Reduced-intensity conditioning significantly improves survival of patients with hemophagocytic lymphohistiocytosis undergoing allogeneic hematopoietic cell transplantation

XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease

(2010) R. A. Marsh et al.   BLOOD

Patterns and kinetics of T-cell chimerism after allo transplant with alemtuzumab-based conditioning: mixed chimerism protects from GVHD, but does not portend disease recurrence

(2010) Koen van Besien et al.   LEUKEMIA & LYMPHOMA

Hematopoietic stem cell transplantation in Griscelli syndrome type 2: a single-center report on 10 patients

(2009) J. Pachlopnik Schmid et al.   BLOOD

Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells

(2009) Marjorie Côte et al.   JOURNAL OF CLINICAL INVESTIGATION

Diagnosis and manifestations of chronic graft-versus-host disease

(2008) Alexandra H. Filipovich   BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY

Hematopoietic cell transplantation for hemophagocytic lymphohistiocytosis: a journey of a thousand miles begins with a single (big) step

(2008) M B Jordan et al.   BONE MARROW TRANSPLANTATION

The use of reduced-intensity stem cell transplantation in haemophagocytic lymphohistiocytosis and Langerhans cell histiocytosis

(2008) N Cooper et al.   BONE MARROW TRANSPLANTATION

Unrelated donor hematopoietic cell transplantation for hemophagocytic lymphohistiocytosis

(2008) K S Baker et al.   BONE MARROW TRANSPLANTATION