Paloma Cabanas

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 · 90 citations · Full text

Hypochondroplasia and acanthosis nigricans: a new syndrome due to the p.Lys650Thr mutation in the fibroblast growth factor receptor 3 gene?

Lidia Castro-Feijóo, Lourdes Loidi, Anxo Vidal et al. · European Journal of Endocrinology · 2008 · 30 citations

Papillary thyroid carcinoma after recombinant GH therapy for Turner syndrome

Paloma Cabanas, Tomás García‐Caballero, J Barreiro et al. · European Journal of Endocrinology · 2005 · 19 citations

Expanding the clinical and molecular spectrum of the CWC27-related spliceosomopathy

Alejandro Brea‐Fernández, Paloma Cabanas, David Dacruz-Álvarez et al. · Journal of Human Genetics · 2019 · 15 citations

Hematology, Pathology, Cytoskeleton +4

Congenital Hypothyroidism with Neurological and Respiratory Alterations: A Case Detected Using a Variable Diagnostic Threshold for Tsh

J.R. Alonso Fernández, Castro-Feijoo Lidia, Cristobal Colón et al. · Journal of Clinical Research in Pediatric Endocrinology · 2011 · 11 citations · Full text