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Critical Care Medicine|March 25, 2006
Insulin reduces the multiple organ injury and dysfunction caused by coadministration of lipopolysaccharide and peptidoglycan independently of blood glucose: role of glycogen synthase kinase-3beta inhibitionLaura Dugo, Marika Collin, David A Allen, et al.
Critical Care Medicine|January 25, 2008
Sphingosylphosphorylcholine reduces the organ injury/dysfunction and inflammation caused by endotoxemia in the ratOliver Murch, Maha Abdelrahman, Massimo Collino, et al.
Shock (Augusta, Ga.)|March 8, 2008
Treatment with the glycogen synthase kinase-3beta inhibitor, TDZD-8, affects transient cerebral ischemia/reperfusion injury in the rat hippocampusMassimo Collino, Christoph Thiemermann, Raffaella Mastrocola, et al.
Archives of Disease in Childhood|February 6, 2024
Wales Infants' and childreN's Genome Service (WINGS): providing rapid genetic diagnoses for unwell childrenEmily Sloper, Jana Jezkova, Joanne Thomas, et al.
American Journal of Respiratory and Critical Care Medicine|January 20, 2007
Selective NOD1 agonists cause shock and organ injury/dysfunction in vivoNeil Cartwright, Oliver Murch, Shaun K McMaster, et al.
European Journal of Human Genetics : EJHG|October 14, 2021
Further delineation of the clinical spectrum of White-Sutton syndrome: 12 new individuals and a review of the literatureOliver Murch, Vani Jain, Andreas Benneche, et al.
American Journal of Medical Genetics. Part A|March 29, 2025
Expanding the SIAH1-Associated Phenotypic Spectrum: Insights From Loss-of-Function VariantsLiza Douiev, Paula Fernandez Alvarez, Marika Frank, et al.
Archives of Disease in Childhood|January 21, 2026
UK consensus guidelines for multidisciplinary care of children and young people with achondroplasia: a modified Delphi processToby P Candler, Kate Ali, Emma Bewick, et al.
International Journal of Molecular Sciences|June 10, 2022
Expanding the Molecular Spectrum of <i>ANKRD11</i> Gene Defects in 33 Patients with a Clinical Presentation of KBG SyndromeIlaria Bestetti, Milena Crippa, Alessandra Sironi, et al.
European Journal of Human Genetics : EJHG|September 13, 2023
Börjeson-Forssman-Lehmann syndrome: delineating the clinical and allelic spectrum in 14 new familiesVani Jain, Seow Hoong Foo, Stephen Chooi, et al.
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