Seri M - Search Results

1

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.

2

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

3

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

4

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

5

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

6

De-novo COL4A5 gene mutations in Alport's syndrome.

Massella L, Rizzoni G, De Blasis R, Barsotti P, Faraggiana T, Renieri A, Seri M, Galli L, De Marchi M. Massella L, et al. Among authors: seri m. Nephrol Dial Transplant. 1994;9(10):1408-11. Nephrol Dial Transplant. 1994. PMID: 7816253

7

Variability of clinical phenotype in a large Alport family with Gly 1143 Ser change of collagen alpha 5(IV)-chain.

Renieri A, Meroni M, Sessa A, Battini G, Serbelloni P, Torri Tarelli L, Seri M, Galli L, De Marchi M. Renieri A, et al. Among authors: seri m. Nephron. 1994;67(4):444-9. doi: 10.1159/000188020. Nephron. 1994. PMID: 7969679

8

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

9

Alport syndrome with type I membranoproliferative glomerulonephritis.

Meroni M, Sessa A, Battini G, Torri Tarelli L, Bertani T, Renieri A, Seri M, De Marchi M. Meroni M, et al. Among authors: seri m. Nephron. 1993;65(3):479-80. doi: 10.1159/000187539. Nephron. 1993. PMID: 8290008 Free article. No abstract available.

10

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

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