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CASP9 germline mutation in a family with multiple brain tumors.
Ronellenfitsch MW, Oh JE, Satomi K, Sumi K, Harter PN, Steinbach JP, Felsberg J, Capper D, Voegele C, Durand G, McKay J, Le Calvez-Kelm F, Schittenhelm J, Klink B, Mittelbronn M, Ohgaki H. Ronellenfitsch MW, et al. Among authors: capper d. Brain Pathol. 2018 Jan;28(1):94-102. doi: 10.1111/bpa.12471. Epub 2017 Apr 17. Brain Pathol. 2018. PMID: 27935156 Free PMC article.
Disseminating anaplastic brainstem oligodendroglioma associated with allelic loss in the tumor suppressor candidate region D19S246 of chromosome 19 mimicking an inflammatory central nervous system disease in a 9-year-old boy.
Mittelbronn M, Wolff M, Bültmann E, Nägele T, Capper D, Beck R, Meyermann R, Beschorner R. Mittelbronn M, et al. Among authors: capper d. Hum Pathol. 2005 Jul;36(7):854-7. doi: 10.1016/j.humpath.2005.05.017. Hum Pathol. 2005. PMID: 16084959
Multiple thromboembolic events in fetofetal transfusion syndrome in triplets contributing to the understanding of pathogenesis of hydranencephaly in combination with polymicrogyria.
Mittelbronn M, Beschorner R, Schittenhelm J, Capper D, Goeppert B, Meyermann R, Meyer-Wittkopf M, Mackensen-Haen S. Mittelbronn M, et al. Among authors: capper d. Hum Pathol. 2006 Nov;37(11):1503-7. doi: 10.1016/j.humpath.2006.07.005. Epub 2006 Sep 25. Hum Pathol. 2006. PMID: 16997352
Rathke's cleft cyst rupture as potential initial event of a secondary perifocal lymphocytic hypophysitis: proposal of an unusual pathogenetic event and review of the literature.
Schittenhelm J, Beschorner R, Psaras T, Capper D, Nägele T, Meyermann R, Saeger W, Honegger J, Mittelbronn M. Schittenhelm J, et al. Among authors: capper d. Neurosurg Rev. 2008 Apr;31(2):157-63. doi: 10.1007/s10143-008-0120-1. Epub 2008 Feb 6. Neurosurg Rev. 2008. PMID: 18253771 Review.
325 results