Janda A - Search Results

1

Early-onset pulmonary and cutaneous vasculitis driven by constitutively active SRC-family kinase HCK.

Kanderova V, Svobodova T, Borna S, Fejtkova M, Martinu V, Paderova J, Svaton M, Kralova J, Fronkova E, Klocperk A, Pruhova S, Lee-Kirsch MA, Hornofova L, Koblizek M, Novak P, Zimmermannova O, Parackova Z, Sediva A, Kalina T, Janda A, Kayserova J, Dvorakova M, Macek M, Pohunek P, Sedlacek P, Poh A, Ernst M, Brdicka T, Hrusak O, Lebl J. Kanderova V, et al. Among authors: janda a. J Allergy Clin Immunol. 2022 Apr;149(4):1464-1472.e3. doi: 10.1016/j.jaci.2021.07.046. Epub 2021 Sep 15. J Allergy Clin Immunol. 2022. PMID: 34536415

2

High antibody levels and reduced cellular response in children up to one year after SARS-CoV-2 infection.

Jacobsen EM, Fabricius D, Class M, Topfstedt F, Lorenzetti R, Janowska I, Schmidt F, Staniek J, Zernickel M, Stamminger T, Dietz AN, Zellmer A, Hecht M, Rauch P, Blum C, Ludwig C, Jahrsdörfer B, Schrezenmeier H, Heeg M, Mayer B, Seidel A, Groß R, Münch J, Kirchhoff F, Bode SFN, Strauss G, Renk H, Elling R, Stich M, Voll RE, Tönshof B, Franz AR, Henneke P, Debatin KM, Rizzi M, Janda A. Jacobsen EM, et al. Among authors: janda a. Nat Commun. 2022 Nov 28;13(1):7315. doi: 10.1038/s41467-022-35055-1. Nat Commun. 2022. PMID: 36437276 Free PMC article.

3

Early development of immunity in diGeorge syndrome.

Sedivá A, Bartůnková J, Zachová R, Poloucková A, Hrusák O, Janda A, Kocárek E, Novotná D, Novotná K, Klein T. Sedivá A, et al. Among authors: janda a. Med Sci Monit. 2005 Apr;11(4):CR182-7. Epub 2005 Mar 24. Med Sci Monit. 2005. PMID: 15795698

4

Unrelated partially matched lymphocyte infusions in a patient with complete DiGeorge/CHARGE syndrome.

Janda A, Sedlacek P, Mejstrikova E, Zdrahalova K, Hrusak O, Kalina T, Sieglova Z, Zizkova H, Formankova R, Keslova P, Hubacek P, Sediva A, Bartunkova J, Dlask K, Stary J. Janda A, et al. Pediatr Transplant. 2007 Jun;11(4):441-7. doi: 10.1111/j.1399-3046.2007.00702.x. Pediatr Transplant. 2007. PMID: 17493228

5

Contiguous X-chromosome deletion syndrome encompassing the BTK, TIMM8A, TAF7L, and DRP2 genes.

Sedivá A, Smith CI, Asplund AC, Hadac J, Janda A, Zeman J, Hansíková H, Dvoráková L, Mrázová L, Velbri S, Koehler C, Roesch K, Sullivan KE, Futatani T, Ochs HD. Sedivá A, et al. Among authors: janda a. J Clin Immunol. 2007 Nov;27(6):640-6. doi: 10.1007/s10875-007-9123-x. Epub 2007 Sep 12. J Clin Immunol. 2007. PMID: 17851739

6

Kinetics of Toll-like receptor-4 splice variants expression in lipopolysaccharide-stimulated antigen presenting cells of healthy donors and patients with cystic fibrosis.

Jaresová I, Rozková D, Spísek R, Janda A, Brázová J, Sedivá A. Jaresová I, et al. Among authors: janda a. Microbes Infect. 2007 Sep;9(11):1359-67. doi: 10.1016/j.micinf.2007.06.009. Epub 2007 Jul 1. Microbes Infect. 2007. PMID: 17890129 Free article.

7

Profiling of polychromatic flow cytometry data on B-cells reveals patients' clusters in common variable immunodeficiency.

Kalina T, Stuchlý J, Janda A, Hrusák O, Růzicková S, Sedivá A, Litzman J, Vlková M. Kalina T, et al. Among authors: janda a. Cytometry A. 2009 Nov;75(11):902-9. doi: 10.1002/cyto.a.20801. Cytometry A. 2009. PMID: 19802875 Free article.

8

Characterization of lymphocyte subsets in patients with common variable immunodeficiency reveals subsets of naive human B cells marked by CD24 expression.

Vlková M, Fronková E, Kanderová V, Janda A, Ruzicková S, Litzman J, Sedivá A, Kalina T. Vlková M, et al. Among authors: janda a. J Immunol. 2010 Dec 1;185(11):6431-8. doi: 10.4049/jimmunol.0903876. Epub 2010 Nov 1. J Immunol. 2010. PMID: 21041728

9

Skin lesions in a boy with X-linked lymphoproliferative disorder: comparison of 5 SH2D1A deletion cases.

Mejstríková E, Janda A, Hrusák O, Bucková H, Vlcková M, Hancárová M, Freiberger T, Ravcuková B, Vesely K, Fajkusová L, Kopecková L, Sumerauer D, Kabícková E, Sedivá A, Stary J, Sedlácek Z. Mejstríková E, et al. Among authors: janda a. Pediatrics. 2012 Feb;129(2):e523-8. doi: 10.1542/peds.2011-0870. Epub 2012 Jan 23. Pediatrics. 2012. PMID: 22271700

10

Diffuse parenchymal lung disease as first clinical manifestation of GATA-2 deficiency in childhood.

Svobodova T, Mejstrikova E, Salzer U, Sukova M, Hubacek P, Matej R, Vasakova M, Hornofova L, Dvorakova M, Fronkova E, Votava F, Freiberger T, Pohunek P, Stary J, Janda A. Svobodova T, et al. Among authors: janda a. BMC Pulm Med. 2015 Feb 10;15:8. doi: 10.1186/s12890-015-0006-2. BMC Pulm Med. 2015. PMID: 25879889 Free PMC article.

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