von Deimling A - Search Results

1

Two molecularly distinct atypical teratoid/rhabdoid tumors (or tumor components) occurring in an infant with rhabdoid tumor predisposition syndrome 1.

Thomas C, Knerlich-Lukoschus F, Reinhard H, Johann PD, Sturm D, Sahm F, Bens S, Vogt J, Nemes K, Oyen F, Kordes U, Siebert R, Schneppenheim R, Messing-Jünger M, Pietsch T, von Deimling A, Paulus W, Pfister SM, Kool M, Frühwald MC, Hasselblatt M. Thomas C, et al. Among authors: von deimling a. Acta Neuropathol. 2019 May;137(5):847-850. doi: 10.1007/s00401-019-02001-3. Epub 2019 Apr 3. Acta Neuropathol. 2019. PMID: 30945057 No abstract available.

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: von deimling a, von schweinitz d. 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: 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

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: von deimling a. 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

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

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: von deimling a, von bakel i. 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. Among authors: von deimling a. Acta Neuropathol. 1997 Feb;93(2):109-17. doi: 10.1007/s004010050591. Acta Neuropathol. 1997. PMID: 9039457

8

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

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: von deimling a, von haken m. 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: von deimling a, von schweinitz d. 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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