Sumerauer D - Search Results

1

Rare IDH1 variants are common in pediatric hemispheric diffuse astrocytomas and frequently associated with Li-Fraumeni syndrome.

Sumerauer D, Krskova L, Vicha A, Misove A, Mamatjan Y, Jencova P, Vlckova M, Slamova L, Vanova K, Liby P, Taborsky J, Koblizek M, Klubal R, Kyncl M, Zadeh G, Stary J, Zamecnik J, Ramaswamy V, Zapotocky M. Sumerauer D, et al. Acta Neuropathol. 2020 Apr;139(4):795-797. doi: 10.1007/s00401-019-02118-5. Epub 2020 Jan 3. Acta Neuropathol. 2020. PMID: 31897644 No abstract available.

2

Gene aberrations in childhood brain tumors.

Kucerová H, Stejskalová E, Vícha A, Tichý M, Chánová M, Sumerauer D, Koutechký J, Eckschlager T. Kucerová H, et al. Among authors: sumerauer d. Folia Biol (Praha). 2000;46(5):187-90. Folia Biol (Praha). 2000. PMID: 11055797

3

Detection of minimal bone marrow infiltration in patients with localized and metastatic Ewing sarcoma using RT-PCR.

Sumerauer D, Vícha A, Kucerová H, Kodet R, Housková J, Bedrnícek J, Eckschlager T. Sumerauer D, et al. Folia Biol (Praha). 2001;47(6):206-10. Folia Biol (Praha). 2001. PMID: 11768778

4

Malignant peripheral primitive neuroectodermal tumor of the kidney.

Vicha A, Stejskalova E, Sumerauer D, Kodet R, Malis J, Kucerova H, Bedrnicek J, Koutecky J, Eckschlager T. Vicha A, et al. Among authors: sumerauer d. Cancer Genet Cytogenet. 2002 Nov;139(1):67-70. doi: 10.1016/s0165-4608(02)00602-7. Cancer Genet Cytogenet. 2002. PMID: 12547163

5

Rhabdomyosarcoma: molecular diagnostics of patients classified by morphology and immunohistochemistry with emphasis on bone marrow and purged peripheral blood progenitor cells involvement.

Krsková L, Mrhalová M, Sumerauer D, Kodet R. Krsková L, et al. Among authors: sumerauer d. Virchows Arch. 2006 Apr;448(4):449-58. doi: 10.1007/s00428-005-0124-y. Epub 2005 Dec 20. Virchows Arch. 2006. PMID: 16365729

6

Teratoma in an adolescent with malignant transformation into embryonal rhabdomyosarcoma: case report.

Sumerauer D, Vicha A, Zuntova A, Stejskalova E, Krskova L, Kabickova E, Kodet R, Eckschlager T. Sumerauer D, et al. J Pediatr Hematol Oncol. 2006 Oct;28(10):688-92. doi: 10.1097/01.mph.0000212992.72059.eb. J Pediatr Hematol Oncol. 2006. PMID: 17023832

7

A novel variant of SYT-SSX1 fusion gene in a case of spindle cell synovial sarcoma.

Krsková L, Sumerauer D, Stejskalová E, Kodet R. Krsková L, et al. Among authors: sumerauer d. Diagn Mol Pathol. 2007 Sep;16(3):179-83. doi: 10.1097/PDM.0b013e3180340343. Diagn Mol Pathol. 2007. PMID: 17721327

8

Molecular and immunohistochemical analysis of ERBB2 expression in correlation with proliferation rate in synovial sarcoma.

Krsková L, Kalinová M, Brizová H, Mrhalová M, Sumerauer D, Kodet R. Krsková L, et al. Among authors: sumerauer d. Diagn Mol Pathol. 2007 Dec;16(4):211-7. doi: 10.1097/PDM.0b013e3180621995. Diagn Mol Pathol. 2007. PMID: 18043284

9

Somatic TP53 mutation mosaicism in a patient with Li-Fraumeni syndrome.

Prochazkova K, Pavlikova K, Minarik M, Sumerauer D, Kodet R, Sedlacek Z. Prochazkova K, et al. Among authors: sumerauer d. Am J Med Genet A. 2009 Feb;149A(2):206-11. doi: 10.1002/ajmg.a.32574. Am J Med Genet A. 2009. PMID: 19012332

10

Molecular and immunohistochemical analyses of BCL2, KI-67, and cyclin D1 expression in synovial sarcoma.

Krsková L, Kalinová M, Brízová H, Mrhalová M, Sumerauer D, Kodet R. Krsková L, et al. Among authors: sumerauer d. Cancer Genet Cytogenet. 2009 Aug;193(1):1-8. doi: 10.1016/j.cancergencyto.2009.03.008. Cancer Genet Cytogenet. 2009. PMID: 19602458

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