Polymorphous lymphoproliferative disorder with Hodgkin-like features in common γ-chain–deficient severe combined immunodeficiency - 10/08/11
Doi : 10.1016/j.jaci.2010.09.036
Mary A. Slatter, MD a, e, Brian Angus, FRCPath b, Kevin Windebank, MD c, Alison Taylor, MSc d, Cathy Meaney, BSc d, Tracey Lester, FRCPath d, Gail Norbury, FRCPath d, Sophie Hambleton, MD a, e, Mario Abinun, MD a, e, Terence J. Flood, MD a, Andrew J. Cant, MD a, e, Andrew R. Gennery, MD a, e 
a Department of Paediatric Immunology, Newcastle Upon Tyne Hospital, NHS Foundation Trust, Newcastle Upon Tyne, United Kingdom
b Department of Pathology, Newcastle Upon Tyne Hospital, NHS Foundation Trust, Newcastle Upon Tyne, United Kingdom
c Department of Paediatric Oncology, Newcastle Upon Tyne Hospital, NHS Foundation Trust, Newcastle Upon Tyne, United Kingdom
d Molecular Genetics, Great Ormond Street Hospital, NHS Trust, London, United Kingdom
e Institute of Cellular Medicine, Newcastle University, Newcastle Upon Tyne, United Kingdom
| Supported by the National Health Service, United Kingdom. |
|
| Disclosure of potential conflict of interest: The authors have declared that they have no conflict of interest. |
© 2010
American Academy of Allergy, Asthma & Immunology. Publié par Elsevier Masson SAS. Tous droits réservés.
Vol 127 - N° 2
P. 533-535 - février 2011 Retour au numéro
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