Ferrari M - Search Results

1

Very high prevalence of right-to-left shunt on transcranial Doppler in an Italian family with cerebral autosomal dominant angiopathy with subcortical infarcts and leukoencephalopathy.

Angeli S, Carrera P, Del Sette M, Assini A, Grandis M, Biancolini D, Ferrari M, Gandolfo C. Angeli S, et al. Among authors: ferrari m. Eur Neurol. 2001;46(4):198-201. doi: 10.1159/000050804. Eur Neurol. 2001. PMID: 11721126

2

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: ferrari m. Acta Neuropathol. 1996 Aug;92(2):115-22. doi: 10.1007/s004010050498. Acta Neuropathol. 1996. PMID: 8841656

3

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: ferrari m. Neurology. 1997 May;48(5):1200-3. doi: 10.1212/wnl.48.5.1200. Neurology. 1997. PMID: 9153443

4

A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia.

Battistini S, Stenirri S, Piatti M, Gelfi C, Righetti PG, Rocchi R, Giannini F, Battistini N, Guazzi GC, Ferrari M, Carrera P. Battistini S, et al. Among authors: ferrari m. Neurology. 1999 Jul 13;53(1):38-43. doi: 10.1212/wnl.53.1.38. Neurology. 1999. PMID: 10408534

5

Migraine with aura and white matter abnormalities: Notch3 mutation.

Ceroni M, Poloni TE, Tonietti S, Fabozzi D, Uggetti C, Frediani F, Simonetti F, Malaspina A, Alimonti D, Celano M, Ferrari M, Carrera P. Ceroni M, et al. Among authors: ferrari m. Neurology. 2000 May 9;54(9):1869-71. doi: 10.1212/wnl.54.9.1869. Neurology. 2000. PMID: 10802804

6

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: ferrari m. Neurology. 2002 Aug 27;59(4):617-20. doi: 10.1212/wnl.59.4.617. Neurology. 2002. PMID: 12196662

7

Early visual function impairment in CADASIL.

Parisi V, Pierelli F, Fattapposta F, Bianco F, Parisi L, Restuccia R, Malandrini A, Ferrari M, Carrera P. Parisi V, et al. Among authors: ferrari m. Neurology. 2003 Jun 24;60(12):2008-10. doi: 10.1212/01.wnl.0000070411.13217.7e. Neurology. 2003. PMID: 12821756

8

Genetic heterogeneity in Italian families with familial hemiplegic migraine.

Carrera P, Piatti M, Stenirri S, Grimaldi LM, Marchioni E, Curcio M, Righetti PG, Ferrari M, Gelfi C. Carrera P, et al. Among authors: ferrari m. Neurology. 1999 Jul 13;53(1):26-33. doi: 10.1212/wnl.53.1.26. Neurology. 1999. PMID: 10408532

9

Familial hemiplegic migraine: a ion channel disorder.

Carrera P, Stenirri S, Ferrari M, Battistini S. Carrera P, et al. Among authors: ferrari m. Brain Res Bull. 2001 Oct-Nov 1;56(3-4):239-41. doi: 10.1016/s0361-9230(01)00570-6. Brain Res Bull. 2001. PMID: 11719257 Review.

10

Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathy.

Benedetti S, Bertini E, Iannaccone S, Angelini C, Trisciani M, Toniolo D, Sferrazza B, Carrera P, Comi G, Ferrari M, Quattrini A, Previtali SC. Benedetti S, et al. Among authors: ferrari m. J Neurol Neurosurg Psychiatry. 2005 Jul;76(7):1019-21. doi: 10.1136/jnnp.2004.046110. J Neurol Neurosurg Psychiatry. 2005. PMID: 15965218 Free PMC article.

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