Iascone MR - Search Results

1

Association between 5,10-methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and conotruncal heart defects.

Storti S, Vittorini S, Iascone MR, Sacchelli M, Collavoli A, Ripoli A, Cocchi G, Biagini A, Clerico A. Storti S, et al. Among authors: iascone mr. Clin Chem Lab Med. 2003 Mar;41(3):276-80. doi: 10.1515/CCLM.2003.043. Clin Chem Lab Med. 2003. PMID: 12705333

2

Analysis of the variation in the hsp70-1 and hsp90alpha mRNA expression in human myocardial tissue that has undergone surgical stress.

Storti S, Vittorini S, Iascone MR, Sacchelli M, Baroni A, Luisi VS, Crucean A, Vanini V, Biagini A, Clerico A. Storti S, et al. Among authors: iascone mr. Cell Stress Chaperones. 2003 Spring;8(1):18-25. doi: 10.1379/1466-1268(2003)8<18:aotvit>2.0.co;2. Cell Stress Chaperones. 2003. PMID: 12820651 Free PMC article.

3

Molecular characterization of 22q11 deletion in a three-generation family with maternal transmission.

Iascone MR, Vittorini S, Sacchelli M, Spadoni I, Simi P, Giusti S. Iascone MR, et al. Am J Med Genet. 2002 Apr 1;108(4):319-21. Am J Med Genet. 2002. PMID: 11920838

4

Evaluation of the endocrine function of the heart in humans: proposal for an integrated approach for the assessment of production, secretion, distribution and degradation of atrial natriuretic factor and related peptides.

Clerico A, Iervasi G, Iascone MR, Manfredi C, Sabatino L, Bertelli A, Iascone MR, Bertelli AA. Clerico A, et al. Among authors: iascone mr. Int J Clin Pharmacol Res. 1995;15(2):65-86. Int J Clin Pharmacol Res. 1995. PMID: 8593975 Review.

5

Familial occurrence of isolated right ventricular hypoplasia.

Chessa M, Redaelli S, Masszi G, Iascone M, Carminati M. Chessa M, et al. Am J Med Genet. 2000 Feb 28;90(5):356-7. doi: 10.1002/(sici)1096-8628(20000228)90:5<356::aid-ajmg2>3.0.co;2-c. Am J Med Genet. 2000. PMID: 10706354

6

De novo deletion of 1q31.1-q32.1 in a patient with developmental delay and behavioral disorders.

Milani D, Bedeschi MF, Iascone M, Chiarelli G, Cerutti M, Menni F. Milani D, et al. Cytogenet Genome Res. 2012;136(3):167-70. doi: 10.1159/000336979. Epub 2012 Mar 7. Cytogenet Genome Res. 2012. PMID: 22398643

7

Clinical and molecular characterization of two patients with palmoplantar keratoderma-congenital alopecia syndrome type 2.

Castori M, Morlino S, Sana ME, Paradisi M, Tadini G, Angioni A, Malacarne M, Grammatico P, Iascone M, Forzano F. Castori M, et al. Clin Exp Dermatol. 2016 Aug;41(6):632-5. doi: 10.1111/ced.12857. Epub 2016 Jun 24. Clin Exp Dermatol. 2016. PMID: 27339777

8

Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic.

Iascone MR, Marchetti D, Lincesso AR, Iacovoni A, Ferrazzi P. Iascone MR, et al. Hum Genet. 2009 Aug;126(2):351. Hum Genet. 2009. PMID: 19694057 No abstract available.

9

Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.

Marchetti D, Iascone MR, Pezzoli L. Marchetti D, et al. Among authors: iascone mr. Hum Genet. 2009 Aug;126(2):350-1. Hum Genet. 2009. PMID: 19694056 No abstract available.

10

Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.

Marchetti D, Iascone MR, Pezzoli L. Marchetti D, et al. Among authors: iascone mr. Hum Genet. 2009 Aug;126(2):350. Hum Genet. 2009. PMID: 19694055 No abstract available.

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