androstenedione has been researched along with 46, XY Disorders of Sex Development in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 4 (66.67) | 24.3611 |
| 2020's | 2 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Arya, S; Bandgar, T; Barnabas, R; Bhandare, VV; Krishnappa, B; Kumbhar, BV; Kunwar, A; Lila, AR; Memon, SS; Patil, V; Sarathi, V; Shah, NS | 1 |
| Cole, FS; Gale, S; Hollander, A; Luna, SE; Nabhan, ZM; Ory, DS; St Dennis-Feezle, L; Wambach, JA; Wegner, DJ; Yang, P | 1 |
| Al Hamid, AA; Atef, A; El Dayem, SM; El Mougy, F; Galal, A; Hafez, M; Kandil, M | 1 |
| Ali, OS; Essawi, ML; Gad, YZ; Hassan, HA; Mazen, I; Mekkawy, M | 1 |
| Balogh, E; Jakab, J; Kiss, A; Kovács, J; Ladányi, E; Megyeri, T; Papp, J; Ságodi, L; Ujfalusi, A | 1 |
| Abdelhedi, F; Abid, M; Belguith, N; Ben Rhouma, B; Charfi, N; Fakhfakh, F; Hachicha, M; Kamoun, H; Kamoun, M; Kamoun, T; Mnif, MF | 1 |
1 review(s) available for androstenedione and 46, XY Disorders of Sex Development
| Article | Year |
|---|---|
17β hydroxysteroid dehydrogenase 3 deficiency in 46,XY disorders of sex development: Our experience and a gender role-focused systematic review.
Topics: Androstenedione; Disorder of Sex Development, 46,XY; Disorders of Sex Development; Female; Gender Role; Genotype; Humans; Male | 2022 |
5 other study(ies) available for androstenedione and 46, XY Disorders of Sex Development
| Article | Year |
|---|---|
Whole exome sequencing and functional characterization increase diagnostic yield in siblings with a 46, XY difference of sexual development (DSD).
Topics: 17-Hydroxysteroid Dehydrogenases; Androstenedione; Child, Preschool; Disorder of Sex Development, 46,XY; Exome Sequencing; HEK293 Cells; Humans; Male; Testosterone | 2021 |
The role of anti-Mullerian and inhibin B hormones in the evaluation of 46,XY disorders of sex development.
Topics: Adolescent; Androstenedione; Anti-Mullerian Hormone; Child; Child, Preschool; Chorionic Gonadotropin; Cross-Sectional Studies; Dehydroepiandrosterone; Dihydrotestosterone; Disorder of Sex Development, 46,XY; Humans; Infant; Infant, Newborn; Inhibins; Male; Prospective Studies; Sensitivity and Specificity; Testosterone | 2014 |
Mutational Profile of 10 Afflicted Egyptian Families with 17-β-HSD-3 Deficiency.
Topics: 17-Hydroxysteroid Dehydrogenases; Adolescent; Adult; Androstenedione; Child; Child, Preschool; Dihydrotestosterone; Disorder of Sex Development, 46,XY; Egypt; Exons; Female; Homozygote; Humans; Male; Mutation; Testosterone; Young Adult | 2016 |
[Dysgenetic male pseudohermaphroditism].
Topics: 17-alpha-Hydroxyprogesterone; Androstenedione; Biomarkers; Chromosomes, Human, X; Chromosomes, Human, Y; Diagnosis, Differential; Disorder of Sex Development, 46,XY; Disorders of Sex Development; Follicle Stimulating Hormone; Humans; Hypospadias; In Situ Hybridization, Fluorescence; Infant, Newborn; Luteinizing Hormone; Male; Mosaicism; Testis; Testosterone | 2012 |
A novel nonsense mutation in HSD17B3 gene in a Tunisian patient with sexual ambiguity.
Topics: 17-Hydroxysteroid Dehydrogenases; Androstenedione; Biomarkers; Child, Preschool; Codon, Nonsense; Disorder of Sex Development, 46,XY; DNA Mutational Analysis; Exons; Female; Genetic Predisposition to Disease; Gynecomastia; Homozygote; Humans; Male; Pedigree; Phenotype; Polymerase Chain Reaction; Steroid Metabolism, Inborn Errors; Testosterone; Tunisia | 2013 |