Manuel Pombo

Epigenetic Defects of<i>GNAS</i>in Patients with Pseudohypoparathyroidism and Mild Features of Albright’s Hereditary Osteodystrophy

Guiomar Pérez de Nanclares, Eduardo Fernández‐Rebollo, Izortze Santín et al. · The Journal of Clinical Endocrinology & Metabolism · 2007 · 162 citations · Full text

Medicine, Endocrinology, Genetics +15

Functional Consequences of Seven Novel Mutations in the<i>CYP11B1</i>Gene: Four Mutations Associated with Nonclassic and Three Mutations Causing Classic 11β-Hydroxylase Deficiency

Silvia Parajes, Lourdes Loidi, Nicole Reisch et al. · The Journal of Clinical Endocrinology & Metabolism · 2010 · 112 citations · Full text

Life Sciences, Endocrinology, Genetics +17

Genetic diagnosis of X-linked dominant hypophosphatemic rickets in a cohort study: Tubular reabsorption of phosphate and 1,25(OH)2D serum levels are associated with PHEX mutation type

Marcos Morey, Lidia Castro-Feijóo, Jesús Barreiro et al. · BMC Medical Genetics · 2011 · 91 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Influence of sex, age and adrenergic pathways on the growth hormone response to GHRP‐6

A Peñalva, Manuel Pombo, J Barreiro et al. · Clinical Endocrinology · 1993 · 85 citations

Medicine, Endocrinology, Pharmacology +12

Effect of growth hormone (GH)-releasing hormone (GHRH), atropine, pyridostigmine, or hypoglycemia on GHRP-6-induced GH secretion in man.

A Peñalva, Manuel Pombo, Felipe F. Casanueva et al. · The Journal of Clinical Endocrinology & Metabolism · 1993 · 81 citations

Medicine, Endocrinology, Pharmacology +17