Castaño L - Search Results

1

Prevalence of plasma lipid abnormalities and its association with glucose metabolism in Spain: the [email protected] study.

Martinez-Hervas S, Carmena R, Ascaso JF, Real JT, Masana L, Catalá M, Vendrell J, Vázquez JA, Valdés S, Urrutia I, Soriguer F, Serrano-Rios M, Rojo-Martínez G, Pascual-Manich G, Ortega E, Mora-Peces I, Menéndez E, Martínez-Larrad MT, López-Alba A, Gomis R, Goday A, Girbés J, Gaztambide S, Franch J, Delgado E, Castell C, Castaño L, Casamitjana R, Calle-Pascual A, Bordiú E. Martinez-Hervas S, et al. Among authors: castano l. Clin Investig Arterioscler. 2014 May-Jun;26(3):107-14. doi: 10.1016/j.arteri.2013.12.001. Epub 2014 Jan 23. Clin Investig Arterioscler. 2014. PMID: 24461346

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. An Esp Pediatr. 1996 Nov;45(5):541-6. An Esp Pediatr. 1996. PMID: 9036792 Spanish. No abstract available.

3

[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. An Esp Pediatr. 1997 May;46(5):513-8. An Esp Pediatr. 1997. PMID: 9297412 Spanish. No abstract available.

4

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

5

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: castano l. Diabetologia. 1998 Sep;41(9):1121-3. doi: 10.1007/s001250051039. Diabetologia. 1998. PMID: 9754833

6

Multisystem Langerhans cell histiocytosis.

Vázquez JA, Castaño L. Vázquez JA, et al. Among authors: castano l. Acta Paediatr. 1999 Mar;88(3):349-50. doi: 10.1080/08035259950170196. Acta Paediatr. 1999. PMID: 10229054 No abstract available.

7

Influence of sex and age at onset on autoantibodies against insulin, GAD65 and IA2 in recent onset type 1 diabetic patients.

Bilbao JR, Rica I, Vázquez JA, Busturia MA, Castaño L. Bilbao JR, et al. Among authors: castano l. Horm Res. 2000;54(4):181-5. doi: 10.1159/000053256. Horm Res. 2000. PMID: 11416235

8

Conserved extended haplotypes discriminate HLA-DR3-homozygous Basque patients with type 1 diabetes mellitus and celiac disease.

Bilbao JR, Calvo B, Aransay AM, Martin-Pagola A, Perez de Nanclares G, Aly TA, Rica I, Vitoria JC, Gaztambide S, Noble J, Fain PR, Awdeh ZL, Alper CA, Castaño L. Bilbao JR, et al. Among authors: castano l. Genes Immun. 2006 Oct;7(7):550-4. doi: 10.1038/sj.gene.6364328. Epub 2006 Aug 24. Genes Immun. 2006. PMID: 16929349

9

Epigenetic defects of GNAS in patients with pseudohypoparathyroidism and mild features of Albright's hereditary osteodystrophy.

de Nanclares GP, Fernández-Rebollo E, Santin I, García-Cuartero B, Gaztambide S, Menéndez E, Morales MJ, Pombo M, Bilbao JR, Barros F, Zazo N, Ahrens W, Jüppner H, Hiort O, Castaño L, Bastepe M. de Nanclares GP, et al. Among authors: castano l. J Clin Endocrinol Metab. 2007 Jun;92(6):2370-3. doi: 10.1210/jc.2006-2287. Epub 2007 Apr 3. J Clin Endocrinol Metab. 2007. PMID: 17405843

10

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

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