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11-hydroxylase deficiency相关文献:
Challenges in treatment of patients with non-classic congenital adrenal hyperplasia.
Adriaansen BPH, Schröder MAM, Span PN, Sweep FCGJ, van Herwaarden AE, Claahsen-van der Grinten HL.
Front Endocrinol (Lausanne). 2022 Dec 12;13:1064024. doi: 10.3389/fendo.2022.1064024. eCollection 2022.
PMID:36578966
Treatment of Nonclassic 11-Hydroxylase Deficiency with Ashwagandha Root.
Powell D, Inoue T, Bahtiyar G, Fenteany G, Sacerdote A.
Case Rep Endocrinol. 2017;2017:1869560. doi: 10.1155/2017/1869560. Epub 2017 Jun 20.
PMID:28713602
11-Hydroxylase deficiency as a cause of pre-pubertal gynecomastia.
Wasniewska M, Arrigo T, Lombardo F, Crisafulli G, Salzano G, De Luca F.
J Endocrinol Invest. 2009 Apr;32(4):387-8. doi: 10.1007/BF03345731.
PMID:19636210
Partial deficiency of adrenal 11-hydroxylase. A possible cause of primary hypertension.
de Simone G, Tommaselli AP, Rossi R, Valentino R, Lauria R, Scopacasa F, Lombardi G.
Hypertension. 1985 Mar-Apr;7(2):204-10. doi: 10.1161/01.hyp.7.2.204.
PMID:2984117
Congenital adrenal hyperplasia due to 11-hydroxylase deficiency-Compound heterozygous mutations of a prevalent and two novel CYP11B1 mutations.
Gu C, Tan H, Yang J, Lu Y, Ma Y.
Gene. 2017 Aug 30;626:89-94. doi: 10.1016/j.gene.2017.05.029. Epub 2017 May 14.
PMID:28514642
The uncommon forms of congenital adrenal hyperplasia.
Auchus RJ.
Curr Opin Endocrinol Diabetes Obes. 2022 Jun 1;29(3):263-270. doi: 10.1097/MED.0000000000000727.
PMID:35621178
Rare Types of Congenital Adrenal Hyperplasias Other Than 21-hydroxylase Deficiency.
İsakoca M, Erdeve Ş, Çetinkaya S.
J Clin Res Pediatr Endocrinol. 2025 Jan 10;17(Suppl 1):23-32. doi: 10.4274/jcrpe.galenos.2024.2024-6-21-S. Epub 2024 Dec 23.
PMID:39713884
A rare case of steroid 11 beta-hydroxylase deficiency in a child revealed by acute pulmonary edema.
El Haddar Z, El Ouali A, Ghanam A, Benajiba N, Rkain M, Babakhouya A.
Oxf Med Case Reports. 2024 May 20;2024(5):omae042. doi: 10.1093/omcr/omae042. eCollection 2024 May.
PMID:38784773
[Adrenal enzymatic block with late-onset caused by 11-hydroxylase deficiency. Apropos of 29 cases].
Reboul P, Merceron RE, Cordray JP, Guillerd X, Nys P, Rainaut M.
Ann Endocrinol (Paris). 1992;53(5-6):187-95.
PMID:1340685
Congenital adrenal hyperplasia due to 11-hydroxylase deficiency: functional characterization of two novel point mutations and a three-base pair deletion in the CYP11B1 gene.
Krone N, Riepe FG, Götze D, Korsch E, Rister M, Commentz J, Partsch CJ, Grötzinger J, Peter M, Sippell WG.
J Clin Endocrinol Metab. 2005 Jun;90(6):3724-30. doi: 10.1210/jc.2005-0089. Epub 2005 Mar 8.
PMID:15755848
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