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Acta Paediatrica (Oslo, Norway : 1992)|September 25, 2020
Patients with both Langerhans cell histiocytosis and Crohn's disease highlight a common role of interleukin-23Egle Kvedaraite, Magda Lourda, HongYa Han, et al.
Nature Genetics|December 26, 2006
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)Christoph Klein, Magda Grudzien, Giridharan Appaswamy, et al.
Critical Care Medicine|October 4, 2021
Consensus-Based Guidelines for the Recognition, Diagnosis, and Management of Hemophagocytic Lymphohistiocytosis in Critically Ill Children and AdultsMelissa R Hines, Tatiana von Bahr Greenwood, Gernot Beutel, et al.
Blood|February 2, 2012
A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromesYenan T Bryceson, Daniela Pende, Andrea Maul-Pavicic, et al.
Blood|April 18, 2019
Recommendations for the management of hemophagocytic lymphohistiocytosis in adultsPaul La Rosée, AnnaCarin Horne, Melissa Hines, et al.
Blood|July 24, 2024
Diagnostic guidelines for familial hemophagocytic lymphohistiocytosis revisitedJan-Inge Henter, Elena Sieni, Julia Eriksson, et al.
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