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Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2015, Volume 136, Issue 3, pp. 819 - 821.e1
Journal Article
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 2002, Volume 39, Issue 8, pp. 537 - 545
Immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX, OMIM 304790) is a rare, recessive disorder resulting in aggressive autoimmunity and early... 
SCURFY SF MOUSE | IMMUNE DYSREGULATION | AUTOIMMUNE ENTEROPATHY | INTRACTABLE DIARRHEA | MUTANT | NEONATAL DIABETES-MELLITUS | MUTATION | GENETICS & HEREDITY | WISKOTT-ALDRICH SYNDROME | LYMPHORETICULAR DISEASE | FOXP3 | Lymphoproliferative Disorders - radiotherapy | Polyendocrinopathies, Autoimmune - diagnosis | Humans | Polyendocrinopathies, Autoimmune - therapy | Child, Preschool | Autoimmune Diseases - radiotherapy | Male | Protein-Losing Enteropathies - radiotherapy | Protein-Losing Enteropathies - genetics | Diabetes Mellitus, Type 1 - therapy | Lymphoproliferative Disorders - therapy | Protein-Losing Enteropathies - immunology | Autoimmune Diseases - genetics | Protein-Losing Enteropathies - therapy | Diabetes Mellitus, Type 1 - radiotherapy | Polyendocrinopathies, Autoimmune - genetics | Child | Disease Models, Animal | Diagnosis, Differential | Diabetes Mellitus, Type 1 - genetics | Lymphoproliferative Disorders - genetics | Autoimmune Diseases - diagnosis | Syndrome | Diabetes Mellitus, Type 1 - diagnosis | Animals | Lymphoproliferative Disorders - diagnosis | Polyendocrinopathies, Autoimmune - radiotherapy | Adolescent | Autoimmune Diseases - therapy | Syndromes | Care and treatment | Genetic disorders | Research | Pediatrics | Nephrology | Medical imaging | Cytokines | Families & family life | Ear diseases | Diarrhea | Infections | Family medical history | Patients | Children & youth | Inflammatory bowel disease | Hospitals | Immunology | Lymphocytes | Bone marrow | Mutation | Age | Review
Journal Article
Journal Article
Journal Article
Blood, ISSN 0006-4971, 01/2015, Volume 125, Issue 4, pp. 583 - 584
In this issue of Blood, Milner et al(1) and Haapaniemi et al(2) report that STAT3 gain-of-function (GOF) mutations are responsible for multiorgan autoimmunity,... 
HEMATOLOGY | CELLS | MUTATIONS | Autoimmune Diseases - genetics | Humans | Genetic Diseases, Inborn - genetics | Female | Male | Lymphoproliferative Disorders - genetics | STAT3 Transcription Factor - genetics
Journal Article
Journal Article
Histopathology, ISSN 0309-0167, 12/2012, Volume 61, Issue 6, pp. 1183 - 1197
Journal Article