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A genetic diagnosis of HNF1A diabetes alters treatment and improves glycaemic control in the majority of insulin-treated patients

Diabetic medicine, 2009-04, Vol.26 (4), p.437-441

2009

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Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations

European journal of endocrinology, 2010-05, Vol.162 (5), p.987-992

2010

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Testing for monogenic diabetes among children and adolescents with antibody-negative clinically defined Type 1 diabetes

Diabetic medicine, 2009-10, Vol.26 (10), p.1070-1074

2009

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Neuroprotective effect of a new variant of Epo nonhematopoietic against oxidative stress

Redox biology, 2018-04, Vol.14, p.285-294

2018

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Diabetes mellitus en niños y adolescentes: complicaciones crónicas y enfermedades asociadas

Anales de pediatría (Barcelona, Spain : 2003), 2007, Vol.66 (3), p.282-289

2007

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Hipoaldosteronismo primario e hipoacusia bilateral moderada en un niño con una mutación sin sentido en homocigosis (Thr318Met) en el gen CYP11B2

Anales de pediatría (Barcelona, Spain : 2003), 2010, Vol.73 (1), p.31-34

2010

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Diabetes mellitus: formas de presentación clínica y diagnóstico diferencial de la hiperglucemia en la infancia y adolescencia

Anales de pediatría (Barcelona, Spain : 2003), 2012-11, Vol.77 (5), p.344.e1-344.e16

2012

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Pulmonary Paragonimiasis in Native Community, Esmeraldas Province, Ecuador, 2022

Emerging infectious diseases, 2022-10, Vol.28 (10), p.2114-2116

2022

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Permanent neonatal diabetes caused by a homozygous nonsense mutation in the glucokinase gene

Pediatric diabetes, 2008-06, Vol.9 (3pt1), p.245-249

2008

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Aceite de matico (Piper aduncum) en el control de Moniliophthora roreri agente causal de la moniliasis en cacao

Peruvian Agricultural Research, 2020-08, Vol.1 (2)

2020

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A risk-based integrated management for patient safety and quality in healthcare services

VII Latin American Congress on Biomedical Engineering CLAIB 2016, Bucaramanga, Santander, Colombia, October 26th -28th 2016, 2017, Vol.60, p.86-89

2017

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Primary hypoaldosteronism and moderate bilateral deafness in a child with a homozygous missense mutation (Thr318Met) in the CYP11B2 gene

Anales de pediatría (Barcelona, Spain : 2003), 2010-07, Vol.73 (1), p.31-34

2010

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Contenidos de Anatomía en Diseños de Aprendizaje Dispuestos en LAMS e Integrado a Moodle

International journal of morphology, 2011-06, Vol.29 (2), p.363-370

2011

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Demanda de dinero en efectivo: hechos estilizados y sustitución por medios de pago electrónicos

Revista de la CEPAL, 2022-05, Vol.2021 (135), p.129-157

2022

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Hipoaldosteronismo primario e hipoacusia bilateral moderada en un niño con una mutación sin sentido en homocigosis (Thr318Met) en el gen CYP1182

Anales de pediatría (Barcelona, Spain : 2003), 2010, Vol.73 (1), p.31-34

2010

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Treatment with continuous subcutaneous insulin infusion in pediatric patients with type 1 diabetes mellitus

Anales de pediatría (Barcelona, Spain : 2003), 2006-06, Vol.64 (6), p.600-1; author reply 601-2

2006

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Tratamiento con infusión subcutánea continua de insulina en pacientes pediátricos con diabetes mellitus tipo 1

Anales de pediatría (Barcelona, Spain : 2003), 2006, Vol.64 (6), p.600-601

2006

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Increased frequency of phytosanitary pod removal in cacao ( Theobroma cacao) increases yield economically in eastern Peru

Crop protection, 1999-12, Vol.18 (10), p.677-685

1999

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Methodology for sustainability analysis of ships

Ships and offshore structures, 2008-02, Vol.3 (1), p.1-11

2008

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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.953-962

2010

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Terrenos configurados ordenados en la alta montaña mediterránea

Pirineos, 1994, Vol.143-144, p.71-85

1994

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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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Diabetes mellitus: clinical presentation and differential diagnosis of hyperglycemia in childhood and adolescence

Anales de pediatría (Barcelona, Spain : 2003), 2012-11, Vol.77 (5), p.344.e1-344.e16

2012

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A genetic diagnosis of HNF1A diabetes alters treatment and improves glycaemic control in the majority of insulin-treated patients

Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations

Testing for monogenic diabetes among children and adolescents with antibody-negative clinically defined Type 1 diabetes

Neuroprotective effect of a new variant of Epo nonhematopoietic against oxidative stress

Diabetes mellitus en niños y adolescentes: complicaciones crónicas y enfermedades asociadas

Hipoaldosteronismo primario e hipoacusia bilateral moderada en un niño con una mutación sin sentido en homocigosis (Thr318Met) en el gen CYP11B2

Diabetes mellitus: formas de presentación clínica y diagnóstico diferencial de la hiperglucemia en la infancia y adolescencia

Pulmonary Paragonimiasis in Native Community, Esmeraldas Province, Ecuador, 2022

Permanent neonatal diabetes caused by a homozygous nonsense mutation in the glucokinase gene

Aceite de matico (Piper aduncum) en el control de Moniliophthora roreri agente causal de la moniliasis en cacao

A risk-based integrated management for patient safety and quality in healthcare services

Primary hypoaldosteronism and moderate bilateral deafness in a child with a homozygous missense mutation (Thr318Met) in the CYP11B2 gene

Contenidos de Anatomía en Diseños de Aprendizaje Dispuestos en LAMS e Integrado a Moodle

Demanda de dinero en efectivo: hechos estilizados y sustitución por medios de pago electrónicos

Hipoaldosteronismo primario e hipoacusia bilateral moderada en un niño con una mutación sin sentido en homocigosis (Thr318Met) en el gen CYP1182

Treatment with continuous subcutaneous insulin infusion in pediatric patients with type 1 diabetes mellitus

Tratamiento con infusión subcutánea continua de insulina en pacientes pediátricos con diabetes mellitus tipo 1

Increased frequency of phytosanitary pod removal in cacao ( Theobroma cacao) increases yield economically in eastern Peru

Methodology for sustainability analysis of ships

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

Terrenos configurados ordenados en la alta montaña mediterránea

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

Diabetes mellitus: clinical presentation and differential diagnosis of hyperglycemia in childhood and adolescence

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