estriol has been researched along with Genetic Diseases in 6 studies
hormonin: estrogen replacement; each tablet contains 600 ug micronized 17beta-estradiol, 270 ug estriol and 1.4 mg estrone
chlorapatite : A phosphate mineral with the formula Ca5(PO4)3Cl.
Excerpt | Relevance | Reference |
---|---|---|
"Application of topical estriol ointment is an effective treatment for hereditary hemorrhagic telangiectasia (HHT) epistaxis." | 5.22 | Intranasal topical estrogen in the management of epistaxis in hereditary hemorrhagic telangiectasia. ( Haji, T; Minami, K, 2016) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (16.67) | 18.7374 |
1990's | 3 (50.00) | 18.2507 |
2000's | 1 (16.67) | 29.6817 |
2010's | 1 (16.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Minami, K | 1 |
Haji, T | 1 |
Langlois, S | 1 |
Armstrong, L | 1 |
Gall, K | 1 |
Hulait, G | 1 |
Livingston, J | 1 |
Nelson, T | 1 |
Power, P | 1 |
Pugash, D | 1 |
Siciliano, D | 1 |
Steinraths, M | 1 |
Mattman, A | 1 |
Rose, NC | 1 |
Mennuti, MT | 1 |
Mennuti, M | 1 |
Drugan, A | 1 |
O'Brien, JE | 1 |
Gambino, RS | 1 |
Evans, MI | 1 |
Behrman, RE | 1 |
Fisher, D | 1 |
Paton, JB | 1 |
Keller, J | 1 |
3 reviews available for estriol and Genetic Diseases
Article | Year |
---|---|
Maternal serum screening for neural tube defects and fetal chromosome abnormalities.
Topics: alpha-Fetoproteins; Chorionic Gonadotropin; Chromosome Aberrations; Chromosome Disorders; Estriol; F | 1993 |
Prenatal biochemical screening.
Topics: alpha-Fetoproteins; Amniocentesis; Chorionic Gonadotropin; Congenital Abnormalities; Estriol; Female | 1992 |
In utero disease and the newborn infant.
Topics: Acid-Base Equilibrium; Acidosis; Amniotic Fluid; Animals; Bilirubin; Birth Weight; Electrocardiograp | 1970 |
1 trial available for estriol and Genetic Diseases
Article | Year |
---|---|
Intranasal topical estrogen in the management of epistaxis in hereditary hemorrhagic telangiectasia.
Topics: Administration, Intranasal; Epistaxis; Estriol; Estrogens; Female; Genetic Diseases, Inborn; Humans; | 2016 |
2 other studies available for estriol and Genetic Diseases
Article | Year |
---|---|
Steroid sulfatase deficiency and contiguous gene deletion syndrome amongst pregnant patients with low serum unconjugated estriols.
Topics: British Columbia; DNA Mutational Analysis; Estriol; Female; Gene Deletion; Genetic Diseases, Inborn; | 2009 |
A 35-year-old pregnant woman considering maternal serum screening and amniocentesis.
Topics: Adult; alpha-Fetoproteins; Amniocentesis; Biomarkers; Chorionic Gonadotropin; Chorionic Villi Sampli | 1996 |