Marangella M - Search Results

1

Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase gene.

Pirulli D, Puzzer D, Ferri L, Crovella S, Amoroso A, Ferrettini C, Marangella M, Mazzola G, Florian F. Pirulli D, et al. Among authors: marangella m. Hum Genet. 1999 Jun;104(6):523-5. doi: 10.1007/s004390050998. Hum Genet. 1999. PMID: 10453743

2

AGXT gene mutations and their influence on clinical heterogeneity of type 1 primary hyperoxaluria.

Amoroso A, Pirulli D, Florian F, Puzzer D, Boniotto M, Crovella S, Zezlina S, Spanò A, Mazzola G, Savoldi S, Ferrettini C, Berutti S, Petrarulo M, Marangella M. Amoroso A, et al. Among authors: marangella m. J Am Soc Nephrol. 2001 Oct;12(10):2072-2079. doi: 10.1681/ASN.V12102072. J Am Soc Nephrol. 2001. PMID: 11562405

3

Primary hyperoxaluria: genotype-phenotype correlation.

Pirulli D, Marangella M, Amoroso A. Pirulli D, et al. Among authors: marangella m. J Nephrol. 2003 Mar-Apr;16(2):297-309. J Nephrol. 2003. PMID: 12768081 Review.

4

Molecular analysis of the AGXT gene in Italian patients with primary hyperoxaluria type 1 (PH1).

Ferrettini C, Pirulli D, Cosseddu D, Marangella M, Petrarulo M, Mazzola G, Vatta S, Amoroso A. Ferrettini C, et al. Among authors: marangella m. J Nephrol. 1998 Mar-Apr;11 Suppl 1:18-22. J Nephrol. 1998. PMID: 9604804

5

Gene symbol: AGXT. Disease: primary hyperoxaluria type I.

Amoroso A, Pirulli D, Puzzer D, Ferri L, Crovella S, Ferrettini C, Marangella M, Mazzola G, Florian F. Amoroso A, et al. Among authors: marangella m. Hum Genet. 1999 May;104(5):441. doi: 10.1007/s004390050984. Hum Genet. 1999. PMID: 10394939 No abstract available.

6

Detection of AGXT bgene mutations by denaturing high-performance liquid chromatography for diagnosis of hyperoxaluria type 1.

Pirulli D, Giordano M, Lessi M, Spanò A, Puzzer D, Zezlina S, Boniotto M, Crovella S, Florian F, Marangella M, Momigliano-Richiardi P, Savoldi S, Amoroso A. Pirulli D, et al. Among authors: marangella m. Clin Exp Med. 2001 Jun;1(2):99-104. doi: 10.1007/s10238-001-8019-y. Clin Exp Med. 2001. PMID: 11699734

7

Severe course of primary hyperoxaluria and renal failure after domino hepatic transplantation.

Franchello A, Paraluppi G, Romagnoli R, Petrarulo M, Vitale C, Pacitti A, Amoroso A, Marangella M, Salizzoni M. Franchello A, et al. Among authors: marangella m. Am J Transplant. 2005 Sep;5(9):2324-7. doi: 10.1111/j.1600-6143.2005.01014.x. Am J Transplant. 2005. PMID: 16095518 Free article.

8

Updated genetic testing of Italian patients referred with a clinical diagnosis of primary hyperoxaluria.

Pelle A, Cuccurullo A, Mancini C, Sebastiano R, Stallone G, Negrisolo S, Benetti E, Peruzzi L, Petrarulo M, De Marchi M, Marangella M, Amoroso A, Giachino D, Mandrile G. Pelle A, et al. Among authors: marangella m. J Nephrol. 2017 Apr;30(2):219-225. doi: 10.1007/s40620-016-0287-4. Epub 2016 Mar 5. J Nephrol. 2017. PMID: 26946417 Free article.

9

The primary hyperoxalurias.

Marangella M, Petrarulo M, Vitale C, Bagnis C, Berutti S, Ramello A, Amoroso A. Marangella M, et al. Contrib Nephrol. 2001;(136):11-32. doi: 10.1159/000060176. Contrib Nephrol. 2001. PMID: 11688375 Review. No abstract available.

10

High-performance liquid chromatographic microassay for L-alanine:glyoxylate aminotransferase activity in human liver.

Petrarulo M, Pellegrino S, Marangella M, Cosseddu D, Linari F. Petrarulo M, et al. Among authors: marangella m. Clin Chim Acta. 1992 Jun 30;208(3):183-92. doi: 10.1016/0009-8981(92)90075-2. Clin Chim Acta. 1992. PMID: 1499137

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