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1-4 of 4
Keywords: Primary adrenal insufficiency
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Journal Articles
Adrenal Crises in Children: Perspectives and Research Directions
Available to Purchase
Journal:
Hormone Research in Paediatrics
Horm Res Paediatr (2018) 89 (5): 341–351.
Published Online: 06 June 2018
.... Adrenal insufficiency Congenital adrenal hyperplasia Adrenal crisis Hypopituitarism Primary adrenal insufficiency Secondary adrenal insufficiency Epidemiology Glucocorticoid National Institutes of Health (NIH) 10.13039/100000002 An adrenal crisis (AC) is an acute, life...
Journal Articles
Adrenal Insufficiency, Sex Reversal, and Angelman Syndrome due to Uniparental Disomy Unmasking a Mutation in CYP11A1
Available to Purchase
Journal:
Hormone Research in Paediatrics
Horm Res Paediatr (2018) 89 (3): 205–210.
Published Online: 22 March 2018
...Ahlee Kim; Masanobu Fujimoto; Vivian Hwa; Philippe Backeljauw; Andrew Dauber Background/Aims: Cholesterol side-chain cleavage enzyme (P450scc) deficiency is a rare genetic disorder causing primary adrenal insufficiency with or without a 46,XY disorder of sexual development (DSD). Herein, we report...
Journal Articles
Hospitalisation in Children with Adrenal Insufficiency and Hypopituitarism: Is There a Differential Burden between Boys and Girls and between Age Groups?
Available to Purchase
Journal:
Hormone Research in Paediatrics
Horm Res Paediatr (2017) 88 (5): 339–346.
Published Online: 12 September 2017
... to in the content or advertisements. Adrenal insufficiency Congenital adrenal hyperplasia Adrenal crisis Hypopituitarism Primary adrenal insufficiency Hospital admission Adrenal insufficiency (AI) is a rare disorder that is associated with serious morbidity and an increased risk of mortality [ 1...
Journal Articles
Novel Insight into Etiology, Diagnosis and Management of Primary Adrenal Insufficiency
Available to Purchase
Journal:
Hormone Research in Paediatrics
Horm Res Paediatr (2014) 82 (3): 145–157.
Published Online: 01 August 2014
...Jana Malikova; Christa E. Flück Primary adrenal insufficiency (PAI) is a rare condition in childhood which is either inherited (mostly) or acquired. It is characterized by glucocorticoid and maybe mineralocorticoid deficiency. The most common form in children is 21-hydroxylase deficiency, which...