Wilhelm Friedrich

Bone marrow transplantation for autosomal recessive osteopetrosis. A report from the Working Party on Inborn Errors of the European Bone Marrow Transplantation Group.

W. Friedrich, A. Vellodi, A. Fasth, 1994, The Journal of pediatrics.

Influence of severe combined immunodeficiency phenotype on the outcome of HLA non-identical, T-cell-depleted bone marrow transplantation: a retrospective European survey from the European group for bone marrow transplantation and the european society for immunodeficiency.

S. Müller, W. Friedrich, E. Haddad, 1999, The Journal of pediatrics.

Severe combined immunodeficiency: treatment by bone marrow transplantation in 15 infants using HLA-haploidentical donors

W. Friedrich, G. Gaedicke, H. Peter, 1985, European Journal of Pediatrics.

Stem cell transplantation in children with infantile osteopetrosis is associated with a high incidence of VOD, which could be prevented with defibrotide

A. Schulz, W. Friedrich, S. Corbacioglu, 2006, Bone Marrow Transplantation.

Similar pattern of thymic-dependent T-cell reconstitution in infants with severe combined immunodeficiency after human leukocyte antigen (HLA)-identical and HLA-nonidentical stem cell transplantation.

S. Müller, A. Schulz, W. Friedrich, 2000, Blood.

Lymphocyte microvilli are dynamic, actin-dependent structures that do not require Wiskott-Aldrich syndrome protein (WASp) for their morphology.

K. Siminovitch, H. Higgs, Stefan Linder, 2004, Blood.

Hematopoietic stem cell transplantation from matched unrelated donors in chronic granulomatous disease

A. Schulz, W. Friedrich, K. Debatin, 2008, Immunologic research.