JOSE JOAQUIN
LADO ABEAL
Forscher in der Zeit 2003-2019
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Complexo Hospitalario Universitario de Santiago
Santiago de Compostela, EspañaPublikationen in Zusammenarbeit mit Forschern von Complexo Hospitalario Universitario de Santiago (12)
2020
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High prevalence of non-thyroidal illness syndrome in patients at long-term care facilities
Endocrine, Vol. 70, Núm. 2, pp. 348-355
2018
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Lipopolysaccharide (LPS)-induced septic shock causes profound changes in myocardial energy metabolites in pigs
Metabolomics, Vol. 14, Núm. 10
2010
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New insights into thyroglobulin pathophysiology revealed by the study of a family with congenital goiter
Journal of Clinical Endocrinology and Metabolism, Vol. 95, Núm. 7, pp. 3522-3526
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Reduced adipogenic gene expression in fibroblasts from a patient with type 2 congenital generalized lipodystrophy
Diabetic Medicine, Vol. 27, Núm. 10, pp. 1178-1187
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Thyroid hormone receptors are down-regulated in skeletal muscle of patients with non-thyroidal illness syndrome secondary to non-septic shock
European Journal of Endocrinology, Vol. 163, Núm. 5, pp. 765-773
2009
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Prevalence and functional analysis of the S107P polymorphism (rs6647476) of the monocarboxylate transporter 8 (SLC16A2) gene in the male population of north-west Spain (Galicia)
Clinical Endocrinology, Vol. 70, Núm. 4, pp. 636-643
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Site-dependent differences in both prelamin A and adipogenic genes in subcutaneous adipose tissue of patients with type 2 familial partial lipodystrophy
Journal of Medical Genetics, Vol. 46, Núm. 1, pp. 40-48
2008
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A novel phenotypic expression associated with a new mutation in LMNA gene, characterized by partial lipodystrophy, insulin resistance, aortic stenosis and hypertrophic cardiomyopathy
Clinical Endocrinology, Vol. 69, Núm. 1, pp. 61-68
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Identification of molecular mechanisms related to nonthyroidal illness syndrome in skeletal muscle and adipose tissue from patients with septic shock
Clinical Endocrinology, Vol. 68, Núm. 5, pp. 821-827
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Pendred syndrome in two Galician families: Insights into clinical phenotypes through cellular, genetic, and molecular studies
Journal of Clinical Endocrinology and Metabolism, Vol. 93, Núm. 1, pp. 267-277
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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
European Journal of Endocrinology, Vol. 159, Núm. 5, pp. 623-631
2003
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Síndrome de vena cava superior y carcinoma insular de tiroides: El stent como alternativa terapéutica paliativa
Anales de Medicina Interna, Vol. 20, Núm. 6, pp. 301-303