Cappa M - Search Results

1

Multiorgan autoimmunity in a Turner syndrome patient with partial monosomy 2q and trisomy 10p.

Grossi A, Palma A, Zanni G, Novelli A, Loddo S, Cappa M, Fierabracci A. Grossi A, et al. Among authors: cappa m. Gene. 2013 Feb 25;515(2):439-43. doi: 10.1016/j.gene.2012.12.007. Epub 2012 Dec 20. Gene. 2013. PMID: 23262341

2

An 8-year-old boy with autoimmune hepatitis and Candida onychosis as the first symptoms of autoimmune polyglandular syndrome (APS1): identification of a new homozygous mutation in the autoimmune regulator gene (AIRE).

Lintas C, Cappa M, Comparcola D, Nobili V, Fierabracci A. Lintas C, et al. Among authors: cappa m. Eur J Pediatr. 2008 Aug;167(8):949-53. doi: 10.1007/s00431-007-0599-4. Epub 2007 Sep 21. Eur J Pediatr. 2008. PMID: 17891543

3

Cardiovascular fitness, insulin resistance and metabolic syndrome in severely obese prepubertal Italian children.

Brufani C, Grossi A, Fintini D, Fiori R, Ubertini G, Colabianchi D, Ciampalini P, Tozzi A, Barbetti F, Cappa M. Brufani C, et al. Among authors: cappa m. Horm Res. 2008;70(6):349-56. doi: 10.1159/000161865. Epub 2008 Oct 27. Horm Res. 2008. PMID: 18953172

4

Sexual dimorphism of body composition and insulin sensitivity across pubertal development in obese Caucasian subjects.

Brufani C, Tozzi A, Fintini D, Ciampalini P, Grossi A, Fiori R, Kiepe D, Manco M, Schiaffini R, Porzio O, Cappa M, Barbetti F. Brufani C, et al. Among authors: cappa m. Eur J Endocrinol. 2009 May;160(5):769-75. doi: 10.1530/EJE-08-0878. Epub 2009 Feb 16. Eur J Endocrinol. 2009. PMID: 19221173

5

Glucose tolerance status in 510 children and adolescents attending an obesity clinic in Central Italy.

Brufani C, Ciampalini P, Grossi A, Fiori R, Fintini D, Tozzi A, Cappa M, Barbetti F. Brufani C, et al. Among authors: cappa m. Pediatr Diabetes. 2010 Feb;11(1):47-54. doi: 10.1111/j.1399-5448.2009.00527.x. Epub 2009 Apr 30. Pediatr Diabetes. 2010. PMID: 19460122

6

Obese children with low birth weight demonstrate impaired beta-cell function during oral glucose tolerance test.

Brufani C, Grossi A, Fintini D, Tozzi A, Nocerino V, Patera PI, Ubertini G, Porzio O, Barbetti F, Cappa M. Brufani C, et al. Among authors: cappa m. J Clin Endocrinol Metab. 2009 Nov;94(11):4448-52. doi: 10.1210/jc.2009-1079. Epub 2009 Oct 9. J Clin Endocrinol Metab. 2009. PMID: 19820011

7

Blood Pressure and Left Ventricular Characteristics in Young Patients with Classical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency.

Ubertini G, Bizzarri C, Grossi A, Gimigliano F, Ravà L, Fintini D, Cappa M. Ubertini G, et al. Among authors: cappa m. Int J Pediatr Endocrinol. 2009;2009:383610. doi: 10.1155/2009/383610. Epub 2010 Feb 7. Int J Pediatr Endocrinol. 2009. PMID: 20169124 Free PMC article.

8

A case of primary selective hypoaldosteronism carrying three mutations in the aldosterone synthase (Cyp11b2) gene.

Taranta A, Bizzarri C, Masotti A, Sciré G, Pampanini V, Cappa M. Taranta A, et al. Among authors: cappa m. Gene. 2012 May 25;500(1):22-7. doi: 10.1016/j.gene.2012.02.052. Epub 2012 Mar 24. Gene. 2012. PMID: 22465514

9

A novel heterozygous mutation of the AIRE gene in a patient with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED).

Fierabracci A, Bizzarri C, Palma A, Milillo A, Bellacchio E, Cappa M. Fierabracci A, et al. Among authors: cappa m. Gene. 2012 Dec 10;511(1):113-7. doi: 10.1016/j.gene.2012.09.029. Epub 2012 Sep 18. Gene. 2012. PMID: 23000069

10

Analysis of the autoimmune regulator gene in patients with autoimmune non-APECED polyendocrinopathies.

Palma A, Gianchecchi E, Palombi M, Luciano R, Di Carlo P, Crinò A, Cappa M, Fierabracci A. Palma A, et al. Among authors: cappa m. Genomics. 2013 Sep;102(3):163-8. doi: 10.1016/j.ygeno.2013.04.016. Epub 2013 Apr 30. Genomics. 2013. PMID: 23643663 Free article.

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