The DOI matches its Crossref record; 22 of the 23 references it cites were found in a registry or an index.
The adrenogenital syndrome with deficiency of 3β-hydroxysteroid dehydrogenase
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Citations
Cites
Jacob, M. (1989) · Health Education Journal · doi:10.1177/001789698904800401 · Cited by 3,123
A QUANTITATIVE COLOR REACTION FOR CORTISONE AND RELATED 17,21-DIHYDROXY-20-KETOSTEROIDS
Porter, C. C., & SILBER, R. H. (1950) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)56408-5 · Cited by 564
An Enzyme in Endocrine Tissues which Oxidizes Δ 5 -3 Hydroxy Steroids to α,β Unsaturated Ketones
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Kinetics and Mechanism of Solvolysis of Steroid Hydrogen Sulfates1
Burstein, S., & Lieberman, S. (1958) · Journal of the American Chemical Society · doi:10.1021/ja01552a054 · Cited by 121
Allen, W. M., Hayward, S. J., & PINTO, A. (1950) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-10-1-54 · Cited by 112
Chromatographie von sterinen, steroiden und verwandten verbindungen
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DEFECTIVE STEROIDAL BIOGENESIS IN CONGENITAL ADRENAL HYPERPLASIA
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Self-citationA simplified method for the routine determination of pregnanediol and pregnanetriol in urine.
Bongiovanni, A. M., & Gw, C. (1954) · PubMed · Cited by 69
Self-citationImpaired Aldosterone Production in “Salt-losing” Congenital Adrenal Hyperplasia*
Bryan, G. T., Kliman, B., & Bartter, F. C. (1965) · Journal of Clinical Investigation · doi:10.1172/jci105213 · Cited by 66
Cox, R. I. (1952) · Biochemical Journal · doi:10.1042/bj0520339 · Cited by 65
Research works printed but not linked: 10
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- [2]2. Bongiovanni, A. M., and Eberlein, W. R. Defects in steroidal metabolism of subjects with the adreno- genital syndrome. Metabolism 1961, 10, 917.
- [3]3. Bongiovanni, A. M. In zitro hydroxylation of ster- oids by whole adrenal homogenates of beef, nor- mal man, and patients with the adrenogenital syn- drome. J. clin. Invest. 1958, 37, 1342.
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Cited by
Sorted by citations
The Molecular Biology, Biochemistry, and Physiology of Human Steroidogenesis and Its Disorders
Miller, W. L., & Auchus, R. J. (2011) · Endocrine Reviews · doi:10.1210/er.2010-0013 · Cited by 2,458
Congenital adrenal hyperplasia
El-Maouche, D., Arlt, W., & Merke, D. P. (2017) · The Lancet · doi:10.1016/s0140-6736(17)31431-9 · Cited by 669
Familial Incomplete Male Pseudohermaphroditism, Type 2
Walsh, P. C., Madden, J. D., Harrod, M. J., Goldstein, J. L., MacDonald, P. C., & Wilson, J. D. (1974) · New England Journal of Medicine · doi:10.1056/nejm197410312911806 · Cited by 621
Molecular biology of the 3β-hydroxysteroid dehydrogenase/Δ5-Δ4 –isomerase gene family
Simard, J., Ricketts, M.-L., Gingras, S., Soucy, P., Feltus, F. A., & Melner, M. H. (2005) · Endocrine Reviews · doi:10.1210/er.2002-0050 · Cited by 620
17-Hydroxylation deficiency in man
Biglieri, E. G., Herron, M. A., & Brust, N. (1966) · Journal of Clinical Investigation · doi:10.1172/jci105499 · Cited by 561
Metadata
- Authors
- Bongiovanni, A. M.
- Corresponding author
- Bongiovanni, Alfred M.
- Venue
- Journal of Clinical Investigation
- Published
- 1962-11-01
- Volume
- 41
- Issue
- 11
- Pages
- 2086-2092
- ISSN
- 0021-9738 (ISSN-L)
- PMC
- PMC291138
- OpenAlex
- W2035956286
- Semantic Scholar
- 85a4c18457b176afbd5cbfe86fbabef4c77a0ae7
- Cited by
- 304
- References
- 23
- Citations by year
- 2026: 4 · 2024: 1 · 2023: 5 · 2022: 2 · 2020: 1 · 2019: 3 · 2018: 4 · 2017: 8 · 2016: 2 · 2015: 4 · 2014: 7 · 2013: 4 · 2012: 5
- FWCI
- 4.23
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Clinical Investigation (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Sexual Differentiation and Disorders
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
- Keywords
- adrenogenital syndrome, 3β-hydroxysteroid dehydrogenase deficiency, congenital adrenal hyperplasia, steroidogenesis, adrenal cortex
- MeSH terms
- Humans, Hypospadias, Male, Oxidoreductases, 3-Hydroxysteroid Dehydrogenases, Adrenogenital Syndrome
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