Consensus Statement on 21-Hydroxylase Deficiency from The European Society for Paediatric Endocrinol...
Consensus Statement on 21-Hydroxylase Deficiency from The European Society for Paediatric Endocrinology and The Lawson Wilkins Pediatric Endocrine Society
About this item
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Publisher
Basel, Switzerland: S. Karger AG
Journal title
Language
English
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Publication information
Publisher
Basel, Switzerland: S. Karger AG
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More information
Scope and Contents
Contents
Despite over 50 years' experience with steroid replacement therapy, the management of congenital adrenal hyperplasia (CAH) remains difficult, and clinical practice varies substantially throughout the world. To consider the evidence for best practice, formulate management guidelines, and consider innovative therapies, The Lawson Wilkins Pediatric En...
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Full title
Consensus Statement on 21-Hydroxylase Deficiency from The European Society for Paediatric Endocrinology and The Lawson Wilkins Pediatric Endocrine Society
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Record Identifier
TN_cdi_proquest_journals_1069231561
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_1069231561
Other Identifiers
ISSN
1663-2818,0301-0163
E-ISSN
1663-2826
DOI
10.1159/000065490
