Kolexia
Moshous Despina Pédiatrie
Moshous Despina
Pédiatrie
Hôpital Necker Enfants Malades
Paris, France
244 Activités
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{{person.topmesh1.name}} Déficits immunitaires Immunodéficience combinée grave Maladies d'immunodéficience primaire Lymphohistiocytose hémophagocytaire Maladie du greffon contre l'hôte Inflammation Syndrome de Wiskott-Aldrich Granulomatose septique chronique Syndromes lymphoprolifératifs

Collaborateurs

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Neven Benedicte
Neven Benedicte
Hôpital Necker Enfants Malades, Paris, France
Fischer Alain
Fischer Alain
Hôpital Necker Enfants Malades, Paris, France
Blanche Stéphane
Blanche Stéphane
Hôpital Necker Enfants Malades, Paris, France
Picard Capucine
Picard Capucine
Hôpital Necker Enfants Malades, Paris, France

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Shire
1 collaboration(s)
Dernière en 2019
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Dernières activités

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Downregulation of V-ATPase V Sector Induces Microvillus Atrophy Independently of Apical Trafficking in the Mammalian Intestine.
Cellular and molecular gastroenterology and hepatology   16 février 2024
Clinical and functional spectrum of RAC2-related immunodeficiency.
Blood   09 janvier 2024
Characterization of novel mutations in the TEL-patch domain of the telomeric factor TPP1 associated with telomere biology disorders.
Human molecular genetics   04 janvier 2024
Letermovir for CMV Prophylaxis in Very High-Risk Pediatric Hematopoietic Stem Cell Transplantation Recipients for Inborn Errors of Immunity.
Journal of clinical immunology   20 décembre 2023
ARTEGENE: A Phase 1/2 Open Label Non Randomized Study, Multicentric, Single Arm Evaluating the Safety and Efficacy of Gene Therapy of the Severe Combined Immunodeficiency (SCID) Caused by Mutations in the Human DCLRE1C Gene (Artemis) by Transplantation of a Single Dose of Autologous CD34+ Cells Transduced ex Vivo With the G2ARTE Lentiviral Vector Expressing the DCLRE1C cDNA
Essai Clinique (Assistance publique – Hôpitaux de Paris)   24 novembre 2023
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
Fertility and Pregnancy in Patients with Congenital Neutropenia: Experience of the French Severe Chronic Neutropenia Registry in 565 Patients Above Age of 15 Years
65th ASH Annual Meeting Abstracts   02 novembre 2023
Hematological Involvement in Childhood Langerhans Cell Histiocytosis: A Cohort Study of 303 Patients
65th ASH Annual Meeting Abstracts   02 novembre 2023
Preclinical Assessment for Gene Addition Strategy in Familial Hemophagocytic Lymphohistiocytosis Related to Munc 13-4 Deficiency
65th ASH Annual Meeting Abstracts   02 novembre 2023
Human Pro-T-Cell Manufacturing in Vitro Is a Safe Procedure for Hematopoietic Stem Cell Transplantation with Delayed T-Cell Reconstitution: Interim Results from 2 Different Clinical Trials
65th ASH Annual Meeting Abstracts   02 novembre 2023