Diegoli M - Search Results

1

Glomuvenous malformations with smooth muscle and eccrine glands: unusual histopathologic features in a familial setting.

Borroni RG, Grassi S, Concardi M, Puccio I, Giordano C, Agozzino M, Caspani C, Grasso M, Diegoli M, Arbustini E. Borroni RG, et al. Among authors: diegoli m. J Cutan Pathol. 2014 Mar;41(3):308-15. doi: 10.1111/cup.12283. Epub 2014 Jan 20. J Cutan Pathol. 2014. PMID: 24345188

2

Incomplete penetrance of GLMN gene c.395-1G>C mutation in a family with glomuvenous malformations.

Borroni RG, Grassi S, Diegoli M, Grasso M, Arbustini E. Borroni RG, et al. Among authors: diegoli m. Int J Dermatol. 2014 Nov;53(11):1362-4. doi: 10.1111/ijd.12588. Epub 2014 Jun 25. Int J Dermatol. 2014. PMID: 24961656

3

A novel mutation of the glomulin gene in an Italian family with autosomal dominant cutaneous glomuvenous malformations.

Borroni RG, Narula N, Diegoli M, Grasso M, Concardi M, Rosso R, Cerica A, Brazzelli V, Arbustini E. Borroni RG, et al. Among authors: diegoli m. Exp Dermatol. 2011 Dec;20(12):1032-4. doi: 10.1111/j.1600-0625.2011.01387.x. Exp Dermatol. 2011. PMID: 22092580

4

Rare exon 10 deletion in POLH gene in a family with xeroderma pigmentosum variant correlating with protein expression by immunohistochemistry.

Borroni RG, Diegoli M, Grasso M, Concardi M, Agozzino M, Vignini M, Arbustini E. Borroni RG, et al. Among authors: diegoli m. G Ital Dermatol Venereol. 2020 Jun;155(3):349-354. doi: 10.23736/S0392-0488.16.05158-0. G Ital Dermatol Venereol. 2020. PMID: 32635709

5

Barth syndrome associated with compound hemizygosity and heterozygosity of the TAZ and LDB3 genes.

Marziliano N, Mannarino S, Nespoli L, Diegoli M, Pasotti M, Malattia C, Grasso M, Pilotto A, Porcu E, Raisaro A, Raineri C, Dore R, Maggio PP, Brega A, Arbustini E. Marziliano N, et al. Among authors: diegoli m. Am J Med Genet A. 2007 May 1;143A(9):907-15. doi: 10.1002/ajmg.a.31653. Am J Med Genet A. 2007. PMID: 17394203 Free article.

6

Genetic counselling and high-penetrance susceptibility gene analysis reveal the novel CDKN2A p.D84V (c.251A>T) mutation in melanoma-prone families from Italy.

Borroni RG, Manganoni AM, Grassi S, Grasso M, Diegoli M, Giorgianni C, Favalli V, Pavoni L, Cespa M, Arbustini E. Borroni RG, et al. Among authors: diegoli m. Melanoma Res. 2017 Apr;27(2):97-103. doi: 10.1097/CMR.0000000000000324. Melanoma Res. 2017. PMID: 28060055

7

Histopathologic and molecular profile of human cytomegalovirus infections in patients with heart transplants.

Arbustini E, Grasso M, Diegoli M, Percivalle E, Grossi P, Bramerio M, Campana C, Goggi C, Gavazzi A, Vigano M. Arbustini E, et al. Among authors: diegoli m. Am J Clin Pathol. 1992 Aug;98(2):205-13. Am J Clin Pathol. 1992. PMID: 1324600

8

When should cardiologists suspect Anderson-Fabry disease?

Gambarin FI, Disabella E, Narula J, Diegoli M, Grasso M, Serio A, Favalli BM, Agozzino M, Tavazzi L, Fraser AG, Arbustini E. Gambarin FI, et al. Among authors: diegoli m. Am J Cardiol. 2010 Nov 15;106(10):1492-9. doi: 10.1016/j.amjcard.2010.07.016. Am J Cardiol. 2010. PMID: 21059442 Review.

9

Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease.

Arbustini E, Pilotto A, Repetto A, Grasso M, Negri A, Diegoli M, Campana C, Scelsi L, Baldini E, Gavazzi A, Tavazzi L. Arbustini E, et al. Among authors: diegoli m. J Am Coll Cardiol. 2002 Mar 20;39(6):981-90. doi: 10.1016/s0735-1097(02)01724-2. J Am Coll Cardiol. 2002. PMID: 11897440 Free article.

10

Transcriptomic and proteomic analysis in the cardiovascular setting: unravelling the disease?

Marziliano N, Grasso M, Pilotto A, Porcu E, Tagliani M, Disabella E, Diegoli M, Pasotti M, Favalli V, Serio A, Gambarin F, Tavazzi L, Klersy C, Arbustini E. Marziliano N, et al. Among authors: diegoli m. J Cardiovasc Med (Hagerstown). 2009 May;10(5):433-42. doi: 10.2459/jcm.0b013e328324e972. J Cardiovasc Med (Hagerstown). 2009. PMID: 19449458

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