Vasovcak P - Search Results

1

A novel frameshift mutation in the AFG3L2 gene in a patient with spinocerebellar ataxia.

Musova Z, Kaiserova M, Kriegova E, Fillerova R, Vasovcak P, Santava A, Mensikova K, Zumrova A, Krepelova A, Sedlacek Z, Kanovsky P. Musova Z, et al. Among authors: vasovcak p. Cerebellum. 2014 Jun;13(3):331-7. doi: 10.1007/s12311-013-0538-z. Cerebellum. 2014. PMID: 24272953

2

Mutations in STK11 gene in Czech Peutz-Jeghers patients.

Vasovcák P, Puchmajerová A, Roubalík J, Krepelová A. Vasovcák P, et al. BMC Med Genet. 2009 Jul 19;10:69. doi: 10.1186/1471-2350-10-69. BMC Med Genet. 2009. PMID: 19615099 Free PMC article.

3

Multiple primary malignancies and subtle mucocutaneous lesions associated with a novel PTEN gene mutation in a patient with Cowden syndrome: case report.

Vasovčák P, Senkeříková M, Hatlová J, Křepelová A. Vasovčák P, et al. BMC Med Genet. 2011 Mar 15;12:38. doi: 10.1186/1471-2350-12-38. BMC Med Genet. 2011. PMID: 21406108 Free PMC article.

4

Molecular genetic analysis of 103 sporadic colorectal tumours in Czech patients.

Vasovcak P, Pavlikova K, Sedlacek Z, Skapa P, Kouda M, Hoch J, Krepelova A. Vasovcak P, et al. PLoS One. 2011;6(8):e24114. doi: 10.1371/journal.pone.0024114. Epub 2011 Aug 25. PLoS One. 2011. PMID: 21901162 Free PMC article.

5

A novel mutation of PTEN gene in a patient with Cowden syndrome with excessive papillomatosis of the lips, discrete cutaneous lesions, and gastrointestinal polyposis.

Vasovcak P, Krepelova A, Puchmajerova A, Spicak J, Voska L, Musilova A, Mestak J, Martinek J. Vasovcak P, et al. Eur J Gastroenterol Hepatol. 2007 Jun;19(6):513-7. doi: 10.1097/MEG.0b013e3280d6ed4b. Eur J Gastroenterol Hepatol. 2007. PMID: 17489063

6

[Rhabdoid tumours].

Vasovčák P, Puchmajerová A, Křepelová A. Vasovčák P, et al. Klin Onkol. 2012;25 Suppl:S27-9. Klin Onkol. 2012. PMID: 22920203 Slovak.

7

[Juvenile polyposis syndrome].

Vasovčák P, Foretová L, Puchmajerová A, Křepelová A. Vasovčák P, et al. Klin Onkol. 2012;25 Suppl:S16-7. Klin Onkol. 2012. PMID: 22920200 Slovak.

8

Unique mutational profile associated with a loss of TDG expression in the rectal cancer of a patient with a constitutional PMS2 deficiency.

Vasovcak P, Krepelova A, Menigatti M, Puchmajerova A, Skapa P, Augustinakova A, Amann G, Wernstedt A, Jiricny J, Marra G, Wimmer K. Vasovcak P, et al. DNA Repair (Amst). 2012 Jul 1;11(7):616-23. doi: 10.1016/j.dnarep.2012.04.004. Epub 2012 May 17. DNA Repair (Amst). 2012. PMID: 22608206 Free PMC article.

9

[Our experience with analysis of the PTEN gene in patients suspected of having Cowden syndrome].

Vasovcák P, Foretová L, Puchmajerová A, Senkeríková M, Martínek J, Krepelová A. Vasovcák P, et al. Klin Onkol. 2010;23(2):111-4. Klin Onkol. 2010. PMID: 20465090 Slovak.

10

[Birt-Hogg-Dubé syndrome].

Křepelová A, Puchmajerová A, Vasovčák P, Chocholatý M. Křepelová A, et al. Among authors: vasovcak p. Klin Onkol. 2012;25 Suppl:S18-20. Klin Onkol. 2012. PMID: 22920201 Czech.

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