| The diagnosis and management of lipodystrophy syndromes: a multi-society practice guideline RJ Brown, D Araujo-Vilar, PT Cheung, D Dunger, A Garg, M Jack, ... The Journal of Clinical Endocrinology & Metabolism 101 (12), 4500-4511, 2016 | 419 | 2016 |
| Diagnosis and treatment of lipodystrophy: a step-by-step approach D Araújo-Vilar, F Santini Journal of endocrinological investigation 42, 61-73, 2019 | 163 | 2019 |
| Estimating the prevalence of generalized and partial lipodystrophy: findings and challenges E Chiquette, EA Oral, A Garg, D Araújo-Vilar, P Dhankhar Diabetes, metabolic syndrome and obesity: targets and therapy, 375-383, 2017 | 117 | 2017 |
| Functional Consequences of Seven Novel Mutations in the CYP11B1 Gene: Four Mutations Associated with Nonclassic and Three Mutations Causing Classic 11β … S Parajes, L Loidi, N Reisch, V Dhir, IT Rose, R Hampel, M Quinkler, ... The Journal of Clinical Endocrinology & Metabolism 95 (2), 779-788, 2010 | 111 | 2010 |
| Long-term effectiveness and safety of metreleptin in the treatment of patients with generalized lipodystrophy RJ Brown, EA Oral, E Cochran, D Araújo-Vilar, DB Savage, A Long, ... Endocrine 60, 479-489, 2018 | 83 | 2018 |
| A new seipin-associated neurodegenerative syndrome E Guillén-Navarro, S Sánchez-Iglesias, R Domingo-Jiménez, B Victoria, ... Journal of medical genetics 50 (6), 401-409, 2013 | 79 | 2013 |
| Prevalence of mutations in TSHR, GNAS, PRKAR1A and RAS genes in a large series of toxic thyroid adenomas from Galicia, an iodine-deficient area in NW Spain F Palos-Paz, O Perez-Guerra, J Cameselle-Teijeiro, C Rueda-Chimeno, ... European journal of endocrinology 159 (5), 623-631, 2008 | 70 | 2008 |
| Comparison of several insulin sensitivity indices derived from basal plasma insulin and glucose levels with minimal model indices DA Garcia-Estevez, D Araujo-Vilar, G Fiestras-Janeiro, ... Hormone and metabolic research 35 (01), 13-17, 2003 | 69 | 2003 |
| High variability in CYP21A2 mutated alleles in Spanish 21‐hydroxylase deficiency patients, six novel mutations and a founder effect L Loidi, C Quinteiro, S Parajes, J Barreiro, DG Lestón, ... Clinical endocrinology 64 (3), 330-336, 2006 | 65 | 2006 |
| Long-term effectiveness and safety of metreleptin in the treatment of patients with partial lipodystrophy EA Oral, P Gorden, E Cochran, D Araújo-Vilar, DB Savage, A Long, ... Endocrine 64, 500-511, 2019 | 63 | 2019 |
| Analysis of the relationship between body mass index, insulin resistance, and beta-cell function: a cross-sectional study using the minimal model DA Garcı́a-Estévez, D Araújo-Vilar, Á Saavedra-González, ... Metabolism 53 (11), 1462-1466, 2004 | 59 | 2004 |
| Phenotypic gender differences in subjects with familial partial lipodystrophy (Dunnigan variety) due to a nuclear lamin A/C R482W mutation D Araujo-Vilar, L Loidi, F Dominguez, J Cabezas-Cerrato Hormone and metabolic research 35 (01), 29-35, 2003 | 54 | 2003 |
| Commentary: Nonalcoholic or metabolic dysfunction-associated fatty liver disease? The epidemic of the 21st century in search of the most appropriate name SA Polyzos, ES Kang, EA Tsochatzis, S Kechagias, M Ekstedt, ... Metabolism 113, 2020 | 52 | 2020 |
| Type 1 familial partial lipodystrophy: understanding the Köbberling syndrome C Guillín-Amarelle, S Sánchez-Iglesias, A Castro-Pais, ... Endocrine 54, 411-421, 2016 | 50 | 2016 |
| Site-dependent differences in both prelamin A and adipogenic genes in subcutaneous adipose tissue of patients with type 2 familial partial lipodystrophy D Araujo-Vilar, G Lattanzi, B González-Méndez, AT Costa-Freitas, ... Journal of medical genetics 46 (1), 40-48, 2009 | 50 | 2009 |
| Recombinant human leptin treatment in genetic lipodystrophic syndromes: the long-term Spanish experience D Araujo-Vilar, S Sánchez-Iglesias, C Guillín-Amarelle, A Castro, M Lage, ... Endocrine 49, 139-147, 2015 | 49 | 2015 |
| A novel phenotypic expression associated with a new mutation in LMNA gene, characterized by partial lipodystrophy, insulin resistance, aortic stenosis and … D Araújo‐Vilar, J Lado‐Abeal, F Palos‐Paz, G Lattanzi, MA Bandín, ... Clinical endocrinology 69 (1), 61-68, 2008 | 49 | 2008 |
| Prematurely aged children: molecular alterations leading to Hutchinson-Gilford progeria and Werner syndromes L Domínguez-Gerpe, D Araújo-Vilar Current aging science 1 (3), 202-212, 2008 | 44 | 2008 |
| Influence of moderate physical exercise on insulin-mediated and non—insulin-mediated glucose uptake in healthy subjects D Araujo-Vilar, E Osifo, M Kirk, DA García-Estévez, J Cabezas-Cerrato, ... Metabolism 46 (2), 203-209, 1997 | 44 | 1997 |
| Pendred syndrome in two Galician families: insights into clinical phenotypes through cellular, genetic, and molecular studies F Palos, MER Garcia-Rendueles, D Araujo-Vilar, MJ Obregon, RM Calvo, ... The Journal of Clinical Endocrinology & Metabolism 93 (1), 267-277, 2008 | 32 | 2008 |
Giovanna LattanziCNR Institute of Molecular GeneticsПодтвержден адрес электронной почты в домене area.bo.cnr.it
