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Human Gene Therapy|June 3, 2009
Stable nonviral gene transfer into primary human T cellsT Magg, S Hartrampf, M H AlbertNeuromuscular Disorders : NMD|April 13, 2016
Proximal muscular atrophy and weakness: An unusual adverse effect of deferasirox iron chelation therapyK Vill, W Müller-Felber, V Teusch, et al.Genes and Immunity|May 23, 2014
MiRNome and transcriptome aided pathway analysis in human regulatory T cellsM H Albert, J Mannert, K K Fleischmann, et al.Bone Marrow Transplantation|August 18, 2009
Successful SCT for Nijmegen breakage syndromeM H Albert, A R Gennery, J Greil, et al.Bone Marrow Transplantation|August 6, 2003
T-cell-depleted peripheral blood stem cell transplantation for alpha-mannosidosisM H Albert, F Schuster, C Peters, et al.Klinische Padiatrie|November 9, 2010
Successful long-term correction of autosomal recessive hyper-IgE syndrome due to DOCK8 deficiency by hematopoietic stem cell transplantationT C Bittner, U Pannicke, E D Renner, et al.Bone Marrow Transplantation|May 10, 2011
Allogeneic hematopoietic SCT for alpha-mannosidosis: an analysis of 17 patientsM Mynarek, J Tolar, M H Albert, et al.Bone Marrow Transplantation|October 26, 2010
Plerixafor with and without chemotherapy in poor mobilizers: results from the German compassionate use programK Hübel, M M Fresen, H Salwender, et al.Bone Marrow Transplantation|October 30, 2012
Allo-SCT using BU, CY and melphalan for children with AML in second CRR Beier, M H Albert, P Bader, et al.Clinical Immunology (Orlando, Fla.)|August 27, 2013
X-linked inhibitor of apoptosis (XIAP) deficiency: the spectrum of presenting manifestations beyond hemophagocytic lymphohistiocytosisC Speckmann, K Lehmberg, M H Albert, et al.Pageof 2