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dehydroepiandrosterone sulfate and Disorders of Sex Development

dehydroepiandrosterone sulfate has been researched along with Disorders of Sex Development in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19902 (28.57)18.7374
1990's3 (42.86)18.2507
2000's1 (14.29)29.6817
2010's1 (14.29)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Andersen, HR; Andersen, MS; Andersson, AM; Jensen, TK; Johannsen, TH; Juul, A; Ljubicic, ML; Main, KM; Petersen, JH1
Mühlendahl, KE; Wieacker, P1
Fujieda, K; Kouda, N; Miller, WL; Nakae, J; Tajima, T1
Augarten, A; Chayen, R; Gazit, E; Goldfarb, H; Pariente, C; Sack, J1
Gajdusek, DC; Imperato-McGinley, J; Miller, M; Peterson, RE; Shackleton, C; Wilson, JD1
Gautier, T; Imperato-McGinley, J; Peterson, RE; Shackleton, C1
Thijssen, JH; Van den Brande, JL; van Hooff, CO; Wit, JM1

Other Studies

7 other study(ies) available for dehydroepiandrosterone sulfate and Disorders of Sex Development

ArticleYear
Sex Differences in Reproductive Hormones During Mini-Puberty in Infants With Normal and Disordered Sex Development.
    The Journal of clinical endocrinology and metabolism, 2018, 08-01, Volume: 103, Issue:8

    Topics: Androstenedione; Anti-Mullerian Hormone; Cross-Sectional Studies; Dehydroepiandrosterone; Dehydroepiandrosterone Sulfate; Disorders of Sex Development; Female; Follicle Stimulating Hormone; Gonadal Steroid Hormones; Humans; Infant; Klinefelter Syndrome; Luteinizing Hormone; Male; Sex Characteristics; Sex Hormone-Binding Globulin; Sexual Maturation; Turner Syndrome

2018
[Disorder of 17 beta-hydroxysteroid dehydrogenase as the cause of hypergonadotropic hypogonadism in 2 siblings with primary amenorrhea].
    Geburtshilfe und Frauenheilkunde, 1996, Volume: 56, Issue:9

    Topics: 17-Hydroxysteroid Dehydrogenases; Adolescent; Androstenedione; Dehydroepiandrosterone Sulfate; Diagnosis, Differential; Disorders of Sex Development; Gonadal Steroid Hormones; Humans; Hypogonadism; Male

1996
Heterozygous mutation in the cholesterol side chain cleavage enzyme (p450scc) gene in a patient with 46,XY sex reversal and adrenal insufficiency.
    The Journal of clinical endocrinology and metabolism, 2001, Volume: 86, Issue:8

    Topics: 17-alpha-Hydroxyprogesterone; Adrenocortical Hyperfunction; Adrenocorticotropic Hormone; Aldosterone; Amino Acid Sequence; Base Sequence; Cholesterol Side-Chain Cleavage Enzyme; Corticosterone; Dehydroepiandrosterone Sulfate; Disorders of Sex Development; Exons; Female; Heterozygote; Humans; Hydrocortisone; Infant; Introns; Male; Molecular Sequence Data; Pedigree; Renin

2001
Ambiguous genitalia due to partial activity of cytochromes P450c17 and P450c21.
    The Journal of steroid biochemistry and molecular biology, 1992, Volume: 41, Issue:1

    Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Androstenedione; Chorionic Gonadotropin; Chromosomes, Human, Pair 10; Chromosomes, Human, Pair 6; Dehydroepiandrosterone; Dehydroepiandrosterone Sulfate; Disorders of Sex Development; Female; Histocompatibility Testing; Humans; Hydrocortisone; Hydroxyprogesterones; Infant; Male; Mutation; Pedigree; Progesterone; Sincalide; Testosterone

1992
A cluster of male pseudohermaphrodites with 5 alpha-reductase deficiency in Papua New Guinea.
    Clinical endocrinology, 1991, Volume: 34, Issue:4

    Topics: 3-Oxo-5-alpha-Steroid 4-Dehydrogenase; Androstenedione; Dehydroepiandrosterone; Dehydroepiandrosterone Sulfate; Dihydrotestosterone; Disorders of Sex Development; Fibroblasts; Humans; Hydrocortisone; Male; Papua New Guinea; Progesterone; Skin; Testosterone

1991
Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases. A new variant of congenital adrenal hyperplasia.
    The New England journal of medicine, 1985, Nov-07, Volume: 313, Issue:19

    Topics: 17-Hydroxycorticosteroids; 17-Ketosteroids; 18-Hydroxycorticosterone; 18-Hydroxydesoxycorticosterone; Adrenal Hyperplasia, Congenital; Aldehyde-Lyases; Aldosterone; Androstenedione; Corticosterone; Cortodoxone; Dehydroepiandrosterone; Dehydroepiandrosterone Sulfate; Desoxycorticosterone; Dihydrotestosterone; Disorders of Sex Development; Humans; Hydrocortisone; Infant; Male; Mixed Function Oxygenases; Pregnenolone; Progesterone; Steroid Hydroxylases; Testosterone

1985
In vivo and in vitro studies in a 46, XY phenotypically female infant with 17-ketosteroid reductase deficiency.
    Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme, 1988, Volume: 20, Issue:6

    Topics: 17-Hydroxysteroid Dehydrogenases; 3-Hydroxysteroid Dehydrogenases; Androgens; Androstenedione; Chorionic Gonadotropin; Dehydroepiandrosterone; Dehydroepiandrosterone Sulfate; Dihydrotestosterone; Disorders of Sex Development; Female; Humans; Infant; Infant, Newborn; Receptors, Androgen; Testosterone

1988