Guazzi GC - Search Results

1

Cerebrotendinous xanthomatosis (van Bogaert-Scherer-Epstein disease): CT and MR findings.

Dotti MT, Federico A, Signorini E, Caputo N, Venturi C, Filosomi G, Guazzi GC. Dotti MT, et al. Among authors: guazzi gc. AJNR Am J Neuroradiol. 1994 Oct;15(9):1721-6. AJNR Am J Neuroradiol. 1994. PMID: 7847220 Free PMC article. Review.

2

Hypoplasia of the corpus callosum in Niemann-Pick type C disease.

Palmeri S, Battisti C, Federico A, Guazzi GC. Palmeri S, et al. Among authors: guazzi gc. Neuroradiology. 1994;36(1):20-2. doi: 10.1007/BF00599187. Neuroradiology. 1994. PMID: 8107989

3

The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome.

Fabrizi GM, Cardaioli E, Grieco GS, Cavallaro T, Malandrini A, Manneschi L, Dotti MT, Federico A, Guazzi G. Fabrizi GM, et al. J Neurol Neurosurg Psychiatry. 1996 Jul;61(1):47-51. doi: 10.1136/jnnp.61.1.47. J Neurol Neurosurg Psychiatry. 1996. PMID: 8676159 Free PMC article.

4

Cerebro-ocular dysplasia and muscular dystrophy: report of two cases.

Federico A, Dotti MT, Malandrini A, Guazzi GC, Hayek G, Simonati A, Rizzuto N, Toti P. Federico A, et al. Among authors: guazzi gc. Neuropediatrics. 1988 May;19(2):109-12. doi: 10.1055/s-2008-1052412. Neuropediatrics. 1988. PMID: 3374764

5

Optic atrophy in Marinesco-Sjögren syndrome: an additional ocular feature. Report of three cases in two families.

Dotti MT, Bardelli AM, De Stefano N, Federico A, Malandrini A, Vanni M, Guazzi GC. Dotti MT, et al. Among authors: guazzi gc. Ophthalmic Paediatr Genet. 1993 Mar;14(1):5-7. doi: 10.3109/13816819309087616. Ophthalmic Paediatr Genet. 1993. PMID: 8345957

6

Progressive myoclonus epilepsies. Criteria for diagnosis on the basis of the follow-up of 37 cases.

Guazzi GC, Federico A. Guazzi GC, et al. Acta Neurol (Napoli). 1992 Aug-Dec;14(4-6):469-84. Acta Neurol (Napoli). 1992. PMID: 1293989 Review.

7

Congenital lactic acidosis due to a defect of pyruvate dehydrogenase complex (E1). Clinical, biochemical, nerve biopsy study and effect of therapy.

Federico A, Dotti MT, Fabrizi GM, Palmeri S, Massimo L, Robinson BH, Malandrini A, Guazzi GC. Federico A, et al. Among authors: guazzi gc. Eur Neurol. 1990;30(3):123-7. doi: 10.1159/000117327. Eur Neurol. 1990. PMID: 2162773

8

Neurocutaneous syndromes with pigmentary abnormalities and central nervous system involvement. II. Two cases with atypical incontinentia pigmenti.

Federico A, Fabrizi GM, Dotti MT, Palmeri S, Aguglia U, Miracco C, Guazzi GC. Federico A, et al. Among authors: guazzi gc. Acta Neurol (Napoli). 1990 Aug;12(4):264-72. Acta Neurol (Napoli). 1990. PMID: 2251951

9

Infanto-juvenile encephaloneuropathy and pigmentary retinopathy in a girl associated with congenital adrenal insufficiency and altered plasma medium-chain fatty acid levels.

Federico A, Baracchini G, Dotti MT, Ibba L, Malandrini A, Ciacci G, Meloni M, Palmeri S, Pompella A, Guazzi GC. Federico A, et al. Among authors: guazzi gc. J Inherit Metab Dis. 1988;11 Suppl 2:178-82. doi: 10.1007/BF01804229. J Inherit Metab Dis. 1988. PMID: 2846958 No abstract available.

10

Adrenomyeloneurodystrophy with late cerebral involvement and evidence of a multiple autoimmune disorder.

Federico A, Dotti MT, Annunziata P, Bonuccelli U, Fenzi G, Ciacci G, Malandrini A, Meucci G, Guazzi GC. Federico A, et al. Among authors: guazzi gc. J Inherit Metab Dis. 1988;11 Suppl 2:169-72. doi: 10.1007/BF01804227. J Inherit Metab Dis. 1988. PMID: 3141701 No abstract available.

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