Page last updated: 2024-08-17

folic acid and Severe Combined Immunodeficiency

folic acid has been researched along with Severe Combined Immunodeficiency in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's3 (75.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Andersson, BA; Asin-Cayuela, J; Baumgartner, MR; Burda, P; Bürer, C; Christa, L; Fowler, B; Froese, DS; Hjalmarson, O; Holme, E; Kollberg, G; Kuster, A; Lutz, S; Rosenblatt, DS; Roussey, G; Suormala, T; Watkins, D1
Rosenblatt, DS; Watkins, D1
Baxi, S; Bergmann, AK; Borzutzky, A; Crompton, B; Giliani, S; Martin, M; Neufeld, EJ; Notarangelo, LD1
Ganesh, J; Kaplan, BS; Majewski, J; Nunez, LD; Orange, JS; Rosenblatt, DS; Schwartzentruber, JA; Watkins, D1

Reviews

1 review(s) available for folic acid and Severe Combined Immunodeficiency

ArticleYear
Characterization and review of MTHFD1 deficiency: four new patients, cellular delineation and response to folic and folinic acid treatment.
    Journal of inherited metabolic disease, 2015, Volume: 38, Issue:5

    Topics: Anemia, Megaloblastic; Cells, Cultured; Fatal Outcome; Female; Folic Acid; Folic Acid Deficiency; Humans; Hyperhomocysteinemia; Infant; Infant, Newborn; Leucovorin; Male; Methylenetetrahydrofolate Dehydrogenase (NADP); Minor Histocompatibility Antigens; Severe Combined Immunodeficiency; Young Adult

2015

Other Studies

3 other study(ies) available for folic acid and Severe Combined Immunodeficiency

ArticleYear
Lessons in biology from patients with inherited disorders of vitamin B12 and folate metabolism.
    Biochimie, 2016, Volume: 126

    Topics: Anemia, Megaloblastic; ATP-Binding Cassette Transporters; Exome; Female; Folic Acid; Hemolytic-Uremic Syndrome; Host Cell Factor C1; Humans; Male; Methylenetetrahydrofolate Dehydrogenase (NADP); Minor Histocompatibility Antigens; Proto-Oncogene Proteins c-cbl; Severe Combined Immunodeficiency; Vitamin B 12

2016
Reversible severe combined immunodeficiency phenotype secondary to a mutation of the proton-coupled folate transporter.
    Clinical immunology (Orlando, Fla.), 2009, Volume: 133, Issue:3

    Topics: Base Sequence; DNA; Female; Flow Cytometry; Folic Acid; Genetic Variation; Humans; Immunophenotyping; Infant; Intestinal Absorption; Leucovorin; Male; Membrane Transport Proteins; Point Mutation; Polymerase Chain Reaction; Proton-Coupled Folate Transporter; Severe Combined Immunodeficiency; T-Lymphocytes

2009
Novel inborn error of folate metabolism: identification by exome capture and sequencing of mutations in the MTHFD1 gene in a single proband.
    Journal of medical genetics, 2011, Volume: 48, Issue:9

    Topics: Amino Acid Metabolism, Inborn Errors; Anemia, Megaloblastic; Exome; Female; Folic Acid; Humans; Hyperhomocysteinemia; Infant; Metabolism, Inborn Errors; Methylenetetrahydrofolate Dehydrogenase (NADP); Minor Histocompatibility Antigens; Mutation; Severe Combined Immunodeficiency

2011