Muda AO - Search Results

1

Cyclosporine A treatment in patients with Alport syndrome: a single-center experience.

Massella L, Muda AO, Legato A, Di Zazzo G, Giannakakis K, Emma F. Massella L, et al. Among authors: muda ao. Pediatr Nephrol. 2010 Jul;25(7):1269-75. doi: 10.1007/s00467-010-1484-3. Epub 2010 Mar 18. Pediatr Nephrol. 2010. PMID: 20238228 Clinical Trial.

2

Prognostic value of glomerular collagen IV immunofluorescence studies in male patients with X-linked Alport syndrome.

Massella L, Gangemi C, Giannakakis K, Crisafi A, Faraggiana T, Fallerini C, Renieri A, Muda AO, Emma F. Massella L, et al. Among authors: muda ao. Clin J Am Soc Nephrol. 2013 May;8(5):749-55. doi: 10.2215/CJN.07510712. Epub 2013 Jan 31. Clin J Am Soc Nephrol. 2013. PMID: 23371956 Free PMC article.

3

Type VII collagen in Alport syndrome.

Giannakakis K, Massella L, Grassetti D, Dotta F, Perez M, Muda AO. Giannakakis K, et al. Among authors: muda ao. Nephrol Dial Transplant. 2007 Dec;22(12):3501-7. doi: 10.1093/ndt/gfm481. Epub 2007 Aug 1. Nephrol Dial Transplant. 2007. PMID: 17670768

4

Acquired glomerulocystic kidney disease following hemolytic uremic syndrome.

Emma F, Muda AO, Rinaldi S, Boldrini R, Bosman C, Rizzoni G. Emma F, et al. Among authors: muda ao. Pediatr Nephrol. 2001 Jul;16(7):557-60. doi: 10.1007/s004670100608. Pediatr Nephrol. 2001. PMID: 11465804

5

Alpha 5 COLIV chain distribution in glomerular basement membrane in a male with X-linked Alport syndrome and thin basement membrane.

Rizzoni G, Massella L, Muda AO. Rizzoni G, et al. Among authors: muda ao. Pediatr Nephrol. 2000 Dec;15(3-4):325. Pediatr Nephrol. 2000. PMID: 11149132 No abstract available.

6

Confocal microscopy of the skin in the diagnosis of X-linked Alport syndrome.

Muda AO, Massella L, Giannakakis K, Renieri A, Rizzoni G, Faraggiana T. Muda AO, et al. J Invest Dermatol. 2003 Jul;121(1):208-11. doi: 10.1046/j.1523-1747.2003.12322.x. J Invest Dermatol. 2003. PMID: 12839584 Free article. No abstract available.

7

COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement.

Diomedi-Camassei F, Di Giandomenico S, Santorelli FM, Caridi G, Piemonte F, Montini G, Ghiggeri GM, Murer L, Barisoni L, Pastore A, Muda AO, Valente ML, Bertini E, Emma F. Diomedi-Camassei F, et al. Among authors: muda ao. J Am Soc Nephrol. 2007 Oct;18(10):2773-80. doi: 10.1681/ASN.2006080833. Epub 2007 Sep 12. J Am Soc Nephrol. 2007. PMID: 17855635

8

Distribution of alpha-chains of type IV collagen in glomerular basement membranes with ultrastructural alterations suggestive of Alport syndrome.

Barsotti P, Muda AO, Mazzucco G, Massella L, Basolo B, De Marchi M, Rizzoni G, Monga G, Faraggiana T. Barsotti P, et al. Among authors: muda ao. Nephrol Dial Transplant. 2001 May;16(5):945-52. doi: 10.1093/ndt/16.5.945. Nephrol Dial Transplant. 2001. PMID: 11328899

9

Ultrastructural immunocytochemistry of collagenous and non-collagenous proteins in fast-frozen, freeze-substituted, and low-temperature-embedded renal tissue in Alport syndrome.

Muda AO, Rahimi S, Renieri A, Rizzoni G, Massella L, Faraggiana T. Muda AO, et al. J Pathol. 1997 Aug;182(4):465-74. doi: 10.1002/(sici)1096-9896(199708)182:4<465::aid-path465>3.0.co;2-v. J Pathol. 1997. PMID: 9306969

10

COL4A3/COL4A4 mutations: from familial hematuria to autosomal-dominant or recessive Alport syndrome.

Longo I, Porcedda P, Mari F, Giachino D, Meloni I, Deplano C, Brusco A, Bosio M, Massella L, Lavoratti G, Roccatello D, Frascá G, Mazzucco G, Muda AO, Conti M, Fasciolo F, Arrondel C, Heidet L, Renieri A, De Marchi M. Longo I, et al. Among authors: muda ao. Kidney Int. 2002 Jun;61(6):1947-56. doi: 10.1046/j.1523-1755.2002.00379.x. Kidney Int. 2002. PMID: 12028435 Free article.

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