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Journal of Pediatric Endocrinology & Metabolism : JPEM
|
June 11, 2008
Thyroid function in 76 sick preterm infants 30-36 weeks: results from a longitudinal study
Antonio Carrascosa, Pilar Ruiz-Cuevas, María Clemente, et al.
Endocrinology, Diabetes & Metabolism Case Reports
|
May 2, 2017
Hyperinsulinaemic hypoglycaemia, renal Fanconi syndrome and liver disease due to a mutation in the <i>HNF4A</i> gene
María Clemente, Alejandro Vargas, Gema Ariceta, et al.
Diabetes Care
|
March 15, 2008
Glucose intolerance and diabetes are observed in the long-term follow-up of nonpancreatectomized patients with persistent hyperinsulinemic hypoglycemia of infancy due to mutations in the ABCC8 gene
Miquel Gussinyer, María Clemente, Rocio Cebrián, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 11, 2004
Areal bone mineral density of the lumbar spine in 80 premature newborns: a prospective and longitudinal study
Diego Yeste, Jordi Almar, María Clemente, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 22, 2009
Ezetimibe as monotherapy in the treatment of hypercholesterolemia in children and adolescents
Diego Yeste, Pilar Chacón, María Clemente, et al.
Anales De Pediatria
|
May 25, 2020
[Diagnostic accuracy of the tri-ponderal mass index in identifying the unhealthy metabolic obese phenotype in obese patients]
Diego Yeste, María Clemente, Ariadna Campos, et al.
Paediatric Drugs
|
November 7, 2025
Advances in Pharmacotherapy for Congenital Hyperinsulinism
Nuria González-Llorens, Daphne Yau, María Clemente León, et al.
Anales De Pediatria
|
February 14, 2025
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: clinical, biochemical and molecular characteristics and long-term outcomes
Elida Mercado Santis, Ariadna Campos, Paula Fernández, et al.
Frontiers in Endocrinology
|
July 15, 2022
A New <i>MAMLD1</i> Variant in an Infant With Microphallus and Hypospadias With Hormonal Pattern Suggesting Partial Hypogonadotropic Hypogonadism-Case Report
Diego Yeste, Cristina Aguilar-Riera, Gennaro Canestrino, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
September 30, 2011
Engineering cyclic amidases for non-natural amino acid synthesis
Francisco Javier Las Heras-Vázquez, Josefa María Clemente-Jiménez, Sergio Martínez-Rodríguez, et al.
Page
of 9
Search research articles
Search
Showing results (1-10 of 87) with videos related to
Sort By:
Page
of 9
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
June 11, 2008
Thyroid function in 76 sick preterm infants 30-36 weeks: results from a longitudinal study
Antonio Carrascosa, Pilar Ruiz-Cuevas, María Clemente, et al.
Endocrinology, Diabetes & Metabolism Case Reports
|
May 2, 2017
Hyperinsulinaemic hypoglycaemia, renal Fanconi syndrome and liver disease due to a mutation in the <i>HNF4A</i> gene
María Clemente, Alejandro Vargas, Gema Ariceta, et al.
Diabetes Care
|
March 15, 2008
Glucose intolerance and diabetes are observed in the long-term follow-up of nonpancreatectomized patients with persistent hyperinsulinemic hypoglycemia of infancy due to mutations in the ABCC8 gene
Miquel Gussinyer, María Clemente, Rocio Cebrián, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 11, 2004
Areal bone mineral density of the lumbar spine in 80 premature newborns: a prospective and longitudinal study
Diego Yeste, Jordi Almar, María Clemente, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 22, 2009
Ezetimibe as monotherapy in the treatment of hypercholesterolemia in children and adolescents
Diego Yeste, Pilar Chacón, María Clemente, et al.
Anales De Pediatria
|
May 25, 2020
[Diagnostic accuracy of the tri-ponderal mass index in identifying the unhealthy metabolic obese phenotype in obese patients]
Diego Yeste, María Clemente, Ariadna Campos, et al.
Paediatric Drugs
|
November 7, 2025
Advances in Pharmacotherapy for Congenital Hyperinsulinism
Nuria González-Llorens, Daphne Yau, María Clemente León, et al.
Anales De Pediatria
|
February 14, 2025
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: clinical, biochemical and molecular characteristics and long-term outcomes
Elida Mercado Santis, Ariadna Campos, Paula Fernández, et al.
Frontiers in Endocrinology
|
July 15, 2022
A New <i>MAMLD1</i> Variant in an Infant With Microphallus and Hypospadias With Hormonal Pattern Suggesting Partial Hypogonadotropic Hypogonadism-Case Report
Diego Yeste, Cristina Aguilar-Riera, Gennaro Canestrino, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
September 30, 2011
Engineering cyclic amidases for non-natural amino acid synthesis
Francisco Javier Las Heras-Vázquez, Josefa María Clemente-Jiménez, Sergio Martínez-Rodríguez, et al.
Page
of 9