Publications by authors named "Nicolas Wulffraat"

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Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness.
Chantal Lagresle-Peyrou, Emmanuelle M Six, Capucine Picard, Frédéric Rieux-Laucat, Vincent Michel, Nicolas M Wulffraat

Nat Genet· January 2009

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Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1.
Salima Hacein-Bey-Abina, Alexandrine Garrigue, Gary P Wang, Jean Soulier, Annick Lim, Nicolas Wulffraat

J Clin Invest· September 2008

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Case report: severe central nervous system involvement in juvenile dermatomyositis.
Elisabeth F Elst, Sylvia S M Kamphuis, Berent J Prakken, Nicolas M Wulffraat, Janjaap van der Net

J Rheumatol· September 2003

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Long-term survival and transplantation of haemopoietic stem cells for immunodeficiencies: report of the European experience 1968-99.
Corinne Antoine, Susanna Müller, Andrew Cant, Marina Cavazzana-Calvo, Paul Veys, Nicolas Wulffraat

Lancet· February 2003

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A serious adverse event after successful gene therapy for X-linked severe combined immunodeficiency.
Salima Hacein-Bey-Abina, Christof von Kalle, Manfred Schmidt, Françoise Le Deist, Nicolas Wulffraat

N Engl J Med· January 2003

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Sustained correction of X-linked severe combined immunodeficiency by ex vivo gene therapy.
Salima Hacein-Bey-Abina, Françoise Le Deist, Frédérique Carlier, Cécile Bouneaud, Christophe Hue, Nicolas Wulffraat

N Engl J Med· April 2002

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