Plevova P - Search Results

1

Identification of five new families strengthens the link between childhood choroid plexus carcinoma and germline TP53 mutations.

Krutilkova V, Trkova M, Fleitz J, Gregor V, Novotna K, Krepelova A, Sumerauer D, Kodet R, Siruckova S, Plevova P, Bendova S, Hedvicakova P, Foreman NK, Sedlacek Z. Krutilkova V, et al. Among authors: plevova p. Eur J Cancer. 2005 Jul;41(11):1597-603. doi: 10.1016/j.ejca.2005.01.026. Eur J Cancer. 2005. PMID: 15925506

2

Elejalde syndrome--a case report.

Silhánová E, Plevová P, Curík R, Kaspercík I, Krepelová A. Silhánová E, et al. Among authors: plevova p. Am J Med Genet A. 2006 Oct 15;140(20):2223-6. doi: 10.1002/ajmg.a.31419. Am J Med Genet A. 2006. PMID: 16969863

3

Spinocerebellar ataxias type 8, 12, and 17 and dentatorubro-pallidoluysian atrophy in Czech ataxic patients.

Musova Z, Sedlacek Z, Mazanec R, Klempir J, Roth J, Plevova P, Vyhnalek M, Kopeckova M, Apltova L, Krepelova A, Zumrova A. Musova Z, et al. Among authors: plevova p. Cerebellum. 2013 Apr;12(2):155-61. doi: 10.1007/s12311-012-0403-5. Cerebellum. 2013. PMID: 22872568

4

Germline variants of the promyelocytic leukemia tumor suppressor gene in patients with familial cancer.

Plevova P, Walczyskova S, Jeziskova I, Jurckova N, Krepelova A, Puchmajerova A, Pavlikova K, Foretova L, Zapletalova J, Silhanova E. Plevova P, et al. Neoplasma. 2009;56(6):500-7. doi: 10.4149/neo_2009_06_500. Neoplasma. 2009. PMID: 19728758

5

HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain.

Jolly LA, Nguyen LS, Domingo D, Sun Y, Barry S, Hancarova M, Plevova P, Vlckova M, Havlovicova M, Kalscheuer VM, Graziano C, Pippucci T, Bonora E, Sedlacek Z, Gecz J. Jolly LA, et al. Among authors: plevova p. Hum Mol Genet. 2015 Jun 15;24(12):3335-47. doi: 10.1093/hmg/ddv083. Epub 2015 Mar 3. Hum Mol Genet. 2015. PMID: 25740848

6

Expression of the hMLH1 and hMSH2 proteins in normal tissues: relationship to cancer predisposition in hereditary non-polyposis colon cancer.

Plevová P, Sedláková E, Zapletalová J, Krepelová A, Skýpalová P, Kolár Z. Plevová P, et al. Virchows Arch. 2005 Feb;446(2):112-9. doi: 10.1007/s00428-004-1139-5. Epub 2004 Dec 10. Virchows Arch. 2005. PMID: 15735976

7

[Cowden syndrome].

Puchmajerová A, Vasovcák P, Krepelová A, Plevová P. Puchmajerová A, et al. Among authors: plevova p. Klin Onkol. 2009;22 Suppl:S56-7. Klin Onkol. 2009. PMID: 19764399 Review. Czech. No abstract available.

8

[Von Hippel-Lindau disease].

Plevová P, Novotný J, Krepelová A. Plevová P, et al. Klin Onkol. 2009;22 Suppl:S23-4. Klin Onkol. 2009. PMID: 19764389 Review. Czech. No abstract available.

9

Immunohistochemical detection of the hMLH1 and hMSH2 proteins in hereditary non-polyposis colon cancer and sporadic colon cancer.

Plevová P, Krepelová A, Papezová M, Sedláková E, Curík R, Foretová L, Navrátilová M, Novotný J, Zapletalová J, Palas J, Nieslanik J, Horácek J, Dvorácková J, Kolár Z. Plevová P, et al. Neoplasma. 2004;51(4):275-84. Neoplasma. 2004. PMID: 15254659

10

[Gorlin syndrome].

Plevová P, Krutílková V, Puchmajerová A, Foretová L. Plevová P, et al. Klin Onkol. 2009;22 Suppl:S34-5. Klin Onkol. 2009. PMID: 19764393 Review. Czech. No abstract available.

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