de Nanclares GP - Search Results

1

New ABCC8 mutations in relapsing neonatal diabetes and clinical features.

Vaxillaire M, Dechaume A, Busiah K, Cavé H, Pereira S, Scharfmann R, de Nanclares GP, Castano L, Froguel P, Polak M; SUR1-Neonatal Diabetes Study Group. Vaxillaire M, et al. Among authors: de nanclares gp. Diabetes. 2007 Jun;56(6):1737-41. doi: 10.2337/db06-1540. Epub 2007 Mar 27. Diabetes. 2007. PMID: 17389331

2

The first clinical case of a mutation at residue K185 of Kir6.2 (KCNJ11): a major ATP-binding residue.

Shimomura K, de Nanclares GP, Foutinou C, Caimari M, Castaño L, Ashcroft FM. Shimomura K, et al. Among authors: de nanclares gp. Diabet Med. 2010 Feb;27(2):225-9. doi: 10.1111/j.1464-5491.2009.02901.x. Diabet Med. 2010. PMID: 20546268

3

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: de nanclares gp. Ann N Y Acad Sci. 2006 Oct;1079:268-72. doi: 10.1196/annals.1375.040. Ann N Y Acad Sci. 2006. PMID: 17130564

4

Killer cell immunoglobulin-like receptor (KIR) genes in the Basque population: association study of KIR gene contents with type 1 diabetes mellitus.

Santin I, de Nanclares GP, Calvo B, Gaafar A, Castaño L; GEPV-N Group; Bilbao JR. Santin I, et al. Among authors: de nanclares gp. Hum Immunol. 2006 Jan-Feb;67(1-2):118-24. doi: 10.1016/j.humimm.2006.02.036. Epub 2006 Apr 5. Hum Immunol. 2006. PMID: 16698433

5

Genetics of pseudohypoparathyroidism: bases for proper genetic counselling.

de Nanclares GP, Fernández-Rebollo E, Gaztambide S, Castaño L. de Nanclares GP, et al. Endocrinol Nutr. 2008 Dec;55(10):476-83. doi: 10.1016/S1575-0922(08)75844-3. Epub 2009 Jan 7. Endocrinol Nutr. 2008. PMID: 22980463 English, Spanish.

6

New mutation type in pseudohypoparathyroidism type Ia.

Fernandez-Rebollo E, Barrio R, Pérez-Nanclares G, Carcavilla A, Garin I, Castaño L, de Nanclares GP. Fernandez-Rebollo E, et al. Among authors: de nanclares gp. Clin Endocrinol (Oxf). 2008 Nov;69(5):705-12. doi: 10.1111/j.1365-2265.2008.03255.x. Epub 2008 Apr 3. Clin Endocrinol (Oxf). 2008. PMID: 18394017

7

Familial hyperinsulinism-hyperammonemia syndrome in a family with seizures: case report.

de las Heras J, Garin I, de Nanclares GP, Aguayo A, Rica I, Castaño L, Vela A. de las Heras J, et al. Among authors: de nanclares gp. J Pediatr Endocrinol Metab. 2010 Aug;23(8):827-30. doi: 10.1515/jpem.2010.132. J Pediatr Endocrinol Metab. 2010. PMID: 21073125

8

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. Among authors: de nanclares gp. 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.

9

Two-year follow-up of anti-transglutaminase autoantibodies among celiac children on gluten-free diet: comparison of IgG and IgA.

Martín-Pagola A, Ortiz-Paranza L, Bilbao JR, de Nanclares GP, Estevez EP, Castaño L, Vitoria JC. Martín-Pagola A, et al. Among authors: de nanclares gp. Autoimmunity. 2007 Mar;40(2):117-21. doi: 10.1080/08916930601119260. Autoimmunity. 2007. PMID: 17364503

10

Two cases of deletion 2q37 associated with segregation of an unbalanced translocation 2;21: choanal atresia leading to misdiagnosis of CHARGE syndrome.

Fernández-Rebollo E, Pérez O, Martinez-Bouzas C, Cotarelo-Pérez MC, Garin I, Ruibal JL, Pérez-Nanclares G, Castaño L, de Nanclares GP. Fernández-Rebollo E, et al. Among authors: de nanclares gp. Eur J Endocrinol. 2009 Apr;160(4):711-7. doi: 10.1530/EJE-08-0865. Eur J Endocrinol. 2009. PMID: 19332529

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