovric, Svjetlana;
    • Schapiro, David;
    • Schneider, Ronen;
    • Marquez, Jonathan;
    • Asif, Maria;
    • Hussain, Muhammad Sajid;
    • Daga, Ankana;
    • Widmeier, Eugen;
    • Rao, Jia;
    • Ashraf, Shazia;
    • Tan, Weizhen;
    • Lusk, C. Patrick;
    • Kolb, Amy;
    • Jobst-Schwan, Tilman;
    • Schmidt, Johanna Magdalena;
    • Hoogstraten, Charlotte A.;
    • Eddy, Kaitlyn;
    • Kitzler, Thomas M.;
    • Shril, Shirlee
    Publication type:
    journal article
    5

    Advillin acts upstream of phospholipase C ϵ1 in steroid-resistant nephrotic syndrome.

    Published in:
    2017
    By:
    • Weizhen Tan;
    • van der Ven, Amelie T.;
    • Braun, Daniela A.;
    • Won-Il Choi;
    • Jobst-Schwan, Tilman;
    • Schneider, Ronen;
    • Schmidt, Johanna Magdalena;
    • Widmeier, Eugen;
    • Warejko, Jillian K.;
    • Hermle, Tobias;
    • Schapiro, David;
    • Lovric, Svjetlana;
    • Shril, Shirlee;
    • Daga, Ankana;
    • Hildebrandt, Friedhelm;
    • Rao, Jia;
    • Ashraf, Shazia;
    • Heon Yung Gee;
    • Bald, Martin;
    • Helmchen, Udo
    Publication type:
    journal article
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    Guidelines regarding ineffective maintenance of organ functions (futile therapy) in paediatric intensive care units.

    Published in:
    Anaesthesiology Intensive Therapy / Anestezjologia, Intensywna Terapia, 2021, v. 53, n. 5, p. 369, doi. 10.5114/ait.2021.111451
    By:
    • Bartkowska-Śniatkowska, Alicja;
    • Byrska-Maciejasz, Elżbieta;
    • Cettler, Maciej;
    • Damps, Maria;
    • Jarosz, Konrad;
    • Mierzewska-Schmidt, Magdalena;
    • Migdał, Marek;
    • Ożóg-Zabolska, Irena;
    • Piotrowski, Andrzej;
    • Rawicz, Marcin;
    • Świder, Magdalena;
    • Tałałaj, Mariola;
    • Zielińska, Marzena
    Publication type:
    Article
    12

    Stanowisko Sekcji Anestezjologii i Intensywnej Terapii Dziecięcej Polskiego Towarzystwa Anestezjologii i Intensywnej Terapii w sprawie znieczulania dzieci powyżej 3. roku życia. Część II.

    Published in:
    Anaesthesiology Intensive Therapy / Anestezjologia, Intensywna Terapia, 2016, v. 48, n. 3, p. 86, doi. 10.5603/AIT.2016.0023
    By:
    • Bartkowska-Śniatkowska, Alicja;
    • Zielińska, Marzena;
    • Cettler, Maciej;
    • Kobylarz, Krzysztof;
    • Mierzewska-Schmidt, Magdalena;
    • Rawicz, Marcin;
    • Piotrowski, Andrzej
    Publication type:
    Article
    13
    14

    Remarks to The consensus statement of the Paediatric Section of the Polish Society of Anaesthesiology and Intensive Therapy on general anaesthesia in children under 3 years of age.

    Published in:
    Anaesthesiology Intensive Therapy / Anestezjologia, Intensywna Terapia, 2015, v. 47, n. 4, p. 430, doi. 10.5603/AIT.2015.0058
    By:
    • Mierzewska-Schmidt, Magdalena;
    • Rawicz, Marcin;
    • Baranowski, Artur;
    • Manowska, Małgorzata;
    • Bartkowska-Sniatkowska, Alicja;
    • Zielinska, Marzena;
    • Kobylarz, Krzysztof;
    • Piotrowski, Andrzej;
    • Walas, Wojciech;
    • Woloszczuk-Gebicka, Bogumila
    Publication type:
    Article
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    A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral reflux.

    Published in:
    PLoS ONE, 2018, v. 13, n. 1, p. 1, doi. 10.1371/journal.pone.0191224
    By:
    • van der Ven, Amelie T.;
    • Kobbe, Birgit;
    • Kohl, Stefan;
    • Shril, Shirlee;
    • Pogoda, Hans-Martin;
    • Imhof, Thomas;
    • Ityel, Hadas;
    • Vivante, Asaf;
    • Chen, Jing;
    • Hwang, Daw-Yang;
    • Connaughton, Dervla M.;
    • Mann, Nina;
    • Widmeier, Eugen;
    • Taglienti, Mary;
    • Schmidt, Johanna Magdalena;
    • Nakayama, Makiko;
    • Senguttuvan, Prabha;
    • Kumar, Selvin;
    • Tasic, Velibor;
    • Kehinde, Elijah O.
    Publication type:
    Article
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    Mutations in WDR4 as a new cause of Galloway–Mowat syndrome.

    Published in:
    American Journal of Medical Genetics. Part A, 2018, v. 176, n. 11, p. 2460, doi. 10.1002/ajmg.a.40489
    By:
    • Braun, Daniela A.;
    • Shril, Shirlee;
    • Sinha, Aditi;
    • Schneider, Ronen;
    • Tan, Weizhen;
    • Ashraf, Shazia;
    • Hermle, Tobias;
    • Jobst‐Schwan, Tilman;
    • Widmeier, Eugen;
    • Majmundar, Amar J.;
    • Daga, Ankana;
    • Warejko, Jillian K.;
    • Nakayama, Makiko;
    • Schapiro, David;
    • Chen, Jing;
    • Airik, Merlin;
    • Rao, Jia;
    • Schmidt, Johanna Magdalena;
    • Hoogstraten, Charlotte A.;
    • Hugo, Hannah
    Publication type:
    Article
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