Introduction: 11β-hydroxylase (11β-OH) deficiency is the second most frequent cause of classic congenital adrenal hyperplasia (CAH) (5%–8% of cases). Clinically, it is characterized by virilization and arterial hypertension.
Elida Mercado Santis +6 more
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Bringing the Pediatric Endocrine Spanish Speaking Community Together: First Virtual Pediatric Endocrine Meeting in Low- and Middle-Income Countries in Central and South America. [PDF]
Bogarin R +9 more
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Early GH therapy and neurodevelopmental outcome in a child with compound heterozygous <i>IGF1R</i> variants. [PDF]
Sá Pinto M +5 more
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Do GnRH Agonists Really Increase Body Weight Gain? Evaluation of a Multicentric Portuguese Cohort of Patients With Central Precocious Puberty. [PDF]
Leite AL +8 more
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Correction: Digital Health Program to Support Family Caregivers of Children Undergoing Growth Hormone Therapy: Qualitative Feasibility Study. [PDF]
Jiménez-Díaz A +10 more
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Glucocorticoid-prescribing trends in congenital adrenal hyperplasia, 2017 to 2023. [PDF]
Roxas A +70 more
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Positive impact of insulin treatment on clinical trend in cystic fibrosis patients: a retrospective study. [PDF]
Giugno A +8 more
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The role of intermittent continuous glucose monitoring in a successful outpatient transition from insulin to glibenclamide in a patient with transient neonatal diabetes. [PDF]
Lyra A +4 more
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Peripheral precocious puberty in girls with McCune-Albright syndrome: a case series. [PDF]
Faria AG +17 more
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Genotypic Findings in Noonan and Non-Noonan RASopathies and Patient Eligibility for Growth Hormone Treatment. [PDF]
Carcavilla A +14 more
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