Palmeri S - Search Results

1

Neurological presentation of Ehlers-Danlos syndrome type IV in a family with parental mosaicism.

Palmeri S, Mari F, Meloni I, Malandrini A, Ariani F, Villanova M, Pompilio A, Schwarze U, Byers PH, Renieri A. Palmeri S, et al. Clin Genet. 2003 Jun;63(6):510-5. doi: 10.1034/j.1399-0004.2003.00075.x. Clin Genet. 2003. PMID: 12786757

2

PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardation.

Malandrini A, Mari F, Palmeri S, Gambelli S, Berti G, Bruttini M, Bardelli AM, Williamson K, van Heyningen V, Renieri A. Malandrini A, et al. Among authors: palmeri s. Clin Genet. 2001 Aug;60(2):151-4. doi: 10.1034/j.1399-0004.2001.600210.x. Clin Genet. 2001. PMID: 11553050

3

Ataxia, mental deterioration, epilepsy in a family with dominant enamel hypoplasia: a variant of Kohlschütter-Tönz syndrome?

Guazzi G, Palmeri S, Malandrini A, Ciacci G, Di Perri R, Mancini G, Messina C, Salvadori C. Guazzi G, et al. Among authors: palmeri s. Am J Med Genet. 1994 Mar 1;50(1):79-83. doi: 10.1002/ajmg.1320500117. Am J Med Genet. 1994. PMID: 8160757

4

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

5

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

6

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

7

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

8

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

9

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

10

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

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