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Human Mutation|July 22, 2014
Online registry for mutations in hereditary amyloidosis including nomenclature recommendationsDorota M Rowczenio, Islam Noor, Julian D Gillmore, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|May 23, 2023
[Bacterial zoonoses of public health importance in Germany-incidence, distribution, and modes of transmission]Hendrik Wilking, Sandra Beermann, Ides Boone, et al.
The European Journal of Health Economics : HEPAC : Health Economics in Prevention and Care|February 27, 2024
Assessment of health state utilities associated with adult and pediatric acid sphingomyelinase deficiency (ASMD)Louis S Matza, Katie D Stewart, Marie Fournier, et al.
Journal of Internal Medicine|January 27, 2025
Multicenter validation of secondary hemophagocytic lymphohistiocytosis diagnostic criteriaGunnar Lachmann, Patrick Heeren, Friederike S Schuster, et al.
Medrxiv : the Preprint Server for Health Sciences|December 16, 2022
Optimizing COVID-19 testing strategies on college campuses: evaluation of the health and economic costsKaitlyn E Johnson, Remy Pasco, Spencer Woody, et al.
American Journal of Respiratory and Critical Care Medicine|August 29, 2009
Exogenous natural surfactant for treatment of acute lung injury and the acute respiratory distress syndromeJozef Kesecioglu, Richard Beale, Thomas E Stewart, et al.
International Journal of Immunopharmacology|January 1, 1991
Protection against influenza A virus infection in mice by oral immunization with a polyvalent bacterial lysateG J Van Daal, F D Beusenberg, K L So, et al.
Transplantation|April 27, 2013
Elevation of CD4+ differentiated memory T cells is associated with acute cellular and antibody-mediated rejection after liver transplantationUndine A Gerlach, Katrin Vogt, Stephan Schlickeiser, et al.
Critical Care Medicine|October 11, 2005
Open lung ventilation improves functional residual capacity after extubation in cardiac surgeryDinis Reis Miranda, Ard Struijs, Peter Koetsier, et al.
Journal of the American Society of Nephrology : JASN|December 17, 2008
Diagnosis, pathogenesis, treatment, and prognosis of hereditary fibrinogen A alpha-chain amyloidosisJulian D Gillmore, Helen J Lachmann, Dorota Rowczenio, et al.
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