P. Veys

Successful treatment of lymphoproliferative disease complicating primary immunodeficiency/ immunodysregulatory disorders with reduced-intensity allogeneic stem-cell transplantation (2007)

Cohen, J.M., Sebire, N.J., Harvey, J., Gaspar, H.B., Cathy, C., Jones, A., ...

Lymphoproliferative disease (LPD) is a recognized complication of primary immunodeficiency (PID) and immunodysregulatory syndromes. Historically, it has a very poor outcome. For patients surviving...

Serial transplantation of mismatched donor hematopoietic cells between HLA-identical sibling pairs with congenital immunodeficiency: in vivo tolerance permits rapid immune reconstitution following T-replete transplantation without GVHD in the secondary recipient (2006)

Cohen, J.M., Rogers, V., Gaspar, H.B., Jones, A., Davies, E.G., Rao, K., ...

We report serial transplantation procedures in 2 sets of brothers with X-linked primary immunodeficiency. The first boy in each family received a T-cell–depleted transplant from a mismatched donor....

Adoptive immunotherapy with allodepleted donor T-cells improves immune reconstitution after haploidentical stem cell transplantation (2006)

Amrolia, P.J., Muccioli-Casadei, G., Huls, H., Adams, S., Durett, A., Gee, A., ...

Poor T lymphocyte reconstitution limits the use of haploidentical stem cell transplantation (SCT) because it results in a high mortality from viral infections. One approach to overcome this problem...

Haematopoietic cell transplantation (HCT) in combination with enzyme replacement therapy (ERT) in patients with Hurler syndrome (2006)

Brinkman, J., Boelens, J.J., Wraith, J.E., O'Meara, A., Veys, P., Wijburg, F.A., ...

Stem cell transplantation with reduced-intensity conditioning for hemophagocytic lymphohistiocytosis (2005)

Cooper, N., Rao, K., Gilmour, K., Hadad, L., Adams, S., Cale, C., ...

Allogeneic stem cell transplantation (SCT) is curative for hemophagocytic lymphohistiocytosis (HLH). However, patients frequently have significant morbidity before transplantation and there is high...

Resolution of peanut allergy following bone marrow transplantation for primary immunodeficiency (2005)

Hourihane, J.O., Rhodes, H.L., Jones, A.M., Veys, P., Connett, G.J.

Peanut allergy is a severe and life-threatening form of food allergy. Treatments are being developed but the mainstays of current management remain avoidance of peanut and appropriate use of rescue...

Successful treatment of juvenile myelomonocytic leukemia relapsing after stem cell transplantation using donor lymphocyte infusion (2003)

Worth, A., Rao, K., Webb, D., Chessells, J., Passmore, J., Veys, P.

Juvenile myelomonocytic leukemia (JMML) is a rare pediatric malignancy. Hematopoietic stem cell transplantation (SCT) is the only curative approach. However, relapse after SCT remains the major cause...

Reverse and converse ocular bobbing with synkinetic blinking and opsoclonus in a child with Epstein-Barr virus encephalitis after bone marrow transplant for MPS I

CASSIDY, L., TAYLOR, D., WERNER, K., VEYS, P., HARRIS, C.

Immune recovery disease: a case of interstitial keratitis and tonic pupil following bone marrow transplantation

Ioannidis, A S, Forrest, M, Nischal, K K, Veys, P, Davies, E G, Woodruff, G

Severe combined immunodeficiency with abnormalities in expression of the common leucocyte antigen, CD45

Cale, C., Klein, N., Novelli, V., Veys, P., Jones, A., Morgan, G.

Accepted 16 September 1996


Improved prognosis for acquired aplastic anaemia

Pitcher, L, Hann, I, Evans, J, Veys, P, Chessells, J, Webb, D

This study compared the prognosis of patients treated for aplastic anaemia at Great Ormond Street Hospital for Children from 1973-88 (group A; n = 38) with a more recent cohort from 1989-96 (group B;...

Clinical course of patients with major histocompatibility complex class II deficiency

Saleem, M, Arkwright, P, Davies, E, Cant, A, Veys, P

The clinical course of 10 children who have been diagnosed with major histocompatibility complex (MHC) class II deficiency (bare lymphocyte syndrome) in the UK over the past eight years is described....