Oral Presentations

 

  • 2019
  • 2018
  • 2017
  • 2016
  • 2015
  • 2014
  • 2013
  • 2012
  • 2011
  • 2010

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: 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: 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

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