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8 Mahlaoui, N., Ouachee-Chardin, M., de Saint Basile, G., et al. Immunotherapy of familial hemophagocytic lymphohistiocytosis with antithymocyte globulins: a single-center retrospective report of 38 patients. Pediatrics 120 (2007), e622–e628.
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9 Baker, K.S., Filipovich, A.H., Gross, T.G., et al. Unrelated donor hematopoietic cell transplantation for hemophagocytic lymphohistiocytosis. Bone Marrow Transplant 42 (2008), 175–180.
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12 Cooper, N., Stem cell transplantation with reduced-intensity conditioning for hemophagocytic lymphohistiocytosis. Blood 107 (2005), 1233–1236.
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13 Cooper, N., Rao, K., Goulden, N., Webb, D., Amrolia, P., Veys, P., The use of reduced-intensity stem cell transplantation in haemophagocytic lymphohistiocytosis and Langerhans cell histiocytosis. Bone Marrow Transplant 42 (2008), S47–S50.
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14 Marsh, R.A., Vaughn, G., Kim, M.O., et al. Reduced-intensity conditioning significantly improves survival of patients with hemophagocytic lymphohistiocytosis undergoing allogeneic hematopoietic cell transplantation. Blood 116 (2010), 5824–5831.
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15 Marsh, R.A., Rao, M.B., Gefen, A., et al. Experience with alemtuzumab, fludarabine, and melphalan reduced-intensity conditioning hematopoietic cell transplantation in patients with nonmalignant diseases reveals good outcomes and that the risk of mixed chimerism depends on underlying disease, stem cell source, and alemtuzumab regimen. Biol Blood Marrow Transplant 21 (2015), 1460–1470.
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16 Marsh, R.A., Kim, M.-O., Liu, C., et al. An intermediate alemtuzumab schedule reduces the incidence of mixed chimerism following reduced-intensity conditioning hematopoietic cell transplantation for hemophagocytic lymphohistiocytosis. Biol Blood Marrow Transplant 19 (2013), 1625–1631.
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17 Hartz, B., Marsh, R., Rao, K., et al. The minimum required level of donor chimerism in hereditary hemophagocytic lymphohistiocytosis. Blood 127 (2016), 3281–3290.
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18 Bock, A.M., LeVeque, M., Camitta, B., Talano, J.A., Successful treatment of recurrent CNS disease post-bone marrow transplant in children with familial hemophagocytic lymphohistiocytosis. Pediatr Blood Cancer 63 (2016), 2154–2158.
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