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Seite 1 für „Hydroxyl“ · Literaturverweise aus öffentlichen Artikeln
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Coexistence of 21-hydroxylase deficiency and Gitelman syndrome in a neonate presenting with severe hyponatremic seizures: a case report
pubmed · 42358677
Literaturverweis öffnenCongenital Adrenal Hyperplasia due to 11β-Hydroxylase Deficiency Presented With Leydig Cell Tumor and Testicular Adrenal Rest Tumors: A Case Report
pubmed · 42052618
Literaturverweis öffnenClinical pregnancy outcomes with assisted reproduction in patients with 17α-Hydroxylase/17, 20-lyase deficiency: a single center cohort study and integrated analysis with reported cases
pubmed · 42445882
Literaturverweis öffnen17α-hydroxylase deficiency in a 46,XY individual with a hypoplastic uterus: In vitro functional validation of a CYP17A1 mutation
pubmed · 42462819
Literaturverweis öffnenConcurrent Phenylalanine Hydroxylase-Related Disorder and Celiac: A Rare Co-occurrence With Implications for Clinical Management
pubmed · 42205176
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