Muda AO - Search Results

1

Identification of CANT1 mutations in Desbuquois dysplasia.

Huber C, Oulès B, Bertoli M, Chami M, Fradin M, Alanay Y, Al-Gazali LI, Ausems MG, Bitoun P, Cavalcanti DP, Krebs A, Le Merrer M, Mortier G, Shafeghati Y, Superti-Furga A, Robertson SP, Le Goff C, Muda AO, Paterlini-Bréchot P, Munnich A, Cormier-Daire V. Huber C, et al. Among authors: muda ao. Am J Hum Genet. 2009 Nov;85(5):706-10. doi: 10.1016/j.ajhg.2009.10.001. Epub 2009 Oct 22. Am J Hum Genet. 2009. PMID: 19853239 Free PMC article.

2

Podocin inactivation in mature kidneys causes focal segmental glomerulosclerosis and nephrotic syndrome.

Mollet G, Ratelade J, Boyer O, Muda AO, Morisset L, Lavin TA, Kitzis D, Dallman MJ, Bugeon L, Hubner N, Gubler MC, Antignac C, Esquivel EL. Mollet G, et al. Among authors: muda ao. J Am Soc Nephrol. 2009 Oct;20(10):2181-9. doi: 10.1681/ASN.2009040379. Epub 2009 Aug 27. J Am Soc Nephrol. 2009. PMID: 19713307 Free PMC article.

3

Maternal environment interacts with modifier genes to influence progression of nephrotic syndrome.

Ratelade J, Lavin TA, Muda AO, Morisset L, Mollet G, Boyer O, Chen DS, Henger A, Kretzler M, Hubner N, Théry C, Gubler MC, Montagutelli X, Antignac C, Esquivel EL. Ratelade J, et al. Among authors: muda ao. J Am Soc Nephrol. 2008 Aug;19(8):1491-9. doi: 10.1681/ASN.2007111268. Epub 2008 Apr 2. J Am Soc Nephrol. 2008. PMID: 18385421 Free PMC article.

4

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

5

AKT2 is essential to maintain podocyte viability and function during chronic kidney disease.

Canaud G, Bienaimé F, Viau A, Treins C, Baron W, Nguyen C, Burtin M, Berissi S, Giannakakis K, Muda AO, Zschiedrich S, Huber TB, Friedlander G, Legendre C, Pontoglio M, Pende M, Terzi F. Canaud G, et al. Among authors: muda ao. Nat Med. 2013 Oct;19(10):1288-96. doi: 10.1038/nm.3313. Epub 2013 Sep 22. Nat Med. 2013. PMID: 24056770

6

Glomerular hypertrophy and chronic renal failure in focal segmental glomerulosclerosis.

Muda AO, Feriozzi S, Cinotti GA, Faraggiana T. Muda AO, et al. Am J Kidney Dis. 1994 Feb;23(2):237-41. doi: 10.1016/s0272-6386(12)80978-4. Am J Kidney Dis. 1994. PMID: 8311081

7

Ultrastructural and immunohistochemical findings in Alport's syndrome: a study of 108 patients from 97 Italian families with particular emphasis on COL4A5 gene mutation correlations.

Mazzucco G, Barsotti P, Muda AO, Fortunato M, Mihatsch M, Torri-Tarelli L, Renieri A, Faraggiana T, De Marchi M, Monga G. Mazzucco G, et al. Among authors: muda ao. J Am Soc Nephrol. 1998 Jun;9(6):1023-31. doi: 10.1681/ASN.V961023. J Am Soc Nephrol. 1998. PMID: 9621285

8

Aberrantly glycosylated IgA1 in glomerular immune deposits of IgA nephropathy.

Giannakakis K, Feriozzi S, Perez M, Faraggiana T, Muda AO. Giannakakis K, et al. Among authors: muda ao. J Am Soc Nephrol. 2007 Dec;18(12):3139-46. doi: 10.1681/ASN.2007030259. Epub 2007 Oct 31. J Am Soc Nephrol. 2007. PMID: 17978312 No abstract available.

9

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

10

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.

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