Serum Markers of Bone Turnover and Bone Remodeling in Children with Noonan Syndrome: Genotype-Phenotype Correlation.
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- Genes, 2025, v. 16, n. 6, p. 668, doi. 10.3390/genes16060668
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- Article
Works matching AU Lattanzio, Crescenza
Results: 4
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Increased risk of nephrolithiasis: an emerging issue in children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
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- Endocrine (1355008X), 2024, v. 84, n. 2, p. 727, doi. 10.1007/s12020-024-03792-6
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- Article
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Predictive Factors of Persistent Growth Hormone Deficiency and Impact on Final Height.
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- Children, 2025, v. 12, n. 3, p. 324, doi. 10.3390/children12030324
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- Article
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Sex Hormone-Binding Globulin (SHBG) Reduction: The Alarm Bell for the Risk of Non-Alcoholic Fatty Liver Disease in Adolescents with Polycystic Ovary Syndrome.
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- Children, 2022, v. 9, n. 11, p. 1748, doi. 10.3390/children9111748
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- Article