I. Rica

发表

Exploring the diabetogenicity of the HLA-B18-DR3 CEH: independent association with T1D genetic risk close to HLA-DOA

I. Santin, S. Gaztambide, J. Bilbao, 2009, Genes and Immunity.

Molecular Differences Based on Erythrocyte Fatty Acid Profile to Personalize Dietary Strategies between Adults and Children with Obesity

S. Gaztambide, C. Ferreri, K. Portune, 2021, Metabolites.

Urinary iodine and thyroid function in a population of healthy pregnant women in the North of Spain.

M. Espada, I. Rica, L. Castaño, 2013, Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements.

Association of insulin-dependent diabetes mellitus and celiac disease: a study based on serologic markers.

J. Bilbao, L. Castano, I. Rica, 1998, Journal of pediatric gastroenterology and nutrition.

Evolutionary Analyses of Entire Genomes Do Not Support the Association of mtDNA Mutations with Ras/MAPK Pathway Syndromes

Á. Carracedo, A. Salas, M. Castro‐Gago, 2011, PloS one.

Lower Frequency of HLA-DRB1 Type 1 Diabetes Risk Alleles in Pediatric Patients with MODY

I. Urrutia, J. Bilbao, I. Rica, 2017, PloS one.

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.

Dual Growth Hormone (GH) Response to Repeated GH Releasing Hormone Stimulus in Children and Adults

R. Coya, I. Rica, J. Algorta, 2004, Journal of pediatric endocrinology & metabolism : JPEM.

Intralymphatic Glutamic Acid Decarboxylase With Vitamin D Supplementation in Recent-Onset Type 1 Diabetes: A Double-Blind, Randomized, Placebo-Controlled Phase IIb Trial

A. Nordlund, T. Pelikanova, J. Ludvigsson, 2021, Diabetes Care.

Conserved extended haplotypes discriminate HLA-DR3-homozygous Basque patients with type 1 diabetes mellitus and celiac disease

P. Fain, S. Gaztambide, J. Bilbao, 2006, Genes and Immunity.

The Outcome of Patients with Lupus Nephritis and the Impact of Cardiovascular Risk Factors

I. Rica, A. Bărbulescu, P. Ciurea, 2011, Current health sciences journal.

Influence of Sex and Age at Onset on Autoantibodies against Insulin, GAD65 and IA2 in Recent Onset Type 1 Diabetic Patients

J. Bilbao, J. Vazquez, I. Rica, 2001, Hormone Research in Paediatrics.

Heterozygous glucokinase mutations and birth weight in Spanish children

I. Rica, L. Castaño, R. Martínez, 2009, Diabetic medicine : a journal of the British Diabetic Association.

Clinical Evaluation and Health Care in Childhood and Adolescent Obesity

I. Rica, P. Martul, A. Aguayo, 2005, Journal of pediatric endocrinology & metabolism : JPEM.

Normal intellectual development in children born from women with hypothyroxinemia during their pregnancy.

M. Espada, I. Rica, L. Castaño, 2015, Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements.

Renal tubular handling of potassium in children with insulin-dependent diabetes mellitus

G. Ariceta, I. Rica, P. Martul, 1996, Pediatric Nephrology.

Is routine endocrine evaluation necessary after paediatric traumatic brain injury?

I. Rica, L. Castaño, G. Grau, 2014, Journal of Endocrinological Investigation.

Thyroid hormone resistance from newborns to adults: a Spanish experience

I. Rica, L. Castaño, I. Rios, 2019, Journal of Endocrinological Investigation.

Recessive mutations in the INS gene result in neonatal diabetes through reduced insulin biosynthesis

A. Hattersley, S. Ellard, L. Harries, 2010, Proceedings of the National Academy of Sciences.

Molecular Analysis of Frasier Syndrome: Mutation in the WT1 Gene in a Girl with Gonadal Dysgenesis and Nephronophthisis

J. Bilbao, I. Rica, L. Castaño, 2002, Journal of pediatric endocrinology & metabolism : JPEM.

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

J. Bilbao, I. Rica, L. Castaño, 2007, Clinical endocrinology.

Genetic diagnosis of X-linked dominant hypophosphatemic rickets in a cohort study: Tubular reabsorption of phosphate and 1,25(OH)2D serum levels are associated with PHEX mutation type

J. M. García-Sagredo, G. Ariceta, O. Moldovan, 2011, BMC Medical Genetics.

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

E. Fernandez-Rebollo, I. Rica, L. Castaño, 2008, Clinical endocrinology.

Prospective Population Screening for Celiac Disease: High Prevalence in the First 3 Years of Life

J. Bilbao, I. Rica, L. Castaño, 2004, Journal of pediatric gastroenterology and nutrition.

Fatty Acid Profile of Mature Red Blood Cell Membranes and Dietary Intake as a New Approach to Characterize Children with Overweight and Obesity

C. Ferreri, K. Portune, I. Rica, 2020, Nutrients.

Negative autoimmunity in a Spanish pediatric cohort suspected of type 1 diabetes, could it be monogenic diabetes?

I. Urrutia, I. Rica, L. Castaño, 2019, PloS one.

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

J. Bilbao, E. Fernandez-Rebollo, I. Rica, 2007, Diabetic medicine : a journal of the British Diabetic Association.

GAD65 antigen therapy in recently diagnosed type 1 diabetes mellitus.

Juan Pedro López, F. Cerutti, O. Kordonouri, 2012, The New England journal of medicine.

Ala cannot explain the phenotype of individuals with a 1 difference of sex development . 2 3

C. Flück, N. Camats, I. Esteva, 2023 .

Clinical and genetic characteristics in patients under 30 years with sporadic pituitary adenomas.

S. Gaztambide, L. Hernández-Ramírez, M. I. Hernández, 2021, European journal of endocrinology.

Rare Germline DICER1 Variants in Pediatric Patients With Cushing's Disease: What Is Their Role?

F. Faucz, C. Stratakis, M. Lodish, 2020, Frontiers in Endocrinology.

Forty-one individuals with mutations in the AVP-NPII gene associated with familial neurohypophyseal diabetes insipidus.

I. Urrutia, S. Gaztambide, M. Rodríguez-Arnao, 2020, The Journal of clinical endocrinology and metabolism.

Absence of diabetes mellitus type 2 in obese children and adolescents in the north of Spain

I. Rica, L. Castaño, P. Martul, 2013, Journal of pediatric endocrinology & metabolism : JPEM.

Consensus on the detection and management of prediabetes. Consensus and Clinical Guidelines Working Group of the Spanish Diabetes Society.

J. C. Ferrer-García, J. Escalada, S. Artola, 2015, Revista clinica espanola.

Consenso sobre la detección y el manejo de la prediabetes. Grupo de Trabajo de Consensos y Guías Clínicas de la Sociedad Española de Diabetes☆

J. C. Ferrer-García, J. Escalada, S. Artola, 2014, Atencion primaria.

Clinical and genetic characterization of congenital hyperinsulinism in Spain.

I. Urrutia, I. Rica, L. Castaño, 2016, European journal of endocrinology.

Familial Hyperinsulinism-Hyperammonemia Syndrome in a Family with Seizures: Case Report

I. Rica, L. Castaño, A. Aguayo, 2010, Journal of pediatric endocrinology & metabolism : JPEM.

Panhypopituitarism: Genetic Versus Acquired Etiological Factors

R. Coya, I. Rica, L. Castaño, 2007, Journal of pediatric endocrinology & metabolism : JPEM.

Potential of Erythrocyte Membrane Lipid Profile as a Novel Inflammatory Biomarker to Distinguish Metabolically Healthy Obesity in Children

C. Ferreri, K. Portune, I. Rica, 2021, Journal of personalized medicine.

[Consensus on the detection and management of prediabetes. Consensus and Clinical Guidelines Working Group of the Spanish Diabetes Society].

J. C. Ferrer-García, J. Escalada, S. Artola, 2015, Endocrinologia y nutricion : organo de la Sociedad Espanola de Endocrinologia y Nutricion.

Molecular Analysis of Hereditary Hyperferritinemia-Cataract Syndrome in a Large Basque Family

I. Rica, L. Castaño, G. Pérez de Nanclares, 2001, Journal of pediatric endocrinology & metabolism : JPEM.

Achievement of metabolic control among children and adolescents with type 1 diabetes in Spain

M. Clemente, I. Rica, R. Barrio, 2017, Acta Diabetologica.

Intralymphatic GAD-Alum (Diamyd®) Improves Glycemic Control in Type 1 Diabetes With HLA DR3-DQ2

T. Pelikanova, Z. Šumník, R. Hanås, 2022, The Journal of clinical endocrinology and metabolism.

Incidence of childhood‐onset type 1 diabetes in Biscay, Spain, 1990–2013

I. Rica, E. Arana-Arri, A. Vela, 2017, Pediatric diabetes.

Glucocorticoid resistance syndrome caused by two novel mutations in the NR3C1 gene.

S. Gaztambide, I. Rica, G. Grau, 2016, Endocrinologia y nutricion : organo de la Sociedad Espanola de Endocrinologia y Nutricion.

Genetic reanalysis of patients with a difference of sex development carrying the NR5A1/SF-1 variant p.Gly146Ala has discovered other likely disease-causing variations

C. Flück, N. Camats, I. Esteva, 2023, PloS one.

Oral dexamethasone administration: new pharmacological test for the assessment of growth hormone secretion.

F. Casanueva, C. Diéguez, I. Rica, 1994, European journal of endocrinology.

Physical activity patterns in type 1 diabetes in Spain: The SED1 study

F. Tinahones, S. Gaztambide, I. Conget, 2023, BMC Sports Science, Medicine and Rehabilitation.

Recessive mutations in the INS gene result in neonatal diabetes through reduced insulin biosynthesis

A. Hattersley, S. Ellard, L. Harries, 2010, Proceedings of the National Academy of Sciences of the United States of America.

[Consensus on the detection and management of prediabetes. Consensus and Clinical Guidelines Working Group of the Spanish Diabetes Society].

J. C. Ferrer-García, J. Escalada, S. Artola, 2015, Semergen.

Consensus on the detection and management of prediabetes. Consensus and Clinical Guidelines Working Group of the Spanish Diabetes Society.

J. C. Ferrer-García, S. Artola, I. Rica, 2015, Revista clinica espanola.

[Consensus on the detection and management of prediabetes. Consensus and Clinical Guidelines Working Group of the Spanish Diabetes Society].

J. C. Ferrer-García, J. Escalada, S. Artola, 2015, Endocrinologia y nutricion : organo de la Sociedad Espanola de Endocrinologia y Nutricion.

GAD65 antigen therapy in recently diagnosed type 1 diabetes mellitus.

Juan Pedro López, F. Cerutti, O. Kordonouri, 2012, The New England journal of medicine.