Caroline Thomas

发表

Overall genomic pattern is a predictor of outcome in neuroblastoma.

Gudrun Schleiermacher, Frank Speleman, Jérôme Couturier, 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Herpes-Virus Infection in Patients with Langerhans Cell Histiocytosis: A Case-Controlled Sero-Epidemiological Study, and In Situ Analysis

T. Molina, F. Geissmann, J. Seigneurin, 2008, PloS one.

Strains Responsible for Invasive Meningococcal Disease in Patients With Terminal Complement Pathway Deficiencies

C. Picard, D. Moshous, F. Suarez, 2017, The Journal of infectious diseases.

Circulating cell‐free BRAFV600E as a biomarker in children with Langerhans cell histiocytosis

J. Emile, P. Nizard, V. Taly, 2017, British journal of haematology.

reliable markers of ALPS associated with FAS loss of function FAS-L, IL-10, and double-negative CD4-CD8-TCR alpha/beta+ T cells are

F. Rieux-Laucat, A. Fischer, J. Casanova, 2011 .

Brief report FAS-L, IL-10, and double-negative CD4 (cid:1) CD8 (cid:1) TCR (cid:2) / (cid:3) (cid:4) T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function

F. Rieux-Laucat, A. Fischer, F. Deist, 2009 .

FAS-L, IL-10, and double-negative CD4- CD8- TCR alpha/beta+ T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function.

F. Rieux-Laucat, A. Fischer, J. Casanova, 2009, Blood.

Late effects after hematopoietic stem cell transplantation for β-thalassemia major: the French national experience

P. Auquier, I. Yakoub-Agha, P. Rohrlich, 2018, Haematologica.

Long term follow-up of pediatric-onset Evans syndrome: broad immunopathological manifestations and high treatment burden

F. Rieux-Laucat, C. Picard, G. Leverger, 2021, Haematologica.

Prospective evaluation of the first option, second-line Therapy in childhood chronic immune thrombocytopenia: splenectomy or immunomodulation.

G. Leverger, G. Vassal, T. Leblanc, 2020, The Journal of pediatrics.

Genetic Variants of APOL1 Are Major Determinants of Kidney Failure in People of African Ancestry With HIV

Hongbo Deng, A. Winston, C. Sabin, 2022, Kidney international reports.

Sickle Cell Trait and Kidney Disease in People of African Ancestry With HIV

Hongbo Deng, A. Winston, C. Sabin, 2021, Kidney international reports.

Outcome of children and adolescents with recurrent/refractory classical Hodgkin lymphoma, a study from the Société Française de Lutte contre le Cancer des Enfants et des Adolescents (SFCE)

T. Leblanc, J. Stéphan, O. Oberlin, 2012, British journal of haematology.

Complex constitutional subtelomeric 1p36.3 deletion/duplication in a mentally retarded child with neonatal neuroblastoma.

M. Le Cunff, C. Le Caignec, B. Isidor, 2008, European journal of medical genetics.

D. Hémon, F. Menegaux, C. Bergeron, 2007, International journal of cancer.

Endocrine involvement in pediatric-onset Langerhans' cell histiocytosis: a population-based study.

K. Hoang-Xuan, D. Frappaz, M. Polak, 2004, The Journal of pediatrics.

T‐Cell Receptor Excision Circles in HIV‐Exposed, Uninfected Newborns Measured During a National Newborn Screening Program for Severe Combined Immunodeficiency

R. Tubiana, N. Winer, A. Moine, 2018, The Journal of pediatrics.