ampicillin has been researched along with Bare Lymphocyte Syndrome in 1 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Borkowsky, W; Eng, F; Hirschhorn, R; Nicknam, MN; Yang, DR | 1 |
1 other study(ies) available for ampicillin and Bare Lymphocyte Syndrome
| Article | Year |
|---|---|
Novel deletion and a new missense mutation (Glu 217 Lys) at the catalytic site in two adenosine deaminase alleles of a patient with neonatal onset adenosine deaminase- severe combined immunodeficiency.
Topics: Adenosine Deaminase; Alleles; Ampicillin; Base Sequence; Chromosomes, Human, Pair 2; Concanavalin A; Deoxyadenine Nucleotides; Deoxyadenosines; DNA Probes; Drug Therapy, Combination; Gene Library; Gentamicins; Humans; Infant; Ketoconazole; Lymphocyte Activation; Male; Molecular Sequence Data; Oxacillin; Phytohemagglutinins; Point Mutation; Pokeweed Mitogens; Promoter Regions, Genetic; Restriction Mapping; Sequence Homology, Nucleic Acid; Severe Combined Immunodeficiency; Trimethoprim, Sulfamethoxazole Drug Combination | 1992 |