Díaz De Greñu C - Search Results

1

[Prevalence of diabetes mellitus and glucose intolerance in the population aged 30 to 75 years in Asturias, Spain].

Botas Cervero P, Delgado Alvarez E, Castaño Fernández G, Díaz De Greñu C, Prieto Santiago J, Díaz Cadórniga FJ. Botas Cervero P, et al. Among authors: diaz de grenu c. Rev Clin Esp. 2002 Aug;202(8):421-9. doi: 10.1016/s0014-2565(02)71101-6. Rev Clin Esp. 2002. PMID: 12199991 Spanish.

2

Comparison of the diagnostic criteria for diabetes mellitus, WHO-1985, ADA-1997 and WHO-1999 in the adult population of Asturias (Spain).

Botas P, Delgado E, Castaño G, Díaz de Greñu C, Prieto J, Díaz-Cadórniga FJ. Botas P, et al. Among authors: diaz de grenu c. Diabet Med. 2003 Nov;20(11):904-8. doi: 10.1046/j.1464-5491.2003.01006.x. Diabet Med. 2003. PMID: 14632715

3

[Acute adrenal insufficiency in a case of isolated deficit of the adeno-corticotropic hormone (ACTH)].

Menéndez Torre EL, Díaz de Greñu C, Díaz Cadorniga FJ. Menéndez Torre EL, et al. Among authors: diaz de grenu c. Med Clin (Barc). 1986 May 17;86(19):805-7. Med Clin (Barc). 1986. PMID: 3016421 Spanish. No abstract available.

4

[Acromegaly: clinical medicine and treatment in 15 cases].

Menéndez Torre EL, Aller Granda J, Díaz Cadórniga FJ, Díaz de Greñu C, Antuña de Alaiz R, Sánchez Lorenzo MJ. Menéndez Torre EL, et al. Among authors: diaz de grenu c. Med Clin (Barc). 1985 Feb 16;84(6):211-4. Med Clin (Barc). 1985. PMID: 3982130 Spanish. No abstract available.

5

Novel mutations in MEN1, CDKN1B and AIP genes in patients with multiple endocrine neoplasia type 1 syndrome in Spain.

Belar O, De La Hoz C, Pérez-Nanclares G, Castaño L, Gaztambide S; Spanish MEN1 Group. Belar O, et al. Clin Endocrinol (Oxf). 2012 May;76(5):719-24. doi: 10.1111/j.1365-2265.2011.04269.x. Clin Endocrinol (Oxf). 2012. PMID: 22026581

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. 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

Mutations in MAFA and IAPP are not a common cause of monogenic diabetes.

Garin I, Martinez R, de las Heras J, Perez-Nanclares G, Castano L, Perez de Nanclares G; Spanish GEDIMO Group. Garin I, et al. Diabet Med. 2009 Jul;26(7):746-8. doi: 10.1111/j.1464-5491.2009.02758.x. Diabet Med. 2009. PMID: 19573128 No abstract available.

8

Haploinsufficiency at GCK gene is not a frequent event in MODY2 patients.

Garin I, Rica I, Estalella I, Oyarzabal M, Rodríguez-Rigual M, San Pedro JI, Pérez-Nanclares G, Fernández-Rebollo E, Busturia MA, Castaño L, Pérez de Nanclares G; Spanish MODY Group. Garin I, et al. Clin Endocrinol (Oxf). 2008 Jun;68(6):873-8. doi: 10.1111/j.1365-2265.2008.03214.x. Epub 2008 Feb 1. Clin Endocrinol (Oxf). 2008. PMID: 18248649

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