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Klinische Padiatrie|July 1, 1989
[Intracranial germ cell tumors: analysis of the therapy study MAKEI 83/86 and changes in protocol for the follow-up study]U Göbel, M Bamberg, V Budach, et al.
Journal of Neuropathology and Experimental Neurology|May 26, 1998
Primitive neuroectodermal tumors of the cerebral hemispheres in two siblings with TP53 germline mutationJ Reifenberger, G Janssen, R G Weber, et al.
American Journal of Medical Genetics|October 27, 1998
Megalencephaly, mega corpus callosum, and complete lack of motor development: a previously undescribed syndromeG Göhlich-Ratmann, M Baethmann, P Lorenz, et al.
Journal of Neurosurgery|August 10, 2000
Multiple intracranial juvenile xanthogranulomas. Case reportJ Boström, G Janssen, M Messing-Jünger, et al.
Neurology|February 1, 1995
The syndrome of autosomal recessive pontocerebellar hypoplasia, microcephaly, and extrapyramidal dyskinesia (pontocerebellar hypoplasia type 2): compiled data from 10 pedigreesP G Barth, G Blennow, H G Lenard, et al.
Klinische Padiatrie|July 1, 1991
[Treatment of non-testicular germ cell tumors in children and adolescents with BEP and VIP: initial results of the MAKEI 89 therapy study]U Göbel, M Bamberg, J Engert, et al.
Klinische Padiatrie|July 1, 1993
[Improved prognosis of intracranial germ cell tumors by intensified therapy: results of the MAKEI 89 therapy protocol]U Göbel, M Bamberg, G Calaminus, et al.
Neuropediatrics|February 1, 1994
Intracranial germ cell tumors: a comprehensive update of the European dataG Calaminus, M Bamberg, M C Baranzelli, et al.
Journal of Medical Genetics|August 1, 1984
The clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfectaA C Nicholls, G Osse, H G Schloon, et al.
Lancet (London, England)|July 21, 2000
End-of-life decisions in neonatal intensive care: physicians' self-reported practices in seven European countries. EURONIC Study GroupM Cuttini, M Nadai, M Kaminski, et al.
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