Publicaciones en las que colabora con José Joaquín Lado Abeal (20)

2020

  1. Effect of chemoradiation on the size of the thyroid gland

    Baylor University Medical Center Proceedings, pp. 1-5

  2. High prevalence of non-thyroidal illness syndrome in patients at long-term care facilities

    Endocrine, Vol. 70, Núm. 2, pp. 348-355

2016

  1. An uncommon association of familial partial lipodystrophy, dilated cardiomyopathy, and conduction system disease

    Journal of Investigative Medicine High Impact Case Reports, Vol. 4, Núm. 3

2011

  1. Estudio clínico y molecular de cinco familias con resistencia a la acción de las hormonas tiroideas

    Medicina Clinica, Vol. 137, Núm. 12, pp. 551-554

2010

  1. Identification of a paired box gene 8-peroxisome proliferator-activated receptor gamma (PAX8-PPARγ) rearrangement mosaicism in a patient with an autonomous functioning follicular thyroid carcinoma bearing an activating mutation in the TSH receptor

    Endocrine-Related Cancer, Vol. 17, Núm. 3, pp. 599-610

  2. 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

  3. Reduced adipogenic gene expression in fibroblasts from a patient with type 2 congenital generalized lipodystrophy

    Diabetic Medicine, Vol. 27, Núm. 10, pp. 1178-1187

  4. Regional decrease of subcutaneous adipose tissue in patients with type 2 familial partial lipodystrophy is associated with changes in thyroid hormone metabolism

    Thyroid, Vol. 20, Núm. 4, pp. 419-424

2009

  1. 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

  2. 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

  1. 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

  2. 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

  3. 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

2007

  1. Hyperglycaemic hyperosmolar nonketotic state as a cause of low gonadotrophin levels in postmenopausal diabetic women: A role for severe hypernatraemia

    Journal of Neuroendocrinology, Vol. 19, Núm. 12, pp. 983-987

  2. Pseudomalabsorción de levotiroxina

    Anales de Medicina Interna

2003

  1. 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

  2. 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

1999

  1. Tiroiditis aguda supurada por Streptococcus intermedius.

    Anales de medicina interna (Madrid, Spain : 1984)

1997

  1. L-hydroxytryptophan amplifies pulsatile secretion of LH in the follicular phase of normal women

    Clinical Endocrinology, Vol. 47, Núm. 5, pp. 555-563

1988

  1. Características del dolor en el infarto agudo de miocardio del diabético. Importancia de la neuropatía autonómica cardiovascular.

    Revista clinica espanola, Vol. 183, Núm. 6, pp. 296-299