Pareyson D - Search Results

1

Non-neural phenotype of spinal and bulbar muscular atrophy: results from a large cohort of Italian patients.

Querin G, Bertolin C, Da Re E, Volpe M, Zara G, Pegoraro E, Caretta N, Foresta C, Silvano M, Corrado D, Iafrate M, Angelini L, Sartori L, Pennuto M, Gaiani A, Bello L, Semplicini C, Pareyson D, Silani V, Ermani M, Ferlin A, Sorarù G; Italian Study Group on Kennedy's disease. Querin G, et al. Among authors: pareyson d. J Neurol Neurosurg Psychiatry. 2016 Aug;87(8):810-6. doi: 10.1136/jnnp-2015-311305. Epub 2015 Oct 26. J Neurol Neurosurg Psychiatry. 2016. PMID: 26503015 Free PMC article.

2

Neurogenic muscle hypertrophy. Report of two cases.

Pareyson D, Morandi L, Scaioli V, Marazzi R, Boiardi A, Sghirlanzoni A. Pareyson D, et al. J Neurol. 1989 Jul;236(5):292-5. doi: 10.1007/BF00314459. J Neurol. 1989. PMID: 2760647

3

Kennedy's disease: clinical and molecular study of two Italian families.

Pareyson D, Castellotti B, Botti S, Defanti CA, Gellera C, Taroni F, Sghirlanzoni A. Pareyson D, et al. Ital J Neurol Sci. 1995 Oct;16(7):467-71. doi: 10.1007/BF02229324. Ital J Neurol Sci. 1995. PMID: 8749704

4

Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes.

Pareyson D, Gellera C, Castellotti B, Antonelli A, Riggio MC, Mazzucchelli F, Girotti F, Pietrini V, Mariotti C, Di Donato S. Pareyson D, et al. J Neurol. 1999 May;246(5):389-93. doi: 10.1007/s004150050369. J Neurol. 1999. PMID: 10399872

5

Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 families.

Mariotti C, Castellotti B, Pareyson D, Testa D, Eoli M, Antozzi C, Silani V, Marconi R, Tezzon F, Siciliano G, Marchini C, Gellera C, Donato SD. Mariotti C, et al. Among authors: pareyson d. Neuromuscul Disord. 2000 Aug;10(6):391-7. doi: 10.1016/s0960-8966(99)00132-7. Neuromuscul Disord. 2000. PMID: 10899444

6

Chronic inflammatory demyelinating polyradiculoneuropathy: long-term course and treatment of 60 patients.

Sghirlanzoni A, Solari A, Ciano C, Mariotti C, Fallica E, Pareyson D. Sghirlanzoni A, et al. Among authors: pareyson d. Neurol Sci. 2000 Feb;21(1):31-7. doi: 10.1007/s100720070116. Neurol Sci. 2000. PMID: 10938200 Clinical Trial.

7

Polyneuropathy in POEMS syndrome: role of angiogenic factors in the pathogenesis.

Scarlato M, Previtali SC, Carpo M, Pareyson D, Briani C, Del Bo R, Nobile-Orazio E, Quattrini A, Comi GP. Scarlato M, et al. Among authors: pareyson d. Brain. 2005 Aug;128(Pt 8):1911-20. doi: 10.1093/brain/awh519. Epub 2005 Jun 23. Brain. 2005. PMID: 15975949

8

Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature.

Pareyson D, Fancellu R, Mariotti C, Romano S, Salmaggi A, Carella F, Girotti F, Gattellaro G, Carriero MR, Farina L, Ceccherini I, Savoiardo M. Pareyson D, et al. Brain. 2008 Sep;131(Pt 9):2321-31. doi: 10.1093/brain/awn178. Epub 2008 Aug 6. Brain. 2008. PMID: 18684770 Review.

9

Neurological pictures. Adult-onset leukoencephalopathy with calcifications associated with primary antiphospholipid syndrome.

Salsano E, Chiapparini L, Finocchiaro G, Pareyson D, Savoiardo M. Salsano E, et al. Among authors: pareyson d. J Neurol Neurosurg Psychiatry. 2008 Nov;79(11):1215-7. doi: 10.1136/jnnp.2007.128579. J Neurol Neurosurg Psychiatry. 2008. PMID: 18940989 No abstract available.

10

Rare association of motor neuron disease and spinocerebellar ataxia type 2 (SCA2): a new case and review of the literature.

Nanetti L, Fancellu R, Tomasello C, Gellera C, Pareyson D, Mariotti C. Nanetti L, et al. Among authors: pareyson d. J Neurol. 2009 Nov;256(11):1926-8. doi: 10.1007/s00415-009-5237-9. Epub 2009 Jul 31. J Neurol. 2009. PMID: 19644730 Review.

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