
MARÍA
CLEMENTE LINUESA
Researcher in the period 1983-2020
Publications (119)
2023
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Curriculum Materials in Initial Literacy: An Instrumental Approach in Spain
Didactics in a Changing World, pp. 83-102
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Paciente con insuficiencia suprarrenal por mutación de novo en el gen NR0B1
Advances in Laboratory Medicine
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Patient with adrenal insufficiency due to a de novo mutation in the NR0B1 gene
Advances in Laboratory Medicine
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Physical activity patterns in type 1 diabetes in Spain: The SED1 study
BMC Sports Science, Medicine and Rehabilitation, Vol. 15, Núm. 1
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Prolyl Endopeptidase-like Deficiency Associated with Growth Hormone Deficiency
Journal of clinical research in pediatric endocrinology, Vol. 15, Núm. 2, pp. 205-209
2022
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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
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A retrospective analysis of endocrine disease in sphingosine-1-phosphate lyase insufficiency: case series and literature review
Endocrine Connections, Vol. 11, Núm. 8
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Amistad y compañerismo
Liber Amicorum: Homenaje al Profesor José María Hernández Díaz (Ediciones Universidad de Salamanca), pp. 89-92
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Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry
Clinical Endocrinology, Vol. 97, Núm. 5, pp. 551-561
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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
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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
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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
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Otras historias de la innovación
Márgenes: Revista de Educación de la Universidad de Málaga, Vol. 3, Núm. 3, pp. 230-235
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Thyroid function in < 32 weeks gestation preterm infants
Anales de Pediatria, Vol. 96, Núm. 2, pp. 130-137
2021
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Diagnostic accuracy of the tri-ponderal mass index in identifying the unhealthy metabolic obese phenotype in obese patients
Anales de Pediatria, Vol. 94, Núm. 2, pp. 68-74
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Growth hormone treatment and papilledema: A prospective pilot study
JCRPE Journal of Clinical Research in Pediatric Endocrinology, Vol. 13, Núm. 2, pp. 146-151
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Leer en familia: tertulias digitales en un programa de fomento de la lectura en la biblioteca
Ocnos: revista de estudios sobre lectura, Vol. 20, Núm. 1, pp. 23-37
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Myocardial Geometry and Dysfunction in Morbidly Obese Adolescents (BMI 35–40 kg/m2)
American Journal of Cardiology, Vol. 157, pp. 128-134
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Phenotypic Variability of Patients With PAX8 Variants Presenting With Congenital Hypothyroidism and Eutopic Thyroid
The Journal of clinical endocrinology and metabolism, Vol. 106, Núm. 1, pp. e152-e170
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Seventy eight children born small for gestational age without catch-up growth treated with growth hormone from the prepubertal stage until adult height age. An evaluation of puberty and changes in the metabolic profile
Endocrinologia, Diabetes y Nutricion, Vol. 68, Núm. 9, pp. 612-620