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Trends in Genetics : TIG|October 9, 2017
The Genetics of Multiple Sclerosis: From 0 to 200 in 50 YearsSergio E Baranzini, Jorge R Oksenberg
Pharmacogenomics|May 11, 2005
Genomics and new targets for multiple sclerosisSergio E Baranzini, Jorge R Oksenberg
Pediatrics|November 3, 2019
Neighborhood Poverty and Pediatric Intensive Care UseErica Andrist, Carley L Riley, Cole Brokamp, et al.
The American Journal of Emergency Medicine|January 13, 2023
High risk and low prevalence diseases: Mesenteric ischemiaKevin Molyneux, Jennifer Beck-Esmay, Alex Koyfman, et al.
Tanaffos|September 29, 2025
Methylprednisolone-Induced Hyperlactatemia: A Case ReportSarah Saenz, Anila Bhatti, Aaron Beck, et al.
American Journal of Medical Genetics|September 1, 1992
Deletion of the Hunter gene and both DXS466 and DXS304 in a patient with mucopolysaccharidosis type IIM Beck, C Steglich, B Zabel, et al.
The American Journal of Emergency Medicine|September 12, 2025
High risk and low incidence diseases: Tumor lysis syndromeKevin Molyneux, Jennifer Beck-Esmay, Alex Koyfman, et al.
Human Molecular Genetics|August 1, 1992
Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II (Hunter syndrome)S Bunge, C Steglich, M Beck, et al.
Prenatal Diagnosis|September 1, 1994
Prenatal diagnosis and carrier detection in mucopolysaccharidosis type II by mutation analysis. A 47,XXY male heterozygous for a missense point mutationS Bunge, C Steglich, P Lorenz, et al.
Cureus|December 11, 2023
Perioperative Management of a Donation After Circulatory Death Heart Transplant in a Recipient With a Persistent Left Superior Vena CavaSloan Long, Cole Sorrels, Saravanan Ramamoorthy, et al.
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