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You searched for: Author/Creator Houang, Muriel

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1. A proof of concept of a machine learning algorithm to predict late-onset 21-hydroxylase deficiency in children with premature pubic hair. Issue 220 (June 2022)

2. Analysis of a pitfall in congenital adrenal hyperplasia newborn screening: evidence of maternal use of corticoids detected on dried blood spot. Issue 6 (15th June 2022)

3. Combining metabolomics and machine learning models as a tool to distinguish non-classic 21-hydroxylase deficiency from polycystic ovary syndrome without adrenocorticotropic hormone testing. Issue 2 (25th November 2022)

5. Increasing knowledge in IGF1R defects: lessons from 35 new patients. Issue 3 (5th October 2019)

6. Mutations in the maternally imprinted gene MKRN3 are common in familial central precocious puberty. Issue 1 (January 2016)