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The New England Journal of Medicine, ISSN 0028-4793, 07/2017, Volume 377, Issue 1, pp. 52 - 61
CD55 prevents convertase enzyme formation in the complement cascade, acting as a brake on complement activation. Inactivating mutations in CD55 result in... 
MEDICINE, GENERAL & INTERNAL | ACTIVATION | INFLAMMATORY-BOWEL-DISEASE | HEMOLYTIC-UREMIC SYNDROME | CELL RESPONSES | COMPLEMENT REGULATORY PROTEIN | INAB PHENOTYPE | DECAY-ACCELERATING FACTOR | PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA | MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS | T-CELLS | Intestine, Small - pathology | Humans | CD55 Antigens - genetics | Child, Preschool | Infant | Male | Protein-Losing Enteropathies - genetics | Syndrome | Complement System Proteins - metabolism | CD55 Antigens - blood | Complement Activation - genetics | Homozygote | T-Lymphocytes - metabolism | Complement Inactivating Agents - pharmacology | Pedigree | Protein-Losing Enteropathies - complications | Statistics, Nonparametric | Immunoglobulin A - blood | Female | Thrombosis - genetics | Mutation | Child | Complement Activation - drug effects | Proteins | Molecular targeted therapy | Gene mutations | Gastrointestinal diseases | Analysis | Homeostasis | Research | Thrombosis | Blood clot | Gastrointestinal tract diseases | Complement component C5a | Lymphocytes T | Cell activation | Immunology | Pain | Intestine | Hepatology | Gastroenterology | Malabsorption | Thromboembolism | Digestive tract | Age | Edema | Medical research | Lymphatic system | Hypersensitivity | Diarrhea | Inflammation | Heredity | Protein deficiency | Patients | Hereditary diseases | Complement activation | Infectious diseases | Decay-accelerating factor
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
Medicine, ISSN 0025-7974, 11/2018, Volume 97, Issue 48, p. e13403
Rationale: Nonocclusive mesenteric ischemia (NOMI) is a life-threatening disorder; prompt diagnosis is vital. Surgical treatment is often required, but some... 
nonocclusive mesenteric ischemia | MEDICINE, GENERAL & INTERNAL | CARDIOVASCULAR-SURGERY | protein-losing enteropathy | conservative therapy | Case studies | Complications and side effects | Development and progression | Care and treatment | Ischemia | Gastrointestinal diseases
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 10/2017, Volume 377, Issue 15, pp. 1499 - 1500
To the Editor: Ozen et al. (July 6 issue) 1 describe 11 study participants with loss-of-function variants in CD55 and complement hyperactivation, angiopathic... 
MEDICINE, GENERAL & INTERNAL | DECAY-ACCELERATING FACTOR | COMPLEMENT | Protein-Losing Enteropathies | Fontan Procedure | Humans
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2017, Volume 69, Issue 24, pp. 2929 - 2937
Journal Article
The Pediatric Infectious Disease Journal, ISSN 0891-3668, 12/2018, Volume 37, Issue 12, pp. e345 - e347
Protein-losing enteropathy may develop as a complication of a wide spectrum of diseases. Three cases of giardiasis that presented with acute onset of... 
INFECTIOUS DISEASES | PEDIATRICS | IMMUNOLOGY | giardiasis | protein-losing enteropathy | hypoalbuminemia | Case studies | Complications and side effects | Development and progression | Care and treatment | Protein metabolism disorders | Giardiasis
Journal Article
The American Journal of Gastroenterology, ISSN 0002-9270, 01/2010, Volume 105, Issue 1, pp. 43 - 49
Journal Article