Calevo MG - Search Results

1

A new method for analysis of mitochondrial DNA point mutations and assess levels of heteroplasmy.

Cassandrini D, Calevo MG, Tessa A, Manfredi G, Fattori F, Meschini MC, Carrozzo R, Tonoli E, Pedemonte M, Minetti C, Zara F, Santorelli FM, Bruno C. Cassandrini D, et al. Among authors: calevo mg. Biochem Biophys Res Commun. 2006 Apr 7;342(2):387-93. doi: 10.1016/j.bbrc.2006.01.152. Epub 2006 Feb 8. Biochem Biophys Res Commun. 2006. PMID: 16483543

2

Homocysteine, folate, vitamin B12 levels, and C677T MTHFR mutation in children with renal failure.

Canepa A, Carrea A, Caridi G, Dertenois L, Minniti G, Cerone R, Canini S, Calevo MG, Perfumo F. Canepa A, et al. Among authors: calevo mg. Pediatr Nephrol. 2003 Mar;18(3):225-9. doi: 10.1007/s00467-002-1058-0. Epub 2003 Feb 21. Pediatr Nephrol. 2003. PMID: 12644913

3

Evaluation of a methylenetetrahydrofolate-dehydrogenase 1958G>A polymorphism for neural tube defect risk.

De Marco P, Merello E, Calevo MG, Mascelli S, Raso A, Cama A, Capra V. De Marco P, et al. Among authors: calevo mg. J Hum Genet. 2006;51(2):98-103. doi: 10.1007/s10038-005-0329-6. Epub 2005 Nov 29. J Hum Genet. 2006. PMID: 16315005

4

Mutation pattern of paired immunoglobulin heavy and light variable domains in chronic lymphocytic leukemia B cells.

Ghiotto F, Marcatili P, Tenca C, Calevo MG, Yan XJ, Albesiano E, Bagnara D, Colombo M, Cutrona G, Chu CC, Morabito F, Bruno S, Ferrarini M, Tramontano A, Fais F, Chiorazzi N. Ghiotto F, et al. Among authors: calevo mg. Mol Med. 2011;17(11-12):1188-95. doi: 10.2119/molmed.2011.00104. Epub 2011 Jul 13. Mol Med. 2011. PMID: 21785810 Free PMC article.

5

Metabolic and genetic risk factors for migraine in children.

Bottini F, Celle ME, Calevo MG, Amato S, Minniti G, Montaldi L, Di Pasquale D, Cerone R, Veneselli E, Molinari AC. Bottini F, et al. Among authors: calevo mg. Cephalalgia. 2006 Jun;26(6):731-7. doi: 10.1111/j.1468-2982.2006.01107.x. Cephalalgia. 2006. PMID: 16686913 Clinical Trial.

6

Comparison of patient hospitalization in chronic peritoneal dialysis and hemodialysis: a pediatric multicenter study.

Verrina E, Perfumo F, Zacchello G, Sorino P, Edefonti A, Bassi S, Calevo MG, Caringella DL, Cattarelli D, Lavoratti G, Consalvo G, Andreetta B, Rinaldi S, Longo L, Gusmano R. Verrina E, et al. Among authors: calevo mg. Perit Dial Int. 1996;16 Suppl 1:S574-7. Perit Dial Int. 1996. PMID: 8728274

7

The Italian Pediatric Chronic Peritoneal Dialysis Registry.

Verrina E, Perfumo F, Calevo MG, Rinaldi S, Sorino P, Andreetta B, Bonaudo R, Lavoratti G, Edefonti A. Verrina E, et al. Among authors: calevo mg. Perit Dial Int. 1999;19 Suppl 2:S479-83. Perit Dial Int. 1999. PMID: 10406568 No abstract available.

8

Low total plasma homocysteine concentrations in patients with type 1 diabetes.

Cotellessa M, Minniti G, Cerone R, Prigione F, Calevo MG, Lorini R. Cotellessa M, et al. Among authors: calevo mg. Diabetes Care. 2001 May;24(5):969-71. doi: 10.2337/diacare.24.5.969. Diabetes Care. 2001. PMID: 11347774 No abstract available.

9

Polymorphisms in genes involved in folate metabolism as risk factors for NTDs.

De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Cama A, Finnell RH, Andreussi L, Capra V. De Marco P, et al. Among authors: calevo mg. Eur J Pediatr Surg. 2001 Dec;11 Suppl 1:S14-7. doi: 10.1055/s-2001-19739. Eur J Pediatr Surg. 2001. PMID: 11813127

10

Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population.

De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V. De Marco P, et al. Among authors: calevo mg. J Hum Genet. 2002;47(6):319-24. doi: 10.1007/s100380200043. J Hum Genet. 2002. PMID: 12111380

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