von Deimling A - Search Results

1

Rosette-forming glioneuronal tumors share a distinct DNA methylation profile and mutations in FGFR1, with recurrent co-mutation of PIK3CA and NF1.

Sievers P, Appay R, Schrimpf D, Stichel D, Reuss DE, Wefers AK, Reinhardt A, Coras R, Ruf VC, Schmid S, de Stricker K, Boldt HB, Kristensen BW, Petersen JK, Ulhøi BP, Gardberg M, Aronica E, Hasselblatt M, Brück W, Bielle F, Mokhtari K, Lhermitte B, Wick W, Herold-Mende C, Hänggi D, Brandner S, Giangaspero F, Capper D, Rushing E, Wesseling P, Pfister SM, Figarella-Branger D, von Deimling A, Sahm F, Jones DTW. Sievers P, et al. Among authors: von deimling a. Acta Neuropathol. 2019 Sep;138(3):497-504. doi: 10.1007/s00401-019-02038-4. Epub 2019 Jun 27. Acta Neuropathol. 2019. PMID: 31250151 Free article.

2

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: von deimling a. Neuropathol Appl Neurobiol. 1994 Feb;20(1):74-81. doi: 10.1111/j.1365-2990.1994.tb00959.x. Neuropathol Appl Neurobiol. 1994. PMID: 8208343

3

Amplification of the cyclin-dependent kinase 4 (CDK4) gene is associated with high cdk4 protein levels in glioblastoma multiforme.

Rollbrocker B, Waha A, Louis DN, Wiestler OD, von Deimling A. Rollbrocker B, et al. Among authors: von deimling a. Acta Neuropathol. 1996 Jul;92(1):70-4. doi: 10.1007/s004010050491. Acta Neuropathol. 1996. PMID: 8811128

4

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: von deimling a, von bakel i. Acta Neuropathol. 1997 Jan;93(1):93-6. doi: 10.1007/s004010050587. Acta Neuropathol. 1997. PMID: 9006662

5

Identification of subgroups of high-grade oligodendroglial tumors by comparative genomic hybridization.

Jeuken JW, Sprenger SH, Wesseling P, Macville MV, von Deimling A, Teepen HL, van Overbeeke JJ, Boerman RH. Jeuken JW, et al. Among authors: von deimling a. J Neuropathol Exp Neurol. 1999 Jun;58(6):606-12. doi: 10.1097/00005072-199906000-00005. J Neuropathol Exp Neurol. 1999. PMID: 10374751

6

Quantitative analysis of NF1 and OMGP gene transcripts in sporadic gliomas, sporadic meningiomas and neurofibromatosis type 1-associated plexiform neurofibromas.

Peters N, Waha A, Wellenreuther R, Friedrich RE, Mautner VF, Hoffmeyer S, Lenartz D, Schramm J, Wiestler OD, von Deimling A. Peters N, et al. Among authors: von deimling a. Acta Neuropathol. 1999 Jun;97(6):547-51. doi: 10.1007/s004010051029. Acta Neuropathol. 1999. PMID: 10378372

7

Mutational analysis of INI1 in sporadic human brain tumors.

Weber M, Stockhammer F, Schmitz U, von Deimling A. Weber M, et al. Among authors: von deimling a. Acta Neuropathol. 2001 May;101(5):479-82. doi: 10.1007/s004010000316. Acta Neuropathol. 2001. PMID: 11484819

8

Indications for a tumor suppressor gene at 22q11 involved in the pathogenesis of ependymal tumors and distinct from hSNF5/INI1.

Kraus JA, de Millas W, Sörensen N, Herbold C, Schichor C, Tonn JC, Wiestler OD, von Deimling A, Pietsch T. Kraus JA, et al. Among authors: von deimling a. Acta Neuropathol. 2001 Jul;102(1):69-74. doi: 10.1007/s004010000353. Acta Neuropathol. 2001. PMID: 11547953

9

No preferential loss of paternal 19q alleles in oligodendroglial tumors.

Hartmann C, Mueller W, Lass U, Stockhammer F, von Eckardstein K, Veelken J, Jeuken J, Wick W, von Deimling A. Hartmann C, et al. Among authors: von deimling a, von eckardstein k. Ann Neurol. 2003 Aug;54(2):256-8. doi: 10.1002/ana.10649. Ann Neurol. 2003. PMID: 12891681

10

No evidence of hSNF5/INI1 point mutations in choroid plexus papilloma.

Mueller W, Eum JH, Lass U, Paulus W, Sarkar C, Bruck W, von Deimling A. Mueller W, et al. Among authors: von deimling a. Neuropathol Appl Neurobiol. 2004 Jun;30(3):304-7. doi: 10.1046/j.0305-1846.2004.00538.x. Neuropathol Appl Neurobiol. 2004. PMID: 15175083

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