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Clinical and Experimental Rheumatology|October 1, 1986
The effect of gold salts on casein-induced macrophage activation and serum amyloid protein SAA levelsC E Herman Hernandes, M A Scheinberg, M D Benson, et al.
Cryobiology|October 20, 2010
Melting point equations for the ternary system water/sodium chloride/ethylene glycol revisitedJames D Benson, Aniruddha Bagchi, Xu Han, et al.
Kidney International|May 2, 2008
Leukocyte chemotactic factor 2: A novel renal amyloid proteinMerrill D Benson, Sam James, Katherine Scott, et al.
Physical & Occupational Therapy in Pediatrics|July 29, 2022
Feasibility of Implementing a Modified SENSE Program to Increase Positive Sensory Experiences for Preterm Infants in the Neonatal Intensive Care Unit (NICU): A Pilot StudyKate N de Castro, Jeryl D Benson, Hillary Thomas, et al.
Biochemical and Biophysical Research Communications|April 13, 1999
A novel apolipoprotein A-1 variant, Arg173Pro, associated with cardiac and cutaneous amyloidosisK Hamidi Asl, J J Liepnieks, M Nakamura, et al.
Cryobiology|October 4, 2005
Mercury free operation of the Coulter counter MultiSizer II sampling standJames D Benson, Mark A Haidekker, Corinna M K Benson, et al.
Molecular Cell|December 3, 2004
Does common architecture reveal a viral lineage spanning all three domains of life?Stacy D Benson, Jaana K H Bamford, Dennis H Bamford, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|February 24, 2006
Complement, fetal antigen, and shaking rigors in parturientsMichael D Benson, Hiroshi Kobayashi, Lakshman R Sehgal, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|November 13, 2019
Inotersen therapy of transthyretin amyloid cardiomyopathyNoel R Dasgupta, Stacy M Rissing, Jessica Smith, et al.
Human Genetics|March 1, 1995
Asp187Asn mutation of gelsolin in an American kindred with familial amyloidosis, Finnish type (FAP IV)R D Steiner, T Paunio, T Uemichi, et al.
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