Seri M - Search Results

1

Epstein-Barr virus and gastric cancer: data and unanswered questions.

Leoncini L, Vindigni C, Megha T, Funtò I, Pacenti L, Musarò M, Renieri A, Seri M, Anagnostopoulos J, Tosi P. Leoncini L, et al. Among authors: seri m. Int J Cancer. 1993 Apr 1;53(6):898-901. doi: 10.1002/ijc.2910530605. Int J Cancer. 1993. PMID: 7682538

2

Molecular characterization of the P and I variants of alpha 1-antitrypsin.

Seri M, Magi B, Cellesi C, Olia PM, Renieri A, De Marchi M. Seri M, et al. Int J Clin Lab Res. 1992;22(2):119-21. doi: 10.1007/BF02591409. Int J Clin Lab Res. 1992. PMID: 1504305

3

De novo mutation in the COL4A5 gene converting glycine 325 to glutamic acid in Alport syndrome.

Renieri A, Seri M, Myers JC, Pihlajaniemi T, Massella L, Rizzoni G, De Marchi M. Renieri A, et al. Among authors: seri m. Hum Mol Genet. 1992 May;1(2):127-9. doi: 10.1093/hmg/1.2.127. Hum Mol Genet. 1992. PMID: 1363780

4

Small frameshift deletions within the COL4A5 gene in juvenile-onset Alport syndrome.

Renieri A, Seri M, Galli L, Cosci P, Imbasciati E, Massella L, Rizzoni G, Restagno G, Carbonara AO, Stramignoni E, et al. Renieri A, et al. Among authors: seri m. Hum Genet. 1993 Oct;92(4):417-20. doi: 10.1007/BF01247348. Hum Genet. 1993. PMID: 8225325

5

Alport syndrome caused by a 5' deletion within the COL4A5 gene.

Renieri A, Seri M, Myers JC, Pihlajaniemi T, Sessa A, Rizzoni G, De Marchi M. Renieri A, et al. Among authors: seri m. Hum Genet. 1992 Apr;89(1):120-1. doi: 10.1007/BF00207059. Hum Genet. 1992. PMID: 1577459

6

KCNE1-like gene is deleted in AMME contiguous gene syndrome: identification and characterization of the human and mouse homologs.

Piccini M, Vitelli F, Seri M, Galietta LJ, Moran O, Bulfone A, Banfi S, Pober B, Renieri A. Piccini M, et al. Among authors: seri m. Genomics. 1999 Sep 15;60(3):251-7. doi: 10.1006/geno.1999.5904. Genomics. 1999. PMID: 10493825

7

Autosomal-dominant Alport syndrome: natural history of a disease due to COL4A3 or COL4A4 gene.

Pescucci C, Mari F, Longo I, Vogiatzi P, Caselli R, Scala E, Abaterusso C, Gusmano R, Seri M, Miglietti N, Bresin E, Renieri A. Pescucci C, et al. Among authors: seri m. Kidney Int. 2004 May;65(5):1598-603. doi: 10.1111/j.1523-1755.2004.00560.x. Kidney Int. 2004. PMID: 15086897 Free article.

8

Pseudoxanthoma elasticum: Point mutations in the ABCC6 gene and a large deletion including also ABCC1 and MYH11.

Meloni I, Rubegni P, De Aloe G, Bruttini M, Pianigiani E, Cusano R, Seri M, Mondillo S, Federico A, Bardelli AM, Andreassi L, Fimiani M, Renieri A. Meloni I, et al. Among authors: seri m. Hum Mutat. 2001;18(1):85. doi: 10.1002/humu.1157. Hum Mutat. 2001. PMID: 11439001

9

9q31.1q31.3 deletion in two patients with similar clinical features: a newly recognized microdeletion syndrome?

Mucciolo M, Magini P, Marozza A, Mongelli P, Mencarelli MA, Hayek G, Tavalazzi F, Mari F, Seri M, Renieri A, Graziano C. Mucciolo M, et al. Among authors: seri m. Am J Med Genet A. 2014 Mar;164A(3):685-90. doi: 10.1002/ajmg.a.36361. Epub 2013 Dec 20. Am J Med Genet A. 2014. PMID: 24376033

10

Autosomal dominant aplasia cutis congenita: report of a large Italian family and no hint for candidate chromosomal regions.

Fimiani M, Seri M, Rubegni P, Cusano R, De Aloe G, Forabosco P, Devoto M, Andreassi L, Renieri A. Fimiani M, et al. Among authors: seri m. Arch Dermatol Res. 1999 Dec;291(12):637-42. doi: 10.1007/s004030050468. Arch Dermatol Res. 1999. PMID: 10651164

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