folic acid has been researched along with Severe Combined Immunodeficiency in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 3 (75.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| 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, D | 1 |
| Rosenblatt, DS; Watkins, D | 1 |
| Baxi, S; Bergmann, AK; Borzutzky, A; Crompton, B; Giliani, S; Martin, M; Neufeld, EJ; Notarangelo, LD | 1 |
| Ganesh, J; Kaplan, BS; Majewski, J; Nunez, LD; Orange, JS; Rosenblatt, DS; Schwartzentruber, JA; Watkins, D | 1 |
1 review(s) available for folic acid and Severe Combined Immunodeficiency
| Article | Year |
|---|---|
Characterization and review of MTHFD1 deficiency: four new patients, cellular delineation and response to folic and folinic acid treatment.
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 |
3 other study(ies) available for folic acid and Severe Combined Immunodeficiency
| Article | Year |
|---|---|
Lessons in biology from patients with inherited disorders of vitamin B12 and folate metabolism.
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.
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.
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 |