folic acid has been researched along with Immunologic Deficiency Syndromes in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (57.14) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 2 (28.57) | 24.3611 |
2020's | 1 (14.29) | 2.80 |
Authors | Studies |
---|---|
Acıpayam, C; Başaran, KE; Belkaya, S; Bişgin, A; Canatan, H; Canatan, MF; Eken, A; Erdem, Ş; Gök, V; Haliloğlu, Y; Karakükcü, M; Özcan, A; Patıroğlu, T; Per, H; Ünal, E; Yılmaz, E | 1 |
Chida, N; Kishimoto, K; Kobayashi, K; Kobayashi, R; Maruoka, H; Sano, H; Suzuki, D; Yamada, M; Yasuda, K | 1 |
Field, MS; Kamynina, E; Stover, PJ | 1 |
MARTIN, C | 1 |
Behan, PO; Dick, H; Lambie, DG; Shakir, RA | 1 |
Ament, ME; Davis, SD; Ochs, HD | 1 |
Cazzola, G; Dainotti, E; Maraschio, P; Piantanida, M; Tiepolo, L; Tupler, R | 1 |
7 other study(ies) available for folic acid and Immunologic Deficiency Syndromes
Article | Year |
---|---|
Immunodeficiency associated with a novel functionally defective variant of SLC19A1 benefits from folinic acid treatment.
Topics: Folic Acid; Humans; Immunologic Deficiency Syndromes; Leucovorin; Leukocytes, Mononuclear; Methotrexate; Proton-Coupled Folate Transporter; Reduced Folate Carrier Protein | 2023 |
Impact of folate therapy on combined immunodeficiency secondary to hereditary folate malabsorption.
Topics: Blood Cell Count; Cytokines; Female; Folic Acid; Folic Acid Deficiency; Heterozygote; Humans; Immunoglobulin Isotypes; Immunologic Deficiency Syndromes; Infant; Lymphocyte Activation; Lymphocyte Subsets; Malabsorption Syndromes; Mutation; Proton-Coupled Folate Transporter | 2014 |
MTHFD1 regulates nuclear de novo thymidylate biosynthesis and genome stability.
Topics: Animals; Congenital Abnormalities; Folic Acid; Genomic Instability; Homocysteine; Humans; Immunologic Deficiency Syndromes; Metabolism, Inborn Errors; Methylenetetrahydrofolate Dehydrogenase (NADP); Mice; Minor Histocompatibility Antigens; Thymidine Monophosphate | 2016 |
[Treatment of erythroderma desquamativa by biotin].
Topics: Biotin; Complement C5; Dermatitis, Exfoliative; Folic Acid; Hereditary Complement Deficiency Diseases; Immunologic Deficiency Syndromes; Vitamin B Complex | 1951 |
Metabolism of immunoglobulin A, lymphocyte function, and histocompatibility antigens in patients on anticonvulsants.
Topics: Adolescent; Adult; Aged; Blood Proteins; Epilepsy; Female; Folic Acid; HLA Antigens; Humans; Immunologic Deficiency Syndromes; Lectins; Lymphocytes; Male; Middle Aged; Phenytoin; T-Lymphocytes | 1978 |
Structure and function of the gastrointestinal tract in primary immunodeficiency syndromes (IDS) and in granulocyte dysfunction.
Topics: Carotenoids; Crohn Disease; Digestive System; Disaccharidases; Feces; Female; Folic Acid; Gastrointestinal Diseases; Giardia; Giardiasis; Granulomatous Disease, Chronic; Histiocytes; Humans; Immunologic Deficiency Syndromes; Intestine, Small; Lactose Intolerance; Malabsorption Syndromes; Male; Metronidazole; Protein-Losing Enteropathies; Rectum; Vitamin B 12 | 1975 |
Differential expression of the ICF (immunodeficiency, centromeric heterochromatin, facial anomalies) mutation in lymphocytes and fibroblasts.
Topics: Adenosine; Caffeine; Centromere; Child, Preschool; Chromosome Aberrations; Chromosomes; Chromosomes, Human, Pair 1; Chromosomes, Human, Pair 16; Chromosomes, Human, Pair 9; Facial Expression; Female; Fibroblasts; Folic Acid; Humans; Immunologic Deficiency Syndromes; Lymphocytes; Mutation; Thymidine | 1989 |