Publicaciones (126) Publicaciones de María Clemente Linuesa

2024

  1. Clinical and molecular study of patients with thyroid dyshormogenesis and variants in the thyroglobulin gene

    Frontiers in Endocrinology, Vol. 15

  2. Genetic and Functional Studies of Patients with Thyroid Dyshormonogenesis and Defects in the TSH Receptor (TSHR)

    International Journal of Molecular Sciences, Vol. 25, Núm. 18

  3. Patients with Thyroid Dyshormonogenesis and DUOX2 Variants: Molecular and Clinical Description and Genotype–Phenotype Correlation

    International Journal of Molecular Sciences, Vol. 25, Núm. 15

  4. Phase 3 Trial of Crinecerfont in Pediatric Congenital Adrenal Hyperplasia

    New England Journal of Medicine, Vol. 391, Núm. 6, pp. 493-503

2023

  1. Curriculum Materials in Initial Literacy: An Instrumental Approach in Spain

    Didactics in a Changing World, pp. 83-102

  2. Genetics and Natural History of Non-pancreatectomized Patients With Congenital Hyperinsulinism Due to Variants in ABCC8

    The Journal of clinical endocrinology and metabolism, Vol. 108, Núm. 11, pp. e1316-e1328

  3. Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia: a retrospective multicenter cohort study

    European journal of endocrinology, Vol. 189, Núm. 4, pp. 460-468

  4. Paciente con insuficiencia suprarrenal por mutación de novo en el gen NR0B1

    Advances in Laboratory Medicine, Vol. 4, Núm. 2, pp. 199-202

  5. Patient with adrenal insufficiency due to a de novo mutation in the NR0B1 gene

    Advances in Laboratory Medicine, Vol. 4, Núm. 2, pp. 195-198

  6. Physical activity patterns in type 1 diabetes in Spain: The SED1 study

    BMC Sports Science, Medicine and Rehabilitation, Vol. 15, Núm. 1

  7. Prolyl Endopeptidase-like Deficiency Associated with Growth Hormone Deficiency

    Journal of clinical research in pediatric endocrinology, Vol. 15, Núm. 2, pp. 205-209

2022

  1. A New MAMLD1 Variant in an Infant With Microphallus and Hypospadias With Hormonal Pattern Suggesting Partial Hypogonadotropic Hypogonadism—Case Report

    Frontiers in Endocrinology, Vol. 13

  2. A retrospective analysis of endocrine disease in sphingosine-1-phosphate lyase insufficiency: case series and literature review

    Endocrine Connections, Vol. 11, Núm. 8

  3. Amistad y compañerismo

    Liber Amicorum: Homenaje al Profesor José María Hernández Díaz (Ediciones Universidad de Salamanca), pp. 89-92

  4. Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry

    Clinical Endocrinology, Vol. 97, Núm. 5, pp. 551-561

  5. Increased Presentation of Diabetic Ketoacidosis and Changes in Age and Month of Type 1 Diabetes at Onset during the COVID-19 Pandemic in Spain

    Journal of Clinical Medicine, Vol. 11, Núm. 15

  6. Intralymphatic GAD-Alum (Diamyd®) Improves Glycemic Control in Type 1 Diabetes With HLA DR3-DQ2

    Journal of Clinical Endocrinology and Metabolism, Vol. 107, Núm. 9, pp. 2644-2651

  7. Novel variant in HHAT as a cause of different sex development with partial gonadal dysgenesis associated with microcephaly, eye defects, and distal phalangeal hypoplasia of both thumbs: Case report

    Frontiers in Endocrinology, Vol. 13

  8. Otras historias de la innovación

    Márgenes: Revista de Educación de la Universidad de Málaga, Vol. 3, Núm. 3, pp. 230-235

  9. Thyroid function in < 32 weeks gestation preterm infants

    Anales de Pediatria, Vol. 96, Núm. 2, pp. 130-137