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Journal Abstract Search

208 related items for PubMed ID: 11298858

  • 1. Gene therapy for genetic haematological disorders and immunodeficiencies.
    Kohn DB.
    J Intern Med; 2001 Apr; 249(4):379-90. PubMed ID: 11298858
    [Abstract] [Full Text] [Related]

  • 2. Progress towards hematopoietic stem cell gene therapy.
    Kurre P, Kiem HP.
    Curr Opin Mol Ther; 2000 Aug; 2(4):400-11. PubMed ID: 11249770
    [Abstract] [Full Text] [Related]

  • 3. [Transplantation of genetically modified cells in the treatment of children with SCID: great hopes and recent disappointments].
    Smogorzewska EM, Weinberg KI, Kohn DB.
    Med Wieku Rozwoj; 2003 Aug; 7(1):27-34. PubMed ID: 13130167
    [Abstract] [Full Text] [Related]

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  • 5. Advances in Gene Therapy for Fanconi Anemia.
    Río P, Navarro S, Bueren JA.
    Hum Gene Ther; 2018 Oct; 29(10):1114-1123. PubMed ID: 30117331
    [Abstract] [Full Text] [Related]

  • 6. Gene transfer to hematopoietic cells--the clinical experience.
    Richter J.
    Eur J Haematol; 1997 Aug; 59(2):67-75. PubMed ID: 9293853
    [No Abstract] [Full Text] [Related]

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  • 8. Stem Cell Genetic Therapy for Fanconi Anemia - A New Hope.
    Hanenberg H, Roellecke K, Wiek C.
    Curr Gene Ther; 2017 Aug; 16(5):309-320. PubMed ID: 28067166
    [Abstract] [Full Text] [Related]

  • 9. Gene therapy for hematopoietic and immune disorders.
    Kohn DB.
    Bone Marrow Transplant; 1996 Dec; 18 Suppl 3():S55-8. PubMed ID: 8971410
    [Abstract] [Full Text] [Related]

  • 10. Gene therapy of primary T cell immunodeficiencies.
    Fischer A, Hacein-Bey-Abina S, Cavazzana-Calvo M.
    Gene; 2013 Aug 10; 525(2):170-3. PubMed ID: 23583799
    [Abstract] [Full Text] [Related]

  • 11. Gene therapy for adenosine deaminase deficiency.
    Cappelli B, Aiuti A.
    Immunol Allergy Clin North Am; 2010 May 10; 30(2):249-60. PubMed ID: 20493400
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  • 15. Gene therapy in infants with severe combined immunodeficiency.
    Otsu M, Candotti F.
    BioDrugs; 2002 May 10; 16(4):229-39. PubMed ID: 12196037
    [Abstract] [Full Text] [Related]

  • 16. Gene therapy for inherited immunodeficiency.
    Touzot F, Hacein-Bey-Abina S, Fischer A, Cavazzana M.
    Expert Opin Biol Ther; 2014 Jun 10; 14(6):789-98. PubMed ID: 24823313
    [Abstract] [Full Text] [Related]

  • 17. Treatment of severe combined immunodeficiency disease (SCID) due to adenosine deaminase deficiency with CD34+ selected autologous peripheral blood cells transduced with a human ADA gene. Amendment to clinical research project, Project 90-C-195, January 10, 1992.
    Blaese RM, Culver KW, Chang L, Anderson WF, Mullen C, Nienhuis A, Carter C, Dunbar C, Leitman S, Berger M.
    Hum Gene Ther; 1993 Aug 10; 4(4):521-7. PubMed ID: 7691188
    [Abstract] [Full Text] [Related]

  • 18. Twenty-Five Years of Gene Therapy for ADA-SCID: From Bubble Babies to an Approved Drug.
    Ferrua F, Aiuti A.
    Hum Gene Ther; 2017 Nov 10; 28(11):972-981. PubMed ID: 28847159
    [Abstract] [Full Text] [Related]

  • 19. Amendment to Clinical Research Project. Project 90-C-195. April 1, 1993. Treatment of severe combined immunodeficiency disease (SCID) due to adenosine deaminase deficiency with autologous lymphocytes transduced with a human ADA gene.
    Dunbar C, Chang L, Mullen C, Ramsey WJ, Carter C, Kohn D, Parkman R, Lenarsky C, Weinberg K, Wara D, Culver KW, Anderson WF, Leitman S, Fleisher T, Klein H, Shearer G, Clerici M, McGarrity G, Bastian J, Hershfield MS.
    Hum Gene Ther; 1999 Feb 10; 10(3):477-88. PubMed ID: 10048399
    [No Abstract] [Full Text] [Related]

  • 20. Promising Results with Ex Vivo Lentiviral HSPC Gene Therapy in ADA-SCID.
    Am J Med Genet A; 2021 Aug 10; 185(8):2291-2292. PubMed ID: 34240545
    [No Abstract] [Full Text] [Related]

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