Palmeri S - Search Results

1

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: palmeri s. Eur Neurol. 1990;30(3):123-7. doi: 10.1159/000117327. Eur Neurol. 1990. PMID: 2162773

2

Type 3 (chronic) GM1 gangliosidosis presenting as infanto-choreo-athetotic dementia, without epilepsy, in three sisters.

Guazzi GC, D'Amore I, Van Hoof F, Fruschelli C, Alessandrini C, Palmeri S, Federico A. Guazzi GC, et al. Among authors: palmeri s. Neurology. 1988 Jul;38(7):1124-7. doi: 10.1212/wnl.38.7.1124. Neurology. 1988. PMID: 3133574

3

Dementia, myoclonus, peripheral neuropathy, and lipid-like material in skin biopsy during psychotropic drug treatment.

Federico A, Palmeri S, Malandrini A, Mangano L, Ciacci G, Scarpini C, Tiacci G. Federico A, et al. Among authors: palmeri s. Biol Psychiatry. 1992 Oct 15;32(8):721-7. doi: 10.1016/0006-3223(92)90303-h. Biol Psychiatry. 1992. PMID: 1333826

4

Imipramine induced lipidosis and dexamethasone effect: morphological and biochemical study in normal and chronic GM2 gangliosidosis fibroblasts.

Palmeri S, Mangano L, Battisti C, Malandrini A, Federico A. Palmeri S, et al. J Neurol Sci. 1992 Jul;110(1-2):215-21. doi: 10.1016/0022-510x(92)90030-o. J Neurol Sci. 1992. PMID: 1506862

5

The clinical aspects of adult hexosaminidase deficiencies.

Federico A, Palmeri S, Malandrini A, Fabrizi G, Mondelli M, Guazzi GC. Federico A, et al. Among authors: palmeri s. Dev Neurosci. 1991;13(4-5):280-7. doi: 10.1159/000112174. Dev Neurosci. 1991. PMID: 1840098 Review.

6

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: palmeri s. Acta Neurol (Napoli). 1990 Aug;12(4):264-72. Acta Neurol (Napoli). 1990. PMID: 2251951

7

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: palmeri s. J Inherit Metab Dis. 1988;11 Suppl 2:178-82. doi: 10.1007/BF01804229. J Inherit Metab Dis. 1988. PMID: 2846958 No abstract available.

8

Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathy.

Malandrini A, Carrera P, Ciacci G, Gonnelli S, Villanova M, Palmeri S, Vismara L, Brancolini V, Signorini E, Ferrari M, Guazzi GC. Malandrini A, et al. Among authors: palmeri s. Neurology. 1997 May;48(5):1200-3. doi: 10.1212/wnl.48.5.1200. Neurology. 1997. PMID: 9153443

9

Juvenile Leigh syndrome with protracted course presenting as chronic sensory motor neuropathy, ataxia, deafness and retinitis pigmentosa: a clinicopathological report.

Malandrini A, Palmeri S, Fabrizi GM, Villanova M, Berti G, Salvadori C, Gardini G, Motti L, Solimé F, Guazzi GC. Malandrini A, et al. Among authors: palmeri s. J Neurol Sci. 1998 Mar 5;155(2):218-21. doi: 10.1016/s0022-510x(98)00014-8. J Neurol Sci. 1998. PMID: 9562272

10

CAG repeat expansion in an italian family with spinocerebellar ataxia type 2 (SCA2): a clinical and genetic study.

Malandrini A, Galli L, Villanova M, Palmeri S, Parrotta E, DeFalco D, Cappelli M, Grieco GS, Renieri A, Guazzi G. Malandrini A, et al. Among authors: palmeri s. Eur Neurol. 1998 Oct;40(3):164-8. doi: 10.1159/000007974. Eur Neurol. 1998. PMID: 9748675

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