G. Morgan

发表

Isolated cutaneous response to granulocyte-monocyte colony stimulating factor in fatal idiopathic disseminated Bacillus-Calmette-Guerin infection

O. Sanal, I. Tezcan, N. Klein, 2000, European Journal of Pediatrics.

Autoimmune enteropathy with distinct mucosal features in T-cell activation deficiency: the contribution of T cells to the mucosal lesion.

C. Fertleman, T. Savidge, N. Klein, 1999, Journal of pediatric gastroenterology and nutrition.

Function of the interleukin-2 (IL-2) receptor gamma-chain in biologic responses of X-linked severe combined immunodeficient B cells to IL-2, IL-4, IL-13, and IL-15.

A. Minty, P. Ferrara, D. Caput, 1995, Blood.

The rise in incidence of lymphomas in Europe 1985-1992.

J. Coebergh, S. de Sanjosé, R. Tumino, 1999, European journal of cancer.

The detection and clinical significance of monoclonality in lymphoproliferative disorders

R. Johnson, A. Jack, G. Morgan, 1995 .

A clinical and immunological study of Netherton's syndrome

J. Harper, M. Judge, G. Morgan, 1994, The British journal of dermatology.

Mutation detection in the X-linked agammaglobulinemia gene, BTK, using single strand conformation polymorphism analysis.

R. Lovering, R. Levinsky, C. Kinnon, 1994, Human molecular genetics.

Neurodevelopmental delay and focal seizures as presenting symptoms of human immunodeficiency virus I infection

D. Howells, E. Brett, R. Levinsky, 2004, European Journal of Pediatrics.

Clinical significance of IgG subclass deficiency.

R. Levinsky, G. Morgan, G. Morgan, 1988, Archives of disease in childhood.

Mutation analysis in CD40 ligand deficiency leading to X‐linked hypogammaglobulinemia with hyper IgM syndrome

C. Kinnon, A. Jones, P. Rutland, 1996, Human mutation.

Demonstration of induction of erythrocyte inosine monophosphate dehydrogenase activity in Ribavirin-treated patients using a high performance liquid chromatography linked method.

V. Micheli, J. Duley, L. Fairbanks, 1995, Clinica chimica acta; international journal of clinical chemistry.

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.

Clinical significance of IgA deficiency.

R. Levinsky, G. Morgan, 1988, Archives of disease in childhood.

Central nervous system dysfunction and erythrocyte guanosine triphosphate depletion in purine nucleoside phosphorylase deficiency.

H. Simmonds, P. Timms, L. Fairbanks, 1987, Archives of disease in childhood.

Isoprinosine does not protect against frequent respiratory tract infections in childhood

J. Litzman, G. Morgan, J. Lokaj, 1999, European Journal of Pediatrics.

Omenn’s syndrome: lessons from a red baby

R. Katugampola, S. Blackford, G. Morgan, 2008, Clinical and experimental dermatology.

Early diagnosis of severe combined immunodeficiency syndrome.

R. Hague, A. Cant, S. Rassam, 1994, Archives of disease in childhood.

Successful bone marrow transplantation and treatment of BCG infection in two patients with severe combined immunodeficiency

R. Levinsky, R. Heyderman, S. Strobel, 1991, European Journal of Pediatrics.

Immunological Studies of herpes simplex virus infection in children with atopic eczema

A. Buchan, J. Harper, J. Rolland, 1996, The British journal of dermatology.

Raised IMP-dehydrogenase activity in the erythrocytes of a case of purine nucleoside phosphorylase (PNP) deficiency.

H. Simmonds, S. Strobel, J. Duley, 1991, Advances in experimental medicine and biology.

Mutation analysis in Bruton's tyrosine kinase, the X-linked agammaglobulinaemia gene, including identification of an insertional hotspot.

R. Lovering, R. Levinsky, C. Kinnon, 1995, Human molecular genetics.

Intravenous immunoglobulin, splenectomy, and antibiotic prophylaxis in Wiskott-Aldrich syndrome.

J. Litzman, S. Strobel, H. Chapel, 1996, Archives of disease in childhood.

A prospective study of CD45 isoform expression in haemophagocytic lymphohistiocytosis; an abnormal inherited immunophenotype in one family

S. Strobel, G. Morgan, R. Wagner, 1995, Clinical and Experimental Immunology.

Fatal graft versus host disease after platelet transfusions in a child with purine nucleoside phosphorylase deficiency

R. Levinsky, S. Strobel, A. Simmonds, 2004, European Journal of Pediatrics.

Tumor necrosis factor-alpha inhibits epithelial differentiation and morphogenesis in the mouse metanephric kidney in vitro.

A. Woolf, N. Klein, G. Morgan, 1998, The International journal of developmental biology.

Lecture Notes on Immunology

G. Morgan, 1988 .

Biochemical and immunological status following gene therapy and PEG-ADA therapy for adenosine deaminase (ADA) deficiency.

H. Simmonds, V. V. van Beusechem, H. Gaspar, 1994, Advances in experimental medicine and biology.

Heterogeneity of biochemical, clinical and immunological parameters in severe combined immunodeficiency due to adenosine deaminase deficiency.

H. Simmonds, R. Levinsky, L. Fairbanks, 1987, Clinical and experimental immunology.

Bone marrow gene transfer in three patients with adenosine deaminase deficiency.

A. Fischer, R. Levinsky, V. V. van Beusechem, 1996, Gene therapy.

Identification of deletions in thebtk gene allows unambiguous assessment of carrier status in families with X-linked agammaglobulinaemia

D. Bentley, D. Vetrie, R. Lovering, 1994, Human Genetics.

Carrier determination for X-linked agammaglobulinemia using X inactivation analysis of purified B cells.

R. Lovering, R. Levinsky, S. Malcolm, 1993, Journal of immunological methods.

Prognosis of chronic granulomatous disease.

R. Levinsky, A. Finn, N. Hadžić, 1990, Archives of disease in childhood.

CD40 ligand (CD40L) expression and B cell function in agammaglobulinemia with normal or elevated levels of IgM (HIM). Comparison of X-linked, autosomal recessive, and non-X-linked forms of the disease, and obligate carriers.

R. Callard, S. Lederman, L. Chess, 1994, Journal of immunology.

Hypogammaglobulinaemia associated with normal or increased IgM (the hyper IgM syndrome): a case series review.

N. Banatvala, R. Levinsky, S. Strobel, 1994, Archives of disease in childhood.

Prognosis ofchronic granulomatous disease

R. Levinsky, A. Finn, N. Hadžić, 1990 .

First trimester diagnosis of adenosine deaminase deficiency

K. Nicolaides, P. Stewart, G. Morgan, 1987, Prenatal diagnosis.

Aetiology of chronic suppurative lung disease.

G. Morgan, 1994, Archives of disease in childhood.

Changing trends in the incidence of non-Hodgkin's lymphoma in Europe. Biomed Study Group.

T. Petrella, R. McNally, J. Olsen, 1997, Annals of oncology : official journal of the European Society for Medical Oncology.

The Lymphoproliferative Disorders: Handbook of diagnosis, investigation and management

J. Child, A. Jack, G. Morgan, 1998, British Journal of Cancer.

Monoclonal antibodies in diagnosis and treatment.

R. Levinsky, G. Morgan, G. Morgan, 1985, Archives of disease in childhood.

PROLONGED SURVIVAL AND LATE PRESENTATION OF VERTICALLY TRANSMITTED HIV INFECTION IN CHILDHOOD

R. Levinsky, S. Strobel, R. Hallett, 1987, The Lancet.

Gene transfer to primary chronic granulomatous disease monocytes

R. Levinsky, A. Segal, A. Thrasher, 1995, The Lancet.

A family study of the X-linked lymphoproliferative syndrome: evidence for a B cell defect contributing to the immunodeficiency.

I. Andó, D. Crawford, R. Levinsky, 1986, Clinical and experimental immunology.

Dual meningoencephalitis with echovirus type 11 and adenovirus in combined (common variable) immunodeficiency.

R. Levinsky, S. Strobel, G. Morgan, 1988, The Pediatric infectious disease journal.

Immunodeficiency presenting as hypergammaglobulinaemia with IgG2 subclass deficiency

R. Levinsky, S. Strobel, J. Shield, 1992, The Lancet.

X linked agammaglobulinaemia with a 'leaky' phenotype.

R. Thompson, C. Kinnon, A. Jones, 1996, Archives of disease in childhood.

Kawasaki disease in Canterbury.

M. Lynch, G. Morgan, 1978, Archives of Disease in Childhood.

Normal uric acid concentrations in a purine nucleoside phosphorylase (PNP) deficient child presenting with severe chicken pox, possible immunodeficiency and developmental delay.

H. Simmonds, J. Duley, L. Fairbanks, 1994, Advances in Experimental Medicine and Biology.

Insights into the quaternary association of proteins through structure graphs: a case study of lectins.

Brighton, Bonnie F. Sloane, Avadhesha Surolia, 2005, The Biochemical journal.