Pierre Philippet

Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and Autoimmunity

Gabriela López‐Herrera, Giacomo Tampella, Qiang Pan‐Hammarström et al. · The American Journal of Human Genetics · 2012 · 525 citations · Full text

Life Sciences, Genetics, Immunology +15

Five years of experience with hydroxyurea in children and young adults with sickle cell disease

Alina Ferster, Parvine Tahriri, Christiane Vermylen et al. · Blood · 2001 · 218 citations · Full text

Medicine, Hematology, Pediatrics +8

Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B–severe combined immune deficiency or Omenn syndrome

Barbara Corneo, Despina Moshous, Tayfun Güngör et al. · Blood · 2001 · 216 citations · Full text

Life Sciences, Genetics, Immunology +17

TTC7A mutations disrupt intestinal epithelial apicobasal polarity

Amélie Bigorgne, Henner F. Farin, Roxane Lemoine et al. · Journal of Clinical Investigation · 2013 · 197 citations

Life Sciences, Immunology, Molecular Genetics +17

Dexamethasone (6 mg/m2/day) and prednisolone (60 mg/m2/day) were equally effective as induction therapy for childhood acute lymphoblastic leukemia in the EORTC CLG 58951 randomized trial

Carine Domenech, Stefan Suciu, Barbara De Moerloose et al. · Haematologica · 2014 · 82 citations · Full text

Medicine, Oncology, Pharmacotherapy +13