Rossi A - Search Results

1

Cognitive profile in spastic paraplegia with thin corpus callosum and mutations in SPG11.

Siri L, Battaglia FM, Tessa A, Rossi A, Rocco MD, Facchinetti S, Mascaretti M, Santorelli FM, Veneselli E, Biancheri R. Siri L, et al. Among authors: rossi a. Neuropediatrics. 2010 Feb;41(1):35-8. doi: 10.1055/s-0030-1253352. Epub 2010 Jun 22. Neuropediatrics. 2010. PMID: 20571989

2

[Leukoencephalopathy with swelling, megalencephalopathy and surprisingly mild course. A case report].

Pisaturo C, Biancheri R, Perrone MV, Rossi A, Veneselli E. Pisaturo C, et al. Among authors: rossi a. Minerva Pediatr. 1999 Nov-Dec;51(11-12):399-402. Minerva Pediatr. 1999. PMID: 10768005 Italian.

3

Early-onset combined methylmalonic aciduria and homocystinuria: neuroradiologic findings.

Rossi A, Cerone R, Biancheri R, Gatti R, Schiaffino MC, Fonda C, Zammarchi E, Tortori-Donati P. Rossi A, et al. AJNR Am J Neuroradiol. 2001 Mar;22(3):554-63. AJNR Am J Neuroradiol. 2001. PMID: 11237984 Free PMC article.

4

Cobalamin (Cbl) C/D deficiency: clinical, neurophysiological and neuroradiologic findings in 14 cases.

Biancheri R, Cerone R, Schiaffino MC, Caruso U, Veneselli E, Perrone MV, Rossi A, Gatti R. Biancheri R, et al. Among authors: rossi a. Neuropediatrics. 2001 Feb;32(1):14-22. doi: 10.1055/s-2001-12217. Neuropediatrics. 2001. PMID: 11315197

5

Presence of delayed myelination and macrocephaly in the sister of a patient with vacuolating leukoencephalopathy with subcortical cysts.

Biancheri R, Pisaturo C, Perrone MV, Pessagno A, Rossi A, Veneselli E. Biancheri R, et al. Among authors: rossi a. Neuropediatrics. 2000 Dec;31(6):321-4. doi: 10.1055/s-2000-12949. Neuropediatrics. 2000. PMID: 11508554

6

Magnetic resonance imaging of spinal dysraphism.

Tortori-Donati P, Rossi A, Biancheri R, Cama A. Tortori-Donati P, et al. Among authors: rossi a. Top Magn Reson Imaging. 2001 Dec;12(6):375-409. doi: 10.1097/00002142-200112000-00003. Top Magn Reson Imaging. 2001. PMID: 11744877 Review.

7

Posterior fossa and arterial abnormalities in patients with facial capillary haemangioma: presumed incomplete phenotypic expression of PHACES syndrome.

Rossi A, Bava GL, Biancheri R, Tortori-Donati P. Rossi A, et al. Neuroradiology. 2001 Nov;43(11):934-40. doi: 10.1007/s002340100594. Neuroradiology. 2001. PMID: 11760796

8

The pathogenesis of hydrocephalus in inborn errors of the single carbon transfer pathway.

Rossi A, Biancheri R, Tortori-Donati P. Rossi A, et al. Neuropediatrics. 2001 Dec;32(6):335-6. doi: 10.1055/s-2001-20411. Neuropediatrics. 2001. PMID: 11870591 No abstract available.

9

A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency.

Bruno C, Biancheri R, Garavaglia B, Biedi C, Rossi A, Lamba LD, Bado M, Greco M, Zeviani M, Minetti C. Bruno C, et al. Among authors: rossi a. J Child Neurol. 2002 Mar;17(3):233-6. doi: 10.1177/088307380201700318. J Child Neurol. 2002. PMID: 12026244

10

Early-onset cobalamin C/D deficiency: epilepsy and electroencephalographic features.

Biancheri R, Cerone R, Rossi A, Schiaffino MC, Caruso U, Minniti G, Perrone MV, Tortori-Donati P, Veneselli E. Biancheri R, et al. Among authors: rossi a. Epilepsia. 2002 Jun;43(6):616-22. doi: 10.1046/j.1528-1157.2002.24001.x. Epilepsia. 2002. PMID: 12060021 Free article.

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