MichaelHolgerAlbertMD

PubMed

• 46 citations
  A Novel Gain-of-Function IKBA Mutation Underlies Ectodermal Dysplasia with Immunodeficiency and Polyendocrinopathy
  Lena F. Schimke, Nikolaus Rieber, Stacey Rylaarsdam, Otavio Cabral-Marques, Nicholas Hubbard, Anne Puel, Laura Kallmann, Stephanie Anover Sombke, Gundula Notheis, Hans...> ;Journal of Clinical Immunology. 2013 May 25
• 96 citations
  Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency.
  Melissa C. Mizesko, Pinaki P. Banerjee, Linda Monaco-Shawver, Emily M. Mace, William Bernal, Julie Sawalle-Belohradsky, Bernd H. Belohradsky, Valerie Heinz, Alexandra ...> ;The Journal of Allergy and Clinical Immunology. 2013 Mar 1
• 45 citations
  Sorafenib and cisplatin/doxorubicin (PLADO) in pediatric hepatocellular carcinoma
  Irene Schmid, Beate Häberle, Michael H. Albert, Selim Corbacioglu, Birgit Fröhlich, Norbert Graf, Birgit Kammer, Udo Kontny, Ivo Leuschner, Hans-Gerhard Scheel-Walter,...> ;Pediatric Blood & Cancer. 2012 Apr 1
• 81 citations
  Preemptive immunotherapy in childhood acute myeloid leukemia for patients showing evidence of mixed chimerism after allogeneic stem cell transplantation
  Eva Rettinger, Andre Willasch, Hermann Kreyenberg, Arndt Borkhardt, Wolfgang Holter, Bernhard Kremens, Brigitte Strahm, Wilhelm Woessmann, Christine Mauz-Koerholz, B. ...> ;Blood. 2011 Nov 17
• Long-term outcome and lineage-specific chimerism in 194 Wiskott-Aldrich Syndrome patients treated by hematopoietic cell transplantation between 1980-2009: an internati...
  Moratto, D., Giliani, S., Bonfim, C., Mazzolari, E., Fischer, A., Ochs, H. D., Cant, A. J., Thrasher, A. J., Cowan, M. J., Albert, M. H., Small, T., Pai, S. Y., Haddad...> ;Blood. 2011 Aug 11
• 48 citations
  123I-MIBG scintigraphy/SPECT versus 18F-FDG PET in paediatric neuroblastoma
  Henriette Ingrid Melzer, Eva Coppenrath, Irene Schmid, Michael H. Albert, Dietrich von Schweinitz, Coral F. Tudball, Peter Bartenstein, Thomas Pfluger> ;European Journal of Nuclear Medicine and Molecular Imaging. 2011 May 27
• 64 citations
  Clinical spectrum, pathophysiology and treatment of the Wiskott-Aldrich syndrome.
  Michael H. Albert, Luigi D. Notarangelo, Hans D. Ochs> ;Current Opinion in Hematology. 2011 Jan 1
• 62 citations
  Successful long-term correction of autosomal recessive hyper-IgE syndrome due to DOCK8 deficiency by hematopoietic stem cell transplantation.
  Tanja C. Bittner, Ulrich Pannicke, Ellen D. Renner, Gundula Notheis, Florian Hoffmann, Bernd H. Belohradsky, U. Wintergerst, M. Hauser, B. Klein, Klaus Schwarz, Irene ...> ;Klinische Padiatrie. 2010 Nov 1
• 1 citations
  Reduced methotrexate clearance and renal impairment in a boy with osteosarcoma and earlier undetected autosomal dominant polycystic kidney disease (ADPKD).
  Martin Alberer, Julia Hoefele, Carsten Bergmann, Steffen Hartrampf, Jutta Hilberath, Ingo Pawlita, Michael H. Albert, Marcus R. Benz, Lutz T. Weber, Irene Schmid> ;Journal of Pediatric Hematology/oncology. 2010 Nov 1
• 138 citations
  X-linked thrombocytopenia (XLT) due to WAS mutations: Clinical characteristics, long-term outcome, and treatment options
  Michael H. Albert, Tanja C. Bittner, Shigeaki Nonoyama, Lucia Dora Notarangelo, Siobhan O. Burns, Kohsuke Imai, Teresa Espanol, Anders Fasth, Isabelle Pellier, Gabriel...> ;Blood. 2010 Apr 22
• 40 citations
  Successful SCT for Nijmegen breakage syndrome.
  Michael H. Albert, Andrew R. Gennery, Johann Greil, Catherine M. Cale, Krzysztof Kałwak, I Kondratenko, Wojciech Młynarski, Gundula Notheis, Monika Führer, Irene Schmi...> ;Bone Marrow Transplantation. 2010 Apr 1
• 34 citations
  Therapeutic strategy in p47-phox deficient chronic granulomatous disease presenting as inflammatory bowel disease
  Folke Freudenberg, Uwe Wintergerst, Angela Roesen-Wolff, Michael H. Albert, Christine Prell, Brigitte Strahm, Sibylle Koletzko, Stephan Ehl, Dirk Roos, Alberto Tommasi...> ;The Journal of Allergy and Clinical Immunology. 2010 Apr 1
• 37 citations
  The most frequent DCLRE1C (ARTEMIS) mutations are based on homologous recombination events.
  Ulrich Pannicke, Manfred Hönig, Ilka Schulze, Jan Rohr, Gitta A. Heinz, Sylvia Braun, Ingrid Janz, Eva-Maria Rump, Markus G. Seidel, Susanne Matthes-Martin, Jan Soeren...> ;Human Mutation. 2010 Feb 1
• 242 citations
  ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia
  Christie-Ann McCarl, Capucine Picard, Sara Khalil, Takumi Kawasaki, Jens Röther, Alexander Papolos, Jeffery L. Kutok, Claire Hivroz, Francoise LeDeist, Katrin Plogmann...> ;The Journal of Allergy and Clinical Immunology. 2009 Dec 1
• 3 citations
  Ethylenecarbodiimide-coupled allogeneic antigen presenting cells induce human CD4+ regulatory T cells.
  Michael H. Albert, Xue-Zhong Yu, Thomas Magg> ;Clinical Immunology. 2008 Dec 1
• 43 citations
  Incidence, Predisposing Factors, and Outcome of Engraftment Syndrome in Pediatric Allogeneic Stem Cell Transplant Recipients
  Irene Schmid, Daniel Stachel, Philipp Pagel, Michael H. Albert> ;Biology of Blood and Marrow Transplantation. 2008 Apr 1
• 20 citations
  Tracking cell proliferation using the far red fluorescent dye SNARF-1.
  Thomas Magg, Michael H. Albert> ;Cytometry. Part B, Clinical Cytometry. 2007 Nov 15
• 42 citations
  Intravenous immunoglobulins contain naturally occurring antibodies that mimic antineutrophil cytoplasmic antibodies and activate neutrophils in a TNFalpha-dependent an...
  Sven Jarius, Peter Eichhorn, Michael H. Albert, Stefan Wagenpfeil, Manfred Wick, Bernd H. Belohradsky, Reinhard Hohlfeld, Dieter E. Jenne, Raymond Voltz> ;Blood. 2007 May 15
• 33 citations
  Oral graft vs. host disease in children--treatment with topical tacrolimus ointment.
  Michael H. Albert, B. Becker, Friedhelm R. Schuster, B. Klein, Vera Binder, K. Adam, C. Nienhoff, Monika Führer, Arndt Borkhardt> ;Pediatric Transplantation. 2007 May 1
• 73 citations
  Patients with adenosine deaminase deficiency surviving after hematopoietic stem cell transplantation are at high risk of CNS complications.
  Manfred Hönig, Michael H. Albert, Ansgar Schulz, Monika Sparber-Sauer, Catharina Schütz, Bernd H. Belohradsky, Tayfun Güngör, Markus Rojewski, Harald Bode, Ulrich Pann...> ;Blood. 2007 Apr 15
• 2 citations
  “Hair-on-end” skull induced by long-term G-CSF treatment in severe congenital neutropenia
  Michael H. Albert, Gundula Notheis, Uwe Wintergerst, Christine Born, Karl Schneider> ;Pediatric Radiology. 2007 Jan 12
• 17 citations
  The genotype of the original Wiskott phenotype.
  Vera Binder, Michael H. Albert, Maria Kabus, Marko Bertone, Alfons Meindl, Bernd H. Belohradsky> ;The New England Journal of Medicine. 2006 Oct 26
• 98 citations
  Cytokine profile in PFAPA syndrome suggests continuous inflammation and reduced anti-inflammatory response
  S. Stojanov, Florian Hoffmann, Anja Kéry, Ellen D. Renner, Dominik Hartl, Peter Lohse, Kristina Huss, Peter Fraunberger, James D Malley, Stephanie Zellerer, Michael H....> ;European Cytokine Network. 2006 Jun 1
• 15 citations
  T regulatory cells as an immunotherapy for transplantation.
  Michael H. Albert, Claudio Anasetti, Xue-Zhong Yu> ;Expert Opinion on Biological Therapy. 2006 Mar 21
• 23 citations
  Alloantigen Affinity and CD4 Help Determine Severity of Graft-versus-Host Disease Mediated by CD8 Donor T Cells
  Xue-Zhong Yu, Michael H. Albert, Claudio Anasetti> ;Journal of Immunology. 2006 Mar 15
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