K. Kébaili

发表

Corrigendum: Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome

Yuya Ito, Jun Wang, Mikita Suyama, 2016, Nature Communications.

Pharmacokinetic Drug Interaction Between Cyclosporine and Imatinib in Bone Marrow Transplant Children and Model-Based Reappraisal of Imatinib Drug Interaction Profile

Y. Bertrand, S. Goutelle, K. Kébaili, 2014, Therapeutic drug monitoring.

Effects of Genotypes and Treatment on Oxygenscan Parameters in Sickle Cell Disease

Celeste K. Kanne, Y. Bertrand, V. Sheehan, 2021, Cells.

Childhood Langerhans cell histiocytosis with severe lung involvement: a nationwide cohort study

J. Emile, R. Epaud, H. Ducou le Pointe, 2020, Orphanet Journal of Rare Diseases.

G6PD deficiency and absence of α‐thalassemia increase the risk for cerebral vasculopathy in children with sickle cell anemia

V. Pialoux, Y. Bertrand, P. Joly, 2016, European journal of haematology.

Childhood leukaemia, polymorphisms of metabolism enzyme genes, and interactions with maternal tobacco, coffee and alcohol consumption during pregnancy

M. Loriot, P. Beaune, D. Hémon, 2005, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

hydrocarbons; a case-control study exposure to potential sources of benzene and other Acute childhood leukaemia and environmental

A. Baruchel, K. Kébaili, J. Clavel, 2004 .

Importance of methodological standardization for the ektacytometric measures of red blood cell deformability in sickle cell anemia.

Y. Bertrand, J. Tisdale, P. Joly, 2016, Clinical hemorheology and microcirculation.

Successful salvage chemotherapy for isolated central nervous system (CNS) relapse in Burkitt lymphoma: monocentric experience of 3 pediatric patients.

Y. Bertrand, C. Pondarré, K. Kébaili, 2008, Journal of pediatric hematology/oncology.

Outcome of 27 patients with Hurler's syndrome transplanted from either related or unrelated haematopoietic stem cell sources

Y. Bertrand, Y. Bertrand, J. Bérard, 2003, Bone Marrow Transplantation.

Goal-oriented monitoring of cyclosporine is effective for graft-versus-host disease prevention after Hematopoietic Stem Cell Transplantation in Sickle Cell Disease and Thalassemia major.

Y. Bertrand, I. Mollet, S. Goutelle, 2020, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Effect of Age on Blood Rheology in Sickle Cell Anaemia and Sickle Cell Haemoglobin C Disease: A Cross-Sectional Study

V. Pialoux, Y. Bertrand, P. Joly, 2016, PloS one.

Priming With Red Blood Cells Allows Red Blood Cell Exchange for Sickle Cell Disease in Low-Weight Children

F. Bérard, Y. Bertrand, P. Joly, 2021, Frontiers in Medicine.

Automatic depletion with Spectra Optia allows a safe 16% reduction of red blood cell pack consumption in exchanged sickle cell anemia patients

Y. Bertrand, P. Joly, F. Cognasse, 2019, Transfusion.

BRAF Mutation Correlates With High-Risk Langerhans Cell Histiocytosis and Increased Resistance to First-Line Therapy.

Valérie Rigau, Valérie Taly, Christine Bodemer, 2016, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Comparisons of oxygen gradient ektacytometry parameters between sickle cell patients with or without α‐thalassaemia

V. Sheehan, Y. Bertrand, P. Joly, 2021, British journal of haematology.

Long‐term follow‐up of children with risk organ‐negative Langerhans cell histiocytosis after 2‐chlorodeoxyadenosine treatment

G. Leverger, J. Emile, P. Schneider, 2020, British journal of haematology.

Incidence and risk factors for clinical neurodegenerative Langerhans cell histiocytosis: a longitudinal cohort study

K. Hoang-Xuan, G. Leverger, A. Idbaih, 2018, British journal of haematology.

Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome

M. Suyama, C. Picard, A. Gennery, 2015, Nature Communications.

A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary Immunodeficiency

F. Rieux-Laucat, A. Fischer, J. Jais, 2019, Journal of Clinical Immunology.

Autoimmune and inflammatory manifestations occur frequently in patients with primary immunodeficiencies

F. Rieux-Laucat, A. Fischer, J. Jais, 2017, The Journal of allergy and clinical immunology.

Time to Switch to Second-line Antiretroviral Therapy in Children With Human Immunodeficiency Virus in Europe and Thailand

A. Trkola, P. Tovey, C. Königs, 2018, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Protective effect of IgM against colonization of the respiratory tract by nontypeable Haemophilus influenzae in patients with hypogammaglobulinemia.

A. Fischer, C. Picard, É. Oksenhendler, 2012, The Journal of allergy and clinical immunology.

Cumulative Efficacy and Safety of 5-Year Deferasirox (Exjade®) Treatment in Pediatric Patients with Thalassemia Major: A Phase II Multicenter Prospective Trial

C. Rebischung, R. Galanello, A. Piga, 2008 .

Renal enlargement as presentation of isolated renal relapse in childhood leukemia.

Y. Bertrand, K. Kébaili, N. Philippe, 2000, Journal of pediatric hematology/oncology.

Acute childhood leukaemia and environmental exposure to potential sources of benzene and other hydrocarbons; a case-control study

D. Hémon, A. Baruchel, G. Leverger, 2004, Occupational and Environmental Medicine.

Medication adherence after pediatric allogeneic stem cell transplantation: Barriers and facilitators.

Y. Bertrand, K. Kébaili, N. Bleyzac, 2019, European journal of oncology nursing : the official journal of European Oncology Nursing Society.