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Growth hormone treatment does not to lead to insulin resistance nor excessive rise in IGF‐1 levels, while improving height in patients small for gestational age A long‐term observational study

Clinical endocrinology (Oxford), 2022-04, Vol.96 (4), p.558-568

2022

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Individualised vs fixed dose of oral 17β-oestradiol for induction of puberty in girls with Turner syndrome: an open-randomised parallel trial

European journal of endocrinology, 2012-10, Vol.167 (4), p.523-529

2012

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Early Nutritional Education in the Prevention of Childhood Obesity

International journal of environmental research and public health, 2021-06, Vol.18 (12), p.6569

2021

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Carrier detection and prenatal diagnosis of congenital adrenal hyperplasia must identify 'apparently mild' CYP21A2 alleles which associate neonatal salt-wasting disease

Prenatal diagnosis, 2010-08, Vol.30 (8), p.758-763

2010

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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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The DATAC study: a new growth database. Description of the epidemiology, diagnosis and therapeutic attitude in a group of Spanish children with short stature

Journal of Pediatric Endocrinology and Metabolism, 2014-11, Vol.27 (11-12), p.1201

2014

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Increased incidence of type 1 diabetes in the south of Spain

Diabetes care, 2002-06, Vol.25 (6), p.1099-1099

2002

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Predicted Benign and Synonymous Variants in CYP11A1 Cause Primary Adrenal Insufficiency Through Missplicing

Journal of the Endocrine Society, 2019-01, Vol.3 (1), p.201-221

2019

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Aldosterone synthase deficiency type I: hormonal and genetic analyses of two cases

Hormone research, 1999-01, Vol.52 (6), p.298-300

1999

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Adipose tissue characteristics related to weight z-score in childhood

International journal of endocrinology and metabolism, 2013, Vol.11 (2), p.82-87

2013

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Transient congenital hypoparathyroidism and 22q11 deletion

Journal of Pediatric Endocrinology and Metabolism, 2000-06, Vol.13 (6), p.659

2000

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Neonatal Hyperthyroidism m Infants of Mothers Previously Thyroidectomized due to Graves’ Disease

Journal of Pediatric Endocrinology and Metabolism, 2001-09, Vol.14 (8), p.1169-1172

2001

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Estudio transversal español de crecimiento 2008. Parte II: valores de talla, peso e índice de masa corporal desde el nacimiento a la talla adulta

Anales de pediatría (Barcelona, Spain : 2003), 2008-06, Vol.68 (6), p.552-569

2008

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Propuesta de pauta en el cribado neonatal de hipotiroidismo congénito en grandes prematuros

Anales de pediatría (Barcelona, Spain : 2003), 2020, Vol.92 (1), p.46-47

2020

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Ten years' clinical experience with biosimilar human growth hormone: a review of efficacy data

Drug design, development and therapy, 2017-01, Vol.11, p.1489-1495

2017

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Monitorización del tratamiento del hipogonadismo hipogonadotropo en el lactante

Anales de pediatría (Barcelona, Spain : 2003), 2019-03, Vol.90 (3), p.190-192

2019

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Riesgos metabólicos del consumo excesivo de bebidas con azúcares refinados

Nutrición hospitalaria : organo oficial de la Sociedad Española de Nutrición Parenteral y Enteral, 2016, Vol.33 (2)

López Siguero, Juan Pedro

2016

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Further delineation of neuropsychiatric findings in Tatton-Brown-Rahman syndrome due to disease-causing variants in DNMT3A: seven new patients

European journal of human genetics : EJHG, 2020-04, Vol.28 (4), p.469-479

2020

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Obesidad asociada al receptor 4 de la melanocortina: diferente expresión fenotípica en la misma familia

Anales de pediatría (Barcelona, Spain : 2003), 2016-11, Vol.85 (5), p.279-280

2016

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Evidence for Genetic Heterogeneity of Pseudohypoaldosteronism Type 1: Identification of a Novel Mutation in the Human Mineralocorticoid Receptor in one Sporadic Case and No Mutations in Two Autosomal Dominant Kindreds

The journal of clinical endocrinology and metabolism, 2001-05, Vol.86 (5), p.2056-2059

2001

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A Novel Dysfunctional Growth Hormone Variant (Ile179Met) Exhibits a Decreased Ability to Activate the Extracellular Signal-Regulated Kinase Pathway

The journal of clinical endocrinology and metabolism, 2004-03, Vol.89 (3), p.1068-1075

2004

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Mutación del gen INSR. Insulinorresistencia poco prevalente en edad pediátrica. A propósito de un caso

Endocrinología, diabetes y nutrición, 2019, Vol.66 (9), p.588-589

2019

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Insulina aspart en población pediátrica

Avances en diabetología, 2012-06, Vol.28, p.22-26

2012

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Mutación en el gen SOS1 como nueva causa de síndrome de Noonan

Anales de pediatría (Barcelona, Spain : 2003), 2008-04, Vol.68 (4), p.365-368

2008

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Growth hormone treatment does not to lead to insulin resistance nor excessive rise in IGF‐1 levels, while improving height in patients small for gestational age A long‐term observational study

Individualised vs fixed dose of oral 17β-oestradiol for induction of puberty in girls with Turner syndrome: an open-randomised parallel trial

Early Nutritional Education in the Prevention of Childhood Obesity

Carrier detection and prenatal diagnosis of congenital adrenal hyperplasia must identify 'apparently mild' CYP21A2 alleles which associate neonatal salt-wasting disease

Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy

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

The DATAC study: a new growth database. Description of the epidemiology, diagnosis and therapeutic attitude in a group of Spanish children with short stature

Increased incidence of type 1 diabetes in the south of Spain

Predicted Benign and Synonymous Variants in CYP11A1 Cause Primary Adrenal Insufficiency Through Missplicing

Aldosterone synthase deficiency type I: hormonal and genetic analyses of two cases

Adipose tissue characteristics related to weight z-score in childhood

Transient congenital hypoparathyroidism and 22q11 deletion

Neonatal Hyperthyroidism m Infants of Mothers Previously Thyroidectomized due to Graves’ Disease

Estudio transversal español de crecimiento 2008. Parte II: valores de talla, peso e índice de masa corporal desde el nacimiento a la talla adulta

Propuesta de pauta en el cribado neonatal de hipotiroidismo congénito en grandes prematuros

Ten years' clinical experience with biosimilar human growth hormone: a review of efficacy data

Monitorización del tratamiento del hipogonadismo hipogonadotropo en el lactante

Riesgos metabólicos del consumo excesivo de bebidas con azúcares refinados

Further delineation of neuropsychiatric findings in Tatton-Brown-Rahman syndrome due to disease-causing variants in DNMT3A: seven new patients

Obesidad asociada al receptor 4 de la melanocortina: diferente expresión fenotípica en la misma familia

Evidence for Genetic Heterogeneity of Pseudohypoaldosteronism Type 1: Identification of a Novel Mutation in the Human Mineralocorticoid Receptor in one Sporadic Case and No Mutations in Two Autosomal Dominant Kindreds

A Novel Dysfunctional Growth Hormone Variant (Ile179Met) Exhibits a Decreased Ability to Activate the Extracellular Signal-Regulated Kinase Pathway

Mutación del gen INSR. Insulinorresistencia poco prevalente en edad pediátrica. A propósito de un caso

Insulina aspart en población pediátrica

Mutación en el gen SOS1 como nueva causa de síndrome de Noonan

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