Rica I - Search Results

1

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

Urrutia I, Martínez R, López-Euba T, Velayos T, Martínez de LaPiscina I, Bilbao JR, Rica I, Castaño L; Spanish Group for the Study of MODY and Type 1 diabetes. Urrutia I, et al. Among authors: rica i. PLoS One. 2017 Jan 4;12(1):e0169389. doi: 10.1371/journal.pone.0169389. eCollection 2017. PLoS One. 2017. PMID: 28052112 Free PMC article.

2

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

Vitoria JC, Castaño L, Rica I, Bilbao JR, Arrieta A, García-Masdevall MD. Vitoria JC, et al. Among authors: rica i. J Pediatr Gastroenterol Nutr. 1998 Jul;27(1):47-52. doi: 10.1097/00005176-199807000-00008. J Pediatr Gastroenterol Nutr. 1998. PMID: 9669725

3

Molecular analysis of hereditary hyperferritinemia-cataract syndrome in a large Basque family.

Pérez de Nanclares G, Castaño L, Martul P, Rica I, Vela A, Sanjurjo P, Aldamiz-Echevarría K, Martínez R, Sarrionandia MJ. Pérez de Nanclares G, et al. Among authors: rica i. J Pediatr Endocrinol Metab. 2001 Mar;14(3):295-300. doi: 10.1515/jpem.2001.14.3.295. J Pediatr Endocrinol Metab. 2001. PMID: 11308047

4

Influence of sex and age at onset on autoantibodies against insulin, GAD65 and IA2 in recent onset type 1 diabetic patients.

Bilbao JR, Rica I, Vázquez JA, Busturia MA, Castaño L. Bilbao JR, et al. Among authors: rica i. Horm Res. 2000;54(4):181-5. doi: 10.1159/000053256. Horm Res. 2000. PMID: 11416235

5

Molecular analysis of Frasier syndrome: mutation in the WT1 gene in a girl with gonadal dysgenesis and nephronophthisis.

Pérez de Nanclares G, Castaño L, Bilbao JR, Vallo A, Rica I, Vela A, Martul P. Pérez de Nanclares G, et al. Among authors: rica i. J Pediatr Endocrinol Metab. 2002 Jul-Aug;15(7):1047-50. doi: 10.1515/jpem.2002.15.7.1047. J Pediatr Endocrinol Metab. 2002. PMID: 12199335

6

Prospective population screening for celiac disease: high prevalence in the first 3 years of life.

Castaño L, Blarduni E, Ortiz L, Núñez J, Bilbao JR, Rica I, Martul P, Vitoria JC. Castaño L, et al. Among authors: rica i. J Pediatr Gastroenterol Nutr. 2004 Jul;39(1):80-4. doi: 10.1097/00005176-200407000-00016. J Pediatr Gastroenterol Nutr. 2004. PMID: 15187786

7

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

Bilbao JR, Calvo B, Aransay AM, Martin-Pagola A, Perez de Nanclares G, Aly TA, Rica I, Vitoria JC, Gaztambide S, Noble J, Fain PR, Awdeh ZL, Alper CA, Castaño L. Bilbao JR, et al. Among authors: rica i. Genes Immun. 2006 Oct;7(7):550-4. doi: 10.1038/sj.gene.6364328. Epub 2006 Aug 24. Genes Immun. 2006. PMID: 16929349

8

Panhypopituitarism: genetic versus acquired etiological factors.

Coya R, Vela A, Pérez de Nanclares G, Rica I, Castaño L, Busturia MA, Martul P; GEDPIT group. Coya R, et al. Among authors: rica i. J Pediatr Endocrinol Metab. 2007 Jan;20(1):27-36. doi: 10.1515/jpem.2007.20.1.27. J Pediatr Endocrinol Metab. 2007. PMID: 17315526

9

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

Rica I, Luzuriaga C, Pérez de Nanclares G, Estalella I, Aragonés A, Barrio R, Bilbao JR, Carlés C, Fernández C, Fernández JM, Fernández-Rebollo E, Gastaldo E, Giralt P, Gomez Vida JM, Gutiérrez A, López Siguero JP, Martínez-Aedo MJ, Muñoz M, Prieto J, Rodrigo J, Vargas F, Castano L. Rica I, et al. Diabet Med. 2007 Jul;24(7):707-13. doi: 10.1111/j.1464-5491.2007.02140.x. Epub 2007 May 8. Diabet Med. 2007. PMID: 17490422

10

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

Estalella I, Rica I, Perez de Nanclares G, Bilbao JR, Vazquez JA, San Pedro JI, Busturia MA, Castaño L; Spanish MODY Group. Estalella I, et al. Among authors: rica i. Clin Endocrinol (Oxf). 2007 Oct;67(4):538-46. doi: 10.1111/j.1365-2265.2007.02921.x. Epub 2007 Jun 15. Clin Endocrinol (Oxf). 2007. PMID: 17573900

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