Urrutia I - Search Results

1

An Activating Mutation in STAT3 Results in Neonatal Diabetes Through Reduced Insulin Synthesis.

Velayos T, Martínez R, Alonso M, Garcia-Etxebarria K, Aguayo A, Camarero C, Urrutia I, Martínez de LaPiscina I, Barrio R, Santin I, Castaño L. Velayos T, et al. Among authors: urrutia i. Diabetes. 2017 Apr;66(4):1022-1029. doi: 10.2337/db16-0867. Epub 2017 Jan 10. Diabetes. 2017. PMID: 28073828

2

[Introduction to molecular biology and its application to pediatrics (2): purification of nucleic acids].

Castaño L, Bilbao JR, Urrutia I. Castaño L, et al. Among authors: urrutia i. An Esp Pediatr. 1996 Nov;45(5):541-6. An Esp Pediatr. 1996. PMID: 9036792 Spanish. No abstract available.

3

Anti-insulin activity in normal newborn cord-blood serum: absence of IgG-mediated insulin binding.

Bilbao JR, Calvo B, Urrutia I, Linares A, Castaño L. Bilbao JR, et al. Among authors: urrutia i. Diabetes. 1997 Apr;46(4):713-6. doi: 10.2337/diab.46.4.713. Diabetes. 1997. PMID: 9075816

4

[Introduction to molecular biology and its application to pediatrics (5): clinical cases. Genetic alterations in XY gonadal dysgenesis and in myotonic dystrophy].

Castaño L, Bilbao JR, Urrutia I. Castaño L, et al. Among authors: urrutia i. An Esp Pediatr. 1997 May;46(5):513-8. An Esp Pediatr. 1997. PMID: 9297412 Spanish. No abstract available.

5

Identification of a novel nonsense mutation and a missense substitution in the vasopressin-neurophysin II gene in two Spanish kindreds with familial neurohypophyseal diabetes insipidus.

Calvo B, Bilbao JR, Urrutia I, Eizaguirre J, Gaztambide S, Castaño L. Calvo B, et al. Among authors: urrutia i. J Clin Endocrinol Metab. 1998 Mar;83(3):995-7. doi: 10.1210/jcem.83.3.4658. J Clin Endocrinol Metab. 1998. PMID: 9580132

6

Anomalous behaviour of the 5' insulin gene polymorphism allele 814: lack of association with Type I diabetes in Basques. GEPV-N Group. Basque-Navarre Endocrinology and Paediatrics.

Urrutia I, Calvo B, Bilbao JR, Castaño L. Urrutia I, et al. Diabetologia. 1998 Sep;41(9):1121-3. doi: 10.1007/s001250051039. Diabetologia. 1998. PMID: 9754833

7

Heterozygous glucokinase mutations and birth weight in Spanish children.

de Las Heras J, Martínez R, Rica I, de Nanclares GP, Vela A, Castaño L; Spanish MODY group. de Las Heras J, et al. Diabet Med. 2010 May;27(5):608-10. doi: 10.1111/j.1464-5491.2010.02953.x. Diabet Med. 2010. PMID: 20536962 No abstract available.

8

Identification of a novel insulin receptor gene heterozygous mutation in a patient with type A insulin resistance syndrome.

Domínguez-García A, Martínez R, Urrutia I, Garin I, Castaño L. Domínguez-García A, et al. Among authors: urrutia i. J Pediatr Endocrinol Metab. 2014 May;27(5-6):561-4. doi: 10.1515/jpem-2013-0284. J Pediatr Endocrinol Metab. 2014. PMID: 24468607

9

Clinical and genetic characterization of congenital hyperinsulinism in Spain.

Martínez R, Fernández-Ramos C, Vela A, Velayos T, Aguayo A, Urrutia I, Rica I, Castaño L; Spanish Congenital Hyperinsulinism Group. Martínez R, et al. Among authors: urrutia i. Eur J Endocrinol. 2016 Jun;174(6):717-26. doi: 10.1530/EJE-16-0027. Eur J Endocrinol. 2016. PMID: 27188453

10

Prevalence of diabetes mellitus and impaired glucose metabolism in the adult population of the Basque Country, Spain.

Aguayo A, Urrutia I, González-Frutos T, Martínez R, Martínez-Indart L, Castaño L, Gaztambide S; Diabetes Epidemiology Basque Study Group. Aguayo A, et al. Among authors: urrutia i. Diabet Med. 2017 May;34(5):662-666. doi: 10.1111/dme.13181. Epub 2016 Sep 11. Diabet Med. 2017. PMID: 27353285

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