Palmeri S - Search Results

1

Asymptomatic cores and paracrystalline mitochondrial inclusions in CADASIL.

Malandrini A, Albani F, Palmeri S, Fattapposta F, Gambelli S, Berti G, Bracco A, Tammaro A, Calzavara S, Villanova M, Ferrari M, Rossi A, Carrera P. Malandrini A, et al. Among authors: palmeri s. Neurology. 2002 Aug 27;59(4):617-20. doi: 10.1212/wnl.59.4.617. Neurology. 2002. PMID: 12196662

2

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

3

Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy.

Malandrini A, Carrera P, Palmeri S, Cavallaro T, Fabrizi GM, Villanova M, Fattapposta M, Vismara L, Brancolini V, Tanganelli P, Calì A, Morocutti C, Zeviani M, Ferrari M, Guazzi GC. Malandrini A, et al. Among authors: palmeri s. Acta Neuropathol. 1996 Aug;92(2):115-22. doi: 10.1007/s004010050498. Acta Neuropathol. 1996. PMID: 8841656

4

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

5

Chronic diarrhea associated with the A3243G mtDNA mutation.

Santorelli FM, Villanova M, Malandrini A, Grieco GS, Palmeri S, Merlini L, Casali C. Santorelli FM, et al. Among authors: palmeri s. Neurology. 2000 Jan 11;54(1):266-7. doi: 10.1212/wnl.54.1.266. Neurology. 2000. PMID: 10636171 No abstract available.

6

Type I sialidosis: a clinical, biochemical and neuroradiological study.

Palmeri S, Villanova M, Malandrini A, van Diggelen OP, Huijmans JG, Ceuterick C, Rufa A, DeFalco D, Ciacci G, Martin JJ, Guazzi G. Palmeri S, et al. Eur Neurol. 2000;43(2):88-94. doi: 10.1159/000008141. Eur Neurol. 2000. PMID: 10686466

7

Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type.

Grieco GS, Malandrini A, Comanducci G, Leuzzi V, Valoppi M, Tessa A, Palmeri S, Benedetti L, Pierallini A, Gambelli S, Federico A, Pierelli F, Bertini E, Casali C, Santorelli FM. Grieco GS, et al. Among authors: palmeri s. Neurology. 2004 Jan 13;62(1):103-6. doi: 10.1212/01.wnl.0000104491.66816.77. Neurology. 2004. PMID: 14718707

8

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

9

A syndrome of autosomal recessive pontocerebellar hypoplasia with white matter abnormalities and protracted course in two brothers.

Malandrini A, Palmeri S, Villanova M, Parrotta E, Sicurelli F, Amato D, DeFalco D, Guazzi GC. Malandrini A, et al. Among authors: palmeri s. Brain Dev. 1997 Apr;19(3):209-11. doi: 10.1016/s0387-7604(96)00563-3. Brain Dev. 1997. PMID: 9134193

10

Neuronal intranuclear inclusion disease: neuropathologic study of a case.

Malandrini A, Villanova M, Tripodi S, Palmeri S, Sicurelli F, Parrotta E, Berti G, Salvadori C, Cintorino M, Guazzi GC. Malandrini A, et al. Among authors: palmeri s. Brain Dev. 1998 Aug;20(5):290-4. doi: 10.1016/s0387-7604(98)00032-1. Brain Dev. 1998. PMID: 9760997

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