H. B.

T cell suicide gene therapy to aid haematopoietic stem cell transplantation (2005)

  • Qasim,
  • W.,
  • Gaspar,
  • H.B.,
  • Thrasher,
  • A.J.

Graft versus host disease (GVHD) is a T cell mediated phenomenon that arises following allogeneic haematopoietic stem cell transplantation, and may be particularly severe in the context of human...

Multisystem disease in CAEBV infection (2005)

  • Williams,
  • A.P.,
  • Hourihane,
  • J.O.B.,
  • Hodges,
  • E.,
  • ...

Failure of SCID-X1 gene therapy in older patients (2005)

  • Thrasher,
  • A.J.,
  • Hacein-Bey-Abina,
  • S.,
  • Gaspar,
  • H.B.,
  • ...

Gene therapy has been shown to be a highly effective treatment for infants with typical X-linked severe combined immunodeficiency (SCID-X1, gammac-deficiency). For patients in whom previous...

Improved survival after unrelated donor bone marrow transplantation in children with primary immunodeficiency using a reduced-intensity conditioning regimen (2005)

  • Rao,
  • K.,
  • Amrolia,
  • P.J.,
  • Jones,
  • A.,
  • ...

The optimal approach to stem cell transplantation in children with immunodeficiency who lack a matched family donor is controversial. Unrelated donor stem cell transplantation gives equivalent...

The impact of telomere erosion on memory CD8(+) T cells in patients with X-linked lymphoproliferative syndrome (2005)

  • Plunkett,
  • F.J.,
  • Franzese,
  • O.,
  • Belaramani,
  • L.L.,
  • ...

Patients with X-linked lymphoproliferative syndrome (XLP) experience excessive T cell proliferation after primary Epstein-Barr virus (EBV) infection, due to mutations in the signalling lymphocyte...

Allogeneic stem cell transplantation in X-linked lymphoproliferative disease: two cases in one family and review of the literature (2005)

Summary:X-linked lymphoproliferative disease (XLP) is a rare immunodeficiency caused by mutations in the signaling lymphocyte activating molecule-associated protein/SH2D1A gene and characterized by a...

Gene therapy for severe combined immunodeficiencies (2005)

Severe combined immune deficiencies (SCIDs) are a group of monogenic diseases resulting in profound disturbances of lymphocyte development and function. Affected individuals are prone to...

Improved survival after unrelated donor bone marrow transplant in children with primary immunodeficiency using a reduced intensity conditioning regimen (2004)

  • Rao,
  • K.,
  • Amrolia,
  • P.J.,
  • Jones,
  • A.,
  • ...

The optimal approach to stem cell transplantation in children with immunodeficiency who lack a matched family donor is controversial. Unrelated donor stem cell transplant gives equivalent outcome to...

 
Additional Information

Publishing period:

1997 - 2006 (26)

Co-authors: