Browsing publications by Dr Karin Engelhardt

Newcastle AuthorsTitleYearFull text
Dr Karin Engelhardt
Professor Sophie Hambleton
14 Years after Discovery: Clinical Follow-up on 15 Patients with Inducible Co-Stimulator Deficiency2017
Dr Christopher Duncan
Angela Grainger
Andrew Skelton
Raf Hussain
Dr Joe Willet
et al.
Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20)2017
Dr Karin Engelhardt
Dr Yaobo Xu
Angela Grainger
Dr David Swan
Dr Joe Willet
et al.
Identification of Heterozygous Single- and Multi-exon Deletions in IL7R by Whole Exome Sequencing2017
Dr Tarana Singh Dang
Dr Joe Willet
Helen Griffin
Dr Graeme O'Boyle
Dr Mario Abinun
et al.
Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 Deficiency2016
Dr Tarana Singh Dang
Dr Joe Willet
Helen Griffin
Dr Graeme O'Boyle
Dr Mario Abinun
et al.
Erratum to: Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 Deficiency (vol 36, pg 117, 2016)2016
Dr Mary Slatter
Dr Karin Engelhardt
Dr Zohreh Nademi
Dr Mario Abinun
Dr Andrew Gennery
et al.
Hematopoietic stem cell transplantation for CTLA4 deficiency2016
Nicholas Robertson
Dr Karin Engelhardt
Professor Andrew Cant
Dr Mario Abinun
Dr Yaobo Xu
et al.
A Novel 10bp Frameshift Deletion In ICOS In Two Patients With Combined Immunodeficiency2015
Nicholas Robertson
Dr Karin Engelhardt
Professor Andrew Cant
Dr Mario Abinun
Professor Sophie Hambleton
et al.
Astute Clinician Report: A Novel 10 bp Frameshift Deletion in Exon 2 of ICOS Causes a Combined Immunodeficiency Associated with an Enteritis and Hepatitis2015
Professor Sophie Hambleton
Professor Andrew Cant
Dr Karin Engelhardt
Dr David Swan
Dr Joe Willet
et al.
Autoimmunity In STAT3 Gain Of Function Mutations; Broadening The Phenotype2015
Dr Andrew Gennery
Dr Karin Engelhardt
DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients2015
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