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Australian and New Zealand Journal of Medicine|December 1, 1983
Adrenomyeloneuropathy--clinical and biochemical diagnosisS F Berkovic, J D Zajac, D J Warburton, et al.
The American Journal of Physiology|April 1, 1990
Circulating xanthine oxidase: potential mediator of ischemic injuryY Yokoyama, J S Beckman, T K Beckman, et al.
Pathology|February 10, 2024
Immunohistochemistry screening for TP53 mutation in myeloid neoplasms in AZF-fixed bone marrow biopsiesGuang Yang, Sarah Anderson Williams, Fiona He, et al.
Journal of Medical Screening|May 5, 2021
Women screened for breast cancer are dying from lung cancer: An opportunity to improve lung cancer screening in a mammography populationKim L Sandler, Diane N Haddad, Alexis B Paulson, et al.
The Journal of Biological Chemistry|February 15, 1992
Simultaneous deficiency of sphingolipid activator proteins 1 and 2 is caused by a mutation in the initiation codon of their common geneD Schnabel, M Schröder, W Fürst, et al.
Blood Cells, Molecules & Diseases|December 5, 2021
A case of VEXAS syndrome associated with EBV-associated hemophagocytic lymphohistiocytosisRoy L Kao, Audrey A Jacobsen, Charles J Billington, et al.
European Journal of Pediatrics|April 1, 1989
A case of combined Farber and Sandhoff diseaseC Fusch, R Huenges, H W Moser, et al.
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