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Elbow MR imaging findings in patients with synovial fringe syndrome

Skeletal radiology, 2013-05, Vol.42 (5), p.675-680

2013

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Safety and efficacy of growth hormone treatment: GeNeSIS study in Spain

Anales de pediatría (Barcelona, Spain : 2003), 2016-03, Vol.84 (3), p.139-147

2016

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Gene duplications in 21-hydroxylase deficiency: the importance of accurate molecular diagnosis in carrier detection and prenatal diagnosis

Prenatal diagnosis, 2006-12, Vol.26 (12), p.1172-1178

2006

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Monogenic and polygenic models detected in steroid 21-hydroxylase deficiency-related paediatric hyperandrogenism

Hormone research, 2009-01, Vol.71 (1), p.28-37

2009

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The majority of cases of neonatal diabetes in Spain can be explained by known genetic abnormalities

Diabetic medicine, 2007-07, Vol.24 (7), p.707-713

2007

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Risk for progression to type 1 diabetes in first-degree relatives under 50 years of age

Frontiers in endocrinology (Lausanne), 2024-08, Vol.15, p.1411686

2024

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Seguridad y efectividad del tratamiento con hormona de crecimiento: estudio GeNeSIS en España

Anales de pediatría (Barcelona, Spain : 2003), 2016-03, Vol.84 (3), p.139-147

2016

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Thyroid hormone resistance from newborns to adults: a Spanish experience

Journal of endocrinological investigation, 2019-08, Vol.42 (8), p.941-949

2019

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Ketoacidosis at onset of type 1 diabetes mellitus in pediatric age in Spain and review of the literature

Pediatric endocrinology reviews : PER, 2012-03, Vol.9 (3), p.669

2012

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Clinical and genetic characterization of congenital hyperinsulinism in Spain

European journal of endocrinology, 2016-06, Vol.174 (6), p.717

2016

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Endocrine Profile and Phenotype-(Epi)Genotype Correlation in Spanish Patients with Pseudohypoparathyroidism

The journal of clinical endocrinology and metabolism, 2013-05, Vol.98 (5), p.E996-E1006

2013

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Gsα activity is reduced in erythrocyte membranes of patients with psedohypoparathyroidism due to epigenetic alterations at the GNAS locus

Journal of bone and mineral research, 2011-08, Vol.26 (8), p.1864-1870

2011

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New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidism

European journal of endocrinology, 2010-12, Vol.163 (6), p.953

2010

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Detection of Hypomethylation Syndrome among Patients with Epigenetic Alterations at the GNAS Locus

The journal of clinical endocrinology and metabolism, 2012-06, Vol.97 (6), p.E1060-E1067

2012

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Effectiveness and Safety of rhIGF-1 Therapy in Children: The European Increlex® Growth Forum Database Experience

Hormone research in paediatrics, 2015-01, Vol.83 (5), p.345-357

2015

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Mutations in GCK and HNF-1α explain the majority of cases with clinical diagnosis of MODY in Spain

Clinical endocrinology (Oxford), 2007-10, Vol.67 (4), p.538-546

2007

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Neonatal salt-wasting and 11 β-hydroxylase deficiency in a child carrying a homozygous deletion hybrid CYP11B2 (aldosterone synthase)-CYP11B1 (11 β-hydroxylase)

Clinical genetics, 2004-09, Vol.66 (3), p.229-235

2004

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Estado actual y recomendaciones sobre la utilización de los sistemas de monitorización continua de glucosa en niños y adolescentes con diabetes mellitus tipo 1

Anales de pediatría (Barcelona, Spain : 2003), 2011-08, Vol.75 (2), p.134.e1-134.e6

2011

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Documento de consenso sobre tratamiento con infusión subcutánea continua de insulina de la diabetes tipo 1 en la edad pediátrica

Anales de pediatría (Barcelona, Spain : 2003), 2010, Vol.72 (5), p.352.e1-352.e4

2010

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Haploinsufficiency at GCK gene is not a frequent event in MODY2 patients

Clinical endocrinology (Oxford), 2008-06, Vol.68 (6), p.873-878

2008

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The exon 3-deleted/full-length Growth Hormone Receptor Polymorphism Does Not Influence the Effect of Puberty or Growth Hormone Therapy on Glucose Homeostasis in Short Non-Growth Hormone-Deficient Small-for-Gestational-Age Children: Results from a Two-Year Controlled Prospective Study

The journal of clinical endocrinology and metabolism, 2008-07, Vol.93 (7), p.2709-2715

2008

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Heterozygous glucokinase mutations and birth weight in Spanish children

Diabetic medicine, 2010-05, Vol.27 (5), p.608-610

2010

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Panhypopituitarism: genetic versus acquired etiological factors

Journal of pediatric endocrinology & metabolism : JPEM, 2007-01, Vol.20 (1), p.27

2007

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Mutations in MAFA and IAPP are not a common cause of monogenic diabetes

Diabetic medicine, 2009-07, Vol.26 (7), p.746-748

2009

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CLASSIFICATION AND PRODUCTIVITY OF SIX COSTA RICAN ANDEPTS

Soil science, 1989-05, Vol.147 (5), p.326-338

1989

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Elbow MR imaging findings in patients with synovial fringe syndrome

Safety and efficacy of growth hormone treatment: GeNeSIS study in Spain

Gene duplications in 21-hydroxylase deficiency: the importance of accurate molecular diagnosis in carrier detection and prenatal diagnosis

Monogenic and polygenic models detected in steroid 21-hydroxylase deficiency-related paediatric hyperandrogenism

The majority of cases of neonatal diabetes in Spain can be explained by known genetic abnormalities

Risk for progression to type 1 diabetes in first-degree relatives under 50 years of age

Seguridad y efectividad del tratamiento con hormona de crecimiento: estudio GeNeSIS en España

Thyroid hormone resistance from newborns to adults: a Spanish experience

Ketoacidosis at onset of type 1 diabetes mellitus in pediatric age in Spain and review of the literature

Clinical and genetic characterization of congenital hyperinsulinism in Spain

Endocrine Profile and Phenotype-(Epi)Genotype Correlation in Spanish Patients with Pseudohypoparathyroidism

Gsα activity is reduced in erythrocyte membranes of patients with psedohypoparathyroidism due to epigenetic alterations at the GNAS locus

New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidism

Detection of Hypomethylation Syndrome among Patients with Epigenetic Alterations at the GNAS Locus

Effectiveness and Safety of rhIGF-1 Therapy in Children: The European Increlex® Growth Forum Database Experience

Mutations in GCK and HNF-1α explain the majority of cases with clinical diagnosis of MODY in Spain

Neonatal salt-wasting and 11 β-hydroxylase deficiency in a child carrying a homozygous deletion hybrid CYP11B2 (aldosterone synthase)-CYP11B1 (11 β-hydroxylase)

Estado actual y recomendaciones sobre la utilización de los sistemas de monitorización continua de glucosa en niños y adolescentes con diabetes mellitus tipo 1

Documento de consenso sobre tratamiento con infusión subcutánea continua de insulina de la diabetes tipo 1 en la edad pediátrica

Haploinsufficiency at GCK gene is not a frequent event in MODY2 patients

The exon 3-deleted/full-length Growth Hormone Receptor Polymorphism Does Not Influence the Effect of Puberty or Growth Hormone Therapy on Glucose Homeostasis in Short Non-Growth Hormone-Deficient Small-for-Gestational-Age Children: Results from a Two-Year Controlled Prospective Study

Heterozygous glucokinase mutations and birth weight in Spanish children

Panhypopituitarism: genetic versus acquired etiological factors

Mutations in MAFA and IAPP are not a common cause of monogenic diabetes

CLASSIFICATION AND PRODUCTIVITY OF SIX COSTA RICAN ANDEPTS

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