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Leukemia|February 24, 2001
Results of Dana-Farber Cancer Institute Consortium protocols for children with newly diagnosed acute lymphoblastic leukemia (1981-1995)L B Silverman, L Declerck, R D Gelber, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|December 17, 2008
Murine cardiac mtDNA: effects of transgenic manipulation of nucleoside phosphorylationJames J Kohler, Seyed H Hosseini, Ioan Cucoranu, et al.
Molecular Syndromology|June 27, 2013
CCM3 Mutations Are Associated with Early-Onset Cerebral Hemorrhage and Multiple MeningiomasF Riant, F Bergametti, H-D Fournier, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|January 13, 2010
Transgenic cardiac-targeted overexpression of human thymidylate kinaseJames J Kohler, Seyed H Hosseini, Ioan Cucoranu, et al.
BMC Infectious Diseases|October 29, 2025
Evaluating antimicrobial resistance and clinical outcomes in surgical ICU using a machine learning perspective: a retrospective observational studyB Ziaian, Sh Yousufzai, M Karami, et al.
European Journal of Neurology|January 31, 2020
Should posterior cerebral artery occlusions be recanalized? Insights from the Trevo RegistryF Clarençon, F Baronnet, E Shotar, et al.
Environmental Health Perspectives|July 7, 2012
Childhood lead poisoning associated with gold ore processing: a village-level investigation-Zamfara State, Nigeria, October-November 2010Yi-Chun Lo, Carrie A Dooyema, Antonio Neri, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 14, 2005
mtDNA mutations increase tumorigenicity in prostate cancerJohn A Petros, Amanda K Baumann, Eduardo Ruiz-Pesini, et al.
European Journal of Neurology|March 26, 2018
Impact of intravenous thrombolysis and emergent carotid stenting on reperfusion and clinical outcomes in patients with acute stroke with tandem lesion treated with thrombectomy: a collaborative pooled analysisB Gory, D C Haussen, M Piotin, et al.
Clinical Genetics|June 24, 2010
Comparative analysis of Shwachman-Diamond syndrome to other inherited bone marrow failure syndromes and genotype-phenotype correlationS K Hashmi, C Allen, R Klaassen, et al.
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