His primary scientific interests are in Immunology, Genetics, Antibody, Common variable immunodeficiency and Selective IgA deficiency. Immunology is often connected to Genotype in his work. His Genetics research focuses on Gene, Allele, Mutation, Immunoglobulin class switching and Genetic linkage.
The Antibody study combines topics in areas such as Molecular biology, In vitro and Reoviridae. As a part of the same scientific study, Lennart Hammarström usually deals with the Common variable immunodeficiency, concentrating on MEDLINE and frequently concerns with Antibody deficiency, Clinical immunology and Differential diagnosis. The study incorporates disciplines such as IgA deficiency, Immunoglobulin A deficiency, Disease and Linkage disequilibrium in addition to Selective IgA deficiency.
His scientific interests lie mostly in Immunology, Antibody, Genetics, Gene and Molecular biology. Immunology is a component of his Common variable immunodeficiency, Primary immunodeficiency, Immune system, Immunodeficiency and Selective IgA deficiency studies. His research integrates issues of Hypogammaglobulinemia and Autoimmunity in his study of Common variable immunodeficiency.
His studies deal with areas such as Severe combined immunodeficiency and Pediatrics, Newborn screening as well as Primary immunodeficiency. His biological study deals with issues like Microbiology, which deal with fields such as Lactobacillus. His Molecular biology study integrates concerns from other disciplines, such as Monoclonal antibody, Isotype, Subclass, B cell and Polyclonal antibodies.
Lennart Hammarström mainly focuses on Immunology, Primary immunodeficiency, Common variable immunodeficiency, Immune system and Internal medicine. Single-nucleotide polymorphism is closely connected to Allele in his research, which is encompassed under the umbrella topic of Immunology. The concepts of his Primary immunodeficiency study are interwoven with issues in Severe combined immunodeficiency, Newborn screening, Cohort and Immunodeficiency.
His Common variable immunodeficiency research incorporates elements of Plasma cell, Haploinsufficiency, Gene and B-cell activating factor. The concepts of his Immune system study are interwoven with issues in Phenotype, Antibody and Pathogenesis. His work on Titer as part of general Antibody study is frequently connected to European union, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them.
Immunology, Primary immunodeficiency, Immunodeficiency, Internal medicine and Hypogammaglobulinemia are his primary areas of study. His study on Common variable immunodeficiency is often connected to Tyrosine kinase 2 as part of broader study in Immunology. Lennart Hammarström usually deals with Common variable immunodeficiency and limits it to topics linked to Autoimmunity and Phenotype.
His Primary immunodeficiency study combines topics from a wide range of disciplines, such as Immune dysregulation, Asymptomatic, Newborn screening and Cohort. His Immunodeficiency study incorporates themes from T cell and Disease. His Hypogammaglobulinemia study integrates concerns from other disciplines, such as Virology, Epstein–Barr virus, CD8 and NKG2D, Cytotoxic T cell.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases
Vetrie D;Vorechovský I;Sideras P;Sideras P;Holland J.
Helicobacter pylori SabA adhesin in persistent infection and chronic inflammation.
Jafar Mahdavi;Berit Sondén;Martina Hurtig;Farzad O. Olfat;Farzad O. Olfat.
Common variable immunodeficiency disorders: division into distinct clinical phenotypes
Helen Chapel;Mary Lucas;Martin Lee;Janne Bjorkander.
Clinical spectrum of X-linked hyper-IgM syndrome
Jacov Levy;Teresa Espanol-Boren;Carolin Thomas;Alain Fischer.
The Journal of Pediatrics (1997)
Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans
U Salzer;H M Chapel;A D B Webster;Q Pan-Hammarström.
Nature Genetics (2005)
Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency
Waleed Al-Herz;Aziz Bousfiha;Jean-Laurent Casanova;Jean-Laurent Casanova;Helen Chapel.
Frontiers in Immunology (2014)
Primary immunodeficiency diseases: An update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee
Raif S. Geha;Luigi D. Notarangelo;Jean Laurent Casanova;Helen Chapel.
The Journal of Allergy and Clinical Immunology (2007)
Selective IgA deficiency (SIgAD) and common variable immunodeficiency (CVID)
L Hammarström;I Vorechovsky;D Webster.
Clinical and Experimental Immunology (2000)
International consensus document (icon): common variable immunodeficiency disorders
Francisco A. Bonilla;Isil Barlan;Helen Chapel;Beatriz Tavares Costa-Carvalho.
The Journal of Allergy and Clinical Immunology: In Practice (2016)
Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and Autoimmunity
Gabriela Lopez-Herrera;Giacomo Tampella;Qiang Pan-Hammarström;Peer Herholz.
American Journal of Human Genetics (2012)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: