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Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial disease.
Population-based estimates of the global prevalence and carrier frequency of apparent mineralocorticoid excess caused by 11β-hydroxysteroid dehydrogenase type 2 deficiency.
Rare case of longevity in Hutchinson-Gilford progeria syndrome and literature review.
🥉 Relato de casoEosinophilic meningitis epidemiological data from a national database in Thailand's Department of Disease Control: a pragmatic, retrospective analytical study.
Correction to: Physical and mental growth and development in children with congenital hypothyroidism: a case-control study.