Pietsch T - Search Results

1

PATZ1 fusions define a novel molecularly distinct neuroepithelial tumor entity with a broad histological spectrum.

Alhalabi KT, Stichel D, Sievers P, Peterziel H, Sommerkamp AC, Sturm D, Wittmann A, Sill M, Jäger N, Beck P, Pajtler KW, Snuderl M, Jour G, Delorenzo M, Martin AM, Levy A, Dalvi N, Hansford JR, Gottardo NG, Uro-Coste E, Maurage CA, Godfraind C, Vandenbos F, Pietsch T, Kramm C, Filippidou M, Kattamis A, Jones C, Øra I, Mikkelsen TS, Zapotocky M, Sumerauer D, Scheie D, McCabe M, Wesseling P, Tops BBJ, Kranendonk MEG, Karajannis MA, Bouvier N, Papaemmanuil E, Dohmen H, Acker T, von Hoff K, Schmid S, Miele E, Filipski K, Kitanovski L, Krskova L, Gojo J, Haberler C, Alvaro F, Ecker J, Selt F, Milde T, Witt O, Oehme I, Kool M, von Deimling A, Korshunov A, Pfister SM, Sahm F, Jones DTW. Alhalabi KT, et al. Among authors: pietsch t. Acta Neuropathol. 2021 Nov;142(5):841-857. doi: 10.1007/s00401-021-02354-8. Epub 2021 Aug 21. Acta Neuropathol. 2021. PMID: 34417833 Free PMC article.

2

Loss of maternal alleles on chromosome arm 11p in hepatoblastoma.

Albrecht S, von Schweinitz D, Waha A, Kraus JA, von Deimling A, Pietsch T. Albrecht S, et al. Among authors: pietsch t. Cancer Res. 1994 Oct 1;54(19):5041-4. Cancer Res. 1994. PMID: 7923113

3

Microsatellite analysis of loss of heterozygosity on chromosomes 9q, 11p and 17p in medulloblastomas.

Albrecht S, von Deimling A, Pietsch T, Giangaspero F, Brandner S, Kleihues P, Wiestler OD. Albrecht S, et al. Among authors: pietsch t. Neuropathol Appl Neurobiol. 1994 Feb;20(1):74-81. doi: 10.1111/j.1365-2990.1994.tb00959.x. Neuropathol Appl Neurobiol. 1994. PMID: 8208343

4

Loss of heterozygosity at locus F13B on chromosome 1q in human medulloblastoma.

Kraus JA, Koch A, Albrecht S, Von Deimling A, Wiestler OD, Pietsch T. Kraus JA, et al. Among authors: pietsch t. Int J Cancer. 1996 Jul 3;67(1):11-5. doi: 10.1002/(SICI)1097-0215(19960703)67:1<11::AID-IJC3>3.0.CO;2-2. Int J Cancer. 1996. PMID: 8690510

5

Perilesional neurochemical changes in focal epilepsies.

Wolf HK, Roos D, Blümcke I, Pietsch T, Wiestler OD. Wolf HK, et al. Among authors: pietsch t. Acta Neuropathol. 1996;91(4):376-84. doi: 10.1007/s004010050439. Acta Neuropathol. 1996. PMID: 8928614

6

Tuberous sclerosis-like lesions in epileptogenic human neocortex lack allelic loss at the TSC1 and TSC2 regions.

Wolf HK, Normann S, Green AJ, von Bakel I, Blümcke I, Pietsch T, Wiestler OD, von Deimling A. Wolf HK, et al. Among authors: pietsch t. Acta Neuropathol. 1997 Jan;93(1):93-6. doi: 10.1007/s004010050587. Acta Neuropathol. 1997. PMID: 9006662

7

Expression and distribution of vascular endothelial growth factor protein in human brain tumors.

Pietsch T, Valter MM, Wolf HK, von Deimling A, Huang HJ, Cavenee WK, Wiestler OD. Pietsch T, et al. Acta Neuropathol. 1997 Feb;93(2):109-17. doi: 10.1007/s004010050591. Acta Neuropathol. 1997. PMID: 9039457

8

Neural antigens in oligodendrogliomas and dysembryoplastic neuroepithelial tumors.

Wolf HK, Buslei R, Blümcke I, Wiestler OD, Pietsch T. Wolf HK, et al. Among authors: pietsch t. Acta Neuropathol. 1997 Nov;94(5):436-43. doi: 10.1007/s004010050730. Acta Neuropathol. 1997. PMID: 9386775

9

Molecular genetic analysis of ependymal tumors. NF2 mutations and chromosome 22q loss occur preferentially in intramedullary spinal ependymomas.

Ebert C, von Haken M, Meyer-Puttlitz B, Wiestler OD, Reifenberger G, Pietsch T, von Deimling A. Ebert C, et al. Among authors: pietsch t. Am J Pathol. 1999 Aug;155(2):627-32. doi: 10.1016/S0002-9440(10)65158-9. Am J Pathol. 1999. PMID: 10433955 Free PMC article.

10

Low frequency of SV40, JC and BK polyomavirus sequences in human medulloblastomas, meningiomas and ependymomas.

Weggen S, Bayer TA, von Deimling A, Reifenberger G, von Schweinitz D, Wiestler OD, Pietsch T. Weggen S, et al. Among authors: pietsch t. Brain Pathol. 2000 Jan;10(1):85-92. doi: 10.1111/j.1750-3639.2000.tb00245.x. Brain Pathol. 2000. PMID: 10668898 Free PMC article.

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