A. Jones

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TITLE Improved Survival after Unrelated Donor Bone Marrow Transplant in Children with Primary Immunodeficiency using a Reduced Intensity Conditioning Regimen

P. Veys, P. Amrolia, C. Cale, 2004 .

Cognitive and behavioral abnormalities in children after hematopoietic stem cell transplantation for severe congenital immunodeﬁciencies

P. Veys, A. Thrasher, E. Davies, 2008 .

Host natural killer immunity is a key indicator of permissiveness for donor cell engraftment in patients with severe combined immunodeficiency☆

A. Gennery, P. Veys, A. Worth, 2014, The Journal of allergy and clinical immunology.

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

N. Sebire, P. Veys, P. Amrolia, 2007, Blood.

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

P. Veys, P. Amrolia, C. Cale, 2005, Blood.

Liver disease in children with primary immunodeficiencies.

B. Portmann, F. Rodrigues, G. Mieli-Vergani, 2001, The Journal of pediatrics.

Clinical picture and treatment of 2212 patients with common variable immunodeficiency.

É. Oksenhendler, P. Soler-Palacín, A. Šedivá, 2014, The Journal of allergy and clinical immunology.

Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study

Bodo Grimbacher, James Curtis, Siobhan O. Burns, 2017, The Journal of allergy and clinical immunology.

Immunogenetics: changing the face of immunodeficiency

H. Gaspar, A. Jones, A. Jones, 2000, Journal of clinical pathology.

Immunodeficiency and disseminated mycobacterial infection associated with homozygous nonsense mutation of IKKβ☆

S. Nejentsev, V. Plagnol, S. Burns, 2014, The Journal of allergy and clinical immunology.

Cognitive and behavioral abnormalities in children after hematopoietic stem cell transplantation for severe congenital immunodeficiencies.

T. Cole, P. Veys, A. Thrasher, 2008, Blood.

Diagnosis of X‐linked lymphoproliferative disease by analysis of SLAM‐associated protein expression

K. Nichols, D. Goldblatt, A. Thrasher, 2000, European journal of immunology.

Advances in the Care of Primary Immunodeficiencies (PIDs): from Birth to Adulthood

N. Mahlaoui, K. Warnatz, A. Cant, 2017, Journal of Clinical Immunology.

B-cell-negative severe combined immunodeficiency associated with a common γ chain mutation

P. Clark, C. Kinnon, S. Genet, 1997, Human Genetics.

Clinical and immunological features in a cohort of patients with partial DiGeorge syndrome followed at a single center.

G. Giardino, A. Worth, Winnie Ip, 2019, Blood.

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.

P. Veys, P. Amrolia, E. Davies, 2006, Blood.

The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency.

A. Schäffer, V. Lougaris, R. Geha, 2015, The Journal of allergy and clinical immunology.

Protein assays for diagnosis of Wiskott–Aldrich syndrome and X‐linked thrombocytopenia

A. Finn, A. Thrasher, C. Kinnon, 2001, British journal of haematology.

The many faces of Artemis-deficient combined immunodeficiency - Two patients with DCLRE1C mutations and a systematic literature review of genotype-phenotype correlation.

P. Jeggo, P. Veys, P. Amrolia, 2013, Clinical immunology.

Bronchiectasis secondary to primary immunodeficiency in children: Longitudinal changes in structure and function

S. Sonnappa, A. Jaffe, A. Calder, 2009, Pediatric pulmonology.

Dedicator of cytokinesis 8 deficiency: a predisposition to sclerosing cholangitis.

N. Hadžić, C. Cale, A. Jones, 2014, Clinical immunology.

Cognitive and behavioural abnormalities in children following haematopoietic stem cell transplantation for severe congenital immunodeficiencies

P. Veys, A. Thrasher, E. Davies, 2008 .

Advances in the Care of Primary Immunodeficiencies (PIDs): from Birth to Adulthood

N. Mahlaoui, K. Warnatz, A. Cant, 2017, Journal of Clinical Immunology.

Screening for mutations causing X-linked severe combined immunodeficiency in the IL-2Rγ chain gene by single-strand conformation polymorphism analysis

R. Levinsky, P. Clark, R. Hendriks, 1995, Human Genetics.

Interferon α treatment of molluscum contagiosum in immunodeficiency

J. Hourihane, G. Connett, E. Hodges, 1999, Archives of Disease in Childhood.

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

P. Veys, N. Klein, C. Cale, 1997, Archives of disease in childhood.

Physical mapping in the region of human Xq12-21.1 using pulsed field gel electrophoresis

R. Levinsky, S. Malcolm, C. Kinnon, 1993, Human Genetics.

Haematopoietic Stem Cell Transplantation for DNA Ligase 1 Deficiency

G. Lucchini, P. Jeggo, P. Veys, 2020, Journal of clinical immunology.

Haematopoietic Stem Cell Transplantation for DNA Ligase 1 Deficiency

G. Lucchini, P. Jeggo, P. Veys, 2020, Journal of Clinical Immunology.

PAEDIATRIC SCLEROSING CHOLANGITIS ASSOCIATED WITH PRIMARY IMMUNODEFICIENCIES

M. Rela, N. Heaton, G. Mieli-Vergani, 1999 .

Quality of Life in Children with Primary Antibody Deficiency

C. Cale, H. Gaspar, G. Davies, 2014, Journal of Clinical Immunology.

Recognition, clinical diagnosis and management of patients with primary antibody deficiencies: a systematic review

S. Stanworth, H. Chapel, C. Hyde, 2007, Clinical and experimental immunology.

Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group

V. Lougaris, A. Plebani, G. Driessen, 2018, Journal of Clinical Immunology.

Rituximab for the treatment of autoimmune cytopenias in children with immune deficiency

A. Thrasher, E. Davies, C. Cale, 2007, British journal of haematology.

Clinical spectrum and features of activated phosphoinositide 3-kinase syndrome: Alarge patient cohort study

J. Casanova, S. Nejentsev, P. Palma, 2016 .

Absence of platelet CD40L identifies patients with X‐linked hyper IgM syndrome

N. Klein, D. Inwald, E. Davies, 2000, Clinical and experimental immunology.

Improved outcome for children with disseminated adenoviral infection following allogeneic stem cell transplantation

P. Veys, S. Samarasinghe, P. Amrolia, 2005, British journal of haematology.

Cognitive and behavioral abnormalities in children after hematopoietic stem cell transplantation for severe congenital immunodeficiencies.

P. Veys, A. Thrasher, E. Pink, 2008, Blood.

immunodeficiencies haematopoietic stem cell transplantation for severe congenital Cognitive and behavioural abnormalities in children following

T. Cole, P. Veys, A. Thrasher, 2013 .

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

P. Veys, P. Amrolia, E. Davies, 2013 .

Patients' views on subcutaneous IgG (SCIG) Home Therapy: results from The UK Subgam ® Study.

M. Duddridge, P. Williams, A. Exley, 2000 .