Congenital absence of norepinephrine due to CYB561 mutations
Shibao, Cyndya A, Garland, Emily M, Black, Bonnie K, Mathias, Christopher J, Grant, Maria B, Root, Allen W, Robertson, David, Biaggioni, Italo
Published in Neurology (14.01.2020)
Published in Neurology (14.01.2020)
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Journal Article
A novel CASR mutation associated with neonatal severe hyperparathyroidism transmitted as an autosomal recessive disorder
Diaz-Thomas, Alicia, Cannon, John, Iyer, Pallavi, Al-Maawali, Almundher, Fazalullah, Mohammed, Diamond, Frank, Mueller, O. Thomas, Root, Allen W., Alyaarubi, Saif
Published in Journal of Pediatric Endocrinology & Metabolism (01.09.2014)
Published in Journal of Pediatric Endocrinology & Metabolism (01.09.2014)
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Journal Article
Salutary Effects of Combining Early Very Low-Dose Systemic Estradiol with Growth Hormone Therapy in Girls with Turner Syndrome
Rosenfield, Robert L, Devine, Nancy, Hunold, Joanne Julius, Mauras, Nelly, Moshang, Thomas, Root, Allen W
Published in The journal of clinical endocrinology and metabolism (01.12.2005)
Published in The journal of clinical endocrinology and metabolism (01.12.2005)
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