methotrexate has been researched along with Fragile X Syndrome in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 5 (83.33) | 18.7374 |
1990's | 1 (16.67) | 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 |
---|---|
Erbe, RW; Wang, JC | 1 |
Mikkelsen, M; Poulsen, H; Senanayahe, M; Soysa, P | 1 |
Bertheas, MF; Brizard, CP; De Freminville, B; Delhomme-Bachy, M; Devillard, F; Fraisse, J; Lauras, B; Prieur, F | 1 |
Goitein, R; Kerem, B; Schaap, T | 1 |
Baker, E; Eichenbaum, SZ; Hockey, A; Krumins, E; Purvis-Smith, S; Sutherland, GR | 1 |
Ledbetter, DH; Nussbaum, RL | 1 |
1 review(s) available for methotrexate and Fragile X Syndrome
Article | Year |
---|---|
Fragile X syndrome: a unique mutation in man.
Topics: Caffeine; Chromosome Fragility; Female; Fragile X Syndrome; Genetic Counseling; Genetic Linkage; Genetic Markers; Heterozygote; Humans; Hybrid Cells; Intellectual Disability; Male; Methotrexate; Models, Genetic; Pedigree; Phenotype; Sex Chromosome Aberrations; Thymidine | 1986 |
5 other study(ies) available for methotrexate and Fragile X Syndrome
Article | Year |
---|---|
Folate metabolism in cells from fragile X syndrome patients and carriers.
Topics: Adolescent; Adult; Aged; Cell Line; Child; Clone Cells; Culture Media; Drug Resistance; Female; Fibroblasts; Folic Acid; Fragile X Syndrome; Genetic Markers; Heterozygote; Homocysteine; Humans; Lymphocytes; Male; Methotrexate; Middle Aged; Sex Chromosome Aberrations | 1984 |
Martin-Bell syndrome fra(X) (q28) in a Sri Lankan family.
Topics: Adult; Child; Female; Fragile X Syndrome; Heterozygote; Humans; Male; Methotrexate; Pedigree; Sex Chromosome Aberrations; Sri Lanka; Testis | 1982 |
Cytogenetic experience in prenatal fra(X) detection on amniotic fluid cultures.
Topics: Amniocentesis; Amniotic Fluid; Cells, Cultured; Female; Fetal Blood; Fragile X Syndrome; Humans; Methotrexate; Pregnancy; Reproducibility of Results; Risk Factors | 1992 |
Cytological evidence of defective template in the fragile X chromosome.
Topics: Cell Cycle; Cells, Cultured; Fragile X Syndrome; Humans; Karyotyping; Male; Methotrexate; Mitosis; Sex Chromosome Aberrations; Staining and Labeling; Templates, Genetic | 1988 |
Prenatal diagnosis of the fragile X using thymidine induction.
Topics: Adult; Amniocentesis; Australia; Chorionic Villi; Female; Floxuridine; Fragile X Syndrome; Humans; Male; Methotrexate; Pregnancy; Prenatal Diagnosis; Sex Chromosome Aberrations; Thymidine | 1987 |