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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 1
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1988 1
1992 1
1999 1
2001 1
2004 1
2006 1
2007 2
2008 2
2009 2
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2011 2
2012 2
2013 2
2015 3
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30 results

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Page 1
Risk for progression to type 1 diabetes in first-degree relatives under 50 years of age.
Urrutia I, Martinez R, Calvo B, Marcelo I, Saso-Jimenez L, Martinez de Lapiscina I, Bilbao JR, Castano L, Rica I; Collaborative Working Group. Urrutia I, et al. Front Endocrinol (Lausanne). 2024 Aug 12;15:1411686. doi: 10.3389/fendo.2024.1411686. eCollection 2024. Front Endocrinol (Lausanne). 2024. PMID: 39188918 Free PMC article.
[Idiopathic short stature. A literature review and update].
Carrascosa A, Fernández Longás A, Gracia Bouthelier R, López Siguero JP, Pombo Arias M, Yturriaga R; Grupo Español de Consenso. Carrascosa A, et al. An Pediatr (Barc). 2011 Sep;75(3):204.e1-11. doi: 10.1016/j.anpedi.2011.05.007. An Pediatr (Barc). 2011. PMID: 21723798 Free article. Review. Spanish.
Forty-One Individuals With Mutations in the AVP-NPII Gene Associated With Familial Neurohypophyseal Diabetes Insipidus.
García-Castaño A, Madariaga L, Pérez de Nanclares G, Vela A, Rica I, Gaztambide S, Martínez R, Martinez de LaPiscina I, Urrutia I, Aguayo A, Velasco O; Familial neurohypophyseal diabetes insipidus Spanish working group; Castaño L. García-Castaño A, et al. J Clin Endocrinol Metab. 2020 Apr 1;105(4):dgaa069. doi: 10.1210/clinem/dgaa069. J Clin Endocrinol Metab. 2020. PMID: 32052034
Vitamin D status in children with Down's syndrome.
Del Arco C, Riancho JA, Luzuriaga C, González-Macías J, Flórez J. Del Arco C, et al. Among authors: luzuriaga c. J Intellect Disabil Res. 1992 Jun;36 ( Pt 3):251-7. doi: 10.1111/j.1365-2788.1992.tb00512.x. J Intellect Disabil Res. 1992. PMID: 1535819
Heterozygous NPR2 Mutations Cause Disproportionate Short Stature, Similar to Léri-Weill Dyschondrosteosis.
Hisado-Oliva A, Garre-Vázquez AI, Santaolalla-Caballero F, Belinchón A, Barreda-Bonis AC, Vasques GA, Ramirez J, Luzuriaga C, Carlone G, González-Casado I, Benito-Sanz S, Jorge AA, Campos-Barros A, Heath KE. Hisado-Oliva A, et al. Among authors: luzuriaga c. J Clin Endocrinol Metab. 2015 Aug;100(8):E1133-42. doi: 10.1210/jc.2015-1612. Epub 2015 Jun 15. J Clin Endocrinol Metab. 2015. PMID: 26075495
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
30 results