Publicacións nas que colabora con JOSE MANUEL CAMESELLE TEIJEIRO (23)

2023

  1. Should we suspect primary aldosteronism in patients with hypokalaemic rhabdomyolysis? A systematic review

    Frontiers in Endocrinology, Vol. 14

2022

  1. Adrenal Medullary Hyperplasia: An Under the Radar Cause of Endocrine Hypertension

    American Journal of the Medical Sciences, Vol. 363, Núm. 1, pp. 64-68

2021

  1. PD-L1 expression and immune cells in anaplastic carcinoma and poorly differentiated carcinoma of the human thyroid gland: A retrospective study

    Oncology Letters, Vol. 22, Núm. 1

  2. The Authors Reply PMC and PMT: Real Medicine and Not Just Biology

    American Journal of Surgical Pathology

2020

  1. Evaluation of 177Lu-Dotatate treatment in patients with metastatic neuroendocrine tumors and prognostic factors

    World Journal of Gastroenterology, Vol. 26, Núm. 13, pp. 1513-1524

  2. Thyroid papillary microtumor: Validation of the (updated) porto proposal assessing sex hormone receptor expression and mutational BRAF gene status

    American Journal of Surgical Pathology, Vol. 44, Núm. 9, pp. 1161-1172

2019

  1. Novel TMEM127 Variant Associated to Bilateral Phaeochromocytoma with an Uncommon Clinical Presentation

    Case Reports in Endocrinology, Vol. 2019

2013

  1. Adrenal carcinoma: A retrospective analysis of our series

    Endocrinologia y Nutricion

2011

  1. Utilidad del PET-FDG 18 en la búsqueda del síndrome de Cushing ectópico por carcinoide bronquial oculto

    Endocrinología y nutrición: órgano de la Sociedad Española de Endocrinología y Nutrición, Vol. 58, Núm. 9, pp. 497-499

  2. Utilidad del PET-FDG18 en la búsqueda del síndrome de Cushing ectópico por carcinoide bronquial oculto

    Endocrinologia y Nutricion

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. Primary thyroid tuberculosis

    Endocrinologia y Nutricion

2009

  1. Egfr expression correlates with maximum standardized uptake value of 18- fluorodeoxyglucose-pet in squamous cell lung Carcinoma

    Current Radiopharmaceuticals, Vol. 2, Núm. 3, pp. 175-176

  2. Pegvisomant-induced cholestatic hepatitis with jaundice in a patient with Gilbert's syndrome

    European Journal of Endocrinology, Vol. 160, Núm. 5, pp. 869-872

2008

  1. 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

  2. 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. Hypoploidy defines patients with poor prognosis in breast cancer

    Oncology Reports, Vol. 17, Núm. 5, pp. 1109-1114

2005

  1. Cell-cycle-associated markers and clinical outcome in human epithelial cancers: A tissue microarray study

    Oncology Reports, Vol. 14, Núm. 6, pp. 1527-1531

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