J. Lachenaud

发表

Down syndrome-like acute megakaryoblastic leukemia in a patient with Cornelia de Lange syndrome

A. Baruchel, H. Cavé, A. Verloes, 2017, Haematologica.

Genetic typing of CBL, ASXL1, RUNX1, TET2 and JAK2 in juvenile myelomonocytic leukaemia reveals a genetic profile distinct from chronic myelomonocytic leukaemia

A. Baruchel, H. Cavé, C. Preudhomme, 2010, British journal of haematology.

Inherited CARD9 deficiency in 2 unrelated patients with invasive Exophiala infection.

J. Casanova, C. Picard, L. Abel, 2014, The Journal of infectious diseases.

Juvenile myelomonocytic leukemia displays mutations in components of the RAS pathway and the PRC2 network

A. Baruchel, C. Picard, H. Cavé, 2015, Nature Genetics.

A new recurrent translocation t(11;14)(q24;q32) involving IGH@ and miR-125b-1 in B-cell progenitor acute lymphoblastic leukemia

I Radford-Weiss, P. Brousset, H. Cavé, 2010, Leukemia.

Juvenile myelomonocytic leukaemia and Noonan syndrome

Corinne Alberti, Alain Verloes, Christine Chomienne, 2014, Journal of Medical Genetics.

Germline mutations of the CBL gene define a new genetic syndrome with predisposition to juvenile myelomonocytic leukaemia

A. Baruchel, H. Cavé, N. Philip, 2010, Journal of Medical Genetics.

Report of Two Cases of Aseptic Meningitis with Persistence of Pneumococcal Cell Wall Components in Cerebrospinal Fluid after Pneumococcal Meningitis

E. Bingen, M. Lorrot, F. Angoulvant, 2006, Journal of Clinical Microbiology.

Juvenile myelomonocytic leukaemia and Noonan syndrome

A. Baruchel, H. Cavé, S. Gazal, 2014, Journal of Medical Genetics.