1. 1408: GENETIC VARIANTS ASSOCIATED WITH HYPERINFLAMMATION IN SEPTIC SHOCK. Issue 12 (December 2016) Authors: Kernan, Kate; Ghaloul-Gonzalez, Lina; Sethi, Rahil; Chandran, Uma; Lamb, Janette; Kellum, John; Angus, Derek; Carcillo, Joseph Journal: Critical care medicine Issue: Volume 44:Issue 12(2016)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 1431: ADULTS WITH SEPTIC SHOCK AND EXTREME HYPERFERRITINEMIA EXHIBIT PATHOGENIC IMMUNE VARIATION. (January 2018) Authors: Kernan, Kate; Ghaloul-Gonzalez, Lina; Kellum, John; Angus, Derek; Carcillo, Joseph Journal: Critical care medicine Issue: Volume 46:Supplement 1 1(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. 1441: PATHOGENIC AND POTENTIALLY PATHOGENIC INBORN ERRORS OF IMMUNITY VARIANTS IN PEDIATRIC SEVERE SEPSIS. (16th December 2021) Authors: Kernan, Kate; Ghaloul-Gonzalez, Lina; Vockley, Jerry; Lamb, Janette; Hollingshead, Deborah; Sethi, Rahil; Park, Hyun-Jung; Carcillo, Joseph; Berg, Robert; Wessel, David; Pollack, Murray; Meert, Kathleen; Hall, Mark; Newth, Christopher; Lin, John; Doctor, Allan; Shanley, Tom; Cornell, Timothy; Har... Other Names: other. Journal: Critical care medicine Issue: Volume 50(2022)Supplement 1 Page Start: 723 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. 1441: PATHOGENIC AND POTENTIALLY PATHOGENIC INBORN ERRORS OF IMMUNITY VARIANTS IN PEDIATRIC SEVERE SEPSIS. (January 2022) Authors: Kernan, Kate; Ghaloul-Gonzalez, Lina; Vockley, Jerry; Lamb, Janette; Hollingshead, Deborah; Sethi, Rahil; Park, Hyun-Jung; Carcillo, Joseph; Berg, Robert; Wessel, David; Pollack, Murray; Meert, Kathleen; Hall, Mark; Newth, Christopher; Lin, John; Doctor, Allan; Shanley, Tom; Cornell, Timothy; Har... Journal: Critical care medicine Issue: Volume 50(2022)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. A familial case of CAMK2B mutation with variable expressivity. (February 2021) Authors: Heiman, Paige; Drewes, Sarah; Ghaloul-Gonzalez, Lina Journal: SAGE open medical case reports Issue: Volume 9(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗