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Genetic aetiology of primary adrenal insufficiency in Chinese children.

• Authors : Chang Z; Department of Pediatric Endocrinology and Inherited Metabolic Diseases, Children's Hospital of Fudan University, 399 Wan Yuan Road, Shanghai, 201102, People's Republic of China.; Lu W

Subjects: Adrenal Hyperplasia, Congenital*/Adrenal Hyperplasia, Congenital*/Adrenal Hyperplasia, Congenital*/genetics; Adolescent ; Child Congenital adrenal hyperplasia due to 21 hydroxylase deficiency

• Source: BMC medical genomics [BMC Med Genomics] 2021 Jun 30; Vol. 14 (1), pp. 172. Date of Electronic Publication: 2021 Jun 30.Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794

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Aldosterone signaling defect in young infants: single-center report and review.

• Authors : Wijaya, Melati¹; Ma, Huamei¹ ; Zhang, Jun¹

• Source: BMC Endocrine Disorders. 7/9/2021, Vol. 21 Issue 1, p1-9. 9p.

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Hyperkalemia in a patient with myasthenia gravis: case presentation.

• Authors : Lin, Mi-Chu¹ ; Tsai, Ming-Hsien^1,2 ; Leu, Jyh-Gang^1,2

• Source: BMC Endocrine Disorders. 7/26/2019, Vol. 19 Issue 1, pN.PAG-N.PAG. 1p. 1 Color Photograph, 1 Diagram, 2 Charts.

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