Rossi A - 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: rossi a. Neurology. 2002 Aug 27;59(4):617-20. doi: 10.1212/wnl.59.4.617. Neurology. 2002. PMID: 12196662

2

Mitochondrial abnormalities in genetically assessed oculopharyngeal muscular dystrophy.

Gambelli S, Malandrini A, Ginanneschi F, Berti G, Cardaioli E, De Stefano R, Franci M, Salvadori C, Mari F, Bruttini M, Rossi A, Federico A, Renieri A. Gambelli S, et al. Among authors: rossi a. Eur Neurol. 2004;51(3):144-7. doi: 10.1159/000077070. Epub 2004 Feb 27. Eur Neurol. 2004. PMID: 14988608

3

Ultrastructural findings in the peripheral nerve in a family with the intermediate form of Charcot-Marie-Tooth disease.

Malandrini A, Ceuterick C, Villanova M, Gambelli S, Berti G, Rossi A, Guazzi GC. Malandrini A, et al. Among authors: rossi a. J Submicrosc Cytol Pathol. 2001 Jan-Apr;33(1-2):59-63. J Submicrosc Cytol Pathol. 2001. PMID: 11686409

4

Charcot-Marie-Tooth disease: an intermediate form.

Villanova M, Timmerman V, De Jonghe P, Malandrini A, Rizzuto N, Van Broeckhoven C, Guazzi G, Rossi A. Villanova M, et al. Among authors: rossi a. Neuromuscul Disord. 1998 Aug;8(6):392-3. doi: 10.1016/s0960-8966(98)00044-3. Neuromuscul Disord. 1998. PMID: 9713856 No abstract available.

5

Acute shoulder-girdle neuralgic amyotrophy (Parsonage-Turner syndrome with saphenous nerve involvement.

Ginanneschi F, Malandrini A, Monti L, Rossi A. Ginanneschi F, et al. Among authors: rossi a. Acta Neurol Belg. 2011 Dec;111(4):333-6. Acta Neurol Belg. 2011. PMID: 22368976

6

Neurophysiological study in chronic GM2 gangliosidosis (hexosaminidase A and B deficiency), with motor neuron disease phenotype.

Mondelli M, Rossi A, Palmeri S, Rizzuto N, Federico A. Mondelli M, et al. Among authors: rossi a. Ital J Neurol Sci. 1989 Aug;10(4):433-9. doi: 10.1007/BF02334949. Ital J Neurol Sci. 1989. PMID: 2793417

7

Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum.

Casali C, Valente EM, Bertini E, Montagna G, Criscuolo C, De Michele G, Villanova M, Damiano M, Pierallini A, Brancati F, Scarano V, Tessa A, Cricchi F, Grieco GS, Muglia M, Carella M, Martini B, Rossi A, Amabile GA, Nappi G, Filla A, Dallapiccola B, Santorelli FM. Casali C, et al. Among authors: rossi a. Neurology. 2004 Jan 27;62(2):262-8. doi: 10.1212/wnl.62.2.262. Neurology. 2004. PMID: 14745065

8

Axonal motor and sensory neuropathy in myotonic dystrophy.

Mondelli M, Rossi A, Malandrini A, Della Porta P, Guzaai GC. Mondelli M, et al. Among authors: rossi a. Acta Neurol Scand. 1993 Aug;88(2):141-8. doi: 10.1111/j.1600-0404.1993.tb04206.x. Acta Neurol Scand. 1993. PMID: 8213059

9

Localization of the gene for the intermediate form of Charcot-Marie-Tooth to chromosome 10q24.1-q25.1.

Verhoeven K, Villanova M, Rossi A, Malandrini A, De Jonghe P, Timmerman V. Verhoeven K, et al. Among authors: rossi a. Am J Hum Genet. 2001 Oct;69(4):889-94. doi: 10.1086/323742. Epub 2001 Aug 30. Am J Hum Genet. 2001. PMID: 11533914 Free PMC article.

10

Electrophysiological evidence of "nerve entrapment syndromes" and subclinical peripheral neuropathy in progressive systemic sclerosis (scleroderma).

Mondelli M, Romano C, Della Porta PD, Rossi A. Mondelli M, et al. Among authors: rossi a. J Neurol. 1995 Mar;242(4):185-94. doi: 10.1007/BF00919590. J Neurol. 1995. PMID: 7798116

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