Dionisi Vici C - Search Results

1

Analysis of Sanfilippo A gene mutations in a large pedigree.

Di Natale P, Villani GR, Di Domenico C, Daniele A, Dionisi Vici C, Bartuli A. Di Natale P, et al. Among authors: dionisi vici c. Clin Genet. 2003 Apr;63(4):314-8. doi: 10.1034/j.1399-0004.2003.00053.x. Clin Genet. 2003. PMID: 12702166

2

Fatal infantile liver failure associated with mitochondrial DNA depletion.

Mazziotta MR, Ricci E, Bertini E, Dionisi Vici C, Servidei S, Burlina AB, Sabetta G, Bartuli A, Manfredi G, Silvestri G, et al. Mazziotta MR, et al. Among authors: dionisi vici c. J Pediatr. 1992 Dec;121(6):896-901. doi: 10.1016/s0022-3476(05)80335-x. J Pediatr. 1992. PMID: 1447652 Free article.

3

Aldolase B mutations in Italian families affected by hereditary fructose intolerance.

Sebastio G, de Franchis R, Strisciuglio P, Andria G, Dionisi Vici C, Sabetta G, Gatti R, Cross NC, Cox TM. Sebastio G, et al. Among authors: dionisi vici c. J Med Genet. 1991 Apr;28(4):241-3. doi: 10.1136/jmg.28.4.241. J Med Genet. 1991. PMID: 1856829 Free PMC article.

4

Prenatal exclusion of ornithine transcarbamylase (OTC) by using RFLP analysis.

Liechti S, Dionisi Vici C, Bachmann C, Mazziotta MR, Bartuli A, Sabetta G. Liechti S, et al. Among authors: dionisi vici c. J Inherit Metab Dis. 1990;13(6):888-90. doi: 10.1007/BF01800215. J Inherit Metab Dis. 1990. PMID: 1981921 No abstract available.

5

Early introduction of uncooked cornstarch for the treatment of glycogen storage disease type I.

Dionisi Vici C, Bartuli A, Mazziotta MR, Sabetta G. Dionisi Vici C, et al. Acta Paediatr Scand. 1990 Oct;79(10):978-9. doi: 10.1111/j.1651-2227.1990.tb11366.x. Acta Paediatr Scand. 1990. PMID: 2264476 Clinical Trial. No abstract available.

6

Acute pancreatitis in propionic acidaemia.

Burlina AB, Dionisi-Vici C, Piovan S, Saponara I, Bartuli A, Sabetta G, Zacchello F. Burlina AB, et al. Among authors: dionisi vici c. J Inherit Metab Dis. 1995;18(2):169-72. doi: 10.1007/BF00711758. J Inherit Metab Dis. 1995. PMID: 7564238 No abstract available.

7

Cranial ultrasonography in maple syrup urine disease.

Fariello G, Dionisi-Vici C, Orazi C, Malena S, Bartuli A, Schingo P, Carnevale E, Saponara I, Sabetta G. Fariello G, et al. Among authors: dionisi vici c. AJNR Am J Neuroradiol. 1996 Feb;17(2):311-5. AJNR Am J Neuroradiol. 1996. PMID: 8938303 Free PMC article.

8

A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation.

Fogli A, Dionisi-Vici C, Deodato F, Bartuli A, Boespflug-Tanguy O, Bertini E. Fogli A, et al. Among authors: dionisi vici c. Neurology. 2002 Dec 24;59(12):1966-8. doi: 10.1212/01.wnl.0000041666.76863.47. Neurology. 2002. PMID: 12499492

9

Inborn errors of metabolism: an update on epidemiology and on neonatal-onset hyperammonemia.

Deodato F, Boenzi S, Rizzo C, Abeni D, Caviglia S, Picca S, Bartuli A, Dionisi-Vici C. Deodato F, et al. Among authors: dionisi vici c. Acta Paediatr Suppl. 2004 May;93(445):18-21. doi: 10.1111/j.1651-2227.2004.tb03050.x. Acta Paediatr Suppl. 2004. PMID: 15176714

10

Medical management and dialysis therapy for the infant with an inborn error of metabolism.

Picca S, Bartuli A, Dionisi-Vici C. Picca S, et al. Among authors: dionisi vici c. Semin Nephrol. 2008 Sep;28(5):477-80. doi: 10.1016/j.semnephrol.2008.05.007. Semin Nephrol. 2008. PMID: 18790367 Review.

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