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Mashup Score: 3Angioedema Due to Acquired Deficiency of C1-Inhibitor: a Cohort Study in Spain and a Comparison With Other series. - 3 year(s) ago
Data on acquired angioedema due to C1-inhibitor deficiency (C1-INH-AAE) from 4 European countries (France, Italy, Germany, and Hungary) were recently published.
Categories: Allergy-Immunology, Latest HeadlinesTweet
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Mashup Score: 0Antibody Deficiency, Chronic Lung Disease, and Comorbid Conditions: A Case-Based Approach - 3 year(s) ago
New emerging pulmonary phenotypes associated with antibody deficiency, such as neutrophilic asthma, frequent exacerbations of chronic obstructive pulmonary disease, and unexplained interstitial lung disease, particularly in younger adults, are discussed in this review through a case-based approach. Also discussed in similar fashion are antibody deficiency syndromes that lead to end-stage lung…
Categories: Allergy-Immunology, Latest HeadlinesTweet
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Mashup Score: 1Diversity in Serine/Threonine Protein Kinase-4 Deficiency and Review of the Literature - 3 year(s) ago
Serine/threonine kinase-4 (STK4) deficiency is an autosomal recessive combined immunodeficiency.
Categories: Allergy-Immunology, Latest HeadlinesTweet
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Mashup Score: 1Hematopoietic Cell Transplantation Rescues Inflammatory Bowel Disease and Dysbiosis of Gut Microbiota in XIAP Deficiency - 3 year(s) ago
X-linked inhibitor of apoptosis protein (XIAP) deficiency is an infrequent inborn error of immunity that is often associated with refractory inflammatory bowel disease (IBD). The natural course of XIAP deficiency is typically associated with poor prognosis, and hematopoietic cell transplantation (HCT) is the only curative treatment.
Categories: Allergy-Immunology, Latest HeadlinesTweet
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Mashup Score: 0Antibody deficiency, Chronic Lung Disease, and Comorbid Conditions: A Case Based Approach - 3 year(s) ago
New emerging pulmonary phenotypes associated with antibody deficiency, such as neutrophilic asthma, frequent exacerbations of chronic obstructive pulmonary disease, and unexplained interstitial lung disease, particularly in younger adults, are discussed in this review through a case-based approach. Also discussed in similar fashion are antibody deficiency syndromes that lead to end-stage lung…
Categories: Allergy-Immunology, Latest HeadlinesTweet
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Mashup Score: 0Threshold ferritin and hepcidin concentrations indicating early iron deficiency in young women based on upregulation of iron absorption - 3 year(s) ago
Based on physiological upregulation of iron absorption, a threshold ferritin of <50 µg/L, corresponding to a threshold hepcidin of <3 nmol/l, indicates incipient iron deficiency in young women.
Source: EClinicalMedicineCategories: General Medicine Journals and Societies, Latest HeadlinesTweet
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Mashup Score: 0Health Outcomes of Infants with Vitamin B12 Deficiency Identified by Newborn Screening and Early Treated - 3 year(s) ago
To evaluate the clinical outcomes at age 1.5 ± 0.5 years of infants with vitamin B12 deficiency identified by newborn screening (NBS).
Source: The Journal of PediatricsCategories: Latest Headlines, PediatricsTweet
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Mashup Score: 0Threshold ferritin and hepcidin concentrations indicating early iron deficiency in young women based on upregulation of iron absorption - 3 year(s) ago
Based on physiological upregulation of iron absorption, a threshold ferritin of <50 µg/L, corresponding to a threshold hepcidin of <3 nmol/l, indicates incipient iron deficiency in young women.
Source: EClinicalMedicineCategories: General Medicine Journals and Societies, Latest HeadlinesTweet
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Mashup Score: 4
Primary antibody deficiencies (PAD) are the most frequently diagnosed primary immunodeficiencies and predispose to infections as well as numerous long-term sequelae. The study of PAD has largely been limited to tertiary referral centers that might over-represent ethnic and socioeconomic groups with fewer impediments to health care.1 As well-financed hospitals are more likely to achieve…
Categories: Allergy-Immunology, Latest HeadlinesTweet
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Mashup Score: 0Immune Dysregulation in Human ITCH Deficiency Successfully Treated with Hematopoietic Cell Transplantation - 3 year(s) ago
Mutations in ITCH, which encodes an E3 ubiquitin-protein ligase, can result in systemic autoimmunity and immunodeficiency. The clinical phenotype and mechanism of disease have not been fully characterized, resulting in a paucity of therapeutic options for this potentially fatal disease.
Categories: Allergy-Immunology, Latest HeadlinesTweet
In Press! #Angioedema Due to #Acquired #Deficiency of #C1- #Inhibitor: a Cohort Study in Spain and a Comparison With Other series. https://t.co/YDgd34i7dp