Lourdes Loidi

Santiago De Compostela, GA, Spain

Last Updated: 09/26/2026

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Found 22 publications

Adrenal mixed corticomedullary tumors: report of a case with molecular characterization and systematic review.

Adrenal mixed corticomedullary tumors: report of a case with molecular characterization and systematic review.

Journal: Virchows Archiv : an international journal of pathology

Published: January 21, 2025

New Insights into the Clinical Characterization of SDHAF2-related Familial Paraganglioma Syndrome.

New Insights into the Clinical Characterization of SDHAF2-related Familial Paraganglioma Syndrome.

Journal: The Journal of clinical endocrinology and metabolism

Published: September 24, 2024

A cohort analysis of familial partial lipodystrophy from two Mediterranean countries.

A cohort analysis of familial partial lipodystrophy from two Mediterranean countries.

Journal: Diabetes, obesity & metabolism

Published: May 10, 2024

Bilateral Uveal Melanoma: An Insight into Genetic Predisposition in Four New Unrelated Patients and Review of Published Cases.

Bilateral Uveal Melanoma: An Insight into Genetic Predisposition in Four New Unrelated Patients and Review of Published Cases.

Journal: Journal of clinical medicine

Published: April 15, 2024

Granulomatous rosacea: a clue to the diagnosis of STAT1 gain of function in a child with immunodeficiency.

Granulomatous rosacea: a clue to the diagnosis of STAT1 gain of function in a child with immunodeficiency.

Journal: Clinical and experimental dermatology

Published: October 31, 2023

Natural history and comorbidities of generalised and partial lipodystrophy syndromes in Spain.

Natural history and comorbidities of generalised and partial lipodystrophy syndromes in Spain.

Journal: Frontiers in endocrinology

Published: June 29, 2023

Yao syndrome: a clinical observation of a non-paradigmatic autoinflammatory disease.

Yao syndrome: a clinical observation of a non-paradigmatic autoinflammatory disease.

Journal: Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG

Published: June 11, 2023

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

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

Journal: Endocrine pathology

Published: October 06, 2022

GNAQ and GNA11 Genes: A Comprehensive Review on Oncogenesis, Prognosis and Therapeutic Opportunities in Uveal Melanoma.

GNAQ and GNA11 Genes: A Comprehensive Review on Oncogenesis, Prognosis and Therapeutic Opportunities in Uveal Melanoma.

Journal: Cancers

Published: May 17, 2022

Two cases of familial glomuvenous malformation and description of a novel pathogenic mutation in glomulin gene (GLMN).

Two cases of familial glomuvenous malformation and description of a novel pathogenic mutation in glomulin gene (GLMN).

Journal: International journal of dermatology

Published: October 25, 2021

Variable Expressivity and Allelic Heterogeneity in Type 2 Familial Partial Lipodystrophy: The p.(Thr528Met) LMNA Variant.

Variable Expressivity and Allelic Heterogeneity in Type 2 Familial Partial Lipodystrophy: The p.(Thr528Met) LMNA Variant.

Journal: Journal of clinical medicine

Published: January 30, 2021

Role of somatic mutations and chromosomal aberrations in the prognosis of uveal melanoma in a Spanish patient cohort.

Role of somatic mutations and chromosomal aberrations in the prognosis of uveal melanoma in a Spanish patient cohort.

Journal: Acta ophthalmologica

Published: August 10, 2020

Showing 1-12 of 22

Last Updated: 09/26/2026