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6 in total

1. Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: description of a new mutation, R384X.

Authors: Audrey Mary Matallana-Rhoades; Juan David Corredor-Castro; Francisco Javier Bonilla-Escobar; Bony Valentina Mecias-Cruz; Liliana Mejia de Beldjena
Journal: Colomb Med (Cali) Date: 2016-09-30

Review 2. Cross-sectional imaging features of unusual adrenal lesions: a radiopathological correlation.

Authors: Ali Devrim Karaosmanoglu; Omer Onder; Can Berk Leblebici; Cenk Sokmensuer; Deniz Akata; Mustafa Nasuh Ozmen; Musturay Karcaaltincaba
Journal: Abdom Radiol (NY) Date: 2021-03-18

3. Premature pubarche in a child with abnormal 3β-hydroxysteroid dehydrogenase function and Klinefelter syndrome: the intriguing relationship between androgen deficiency and excess.

Authors: Michele Gortakowski; Rushika Conroy; Luisa Aguiar; Holley Allen
Journal: Clin Case Rep Date: 2016-12-20

Review 4. Clinical outcomes and characteristics of P30L mutations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Authors: Mirjana Kocova; Violeta Anastasovska; Henrik Falhammar
Journal: Endocrine Date: 2020-05-05 Impact factor: 3.633

5. Challenges in the Diagnosis of Simple-Virilizing Congenital Adrenal Hyperplasia: A Case Report.

Authors: Ritu Singh; Mukta Agarwal; Sudwita Sinha
Journal: Cureus Date: 2022-10-05

6. Congenital adrenal hyperplasia presenting as pelvic inflammatory disease in a phenotypic male: A case report.

Authors: Eunsoo Lim; Ja Young Jeon
Journal: Medicine (Baltimore) Date: 2020-01 Impact factor: 1.817

6 in total