Salvatore Scommegna

Molecular Characterization of 6 Unrelated Italian Patients With 5α‐Reductase Type 2 Deficiency

Fulvia Baldinotti, Silvia Majore, Antonella Fogli et al. · Journal of Andrology · 2007 · 46 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Neonatal Identification of Pituitary Aplasia: A Life-Saving Diagnosis

Salvatore Scommegna, Daniela Galeazzi, Simonetta Picone et al. · Hormone Research in Paediatrics · 2004 · 44 citations

Medicine, Endocrinology, Pediatrics +16

Bone mineral density at diagnosis and following successful treatment of pediatric Cushing’s disease

Salvatore Scommegna, Janelle Greening, Helen L. Storr et al. · Journal of Endocrinological Investigation · 2005 · 39 citations

Medicine, Endocrinology, Pediatrics +15

Longitudinal hormonal evaluation in a patient with disorder of sexual development, 46,XY karyotype and one <i>NR5A1</i> mutation

Lucia Pedace, Luigi Laino, Nicoletta Preziosi et al. · American Journal of Medical Genetics Part A · 2014 · 36 citations

Medicine, Endocrinology, Genetics +17

Endocrine and neuropsychological assessment in a child with a novel mutation of thyroid hormone receptor: Response to 12- month triiodothyroacetic acid (TRIAC) therapy

Pasquale La Torre, M Bertoli, Simone Di Giovanni et al. · Journal of Endocrinological Investigation · 2005 · 33 citations

Medicine, Endocrinology, Neurology +17