Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ariane Hai Ha Nguyen"'
Autor:
Syed Fakhar‐ul‐Hassnain Waqas, Aaqib Sohail, Ariane Hai Ha Nguyen, Abdulai Usman, Tobias Ludwig, Andre Wegner, Muhammad Nasir Hayat Malik, Sven Schuchardt, Robert Geffers, Moritz Winterhoff, Sylvia Merkert, Ulrich Martin, Ruth Olmer, Nico Lachmann, Frank Pessler
Publikováno v:
Clinical and Translational Medicine, Vol 12, Iss 7, Pp n/a-n/a (2022)
Abstract Background Congenital ISG15 deficiency is a rare autoinflammatory disorder that is driven by chronically elevated systemic interferon levels and predominantly affects central nervous system and skin. Methods and results We have developed ind
Externí odkaz:
https://doaj.org/article/8d6059a843714b79980249a16907b0fe
Autor:
Katharina Hahn, Liart Pollmann, Juliette Nowak, Ariane Hai Ha Nguyen, Kathrin Haake, Anna-Lena Neehus, Syed F. Hassnain Waqas, Frank Pessler, Ulrich Baumann, Miriam Hetzel, Jean-Laurent Casanova, Ansgar Schulz, Jacinta Bustamante, Mania Ackermann, Nico Lachmann
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 17, Iss , Pp 785-795 (2020)
Autosomal recessive (AR) complete interferon-γ receptor 1 (IFN-γR1) deficiency, also known as one genetic etiology of Mendelian susceptibility to mycobacterial disease (MSMD), is a life-threatening congenital disease leading to premature death. Aff
Externí odkaz:
https://doaj.org/article/402b38c898664b7e8e2c466f01b1aa11
Autor:
Miriam Hetzel, Elena Lopez-Rodriguez, Adele Mucci, Ariane Hai Ha Nguyen, Takuji Suzuki, Kenjiro Shima, Theresa Buchegger, Sabine Dettmer, Thomas Rodt, Jens P. Bankstahl, Punam Malik, Lars Knudsen, Axel Schambach, Gesine Hansen, Bruce C. Trapnell, Nico Lachmann, Thomas Moritz
Publikováno v:
Haematologica, Vol 105, Iss 4 (2020)
Hereditary pulmonary alveolar proteinosis due to GM-CSF receptor deficiency (herPAP) constitutes a life-threatening lung disease characterized by alveolar deposition of surfactant protein secondary to defective alveolar macrophage function. As curren
Externí odkaz:
https://doaj.org/article/42eb50b712764660ad306648570ef7bd
Autor:
Liart Pollmann, Nico Lachmann, Katharina Hahn, Miriam Hetzel, Ulrich Baumann, Juliette Nowak, Anna-Lena Neehus, Jacinta Bustamante, Ariane Hai Ha Nguyen, Ansgar Schulz, Jean-Laurent Casanova, Frank Pessler, Kathrin Haake, Syed F. Hassnain Waqas, Mania Ackermann
Publikováno v:
Molecular therapy. Methods & clinical development
United States
Molecular Therapy-Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 17, Iss, Pp 785-795 (2020)
Molecular Therapy. Methods & Clinical Development
United States
Molecular Therapy-Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 17, Iss, Pp 785-795 (2020)
Molecular Therapy. Methods & Clinical Development
Autosomal recessive (AR) complete interferon-γ receptor 1 (IFN-γR1) deficiency, also known as one genetic etiology of Mendelian susceptibility to mycobacterial disease (MSMD), is a life-threatening congenital disease leading to premature death. Aff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6993d2462ff4f5b72df8b06b6f2625e4
https://doi.org/10.1016/j.omtm.2020.04.002
https://doi.org/10.1016/j.omtm.2020.04.002
Autor:
Punam Malik, Thomas Moritz, Axel Schambach, Thomas Rodt, Theresa Buchegger, Adele Mucci, Nico Lachmann, Kenjiro Shima, Elena Lopez-Rodriguez, Jens P. Bankstahl, Takuji Suzuki, Miriam Hetzel, Ariane Hai Ha Nguyen, Gesine Hansen, Sabine Dettmer, Bruce C. Trapnell, Lars Knudsen
Publikováno v:
Haematologica
Hereditary pulmonary alveolar proteinosis due to GM-CSF receptor deficiency (herPAP) constitutes a life-threatening lung disease characterized by alveolar deposition of surfactant protein secondary to defective alveolar macrophage function. As curren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5b683113b567058c64e2967aab82ad8
http://europepmc.org/articles/PMC7109724
http://europepmc.org/articles/PMC7109724
Autor:
Adele Mucci, Bernhard Gentner, Wolfgang Baumgärtner, Mark-Philipp Kühnel, Reinhold Förster, Sandra Billig, Nico Lachmann, Jacinta Bustamante, Axel Schambach, Daniel Brand, Jean-Laurent Casanova, Ralph Goethe, Patrick Blank, Danny Jonigk, Olga Halle, Robert Meineke, Ulrich Kalinke, Vanessa Herder, Miriam Hetzel, Franz-Christoph Bange, Ariane Hai Ha Nguyen, Jan Schiller
Mendelian susceptibility to mycobacterial disease is a rare primary immunodeficiency characterized by severe infections caused by weakly virulent mycobacteria. Biallelic null mutations in genes encoding interferon gamma receptor 1 or 2 (IFNGR1 or IFN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3365f518b16988b1a588e6d92a5c25b
https://hdl.handle.net/10033/621335
https://hdl.handle.net/10033/621335
