Calvo B - Search Results

1

[Introduction to molecular biology and its application to pediatrics (6): clinical case: molecular disorder in central diabetes insipidus. Analysis of polymorphic gene: HLA type].

Castaño L, Bilbao JR, Calvo B. Castaño L, et al. Among authors: calvo b. An Esp Pediatr. 1997 Aug;47(2):201-6. An Esp Pediatr. 1997. PMID: 9382358 Spanish. No abstract available.

2

[Introduction to molecular biology and its application to pediatrics (3): restriction enzymes. Polymerase chain reaction. Ways to study mutations].

Castaño L, Bilbao JR, Calvo B. Castaño L, et al. Among authors: calvo b. An Esp Pediatr. 1997 Jan;46(1):87-92. An Esp Pediatr. 1997. PMID: 9082901 Spanish. No abstract available.

3

Molecular analysis in familial neurohypophyseal diabetes insipidus: early diagnosis of an asymptomatic carrier.

Calvo B, Bilbao JR, Rodríguez A, Rodríguez-Arnao MD, Castaño L. Calvo B, et al. J Clin Endocrinol Metab. 1999 Sep;84(9):3351-4. doi: 10.1210/jcem.84.9.5979. J Clin Endocrinol Metab. 1999. PMID: 10487710

4

Contribution of MIC-A polymorphism to type 1 diabetes mellitus in Basques.

Bilbao JR, Martín-Pagola A, Calvo B, Perez de Nanclares G, Gepv-N, Castaño L. Bilbao JR, et al. Among authors: calvo b. Ann N Y Acad Sci. 2002 Apr;958:321-4. doi: 10.1111/j.1749-6632.2002.tb02996.x. Ann N Y Acad Sci. 2002. PMID: 12021133

5

HLA-DRB1 and MICA in autoimmunity: common associated alleles in autoimmune disorders.

Bilbao JR, Martín-Pagola A, Pérez De Nanclares G, Calvo B, Vitoria JC, Vázquez F, Castaño L. Bilbao JR, et al. Among authors: calvo b. Ann N Y Acad Sci. 2003 Nov;1005:314-8. doi: 10.1196/annals.1288.049. Ann N Y Acad Sci. 2003. PMID: 14679082

6

5'-Insulin gene VNTR polymorphism is specific for type 1 diabetes: no association with celiac or Addison's disease.

Pérez De Nanclares G, Bilbao JR, Calvo B, Vitoria JC, Vázquez F, Castaño L. Pérez De Nanclares G, et al. Among authors: calvo b. Ann N Y Acad Sci. 2003 Nov;1005:319-23. doi: 10.1196/annals.1288.050. Ann N Y Acad Sci. 2003. PMID: 14679083

7

No association of TLR2 and TLR4 polymorphisms with type I diabetes mellitus in the Basque population.

Santin I, Bilbao JR, de Nanclares GP, Calvo B, Castaño L. Santin I, et al. Among authors: calvo b. Ann N Y Acad Sci. 2006 Oct;1079:268-72. doi: 10.1196/annals.1375.040. Ann N Y Acad Sci. 2006. PMID: 17130564

8

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: calvo b. Diabetes. 1997 Apr;46(4):713-6. doi: 10.2337/diab.46.4.713. Diabetes. 1997. PMID: 9075816

9

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. J Clin Endocrinol Metab. 1998 Mar;83(3):995-7. doi: 10.1210/jcem.83.3.4658. J Clin Endocrinol Metab. 1998. PMID: 9580132

10

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. Among authors: calvo b. Diabetologia. 1998 Sep;41(9):1121-3. doi: 10.1007/s001250051039. Diabetologia. 1998. PMID: 9754833

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