Castano L - 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: castano l. Diabetes. 2007 Jun;56(6):1737-41. doi: 10.2337/db06-1540. Epub 2007 Mar 27. Diabetes. 2007. PMID: 17389331

2

Cyclosporin A suppresses insulin autoantibodies and heterologous insulin antibodies in type I diabetic children.

Castaño L, Boîtard C, Bougnères PF. Castaño L, et al. Diabetes. 1988 Aug;37(8):1049-52. doi: 10.2337/diab.37.8.1049. Diabetes. 1988. PMID: 3292324

3

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: castano l. 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

4

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

5

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: castano l. 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

6

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: castano l. 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.

7

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: castano l. Diabet Med. 2010 Feb;27(2):225-9. doi: 10.1111/j.1464-5491.2009.02901.x. Diabet Med. 2010. PMID: 20546268

8

Neonatal diabetes caused by mutations in sulfonylurea receptor 1: interplay between expression and Mg-nucleotide gating defects of ATP-sensitive potassium channels.

Zhou Q, Garin I, Castaño L, Argente J, Muñoz-Calvo MT, Perez de Nanclares G, Shyng SL. Zhou Q, et al. Among authors: castano l. J Clin Endocrinol Metab. 2010 Dec;95(12):E473-8. doi: 10.1210/jc.2010-1231. Epub 2010 Sep 1. J Clin Endocrinol Metab. 2010. PMID: 20810569 Free PMC article.

9

New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidism.

Fernández-Rebollo E, Lecumberri B, Garin I, Arroyo J, Bernal-Chico A, Goñi F, Orduña R; Spanish PHP Group; Castaño L, de Nanclares GP. Fernández-Rebollo E, et al. Among authors: castano l. Eur J Endocrinol. 2010 Dec;163(6):953-62. doi: 10.1530/EJE-10-0435. Epub 2010 Sep 13. Eur J Endocrinol. 2010. PMID: 20837711

10

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: castano l. J Pediatr Endocrinol Metab. 2010 Aug;23(8):827-30. doi: 10.1515/jpem.2010.132. J Pediatr Endocrinol Metab. 2010. PMID: 21073125

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