Fine-Scale Mapping at IGAD1 and Genome-Wide Genetic Linkage Analysis Implicate HLA-DQ/DR as a Major Susceptibility Locus in Selective IgA Deficiency and Common Variable Immunodefic... von Kralovicova, Jana, Hammarstrom, Lennart, Plebani, Alessandro, Webster, A. David B, Vorechovsky, Igor

Volltext

Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4q von FINCK, Anemone, VAN DER MEER, Jos W. M, SCHÄFFER, Alejandro A, PFANNSTIEL, Jessica, FIESCHI, Claire, PLEBANI, Alessandro, WEBSTER, A. David B, HAMMARSTRÖM, Lennart, GRIMBACHER, Bodo

Volltext

Role for Mannose Binding Lectin in the Prevention of Mycoplasma Infection von Hamvas, Renata M. J, Johnson, Marina, Vlieger, Arine M, Ling, Clare, Sherriff, Andrea, Wade, Angela, Klein, Nigel J, Turner, Malcolm W, Webster, A. David B

Volltext

Selective deficits in blood dendritic cell subsets in common variable immunodeficiency and X-linked agammaglobulinaemia but not specific polysaccharide antibody deficiency von Yong, Patrick F.K, Workman, Sarita, Wahid, Faisal, Exley, Andrew, Webster, A. David B, Ibrahim, Mohammad A.A

Volltext

A 9-yr evaluation of carrier erythrocyte encapsulated adenosine deaminase (ADA) therapy in a patient with adult-type ADA deficiency von Bax, Bridget E., Bain, Murray D., Fairbanks, Lynette D., Webster, A David B., Ind, Philip W., Hershfield, Michael S., Chalmers, Ronald A.

Volltext

Analysis of families with common variable immunodeficiency (VID) and IgA deficiency suggests linkage of CVID to chromosome 16q von SCHÄFFER, Alejandro A, PFANNSTIEL, Jessica, WEBSTER, A. David B, PLEBANI, Alessandro, HAMMARSTRÖM, Lennart, GRIMBACHER, Bodo

Volltext

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes von Salzer, Ulrich, Bacchelli, Chiara, Buckridge, Sylvie, Pan-Hammarström, Qiang, Jennings, Stephanie, Lougaris, Vassilis, Bergbreiter, Astrid, Hagena, Tina, Birmelin, Jennifer, Plebani, Alessandro, Webster, A. David B., Peter, Hans-Hartmut, Suez, Daniel, Chapel, Helen, McLean-Tooke, Andrew, Spickett, Gavin P., Anover-Sombke, Stephanie, Ochs, Hans D., Urschel, Simon, Belohradsky, Bernd H., Ugrinovic, Sanja, Kumararatne, Dinakantha S., Lawrence, Tatiana C., Holm, Are M., Franco, Jose L., Schulze, Ilka, Schneider, Pascal, Gertz, E. Michael, Schäffer, Alejandro A., Hammarström, Lennart, Thrasher, Adrian J., Gaspar, H. Bobby, Grimbacher, Bodo

Volltext

Effect of anti‐CD20 (rituximab) on resistant thrombocytopenia in autoimmune lymphoproliferative syndrome von Heelan, Bridget T., Tormey, Vincent, Amlot, Peter, Payne, Elspeth, Mehta, Atul, Webster, A. David B.

Volltext

The immunocompromised patient: primary immunodeficiencies von Webster, A. David B

Volltext

The immunocompromised patient: primary immunodeficiencies von Webster, A. David B

Volltext

Up-Regulation of IL-12 in Monocytes: A Fundamental Defect in Common Variable Immunodeficiency von Cambronero, Rosario, Sewell, W. A. Carrock, North, Margaret E, Webster, A. David B, Farrant, John

Volltext

ATM Mutations in cancer families von VORECHOVSKY, I, LUO, L, LINDBLOM, A, NEGRINI, M, WEBSTER, A. D. B, CROCE, C. M, HAMMARSTRÖM, L

Volltext

Infection in patients with congenital immune deficiencies von Carrock Sewell, W A, B. Webster, A David

Volltext

Short tandem repeat (STR) haplotypes in HLA: an integrated 50-kb STR/linkage disequilibrium/gene map between the RING3 and HLA-B genes and identification of STR haplotype diversifi... von Vorechovsky, I, Kralovicova, J, Laycock, M D, Webster, A D, Marsh, S G, Madrigal, A, Hammarström, L

Volltext

Ataxia-telangiectasia and T-cell leukemias : No evidence for somatic ATM mutation in sporadic T-ALL or for hypermethylation of the ATM-NPAT/E14 bidirectional promoter in T-PLL von LIPING LUO, LU, F.-M, HART, S, FORONI, L, RABBANI, H, HAMMARSTRÖM, L, WEBSTER, A. D. B, VORECHOVSKY, I

Volltext

Structural Basis for Chromosome X-Linked Agammaglobulinemia: A Tyrosine Kinase Disease von Vihinen, Mauno, Vetrie, David, Maniar, Hina S., Ochs, Hans D., Zhu, Qili, Vorechovsky, Igor, A. David B. Webster, Notarangelo, Luigi D., Nilsson, Lennart, Sowadski, Janusz M., C. I. Edvard Smith

Volltext

A Putative Susceptibility Locus on Chromosome 18 Is Not a Major Contributor to Human Selective IgA Deficiency: Evidence from Meiotic Mapping of 83 Multiple-Case Families von Vorechovsky, Igor, Blennow, Elisabeth, Nordenskjold, Magnus, Webster, A. David B, Hammarstrom, Lennart

Volltext

Mutation pattern in the Bruton's tyrosine kinase gene in 26 unrelated patients with X-linked agammaglobulinemia von Vorřechovský, Igor, Luo, Liping, Hertz, Jens M., Frøland, Stig S., Klemola, Timo, Fiorini, Maurilia, Quinti, Isabella, Paganelli, Roberto, Ozsahin, Hulya, Hammarström, Lennart, Webster, A. David B., Smith, C. I. Edvard

Volltext

Genetic Linkage of IgA Deficiency to the Major Histocompatibility Complex: Evidence for Allele Segregation Distortion, Parent-of-Origin Penetrance Differences, and the Role of Anti... von Vořechovský, Igor, Webster, A. David B., Plebani, Alessandro, Hammarström, Lennart

Volltext

Clustering of missense mutations in the ataxia-telangiectasia gene in a sporadic T-cell leukaemia von VORECHOVSKY, I, LUO, L, DYER, M. J. S, CATOVSKY, D, AMLOT, P. L, YAXLEY, J. C, FORONI, L, HAMMARSTRÖM, L, WEBSTER, A. D. B, YUILLE, M. A. R

Volltext