Unanue G - Search Results

Year	Number of Results
2008	1
2009	1
2010	2
2011	1
2012	1
2013	2
2025	0

1

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.

2

[Usage analysis of the Nursing Activities Score in two Spanish ICUS].

Carmona-Monge FJ, Uranga IU, Gómez SG, Herranz CQ, Bengoetxea MB, Unanue GE, Martin AI, Hernando ME, Saralegui EB, Irazoqui MA. Carmona-Monge FJ, et al. Among authors: unanue ge. Rev Esc Enferm USP. 2013 Oct;47(5):1108-16. doi: 10.1590/S0080-623420130000500014. Rev Esc Enferm USP. 2013. PMID: 24346450 Free article. Spanish.

3

Endocrine profile and phenotype-(epi)genotype correlation in Spanish patients with pseudohypoparathyroidism.

Fernández-Rebollo E, Lecumberri B, Gaztambide S, Martinez-Indart L, Perez de Nanclares G, Castaño L; Spanish PHP Group. Fernández-Rebollo E, et al. J Clin Endocrinol Metab. 2013 May;98(5):E996-1006. doi: 10.1210/jc.2012-4164. Epub 2013 Mar 26. J Clin Endocrinol Metab. 2013. PMID: 23533243

4

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

5

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. 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

6

Detection of hypomethylation syndrome among patients with epigenetic alterations at the GNAS locus.

Perez-Nanclares G, Romanelli V, Mayo S, Garin I, Zazo Seco C, Fernandez-Rebollo E, Martínez F, Lapunzina P, de Nanclares GP; Spanish PHP Group. Perez-Nanclares G, et al. J Clin Endocrinol Metab. 2012 Jun;97(6):E1060-7. doi: 10.1210/jc.2012-1081. Epub 2012 Apr 4. J Clin Endocrinol Metab. 2012. PMID: 22492776

7

Gsα activity is reduced in erythrocyte membranes of patients with psedohypoparathyroidism due to epigenetic alterations at the GNAS locus.

Zazo C, Thiele S, Martín C, Fernandez-Rebollo E, Martinez-Indart L, Werner R, Garin I; Spanish PHP Group; Hiort O, Perez de Nanclares G. Zazo C, et al. J Bone Miner Res. 2011 Aug;26(8):1864-70. doi: 10.1002/jbmr.369. J Bone Miner Res. 2011. PMID: 21351142 Free article.

8

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.

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