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25(OH)Vitamin D Deficiency and Calcifediol Treatment in Pediatrics

Nutrients, 2022-04, Vol.14 (9), p.1854

2022

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Changing trends in transgender demographics and morbidity: baseline data from a Spanish cohort

Sexual health, 2023-02, Vol.20 (1), p.96-98

2023

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Fatty Acid Profile of Mature Red Blood Cell Membranes and Dietary Intake as a New Approach to Characterize Children with Overweight and Obesity

Nutrients, 2020-11, Vol.12 (11), p.3446

2020

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Is Polymerase Chain Reaction in Neonatal Dried Blood Spots Reliable for the Diagnosis of Congenital Cytomegalovirus Infection?

The Pediatric infectious disease journal, 2019-05, Vol.38 (5), p.520-524

2019

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Genetic profile of a large Spanish cohort with hypercalcemia

Frontiers in endocrinology (Lausanne), 2024, Vol.15, p.1297614-1297614

2024

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Molecular Differences Based on Erythrocyte Fatty Acid Profile to Personalize Dietary Strategies between Adults and Children with Obesity

Metabolites, 2021-01, Vol.11 (1), p.43

2021

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Recomendaciones para el diagnóstico y seguimiento del feto y del recién nacido hijo de madre con patología tiroidea autoinmune

Anales de pediatría (Barcelona, Spain : 2003), 2018-10, Vol.89 (4), p.254.e1-254.e7

2018

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Genetic reanalysis of patients with a difference of sex development carrying the NR5A1/SF-1 variant p.Gly146Ala has discovered other likely disease-causing variations

PloS one, 2023-07, Vol.18 (7), p.e0287515-e0287515

2023

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Urinary iodine and thyroid function in a population of healthy pregnant women in the North of Spain

Journal of trace elements in medicine and biology, 2013-10, Vol.27 (4), p.302-306

2013

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Negative autoimmunity in a Spanish pediatric cohort suspected of type 1 diabetes, could it be monogenic diabetes?

PloS one, 2019-07, Vol.14 (7), p.e0220634-e0220634

2019

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Potential of Erythrocyte Membrane Lipid Profile as a Novel Inflammatory Biomarker to Distinguish Metabolically Healthy Obesity in Children

Journal of personalized medicine, 2021-04, Vol.11 (5), p.337

2021

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Reiterative infusions of MSCs improve pediatric osteogenesis imperfecta eliciting a pro‐osteogenic paracrine response: TERCELOI clinical trial

Clinical and translational medicine, 2021-01, Vol.11 (1), p.e265-n/a

2021

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Utilidad diagnóstica de la detección de ácidos nucleicos mediante la reacción en cadena de la polimerasa realizada en tiempo real

Enfermedades infecciosas y microbiología clínica, 2006, Vol.24 (9), p.539-540

2006

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Normal intellectual development in children born from women with hypothyroxinemia during their pregnancy

Journal of trace elements in medicine and biology, 2015-07, Vol.31, p.18-24

2015

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Glucocorticoid resistance syndrome caused by two novel mutations in the NR3C1 gene

Endocrinologia y nutricion, 2016-08, Vol.63 (7), p.369-371

2016

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Clinical and molecular characterization of five Spanish kindreds with X-linked adrenal hypoplasia congenita: atypical findings and a novel mutation in NR0B1

Journal of Pediatric Endocrinology and Metabolism, 2015-09, Vol.28 (9-10), p.1129

2015

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Absence of diabetes mellitus type 2 in obese children and adolescents in the north of Spain

Journal of Pediatric Endocrinology and Metabolism, 2013, Vol.26 (1-2), p.25-29

2013

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Recommendations for the diagnosis and followup of the foetus and newborn child born to mothers with autoimmune thyroid disease

Anales de Pediatría, 2018-10, Vol.89 (4), p.254.e1-254.e7

2018

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Diagnostic utility of nucleic acid detection by real-time polymerase chain reaction

Enfermedades infecciosas y microbiología clínica, 2006-11, Vol.24 (9), p.539-540

2006

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Recommendations for the diagnosis and follow up of the foetus and newborn child born to mothers with autoimmune thyroid disease

Anales de Pediatría, 2018-10, Vol.89 (4), p.254.e1-254.e7

2018

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Demographic trends and morbidity in the basque country transgender population (2009-2020)

Endocrine Abstracts, 2022-05

2022

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Recommendations for the diagnosis and followup of the foetus and newborn child born to mothers with autoimmune thyroid disease

Anales de Pediatría, 2018-10, Vol.89 (4), p.254.e1-254.e7

2018

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Glucocorticoid resistance syndrome caused by two novel mutations in the NR3C1 gene

Endocrinologia y nutrición (English ed.), 2016-08, Vol.63 (7), p.369-371

2016

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25(OH)Vitamin D Deficiency and Calcifediol Treatment in Pediatrics

Changing trends in transgender demographics and morbidity: baseline data from a Spanish cohort

Fatty Acid Profile of Mature Red Blood Cell Membranes and Dietary Intake as a New Approach to Characterize Children with Overweight and Obesity

Is Polymerase Chain Reaction in Neonatal Dried Blood Spots Reliable for the Diagnosis of Congenital Cytomegalovirus Infection?

Genetic profile of a large Spanish cohort with hypercalcemia

Molecular Differences Based on Erythrocyte Fatty Acid Profile to Personalize Dietary Strategies between Adults and Children with Obesity

Recomendaciones para el diagnóstico y seguimiento del feto y del recién nacido hijo de madre con patología tiroidea autoinmune

Genetic reanalysis of patients with a difference of sex development carrying the NR5A1/SF-1 variant p.Gly146Ala has discovered other likely disease-causing variations

Urinary iodine and thyroid function in a population of healthy pregnant women in the North of Spain

Negative autoimmunity in a Spanish pediatric cohort suspected of type 1 diabetes, could it be monogenic diabetes?

Potential of Erythrocyte Membrane Lipid Profile as a Novel Inflammatory Biomarker to Distinguish Metabolically Healthy Obesity in Children

Reiterative infusions of MSCs improve pediatric osteogenesis imperfecta eliciting a pro‐osteogenic paracrine response: TERCELOI clinical trial

Utilidad diagnóstica de la detección de ácidos nucleicos mediante la reacción en cadena de la polimerasa realizada en tiempo real

Normal intellectual development in children born from women with hypothyroxinemia during their pregnancy

Glucocorticoid resistance syndrome caused by two novel mutations in the NR3C1 gene

Clinical and molecular characterization of five Spanish kindreds with X-linked adrenal hypoplasia congenita: atypical findings and a novel mutation in NR0B1

Absence of diabetes mellitus type 2 in obese children and adolescents in the north of Spain

Recommendations for the diagnosis and followup of the foetus and newborn child born to mothers with autoimmune thyroid disease

Diagnostic utility of nucleic acid detection by real-time polymerase chain reaction

Adaptation, reliability and validity of health-related quality of life questionnaires: Disabkids chronic and specific diabetes disease in children and adolescents with diabetes mellitus type 1

Adaptación, fiabilidad y validez de los cuestionarios de calidad de vida relacionada con la salud: DISABKIDS, enfermedad crónica y específico de diabetes, en niños y adolescentes con diabetes mellitus tipo 1

Recommendations for the diagnosis and follow up of the foetus and newborn child born to mothers with autoimmune thyroid disease

Demographic trends and morbidity in the basque country transgender population (2009-2020)

Recommendations for the diagnosis and followup of the foetus and newborn child born to mothers with autoimmune thyroid disease

Glucocorticoid resistance syndrome caused by two novel mutations in the NR3C1 gene

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