Slamova I - Search Results

1

Antibody-Associated Reversal of ATTR Amyloidosis-Related Cardiomyopathy.

Fontana M, Gilbertson J, Verona G, Riefolo M, Slamova I, Leone O, Rowczenio D, Botcher N, Ioannou A, Patel RK, Razvi Y, Martinez-Naharro A, Whelan CJ, Venneri L, Duhlin A, Canetti D, Ellmerich S, Moon JC, Kellman P, Al-Shawi R, McCoy L, Simons JP, Hawkins PN, Gillmore JD. Fontana M, et al. Among authors: slamova i. N Engl J Med. 2023 Jun 8;388(23):2199-2201. doi: 10.1056/NEJMc2304584. N Engl J Med. 2023. PMID: 37285532 No abstract available.

2

Plasmin activity promotes amyloid deposition in a transgenic model of human transthyretin amyloidosis.

Slamova I, Adib R, Ellmerich S, Golos MR, Gilbertson JA, Botcher N, Canetti D, Taylor GW, Rendell N, Tennent GA, Verona G, Porcari R, Mangione PP, Gillmore JD, Pepys MB, Bellotti V, Hawkins PN, Al-Shawi R, Simons JP. Slamova I, et al. Nat Commun. 2021 Dec 7;12(1):7112. doi: 10.1038/s41467-021-27416-z. Nat Commun. 2021. PMID: 34876572 Free PMC article.

3

The effects of short-term JNK inhibition on the survival and growth of aged sympathetic neurons.

Guha I, Slamova I, Chun S, Clegg A, Golos M, Thrasivoulou C, Simons JP, Al-Shawi R. Guha I, et al. Among authors: slamova i. Neurobiol Aging. 2016 Oct;46:138-48. doi: 10.1016/j.neurobiolaging.2016.06.016. Epub 2016 Jul 5. Neurobiol Aging. 2016. PMID: 27490965

4

A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms.

Hladilkova E, Barøy T, Fannemel M, Vallova V, Misceo D, Bryn V, Slamova I, Prasilova S, Kuglik P, Frengen E. Hladilkova E, et al. Among authors: slamova i. Mol Cytogenet. 2015 Jul 31;8:57. doi: 10.1186/s13039-015-0157-0. eCollection 2015. Mol Cytogenet. 2015. PMID: 26236398 Free PMC article.

5

Unique Combination of 22q11 and 14qter Microdeletion Syndromes Detected Using Oligonucleotide Array-CGH.

Zrnová E, Vranová V, Soukalová J, Slámová I, Vilémová M, Gaillyová R, Kuglík P. Zrnová E, et al. Among authors: slamova i. Mol Syndromol. 2012 Jan;2(2):88-93. doi: 10.1159/000335334. Epub 2012 Jan 26. Mol Syndromol. 2012. PMID: 22511897 Free PMC article.

6

Analysis of chromosomal aberrations in patients with mental retardation using the array-CGH technique: a single Czech centre experience.

Zrnová E, Vranová V, Slámová I, Gaillyová R, Kuglík P. Zrnová E, et al. Among authors: slamova i. Folia Biol (Praha). 2011;57(5):206-15. Folia Biol (Praha). 2011. PMID: 22123463 Free article.

7

Monozygotic twins with discordant karyotypes following preimplantation genetic screening and single embryo transfer: case report.

Tauwinklova G, Gaillyova R, Travnik P, Oracova E, Vesela K, Hromadova L, Vesely J, Musilova P, Rubes J, Kadlecova J, Slamova I, Makaturova E, Vranova V. Tauwinklova G, et al. Among authors: slamova i. J Assist Reprod Genet. 2010 Nov;27(11):649-55. doi: 10.1007/s10815-010-9462-z. Epub 2010 Aug 11. J Assist Reprod Genet. 2010. PMID: 20700760 Free PMC article.

8

Low-level copy number changes of MYC genes have a prognostic impact in medulloblastoma.

Zitterbart K, Filkova H, Tomasikova L, Necesalova E, Zambo I, Kantorova D, Slamova I, Vranova V, Zezulkova D, Pesakova M, Pavelka Z, Veselska R, Kuglik P, Sterba J. Zitterbart K, et al. Among authors: slamova i. J Neurooncol. 2011 Mar;102(1):25-33. doi: 10.1007/s11060-010-0289-3. Epub 2010 Jul 8. J Neurooncol. 2011. PMID: 20607354

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

8 results

Search Page