Petrak B - Search Results

1

Novel mutations in the NF1 gene in Czech patients with neurofibromatosis type 1.

Bendova S, Krepelova A, Petrak B, Kinstova L, Musova Z, Rausova E, Marikova T. Bendova S, et al. Among authors: petrak b. J Mol Neurosci. 2007;31(3):273-9. doi: 10.1385/jmn:31:03:273. J Mol Neurosci. 2007. PMID: 17726231

2

A girl with neurofibromatosis type 1, atypical autism and mosaic ring chromosome 17.

Havlovicova M, Novotna D, Kocarek E, Novotna K, Bendova S, Petrak B, Hrdlicka M, Sedlacek Z. Havlovicova M, et al. Among authors: petrak b. Am J Med Genet A. 2007 Jan 1;143A(1):76-81. doi: 10.1002/ajmg.a.31569. Am J Med Genet A. 2007. PMID: 17163520

3

Mid-aortic syndrome with renovascular hypertension and multisystem involvement in a girl with familiar neurofibromatosis von Recklinghausen type 1.

Petrak B, Bendova S, Seeman T, Klein T, Lisy J, Zatrapa T, Marikova T. Petrak B, et al. Neuro Endocrinol Lett. 2007 Dec;28(6):734-8. Neuro Endocrinol Lett. 2007. PMID: 18063929

4

[Neurofibromatosis von Recklinghausen].

Petrák B, Plevová P, Novotný J, Foretová L. Petrák B, et al. Klin Onkol. 2009;22 Suppl:S38-44. Klin Onkol. 2009. PMID: 19764395 Review. Czech. No abstract available.

5

The importance of advanced parental age in the origin of neurofibromatosis type 1.

Snajderova M, Riccardi VM, Petrak B, Zemkova D, Zapletalova J, Mardesic T, Petrakova A, Lanska V, Marikova T, Bendova S, Havlovicova M, Kaluzova M. Snajderova M, et al. Among authors: petrak b. Am J Med Genet A. 2012 Mar;158A(3):519-23. doi: 10.1002/ajmg.a.34413. Epub 2012 Feb 2. Am J Med Genet A. 2012. PMID: 22302476

6

[Neurofibromatosis von Recklinghausen type 1 (NF1) - clinical picture and molecular-genetics diagnostic].

Petrák B, Bendová Š, Lisý J, Kraus J, Zatrapa T, Glombová M, Zámečník J. Petrák B, et al. Cesk Patol. 2015;51(1):34-40. Cesk Patol. 2015. PMID: 25671360 Review. Czech.

7

Anti-vimentin antibodies and neuron-specific enolase in children with neurofibromatosis type-1.

Kotaska K, Petrak B, Kukacka J, Kraus J, Prusa R. Kotaska K, et al. Among authors: petrak b. Neuro Endocrinol Lett. 2007 Dec;28(6):761-4. Neuro Endocrinol Lett. 2007. PMID: 18063947

8

Homozygous EXOSC3 mutation c.92G→C, p.G31A is a founder mutation causing severe pontocerebellar hypoplasia type 1 among the Czech Roma.

Schwabova J, Brozkova DS, Petrak B, Mojzisova M, Pavlickova K, Haberlova J, Mrazkova L, Hedvicakova P, Hornofova L, Kaluzova M, Fencl F, Krutova M, Zamecnik J, Seeman P. Schwabova J, et al. Among authors: petrak b. J Neurogenet. 2013 Dec;27(4):163-9. doi: 10.3109/01677063.2013.814651. Epub 2013 Jul 25. J Neurogenet. 2013. PMID: 23883322

9

Brain gliomas, hydrocephalus and idiopathic aqueduct stenosis in children with neurofibromatosis type 1.

Glombova M, Petrak B, Lisy J, Zamecnik J, Sumerauer D, Liby P. Glombova M, et al. Among authors: petrak b. Brain Dev. 2019 Sep;41(8):678-690. doi: 10.1016/j.braindev.2019.04.003. Epub 2019 Apr 15. Brain Dev. 2019. PMID: 31000370

10

Chromosome 12q13.13 deletions involving the HOXC gene cluster: phenotype and candidate genes.

Hancarova M, Simandlova M, Drabova J, Petrak B, Koudova M, Havlovicova M, Sedlacek Z. Hancarova M, et al. Among authors: petrak b. Eur J Med Genet. 2013 Mar;56(3):171-3. doi: 10.1016/j.ejmg.2012.12.003. Epub 2012 Dec 27. Eur J Med Genet. 2013. PMID: 23274590 No abstract available.

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

25 results

Search Page