J. Labarta

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Growth hormone does not alter CYP2A6 activity in growth hormone-deficient children.

B. Sinúes, A. Fanlo, E. Mayayo, 2007, Basic & clinical pharmacology & toxicology.

Content Analysis of Apps for Growth Monitoring and Growth Hormone Treatment: Systematic Search in the Android App Store

L. Fernández-Luque, E. Koledova, J. Labarta, 2020, JMIR mHealth and uHealth.

Novel (60%) and recurrent (40%) androgen receptor gene mutations in a series of 59 patients with a 46,XY disorder of sex development.

P. Lapunzina, M. Campo, J. Calaf, 2010, The Journal of clinical endocrinology and metabolism.

Growth and metabolic effects of long-term recombinant human growth hormone (rhGH) treatment in short children born small for gestational age: GH-RAST study

Antonio de Arriba, J. Labarta, Amparo Rodríguez, 2020, Journal of pediatric endocrinology & metabolism : JPEM.

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

I. Rica, J. López-Siguero, J. Labarta, 2012, European journal of endocrinology.

Study of apoptosis and related proteins, CRH and hpGH in placentas of newborns small for gestational age (SGA).

E. Mayayo, J. Labarta, M. Miramar, 2009, Pediatric endocrinology reviews : PER.

Insulin-like growth factor binding protein-I levels are strongly associated with insulin sensitivity and obesity in early pubertal children.

R. Eckel, R. Rosenfeld, B. Jeffers, 1998, The Journal of clinical endocrinology and metabolism.

Effects of growth hormone deficiency and rhGH replacement therapy on the 6β-hydroxycortisol/free cortisol ratio, a marker of CYP3A activity, in growth hormone-deficient children

M. L. Bernal, B. Sinúes, A. Fanlo, 2004, European Journal of Clinical Pharmacology.

Central precocious puberty in children living in Spain: incidence, prevalence, and influence of adoption and immigration.

J. Argente, L. Soriano-Guillén, R. Corripio, 2010, The Journal of clinical endocrinology and metabolism.

IGF-II and IGF-binding proteins increase dramatically during rabbit pregnancy.

N. Binder, R. Rosenfeld, S. Gargosky, 1996, The Journal of endocrinology.

Important Tools for Use by Pediatric Endocrinologists in the Assessment of Short Stature

M. Maghnie, J. Wit, M. Ranke, 2020, Journal of clinical research in pediatric endocrinology.

Evidence for insulin-like growth factor (IGF)-independent transcriptional regulation of IGF binding protein-3 by growth hormone in SKHEP-1 human hepatocarcinoma cells.

Z. Gucev, R. Rosenfeld, Y. Oh, 1997, Endocrinology.

Lack of effect of growth hormone replacement therapy on CYP1A2 and xanthine oxidase activities in growth hormone–deficient children

B. Sinúes, A. Fanlo, E. Mayayo, 2006, European Journal of Clinical Pharmacology.

Immunoblot studies of the acid‐labile subunit (ALS) in biological fluids, normal human serum and in children with GH deficiency and GH receptor deficiency before and after long‐term therapy with GH or IGF‐I respectively

J. Argente, J. Guevara-Aguirre, Phillip D. K. Lee, 1997, Clinical endocrinology.

Changes in Body Mass Index in Girls with Idiopathic Central Precocious Puberty under Gonadotropin-Releasing Hormone Analogue Therapy: The Spanish Registry

J. Argente, L. Soriano-Guillén, R. Corripio, 2016, Hormone Research in Paediatrics.

Identification of miRNAs Involved in Foetal Growth Restriction Due to Maternal Smoking during Pregnancy

A. Gascón-Catalán, J. Labarta, E. Barrio, 2022, Journal of clinical medicine.

Longitudinal Pubertal Growth According to Age at Pubertal Growth Spurt Onset: Data from a Spanish Study Including 458 Children (223 Boys and 235 Girls)

M. Fernández-Cancio, M. Clemente, M. Gussinyé, 2009, Journal of pediatric endocrinology & metabolism : JPEM.

Psychomotor and intellectual development (Neurocognitive Function) of children born small for gestational age (SGA). Transversal and longitudinal study.

Antonio de Arriba, J. Labarta, Á. F. Longás, 2009, Pediatric endocrinology reviews : PER.

Noonan syndrome: genetic and clinical update and treatment options

M. Ramón-Krauel, J. López-Siguero, A. Carcavilla, 2020, Anales de Pediatría (English Edition).

[Noonan syndrome: genetic and clinical update and treatment options].

M. Ramón-Krauel, I. Riaño Galán, J. López-Siguero, 2020, Anales de pediatria.

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

Miguel Ángel Martínez, N. Rahman, Pablo I Alarcón, 2019, European Journal of Human Genetics.

Novel Genetic and Biochemical Findings of DLK1 in Children with Central Precocious Puberty: A Brazilian-Spanish Study.

J. Argente, V. Barrios, A. Latronico, 2020, The Journal of clinical endocrinology and metabolism.

Short Stature Diagnosis and Referral

M. Maghnie, T. Rohrer, E. Koledova, 2018, Front. Endocrinol..

Recommendations for the diagnosis and treatment of classic forms of 21-hydroxylase-deficient congenital adrenal hyperplasia

B. Ezquieta, M. Clemente, J. Labarta, 2017 .

Recommendations for the diagnosis and treatment of classic forms of 21-hydroxylase-deficient congenital adrenal hyperplasia

B. Ezquieta, M. Clemente, J. Labarta, 2017 .

A Follow-up Study to Monitor Adult Height Among Spanish Children with Growth Hormone Deficiency Who Received Biosimilar Human Recombinant Growth Hormone (Omnitrope®) During a Phase III Clinical Trial

M. Ramón-Krauel, F. Rebollo, R. Corripio, 2015, Advances in Therapy.

Insulin-Like Growth Factors in Childhood-Onset Gaucher Disease

Á. Ferrández, M. Pocovi, P. Giraldo, 2002, Pediatric Research.

Physical Repercussions of Childhood-Onset Growth Hormone (GH) Deficiency and hGH Treatment in Adulthood

J. Casajús, Á. Ferrández Longás, J. Labarta, 2003, Journal of pediatric endocrinology & metabolism : JPEM.

Familial short stature and intrauterine growth retardation associated with a novel mutation in the IGF‐I receptor (IGF1R) gene

M. Fernández-Cancio, A. Carrascosa, L. Audí, 2013, Clinical endocrinology.

Metabolic syndrome and endothelial dysfunction in a population born small for gestational age relationship to growth and Gh therapy.

E. Mayayo, J. Labarta, Á. F. Longás, 2013, Pediatric Endocrinology Reviews: diabetes, nutrition, metabolism.

Monogenic and Polygenic Models Detected in Steroid 21-Hydroxylase Deficiency-Related Paediatric Hyperandrogenism

B. Ezquieta, F. Hermoso, M. Gallego, 2008, Hormone Research in Paediatrics.

Genotype-phenotype correlations in central precocious puberty caused by MKRN3 mutations.

J. Argente, U. Kaiser, A. Latronico, 2020, The Journal of clinical endocrinology and metabolism.

[Recommendations for the diagnosis and treatment of classic forms of 21-hydroxylase-deficient congenital adrenal hyperplasia].

B. Ezquieta, M. Clemente, J. Labarta, 2017, Anales de Pediatría.

Growth and growth hormone treatment in short stature children born small for gestational age.

E. Mayayo, J. Labarta, Á. F. Longás, 2009, Pediatric endocrinology reviews : PER.

Evaluating the Usefulness and Ease of Use of a Next-Generation–Connected Drug Delivery Device for Growth Hormone Therapy: Qualitative Study of Health Care Professionals’ Perceptions

E. Koledova, P. Dimitri, J. Labarta, 2023, JMIR human factors.

Growth hormone and treatment outcomes: expert review of current clinical practice.

M. Maghnie, V. Mericq, S. Norgren, 2011, Pediatric endocrinology reviews : PER.

Epigenetic modifications in the ferroptosis pathway in cord blood cells from newborns of smoking mothers and their influence on fetal growth.

J. Labarta, Diego Lerma-Puertas, Eva Barrio, 2024, Reproductive toxicology.