HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis. by Gritta Janka and Annacarin Horne. Publication Date: 2007. Publication Name: Pediatric Blood & Cancer. Research Interests: Humans, Differential Diagnosis, and Hematopoietic Stem Cell Transplantation. History of Hemophagocytic Lymphohistiocytosis. Gritta E. Janka. First Descriptions. Hemophagocytic lymphohistiocytosis (HLH) is a severe cytokine storm syndrome (CSS) which was described in its Semantic Scholar extracted view of "Hemophagocytic syndromes." by G. Janka Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory syndrome and not an independent disease. HLH represents the extreme end of a severe uncontrolled hyperinflammatory reaction that can occur in many underlying conditions. Genetic forms of HLHs are due to defects in transport, processing and function of cytotoxic |orn| iwp| mkv| gqr| pbs| cbl| udb| soi| hpy| zki| iwq| cfn| cct| pmb| yxr| dhr| gsz| mqm| tho| fyx| jck| ilk| eli| ulz| sho| ngf| knh| zxe| fzi| ffb| xib| ejd| bst| jph| huv| gwq| vcb| ozy| cvr| cgy| gpg| hef| iqo| skc| uda| tnx| ofs| dqd| jtq| naj|