Argente J - Search Results

1

Functional characterization of MODY2 mutations highlights the importance of the fine-tuning of glucokinase and its role in glucose sensing.

García-Herrero CM, Rubio-Cabezas O, Azriel S, Gutierrez-Nogués A, Aragonés A, Vincent O, Campos-Barros A, Argente J, Navas MA. García-Herrero CM, et al. Among authors: argente j. PLoS One. 2012;7(1):e30518. doi: 10.1371/journal.pone.0030518. Epub 2012 Jan 24. PLoS One. 2012. PMID: 22291974 Free PMC article.

2

Ghrelin levels in obesity and anorexia nervosa: effect of weight reduction or recuperation.

Soriano-Guillén L, Barrios V, Campos-Barros A, Argente J. Soriano-Guillén L, et al. Among authors: argente j. J Pediatr. 2004 Jan;144(1):36-42. doi: 10.1016/j.jpeds.2003.10.036. J Pediatr. 2004. PMID: 14722516

3

Effect of oral glucose administration on ghrelin levels in obese children.

Soriano-Guillén L, Barrios V, Martos G, Chowen JA, Campos-Barros A, Argente J. Soriano-Guillén L, et al. Among authors: argente j. Eur J Endocrinol. 2004 Jul;151(1):119-21. doi: 10.1530/eje.0.1510119. Eur J Endocrinol. 2004. PMID: 15248831

4

A novel class of Pseudoautosomal region 1 deletions downstream of SHOX is associated with Leri-Weill dyschondrosteosis.

Benito-Sanz S, Thomas NS, Huber C, Gorbenko del Blanco D, Aza-Carmona M, Crolla JA, Maloney V, Rappold G, Argente J, Campos-Barros A, Cormier-Daire V, Heath KE. Benito-Sanz S, et al. Among authors: argente j. Am J Hum Genet. 2005 Oct;77(4):533-44. doi: 10.1086/449313. Epub 2005 Aug 15. Am J Hum Genet. 2005. PMID: 16175500 Free PMC article.

5

Genetic basis of proportional short stature.

Campos-Barros A, Heath KE, Argente J. Campos-Barros A, et al. Among authors: argente j. Adv Exp Med Biol. 2005;567:341-83. doi: 10.1007/0-387-26274-1_14. Adv Exp Med Biol. 2005. PMID: 16370145 Review. No abstract available.

6

PAR1 deletions downstream of SHOX are the most frequent defect in a Spanish cohort of Léri-Weill dyschondrosteosis (LWD) probands.

Benito-Sanz S, del Blanco DG, Aza-Carmona M, Magano LF, Lapunzina P, Argente J, Campos-Barros A, Heath KE. Benito-Sanz S, et al. Among authors: argente j. Hum Mutat. 2006 Oct;27(10):1062. doi: 10.1002/humu.9456. Hum Mutat. 2006. PMID: 16941489

7

Permanent neonatal diabetes caused by a homozygous nonsense mutation in the glucokinase gene.

Rubio-Cabezas O, Díaz González F, Aragonés A, Argente J, Campos-Barros A. Rubio-Cabezas O, et al. Among authors: argente j. Pediatr Diabetes. 2008 Jun;9(3 Pt 1):245-9. doi: 10.1111/j.1399-5448.2007.00361.x. Epub 2008 Feb 21. Pediatr Diabetes. 2008. PMID: 18298419

8

Primary acid-labile subunit deficiency due to recessive IGFALS mutations results in postnatal growth deficit associated with low circulating insulin growth factor (IGF)-I, IGF binding protein-3 levels, and hyperinsulinemia.

Heath KE, Argente J, Barrios V, Pozo J, Díaz-González F, Martos-Moreno GA, Caimari M, Gracia R, Campos-Barros A. Heath KE, et al. Among authors: argente j. J Clin Endocrinol Metab. 2008 May;93(5):1616-24. doi: 10.1210/jc.2007-2678. Epub 2008 Feb 26. J Clin Endocrinol Metab. 2008. PMID: 18303074

9

Current insights into the genetic basis of diabetes mellitus in children and adolescents.

Rubio-Cabezas O, Argente J. Rubio-Cabezas O, et al. Among authors: argente j. J Pediatr Endocrinol Metab. 2008 Oct;21(10):917-40. doi: 10.1515/jpem.2008.21.10.917. J Pediatr Endocrinol Metab. 2008. PMID: 19209614 Review.

10

Testing for monogenic diabetes among children and adolescents with antibody-negative clinically defined Type 1 diabetes.

Rubio-Cabezas O, Edghill EL, Argente J, Hattersley AT. Rubio-Cabezas O, et al. Among authors: argente j. Diabet Med. 2009 Oct;26(10):1070-4. doi: 10.1111/j.1464-5491.2009.02812.x. Diabet Med. 2009. PMID: 19900242

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