Clinical Phenotypes and Immunological Characteristics of 18 Egyptian LRBA Deficiency Patients
Sign Up to like & getrecommendations! Published in 2020 at "Journal of Clinical Immunology"
DOI: 10.1007/s10875-020-00799-2
Abstract: LPS-responsive beige-like anchor (LRBA) deficiency is an autosomal recessive primary immunodeficiency disorder, OMIM (#614700). LRBA deficiency patients suffer from variable manifestations including recurrent infections, immune dysregulation, autoimmunity, cytopenias, and enteropathy. This study describes different clinical… read more here.
Keywords: deficiency patients; phenotypes immunological; immunological characteristics; clinical phenotypes ... See more keywords
Vitamin D deficiency in patients with alopecia areata: A systematic review and meta‐analysis
Sign Up to like & getrecommendations! Published in 2018 at "Journal of the American Academy of Dermatology"
DOI: 10.1016/j.jaad.2017.07.051
Abstract: on diphenylcyclopropenone (DPCP) maintenance treatment (MT), we first compared the treatment interval of patients who a had relapse with those who did not. Because there was a significant difference in Intervalmnt itself (P 1⁄4 .022),… read more here.
Keywords: deficiency patients; alopecia areata; treatment; patients alopecia ... See more keywords
Vitamin B1 deficiency in patients with postural tachycardia syndrome (POTS)
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DOI: 10.1080/01616412.2017.1331895
Abstract: Abstract Objective: POTS is a heterogeneous disorder of the autonomic nervous system that can result from multiple etiologies. An increased prevalence of vitamin B12, vitamin D 25-OH and iron deficiencies has been observed in patients… read more here.
Keywords: deficiency patients; deficiency; patients postural; patients pots ... See more keywords
Daily Vitamin D Supplementation Improves Vitamin D Deficiency in Patients With Chronic Liver Disease
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DOI: 10.1097/mpg.0000000000003769
Abstract: Objective: The objective of this article is to evaluate the response to 6000 IU oral cholecalciferol (OC) treatment in children with chronic liver disease (CLD) and 25(OH)D deficiency. Methods: This historical cohort included non-transplanted CLD… read more here.
Keywords: deficiency patients; treatment; liver disease; deficiency ... See more keywords
ASXL1 and STAG2 are Common Mutations in GATA2 Deficiency Patients with Bone Marrow Disease and Myelodysplastic Syndrome.
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DOI: 10.1182/bloodadvances.2021005065
Abstract: GATA2 Deficiency patients harbor de novo or inherited germline mutations in the GATA2 transcription factor gene, predisposing them to myeloid malignancies. There is considerable variation in disease progression, even among family members with the same… read more here.
Keywords: deficiency patients; mutations gata2; disease; somatic mutations ... See more keywords