Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Martina Fejtkova"'
Autor:
Veronika Kanderova, Hana Grombirikova, Irena Zentsova, Kamila Reblova, Adam Klocperk, Martina Fejtkova, Marketa Bloomfield, Barbora Ravcukova, Tomas Kalina, Tomas Freiberger, Anna Sediva
Publikováno v:
Haematologica, Vol 104, Iss 1 (2019)
Externí odkaz:
https://doaj.org/article/e499ab134e854d8c9b7d672745285506
Autor:
Tomas Milota, Jitka Smetanova, Aneta Skotnicova, Michal Rataj, Jan Lastovicka, Hana Zelena, Zuzana Parackova, Martina Fejtkova, Veronika Kanderova, Eva Fronkova, Katerina Rejlova, Anna Sediva, Tomas Kalina
Publikováno v:
The journal of allergy and clinical immunology. In practice. 11(1)
Common variable immunodeficiency (CVID) is characterized by an impaired postvaccination response, high susceptibility to respiratory tract infections, and a broad spectrum of noninfectious complications. Thus, patients with CVID may be at high risk f
Autor:
Zofia Klimova, Linh Truong, Martina Fejtkova, Venetia Bigley, Dusana Moravcikova, Catherine F Hatton, Dipayan Mitra, Angela Grainger, Florian Gothe, Veronika Kanderova, Sophie Hambleton, Ales Janda, Joanna E. Perthen, Christopher J A Duncan, Eva Fronkova
Publikováno v:
Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America
We present a case of complete deficiency of the interferon alpha/beta receptor alpha chain (IFNAR1) in a child with fatal systemic hyperinflammation, apparently provoked by live-attenuated viral vaccination. Such pathologic hyperinflammation, fulfill
Early-onset pulmonary and cutaneous vasculitis driven by constitutively active SRC-family kinase HCK
Autor:
Jan Lebl, Eva Fronkova, Petr Novák, Tomas Brdicka, Marcela Dvorakova, Min Ae Lee-Kirsch, Jarmila Králová, Milan Macek, Ludmila Hornofova, Anna Sediva, Vendula Martinu, Jana Kayserova, Miroslav Koblizek, Michael Svaton, Petr Sedlacek, Ashleigh R Poh, Olga Zimmermannova, Ales Janda, Jana Paderova, Matthias Ernst, Tomas Kalina, Zuzana Parackova, Tamara Svobodová, Adam Klocperk, Stepanka Pruhova, Ondrej Hrusak, Veronika Kanderova, Simon Borna, Petr Pohunek, Martina Fejtkova
Background Inborn errors of immunity are genetic disorders characterized by various degrees of immune dysregulation that can manifest as immune deficiency, autoimmunity, or autoinflammation. The routine use of next-generation sequencing in the clinic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::661be0062cb1ee5200e3673fa2a750d8
Autor:
Martina Fejtkova, Martina Sukova, Katerina Hlozkova, Karolina Skvarova Kramarzova, Marketa Rackova, David Jakubec, Marina Bakardjieva, Marketa Bloomfield, Adam Klocperk, Zuzana Parackova, Anna Sediva, Jahnavi Aluri, Michaela Novakova, Tomas Kalina, Eva Fronkova, Ondrej Hrusak, Hana Malcova, Petr Sedlacek, Zuzana Liba, Martin Kudr, Jan Stary, Megan A. Cooper, Michael Svaton, Veronika Kanderova
Publikováno v:
American journal of hematologyREFERENCES. 97(3)
Our study presents a novel germline c.1715GT (p.G572V) mutation in the gene encoding Toll-like receptor 8 (TLR8) causing an autoimmune and autoinflammatory disorder in a family with monozygotic male twins, who suffer from severe autoimmune hemolytic
Autor:
Petra Vrabcova, Martina Fejtkova, Irena Zentsova, Marketa Bloomfield, Radana Zachova, Adam Klocperk, Anna Sediva, Tomas Kalina, Tomas Milota, Veronika Kanderova, Michal Rataj, Eva Froňková, Michael Svatoň, Zuzana Parackova
Publikováno v:
Journal of Clinical Immunology. 38:589-601
Signal transducer and activator of transcription 1 gain-of-function (STAT1 GOF) mutations are the most common cause of chronic mucocutaneous candidiasis (CMC). We aim to report the effect of oral ruxolitinib, the Janus kinase (JAK) family tyrosine ki