Foretová L - Search Results

1

BAP1 Syndrome - Predisposition to Malignant Mesothelioma, Skin and Uveal Melanoma, Renal and Other Cancers.

Foretová L, Navrátilová M, Svoboda M, Házová J, Vašíčková P, Sťahlová EH, Fabian P, Schneiderová M, Macháčková E. Foretová L, et al. Klin Onkol. 2019 Summer;32(Supplementum2):118-122. doi: 10.14735/amko2019S118. Klin Onkol. 2019. PMID: 31409087 English.

2

A high occurrence of BRCA1 and BRCA2 mutations among Czech hereditary breast and breast-ovarian cancer families.

Machácková E, Foretová L, Navrátilová M, Valík D, Claes K, Messiaen L. Machácková E, et al. Among authors: foretova l. Cas Lek Cesk. 2000 Oct 11;139(20):635-7. Cas Lek Cesk. 2000. PMID: 11192759

3

Novel germline BRCA1 and BRCA2 mutations in breast and breast/ovarian cancer families from the Czech Republic.

Machackova E, Damborsky J, Valik D, Foretova L. Machackova E, et al. Among authors: foretova l. Hum Mutat. 2001 Dec;18(6):545. doi: 10.1002/humu.1232. Hum Mutat. 2001. PMID: 11748848

4

Differentiating pathogenic mutations from polymorphic alterations in the splice sites of BRCA1 and BRCA2.

Claes K, Poppe B, Machackova E, Coene I, Foretova L, De Paepe A, Messiaen L. Claes K, et al. Among authors: foretova l. Genes Chromosomes Cancer. 2003 Jul;37(3):314-20. doi: 10.1002/gcc.10221. Genes Chromosomes Cancer. 2003. PMID: 12759930

5

BRCA1 and BRCA2 mutations in women with familial or early-onset breast/ovarian cancer in the Czech Republic.

Foretova L, Machackova E, Navratilova M, Pavlu H, Hruba M, Lukesova M, Valik D. Foretova L, et al. Hum Mutat. 2004 Apr;23(4):397-8. doi: 10.1002/humu.9226. Hum Mutat. 2004. PMID: 15024741

6

High occurrence of BRCA1 intragenic rearrangements in hereditary breast and ovarian cancer syndrome in the Czech Republic.

Vasickova P, Machackova E, Lukesova M, Damborsky J, Horky O, Pavlu H, Kuklova J, Kosinova V, Navratilova M, Foretova L. Vasickova P, et al. Among authors: foretova l. BMC Med Genet. 2007 Jun 11;8:32. doi: 10.1186/1471-2350-8-32. BMC Med Genet. 2007. PMID: 17561994 Free PMC article.

7

PML protein expression in hereditary and sporadic breast cancer.

Plevová P, Bouchal J, Fiurásková M, Foretová L, Navrátilová M, Zapletalová J, Curík R, Kubala O, Prokop J, Kolár Z. Plevová P, et al. Among authors: foretova l. Neoplasma. 2007;54(4):263-8. Neoplasma. 2007. PMID: 17822314

8

Spectrum and characterisation of BRCA1 and BRCA2 deleterious mutations in high-risk Czech patients with breast and/or ovarian cancer.

Machackova E, Foretova L, Lukesova M, Vasickova P, Navratilova M, Coene I, Pavlu H, Kosinova V, Kuklova J, Claes K. Machackova E, et al. Among authors: foretova l. BMC Cancer. 2008 May 20;8:140. doi: 10.1186/1471-2407-8-140. BMC Cancer. 2008. PMID: 18489799 Free PMC article.

9

[Hereditary breast and ovarian cancer syndrome].

Plevová P, Novotný J, Petráková K, Palácová M, Kalábová R, Schneiderová M, Foretová L. Plevová P, et al. Among authors: foretova l. Klin Onkol. 2009;22 Suppl:S8-11. Klin Onkol. 2009. PMID: 19764385 Review. Czech. No abstract available.

10

[Limitations of genetic testing in oncology].

Foretová L, Navrátilová M, Machácková E. Foretová L, et al. Klin Onkol. 2009;22 Suppl:S65-8. Klin Onkol. 2009. PMID: 19764402 Review. Czech.

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