D'Adamo M - Search Results

1

Relationship between Regional Fat Distribution and Hypertrophic Cardiomyopathy Phenotype.

Guglielmi V, Maresca L, Lanzillo C, Marinoni GM, D'Adamo M, Di Roma M, Preziosi P, Bellia A, Calò L, Sbraccia P. Guglielmi V, et al. PLoS One. 2016 Jul 7;11(7):e0158892. doi: 10.1371/journal.pone.0158892. eCollection 2016. PLoS One. 2016. PMID: 27388274 Free PMC article.

2

Expression of insulin/IGF-I hybrid receptors is increased in skeletal muscle of patients with chronic primary hyperinsulinemia.

Federici M, Lauro D, D'Adamo M, Giovannone B, Porzio O, Mellozzi M, Tamburrano G, Sbraccia P, Sesti G. Federici M, et al. Diabetes. 1998 Jan;47(1):87-92. doi: 10.2337/diab.47.1.87. Diabetes. 1998. PMID: 9421379

3

Expression of the two insulin receptor isoforms is not altered in the skeletal muscle and liver of diabetic rats.

Sbraccia P, Giaccari A, D'Adamo M, Caiola S, Morviducci L, Zorretta D, Maroccia E, Buongiorno A, Tamburrano G. Sbraccia P, et al. Metabolism. 1998 Feb;47(2):129-32. doi: 10.1016/s0026-0495(98)90207-4. Metabolism. 1998. PMID: 9472957

4

Relationship between plasma free fatty acids and uncoupling protein-3 gene expression in skeletal muscle of obese subjects: in vitro evidence of a causal link.

Sbraccia P, D'Adamo M, Leonetti F, Buongiorno A, Silecchia G, Basso MS, Tamburrano G, Lauro D, Federici M, Di Daniele N, Lauro R. Sbraccia P, et al. Clin Endocrinol (Oxf). 2002 Aug;57(2):199-207. doi: 10.1046/j.1365-2265.2002.01593.x. Clin Endocrinol (Oxf). 2002. PMID: 12153598

5

The -866A/A genotype in the promoter of the human uncoupling protein 2 gene is associated with insulin resistance and increased risk of type 2 diabetes.

D'Adamo M, Perego L, Cardellini M, Marini MA, Frontoni S, Andreozzi F, Sciacqua A, Lauro D, Sbraccia P, Federici M, Paganelli M, Pontiroli AE, Lauro R, Perticone F, Folli F, Sesti G. D'Adamo M, et al. Diabetes. 2004 Jul;53(7):1905-10. doi: 10.2337/diabetes.53.7.1905. Diabetes. 2004. PMID: 15220218

6

Gene expression profiling of fibroblasts from a human progeroid disease (mandibuloacral dysplasia, MAD #248370) through cDNA microarrays.

Amati F, Biancolella M, D'Apice MR, Gambardella S, Mango R, Sbraccia P, D'Adamo M, Margiotti K, Nardone A, Lewis M, Novelli G. Amati F, et al. Gene Expr. 2004;12(1):39-47. doi: 10.3727/000000004783992189. Gene Expr. 2004. PMID: 15473259 Free PMC article.

7

Compound heterozygosity for mutations in LMNA in a patient with a myopathic and lipodystrophic mandibuloacral dysplasia type A phenotype.

Lombardi F, Gullotta F, Columbaro M, Filareto A, D'Adamo M, Vielle A, Guglielmi V, Nardone AM, Azzolini V, Grosso E, Lattanzi G, D'Apice MR, Masala S, Maraldi NM, Sbraccia P, Novelli G. Lombardi F, et al. J Clin Endocrinol Metab. 2007 Nov;92(11):4467-71. doi: 10.1210/jc.2007-0116. Epub 2007 Sep 11. J Clin Endocrinol Metab. 2007. PMID: 17848409

8

Increased release and activity of matrix metalloproteinase-9 in patients with mandibuloacral dysplasia type A, a rare premature ageing syndrome.

Lombardi F, Fasciglione GF, D'Apice MR, Vielle A, D'Adamo M, Sbraccia P, Marini S, Borgiani P, Coletta M, Novelli G. Lombardi F, et al. Clin Genet. 2008 Oct;74(4):374-83. doi: 10.1111/j.1399-0004.2008.01034.x. Epub 2008 Jun 28. Clin Genet. 2008. PMID: 18554282 Free article.

9

A rare cardiac finding in a morbidly obese patient with severe hypertension.

Fiore AM, Marinoni GM, Piccione A, Marini MA, D'Adamo M, Lauro R, Sbraccia P. Fiore AM, et al. Intern Emerg Med. 2011 Jun;6(3):241-4. doi: 10.1007/s11739-010-0472-8. Epub 2010 Oct 9. Intern Emerg Med. 2011. PMID: 20936437 No abstract available.

10

Elbow deformities in a patient with mandibuloacral dysplasia type A.

Guglielmi V, D'Adamo M, D'Apice MR, Bellia A, Lauro D, Federici M, Lauro R, Novelli G, Sbraccia P. Guglielmi V, et al. Am J Med Genet A. 2010 Nov;152A(11):2711-3. doi: 10.1002/ajmg.a.33700. Am J Med Genet A. 2010. PMID: 20949529 No abstract available.

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