Kotlas J - Search Results

1

[Hereditary forms of colorectal adenomatous polyposis].

Kohoutová M, Stekrová J, Sulová M, Zidková K, Kleibl Z, Vandrovcová J, Kebrdlová V, Kotlas J, Jirásek V. Kohoutová M, et al. Among authors: kotlas j. Cas Lek Cesk. 2006;145(6):475-9. Cas Lek Cesk. 2006. PMID: 16836001 Czech.

2

Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects.

Stekrova J, Sulova M, Kebrdlova V, Zidkova K, Kotlas J, Ilencikova D, Vesela K, Kohoutova M. Stekrova J, et al. Among authors: kotlas j. BMC Med Genet. 2007 Apr 5;8:16. doi: 10.1186/1471-2350-8-16. BMC Med Genet. 2007. PMID: 17411426 Free PMC article.

3

[Human gene therapy].

Kohoutová M, Kotlas J. Kohoutová M, et al. Among authors: kotlas j. Cas Lek Cesk. 1994 Mar 21;133(6):164-6. Cas Lek Cesk. 1994. PMID: 8156570 Review. Czech.

4

Two Czech patients with familial adenomatous polyposis presenting mosaicism in APC gene.

Urbanova M, Hirschfeldova K, Obeidova L, Janosikova B, Lastuvkova J, Lukas M, Kotlas J, Stekrova J. Urbanova M, et al. Among authors: kotlas j. Neoplasma. 2019 Mar 5;66(2):294-300. doi: 10.4149/neo_2018_180731N559. Epub 2018 Dec 12. Neoplasma. 2019. PMID: 30569724

5

Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families.

Schwarzová L, Štekrová J, Florianová M, Novotný A, Schneiderová M, Lněnička P, Kebrdlová V, Kotlas J, Veselá K, Kohoutová M. Schwarzová L, et al. Among authors: kotlas j. Fam Cancer. 2013 Mar;12(1):35-42. doi: 10.1007/s10689-012-9569-8. Fam Cancer. 2013. PMID: 22987206

6

High proportion of recurrent germline mutations in the BRCA1 gene in breast and ovarian cancer patients from the Prague area.

Pohlreich P, Zikan M, Stribrna J, Kleibl Z, Janatova M, Kotlas J, Zidovska J, Novotny J, Petruzelka L, Szabo C, Matous B. Pohlreich P, et al. Among authors: kotlas j. Breast Cancer Res. 2005;7(5):R728-36. doi: 10.1186/bcr1282. Epub 2005 Jul 19. Breast Cancer Res. 2005. PMID: 16168118 Free PMC article.

7

Autosomal dominant polycystic kidney disease in a family with mosaicism and hypomorphic allele.

Reiterová J, Štekrová J, Merta M, Kotlas J, Elišáková V, Lněnička P, Korabečná M, Kohoutová M, Tesař V. Reiterová J, et al. Among authors: kotlas j. BMC Nephrol. 2013 Mar 15;14:59. doi: 10.1186/1471-2369-14-59. BMC Nephrol. 2013. PMID: 23496908 Free PMC article.

8

Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease - a case report.

Elisakova V, Merta M, Reiterova J, Baxova A, Kotlas J, Hirschfeldova K, Obeidova L, Tesar V, Stekrova J. Elisakova V, et al. Among authors: kotlas j. BMC Nephrol. 2018 Jul 4;19(1):163. doi: 10.1186/s12882-018-0978-2. BMC Nephrol. 2018. PMID: 29973168 Free PMC article.

9

[Prerequisites for preimplantation genetic diagnosis (PGD in carriers of mutations responsible for hereditary cancers].

Hüttelová R, Kleibl Z, Rezátová J, Krutílková V, Foretová L, Novotný J, Kotlas J, Zikán M, Pohlreich P. Hüttelová R, et al. Among authors: kotlas j. Klin Onkol. 2009;22 Suppl:S69-74. Klin Onkol. 2009. PMID: 19764403 Czech.

10

[Hereditary ovarian cancer].

Zikán M, Foretová L, Cibula D, Kotlas J, Pohlreich P. Zikán M, et al. Among authors: kotlas j. Ceska Gynekol. 2006 May;71(3):246-51. Ceska Gynekol. 2006. PMID: 16768054 Review. Czech.

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