Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2011 1
2013 1
2014 1
2015 1
2016 1
2017 2
2018 2
2019 1
2020 1
2021 2
2022 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

11 results

Results by year

Filters applied: . Clear all
Page 1
[Soft tissue tumors - the view of the molecular biologist].
Krsková L, Mrhalová M, Kalinová M, Campr V, Capková L, Grega M, Háček J, Hornofová L, Chadimová M, Chmelová R, Kodetová D, Zámečník J, Kodet R. Krsková L, et al. Among authors: hornofova l. Cesk Patol. 2014 Jul;50(3):132-40. Cesk Patol. 2014. PMID: 25186594 Review. Czech.
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: hornofova l. 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
Congenital bronchopulmonary malformation: CT histopathological correlation.
Kyncl M, Koci M, Ptackova L, Hornofova L, Ondrej F, Snajdauf J, Pychova M. Kyncl M, et al. Among authors: hornofova l. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2016 Dec;160(4):533-537. doi: 10.5507/bp.2016.051. Epub 2016 Oct 17. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2016. PMID: 27752149 Free article.
Homozygous EXOSC3 mutation c.92G→C, p.G31A is a founder mutation causing severe pontocerebellar hypoplasia type 1 among the Czech Roma.
Schwabova J, Brozkova DS, Petrak B, Mojzisova M, Pavlickova K, Haberlova J, Mrazkova L, Hedvicakova P, Hornofova L, Kaluzova M, Fencl F, Krutova M, Zamecnik J, Seeman P. Schwabova J, et al. Among authors: hornofova l. J Neurogenet. 2013 Dec;27(4):163-9. doi: 10.3109/01677063.2013.814651. Epub 2013 Jul 25. J Neurogenet. 2013. PMID: 23883322
11 results