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Diseases of the Colon and Rectum|April 1, 1982
Serial CEA assays and liver scintigraphy for the detection of hepatic metastases from colorectal carcinomaJ J Szymendera, J E Wilczyńska, M P Nowacki, et al.Archivum Immunologiae Et Therapiae Experimentalis|January 1, 1979
Studies on the derivatives of thiazole acetic acid. II. Syntheses and pharmacological analysis of 2-N-aralkylidene and 2-N-aralkyl derivatives of 2-amino-4-p-chlorophenylthiazole-5-acetic acidT Jakóbiec, S H Kowalczyk-Bronisz, J Stankiewicz, et al.Neurology|March 23, 2005
Levetiracetam for seizures after liver transplantationG A Glass, J Stankiewicz, A Mithoefer, et al.Magnetic Resonance in Medicine|August 1, 1986
Pulse techniques for the suppression of individual components in multiexponential relaxation curvesK R Metz, P J Stankiewicz, J W Sassani, et al.Archivum Immunologiae Et Therapiae Experimentalis|January 1, 1979
Studies on the derivatives of 2-amino-4-p-chlorophenylthiazole-5-acetic acid. I. Syntheses and pharmacological analysis of acylderivatives of 2-amino-4-p-chlorophenylthiazole-5-acetic acidT Jakóbiec, I Glama, S H Kowalczyk-Bronisz, et al.Journal of Experimental Psychology. Human Perception and Performance|July 11, 2006
Lost in virtual space: studies in human and ideal spatial navigationBrian J Stankiewicz, Gordon E Legge, J Stephen Mansfield, et al.Biochemistry|March 10, 1987
2,3-diphosphoglycerate phosphatase activity of phosphoglycerate mutase: stimulation by vanadate and phosphateP J Stankiewicz, M J Gresser, A S Tracey, et al.Journal of Intellectual Disability Research : JIDR|January 25, 2003
Different presentations of late-detected phenylketonuria in two brothers with the same R408W/R111X genotype in the PAH geneM Gizewska, B Cabalska, L Cyrytowski, et al.Blood|February 12, 2015
Aurora kinase A is required for hematopoiesis but is dispensable for murine megakaryocyte endomitosis and differentiationBenjamin Goldenson, Gina Kirsammer, Monika J Stankiewicz, et al.Folia Neuropathologica|March 8, 2000
Microglia and neuritic plaques in familial Alzheimer's disease induced by a new mutation of presenilin-1 gene. An ultrastructural studyE Lewandowska, E Bertrand, J Kulczycki, et al.Pageof 17