Oral Presentations

 

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Title: Gene therapy in Fanconi anemia (FA)
Speakers: J. Bueren
DateOctober 10-12, 2019
Place: Prague, Czesh Republic
Organizing institucion: Stem Cell transplantation in childhood biotechnological advances, ethical issues and worldwide equal access

Title: Stem Cell transplantation in childhood biotechnological advances, ethical issues and worldwide equal access
Speakers: J. Bueren
Date26-28 september 2019
Place: Roma, Italy
Organizing institucion: Stem Cell transplantation in childhood biotechnological advances, ethical issues and worldwide equal access

Title: NHEJ-mediated gene editing: an alternative approach to efficiently correct hspcs from patients with fanconi anemia
Speakers: P. Río
Date12 september 2019
Place: Madison, WI, USA
Organizing institucion: ISCT

Title: Lentiviral gene therapy and genome editing for the treatment of a rare hemolytic disease, Pyruvate Kinase Deficiency
Speakers: Jose Carlos Segovia
Date: july 14 2019
Place: Barcelona, Spain
Organizing institucion: CRG y upf

Title: Gene Therapy Panel
Speakers: P. Río
Date21-26 June 2019
Place: Camp Sunshine, Casco, Maine
Organizing institucion: 28th Annual Family Meeting

Title: Pyruvate kinase deficiency gene therapy.
Speakers: Jose Carlos Segovia
Date: may 17 2019
Place: Athens, Greece
Organizing institucion: 4th Congress gene therapy and regenerative medicine

Title: Genome-wide assessment of lentiviral integration sites of gene-corrected lympho-hematopoietic cells in FA-A patients
Speakers: S. Navarro
Date: april 29-may 2 2019
Place: Washington D.C., USA
Organizing institucion: 22nd Annual Meeting of the American Society of Gene and Cell Therapy

Title: Update on the Fanconi anaemia clinical trial
Speakers: P. Río
Date17 May 2019
Place: Paris, France
Organizing institucion: SFTCG: Societe francaise de therapie cellulaire et genique

Title: Preliminary conclusions obtained in Fanconi anemia patients treated by lentiviral-mediated gene therapy after 2 years of follow-up
Speakers: Paula Rio
Date: April 29-May 2 2019
Place: Washington D.C., USA
Organizing institucion: 22nd Annual Meeting of the American Society of Gene and Cell Therapy

Title: Advanced therapies for the treatment of PH1: cellular reprogramming and gene editing
Speakers: Virginia Nieto Romero
Date: 21-22 june 2019
Place: Boston, EEUU.
Organizing institucion: OHF International Hyperoxaluria Workshop

Title: Preclinical Studies towards the Gene Therapy of Diamond-Blackfan Anemia
Speakers: Susana Navarro
Date: 10-12 june 2019
Place: Amsterdam, Holland.
Organizing institucion: The european Diamond-Blackfan anemia symposium

Title: Efficient genome editing of the PKLR locus in human long-term hematopietic stem cells using specific CRISPR/CAS9 RNP and AAV6-delivery of donor templates to treat pyruvate kinase deficiency
Speakers: S. Fañanas Baquero
Date: April 29-May 2 2019
Place: Washington, D.C., USA
Organizing institucion: 22nd Annual Meeting of the American Society of Gene and Cell Therapy

Title: Gene therapy for bone marrow failure syndromes
Speakers: J. Bueren
DateApril 26th 2019
Place: Zürich, Switzerland.
Organizing institucion: INTERNATIONAL SYMPOSIUM GENE AND CELL THERAPIES

Title: Fanconi Anaemia and other inherited bone marrow failure syndromes
Speakers: J. Bueren
Date22-25 march 2019
Place: Madrid, Spain.
Organizing institucion: 46th Annual meeting of the european society for blood and marrow transplantation

Title: Conferences on haematological diseases
Speakers: J. Bueren
Date: 7 february 2019
Place: Paris, France
Organizing institucion: Gene Therapy for Rare monogenic Diseases (GTRD)-1st EDITION

Title: Therapie genique dans I`Anemia de Fanconi
Speakers: J. Bueren
Date: 24-25 Jannuary 2019
Place: Chamonix, France
Organizing institucion: CONGRES SOCIETE D`HEMATOLOGIE ET D`IMMUNOLOGIE PEDIATRIQUE