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Journal of Pediatric Endocrinology & Metabolism : JPEM|May 24, 2014
A novel CASR mutation associated with neonatal severe hyperparathyroidism transmitted as an autosomal recessive disorderAlicia Diaz-Thomas, John Cannon, Pallavi Iyer, et al.Neurology|December 12, 2019
Congenital absence of norepinephrine due to <i>CYB561</i> mutationsCyndya A Shibao, Emily M Garland, Bonnie K Black, et al.JCEM Case Reports|February 16, 2026
Preventing Cushing Syndrome: Adrenalectomy in <i>PDE11A</i>-Positive Primary Pigmented Nodular Adrenocortical DiseaseTobias Carling, Meredith LaRue, Anne M Lenz, et al.Pediatrics|August 18, 2010
Bicalutamide and third-generation aromatase inhibitors in testotoxicosisAnne M Lenz, Dorothy Shulman, Erica A Eugster, et al.Pageof 2