Publicacións nas que colabora con Lourdes Loidi (10)

2022

  1. Histopathological Features of Pendred Syndrome Thyroids Align with Differences in the Expression of Thyroid-Specific Markers, Apical Iodide Transporters, and Ciliogenesis Process

    Endocrine Pathology, Vol. 33, Núm. 4, pp. 484-493

2019

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

    Case Reports in Endocrinology, Vol. 2019

2017

  1. Autosomal recessive agammaglobulinemia due to defect in μ heavy chain caused by a novel mutation in the IGHM gene

    Genes and Immunity, Vol. 18, Núm. 3, pp. 197-199

2016

  1. A Calcitonin Non-producing Neuroendocrine Tumor of the Thyroid Gland

    Endocrine Pathology, Vol. 27, Núm. 4, pp. 325-331

2011

  1. CAMT in a female with developmental delay, facial malformations and central nervous system anomalies

    Pediatric Blood and Cancer, Vol. 56, Núm. 3, pp. 452-453

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

2001

  1. Somatic but not germline mutation of the APC gene in a case of cribriform-morular variant of papillary thyroid carcinoma

    American Journal of Clinical Pathology, Vol. 115, Núm. 4, pp. 486-493

2000

  1. Rapid real-time fluorescent PCR gene dosage test for the diagnosis of DNA duplications and deletions

    Clinical Chemistry, Vol. 46, Núm. 10, pp. 1574-1582

1998

  1. Progress in methodology and standards in European molecular genetics laboratories

    Clinica Chimica Acta

1993

  1. Tissue concentrations of prothymosin alpha: A novel proliferation index of primary breast cancer

    European Journal of Cancer, Vol. 29, Núm. 6, pp. 893-897