Castano L - Search Results

1

Functional analysis of six Kir6.2 (KCNJ11) mutations causing neonatal diabetes.

Girard CA, Shimomura K, Proks P, Absalom N, Castano L, Perez de Nanclares G, Ashcroft FM. Girard CA, et al. Among authors: castano l. Pflugers Arch. 2006 Dec;453(3):323-32. doi: 10.1007/s00424-006-0112-3. Epub 2006 Sep 22. Pflugers Arch. 2006. PMID: 17021801

2

[Introduction to molecular biology and its application to pediatrics (8): additional methods for the detection of mutations. Clinical case: hemochromatosis in a family. Transgenic animals].

Castaño L, Bilbao JR, Pérez de Nanclares G. Castaño L, et al. An Esp Pediatr. 1997 Dec;47(6):653-8. An Esp Pediatr. 1997. PMID: 9580072 Spanish. No abstract available.

3

Nonisotopic, PCR-based method for 5' insulin gene VNTR allele class assignment.

Calvo B, Bilbao JR, Pérez de Nanclares G, Vázquez JA, Castaño L. Calvo B, et al. Among authors: castano l. Biotechniques. 2000 Nov;29(5):944-6, 948. doi: 10.2144/00295bm03. Biotechniques. 2000. PMID: 11084851 Free article. No abstract available.

4

Analysis of chromosome 6q in Basque families with type 1 diabetes. GEPV-N. Basque-Navarre Endocrinology and Paediatric Group.

Pérez De Nanclares G, Bilbao JR, Calvo B, Castaño L. Pérez De Nanclares G, et al. Among authors: castano l. Autoimmunity. 2000;33(1):33-6. doi: 10.3109/08916930108994107. Autoimmunity. 2000. PMID: 11204251

5

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: castano l. Ann N Y Acad Sci. 2003 Nov;1005:319-23. doi: 10.1196/annals.1288.050. Ann N Y Acad Sci. 2003. PMID: 14679083

6

No association of INS-VNTR genotype and IAA autoantibodies.

Pérez de Nanclares G, Bilbao JR, Castano L. Pérez de Nanclares G, et al. Among authors: castano l. Ann N Y Acad Sci. 2004 Dec;1037:127-30. doi: 10.1196/annals.1337.020. Ann N Y Acad Sci. 2004. PMID: 15699505

7

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. Among authors: castano l. 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

8

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: castano l. 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

9

ACTH-dependent precocious pseudopuberty in an infant with DAX1 gene mutation.

Yeste D, González-Niño C, Pérez de Nanclares G, Pérez-Nanclares G, Audi L, Castaño L, Carrascosa A. Yeste D, et al. Among authors: castano l. Eur J Pediatr. 2009 Jan;168(1):65-9. doi: 10.1007/s00431-008-0710-5. Epub 2008 Apr 15. Eur J Pediatr. 2009. PMID: 18414894

10

Neonatal diabetes with end-stage nephropathy: pancreas transplantation decision.

Esmatjes E, Jimenez A, Diaz G, Mora M, Casamitjana R, Pérez de Nanclares G, Castaño L, José Ricart M. Esmatjes E, et al. Among authors: castano l. Diabetes Care. 2008 Nov;31(11):2116-7. doi: 10.2337/dc08-0823. Epub 2008 Aug 4. Diabetes Care. 2008. PMID: 18678608 Free PMC article.

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