The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.
Congenital Adrenal Hyperplasia
Abstract
(First of Two Parts)CONGENITAL adrenal hyperplasia results from an inherited defect in any of the five enzymatic steps required to synthesize Cortisol from cholesterol. A defect in a particular step may be manifested clinically, not only because cortisol and other steroid hormones are not synthesized effectively but also because precursor steroids proximal to the blocked step may accumulate and be shunted into other metabolic pathways, particularly that of androgen biosynthesis. For example, in one of the earliest reports (in 1865) of a case of congenital adrenal hyperplasia, de Crecchio described a person who was considered to be a female . . .
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Citations
Cites
Genotyping steroid 21-hydroxylase deficiency: hormonal reference data
NEW, M. I., LORENZEN, F., LERNER, A. J., KOHN, B., OBERFIELD, S. E., POLLACK, M. S., DUPONT, B., STONER, E., LEVY, D. J., PANG, S., et al. (1983) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-57-2-320 · Cited by 624
Self-citationLate-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia
KOHN, B., LEVINE, L. S., POLLACK, M. S., PANG, S., LORENZEN, F., LEVY, D., LERNER, A. J., RONDANINI, G. F., DUPONT, B., & NEW, M. I. (1982) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-55-5-817 · Cited by 204
Self-citationYanagibashi, K., Haniu, M., Shively, J. E., Shen, W. H., & Hall, P. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)35682-x · Cited by 172
Genetic and Hormonal Characterization of Cryptic 21-Hydroxylase Deficiency*
LEVINE, L. S., DUPONT, B., LORENZEN, F., PANG, S., POLLACK, M., OBERFIELD, S. E., KOHN, B., LERNER, A., CACCIARI, E., MANTERO, F., et al. (1981) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-53-6-1193 · Cited by 81
Self-citationBovine steroid 21-hydroxylase: regulation of biosynthesis
John, M. E., Okamura, T., Dee, A., Adler, B., John, M. C., White, P. C., Simpson, E. R., & Waterman, M. R. (1986) · Biochemistry · doi:10.1021/bi00358a016 · Cited by 61
Self-citationIS SALT‐WASTING IN CONGENITAL ADRENAL HYPERPLASIA DUE TO THE SAME GENE AS THE FASCICULATA DEFECT?
STONER, E., DIMARTINO‐NARDI, J., KUHNLE, U., LEVINE, L. S., OBERFIELD, S. E., & NEW, M. I. (1986) · Clinical Endocrinology · doi:10.1111/j.1365-2265.1986.tb03249.x · Cited by 54
Self-citation
Cited by
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency*
White, P. C., & Speiser, P. W. (2000) · Endocrine Reviews · doi:10.1210/edrv.21.3.0398 · Cited by 1,432
Self-citationCongenital adrenal hyperplasia
Speiser, P. W., & White, P. C. (2003) · New England Journal of Medicine · doi:10.1056/nejmra021561 · Cited by 1,405
Self-citationCharacterization of Two Genes Encoding Human Steroid 11β-Hydroxylase (P-45011β)
Mornet, E., Dupont, J., Vitek, A., & White, P. C. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)30030-4 · Cited by 405
Self-citationAdrenomedullary dysplasia and hypofunction in patients with classic 21-hydroxylase deficiency.
Merke, D. P., Chrousos, G. P., Eisenhofer, G., Weise, M., Keil, M. F., Rogol, A. D., Van Wyk, J. J., & Bornstein, S. R. (2000) · New England Journal of Medicine · doi:10.1056/nejm200011093431903 · Cited by 266
Tusie-Luna, M. T., Traktman, P., & White, P. C. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)45304-x · Cited by 254
Self-citation
Metadata
- Authors
- White, P. C., New, M. I., & Dupont, B.
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 1987-06-11
- Volume
- 316
- Issue
- 24
- Pages
- 1519-1524
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W2413525758
- Cited by
- 288
- References
- 6
- FWCI
- 7.93
- Type
- journal article
- Language
- en
- Open access
- closed
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.