Kotlín R - Search Results

1

CCAAT/enhancer-binding protein alpha (CEBPA) polymorphisms and mutations in healthy individuals and in patients with peripheral artery disease, ischaemic heart disease and hyperlipidaemia.

Fuchs O, Kostecka A, Provazníková D, Krásná B, Kotlín R, Stanková M, Kobylka P, Dostálová G, Zeman M, Chochola M. Fuchs O, et al. Among authors: kotlin r. Folia Biol (Praha). 2010;56(2):51-7. Folia Biol (Praha). 2010. PMID: 20492756 Free article.

2

High-resolution melting analysis for detection of MYH9 mutations.

Provaznikova D, Kumstyrova T, Kotlin R, Salaj P, Matoska V, Hrachovinova I, Rittich S. Provaznikova D, et al. Among authors: kotlin r. Platelets. 2008 Sep;19(6):471-5. doi: 10.1080/09537100802140013. Platelets. 2008. PMID: 18925516

3

Clinical manifestation and molecular genetic characterization of MYH9 disorders.

Provaznikova D, Geierova V, Kumstyrova T, Kotlin R, Mikulenkova D, Zurkova K, Matoska V, Hrachovinova I, Rittich S. Provaznikova D, et al. Among authors: kotlin r. Platelets. 2009 Aug;20(5):289-96. doi: 10.1080/09537100902993022. Platelets. 2009. PMID: 19557653

4

Nature of frequent deletions in CEBPA.

Fuchs O, Kostecka A, Provaznikova D, Krasna B, Brezinova J, Filkukova J, Kotlin R, Kouba M, Kobylka P, Neuwirtova R, Jonasova A, Caniga M, Schwarz J, Markova J, Maaloufova J, Sponerova D, Novakova L, Cermak J. Fuchs O, et al. Among authors: kotlin r. Blood Cells Mol Dis. 2009 Nov-Dec;43(3):260-3. doi: 10.1016/j.bcmd.2009.07.001. Epub 2009 Aug 3. Blood Cells Mol Dis. 2009. PMID: 19651529

5

Diagnosing Czech Patients with Inherited Platelet Disorders.

Louzil J, Stikarova J, Provaznikova D, Hrachovinova I, Fenclova T, Musil J, Radek M, Kaufmanova J, Geierova V, Ceznerova E, Salaj P, Kotlin R. Louzil J, et al. Among authors: kotlin r. Int J Mol Sci. 2022 Nov 19;23(22):14386. doi: 10.3390/ijms232214386. Int J Mol Sci. 2022. PMID: 36430862 Free PMC article.

6

A novel fibrinogen variant--Liberec: dysfibrinogenaemia associated with gamma Tyr262Cys substitution.

Kotlín R, Sobotková A, Suttnar J, Salaj P, Walterová L, Riedel T, Reicheltová Z, Dyr JE. Kotlín R, et al. Eur J Haematol. 2008 Aug;81(2):123-9. doi: 10.1111/j.1600-0609.2008.01094.x. Epub 2008 May 11. Eur J Haematol. 2008. PMID: 18485115

7

Dysfibrinogenemia in childhood: two cases of congenital dysfibrinogens.

Kotlín R, Blažek B, Suttnar J, Malý M, Kvasnička J, Dyr JE. Kotlín R, et al. Blood Coagul Fibrinolysis. 2010 Oct;21(7):640-8. doi: 10.1097/MBC.0b013e32833e4284. Blood Coagul Fibrinolysis. 2010. PMID: 20829681

8

Enhanced plasma protein carbonylation in patients with myelodysplastic syndromes.

Hlaváčková A, Štikarová J, Pimková K, Chrastinová L, Májek P, Kotlín R, Čermák J, Suttnar J, Dyr JE. Hlaváčková A, et al. Among authors: kotlin r. Free Radic Biol Med. 2017 Jul;108:1-7. doi: 10.1016/j.freeradbiomed.2017.03.007. Epub 2017 Mar 12. Free Radic Biol Med. 2017. PMID: 28300669

9

Fibrinogen Nový Jicín and Praha II: cases of hereditary Aalpha 16 Arg-->Cys and Aalpha 16 Arg-->His dysfibrinogenemia.

Kotlín R, Chytilová M, Suttnar J, Riedel T, Salaj P, Blatný J, Santrůcek J, Klener P, Dyr JE. Kotlín R, et al. Thromb Res. 2007;121(1):75-84. doi: 10.1016/j.thromres.2007.02.011. Epub 2007 Apr 3. Thromb Res. 2007. PMID: 17408725

10

Two novel mutations in the fibrinogen γ nodule.

Kotlín R, Pastva O, Stikarová J, Hlaváčková A, Suttnar J, Chrastinová L, Riedel T, Salaj P, Dyr JE. Kotlín R, et al. Thromb Res. 2014 Oct;134(4):901-8. doi: 10.1016/j.thromres.2014.07.021. Epub 2014 Jul 21. Thromb Res. 2014. PMID: 25074738

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

30 results

Search Page