Jose C. Moreno
Majadahonda, MD 28220, Spain
Last Updated: 09/26/2026
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Found 23 publications
New Insights into Iodide Transport Defects (ITDs) from the Characterization of a Heterozygous NIS Missense Variant (p.G288S) Identified in a Family with Thyroid Dysfunction During Pregnancy.
Journal: International journal of molecular sciences
Published: March 24, 2026
International Registry of NKX2-1-Related Disorders: Clinical, Genetic, and Imaging Perspectives.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: September 03, 2025
Identification and determination of the urinary metabolite of iodotyrosine invivo.
Journal: Biochemical and biophysical research communications
Published: October 01, 2024
A Novel Missense Variant in the NKX2-1 Homeodomain Prevents Transcriptional Rescue by TAZ.
Journal: Thyroid : official journal of the American Thyroid Association
Published: May 17, 2024
Multimodal Mobile Robotic Dataset for a Typical Mediterranean Greenhouse: The GREENBOT Dataset.
Journal: Sensors (Basel, Switzerland)
Published: January 31, 2024
Assisted Robots in Therapies for Children with Autism in Early Childhood.
Journal: Sensors (Basel, Switzerland)
Published: December 31, 2023
Systematic review of thyroid function in NKX2-1-related disorders: Screening and diagnosis.
Journal: PloS one
Published: December 30, 2023
Iodotyrosines Are Biomarkers for Preclinical Stages of Iodine-Deficient Hypothyroidism in Dehal1-Knockout Mice.
Journal: Thyroid : official journal of the American Thyroid Association
Published: March 07, 2023
Identification of Resistance to Exogenous Thyroxine in Humans.
Journal: Thyroid : official journal of the American Thyroid Association
Published: June 06, 2020
Central Hypothyroidism and Novel Clinical Phenotypes in Hemizygous Truncation of TBL1X.
Journal: Journal of the Endocrine Society
Published: May 12, 2018
Transient PAX8 Expression in Islets During Pregnancy Correlates With β-Cell Survival, Revealing a Novel Candidate Gene in Gestational Diabetes Mellitus.
Journal: Diabetes
Published: March 08, 2018
The Brain-Lung-Thyroid syndrome (BLTS): A novel deletion in chromosome 14q13.2-q21.1 expands the phenotype to humoral immunodeficiency.
Journal: European journal of medical genetics
Published: October 10, 2017
Last Updated: 09/26/2026