Kolexia
Touzot Fabien
Pédiatrie
Hôpital Necker Enfants Malades
Paris, France
103 Activités
0 Followers

Scientifique
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{{person.topmesh1.name}} Déficits immunitaires Granulomatose septique chronique Immunodéficience combinée grave Immunodéficiences combinées graves liées à l'X Drépanocytose Dyskératose congénitale Thalassémie Bêta-Thalassémie Microcéphalie

Industries

Novartis
4 collaboration(s)
Dernière en 2022
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Dernières activités

Allogeneic hematopoietic cell transplantation is effective for p47phox chronic granulomatous disease: A Primary Immune Deficiency Treatment Consortium study.
The Journal of allergy and clinical immunology   28 janvier 2024
Long-term Follow-up of Subjects With Sickle Cell Disease Treated With Ex Vivo Gene Therapy Using Autologous Hematopoietic Stem Cells Transduced With a Lentiviral Vector
Essai Clinique (Bluebird)   08 janvier 2024
Gene Transfer for Severe Combined Immunodeficiency, X-linked (SCID-X1) Using a Self-inactivating (SIN) Gammaretroviral Vector: Multi-site Phase I/II Trial Evaluating the Treatment of SCID-X1 Patients With Retrovirus-mediated Gene Transfer
Essai Clinique (David Williams)   11 novembre 2023
JAK-inhibitor treatment for inborn errors of JAK/STAT signaling: An ESID and EBMT IEWP retrospective study.
The Journal of allergy and clinical immunology   05 novembre 2023
Case report: Success of allogeneic hematopoietic stem cell transplantation for refractory systemic-onset juvenile idiopathic arthritis.
Frontiers in medicine   16 octobre 2023
Long-term Follow-up of Subjects With Transfusion-Dependent β-Thalassemia (TDT) Treated With Ex Vivo Gene Therapy Using Autologous Hematopoietic Stem Cells Transduced With a Lentiviral Vector
Essai Clinique (Bluebird)   13 octobre 2023
NOX2 deficiency enhances priming and activation of the NLRP3 inflammasome.
The Journal of allergy and clinical immunology   05 octobre 2023
Intestinal microbiome and metabolome signatures in patients with chronic granulomatous disease.
The Journal of allergy and clinical immunology   01 septembre 2023
Genotype, Oxidase Status, and Preceding Infection or Autoinflammation Do Not Affect Allogeneic HCT Outcomes for CGD.
Blood   10 août 2023
A novel variant in caspase recruitment domain family member 11 highlights the variability of clinical manifestations and management in a three generation family.
The journal of allergy and clinical immunology. In practice   28 juin 2023