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Journal of Neuro-Oncology|February 7, 2024
Treatment outcome of IDH1/2 wildtype CNS WHO grade 4 glioma histologically diagnosed as WHO grade II or III astrocytomasNaureen Keric, Harald Krenzlin, Darius Kalasauskas, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 20, 2001
A whole genome scan for differences in recombination rates among three Bos taurus breedsH Thomsen, N Reinsch, N Xu, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 1, 2005
Treatment results in localized primary gastric lymphoma: data of patients registered within the German multicenter study (GIT NHL 02/96)Peter Koch, Andreas Probst, Wolfgang E Berdel, et al.
Neurology|October 23, 2020
Phenylalanine Effects on Brain Function in Adult PhenylketonuriaAndrea Pilotto, Carl M Zipser, Edytha Leks, et al.
American Journal of Human Genetics|August 24, 2010
Recessive mutations in the gene encoding the tight junction protein occludin cause band-like calcification with simplified gyration and polymicrogyriaMary C O'Driscoll, Sarah B Daly, Jill E Urquhart, et al.
Neuropediatrics|October 16, 2012
Early-onset LBSL: how severe does it get?M E Steenweg, L van Berge, C G M van Berkel, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 18, 2001
Primary gastrointestinal non-Hodgkin's lymphoma: I. Anatomic and histologic distribution, clinical features, and survival data of 371 patients registered in the German Multicenter Study GIT NHL 01/92P Koch, F del Valle, W E Berdel, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 18, 2001
Primary gastrointestinal non-Hodgkin's lymphoma: II. Combined surgical and conservative or conservative management only in localized gastric lymphoma--results of the prospective German Multicenter Study GIT NHL 01/92P Koch, F del Valle, W E Berdel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 7, 2020
Heterozygous truncating variants in SUFU cause congenital ocular motor apraxiaSimone Schröder, Yun Li, Gökhan Yigit, et al.
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