Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 78

1.

Impaired copper and iron metabolism in blood cells and muscles of patients affected by copper deficiency myeloneuropathy.

Spinazzi M, Sghirlanzoni A, Salviati L, Angelini C.

Neuropathol Appl Neurobiol. 2014 Dec;40(7):888-98. doi: 10.1111/nan.12111.

PMID:
24708542
2.

Effects of manidipine and delapril in hypertensive patients with type 2 diabetes mellitus: the delapril and manidipine for nephroprotection in diabetes (DEMAND) randomized clinical trial.

Ruggenenti P, Lauria G, Iliev IP, Fassi A, Ilieva AP, Rota S, Chiurchiu C, Barlovic DP, Sghirlanzoni A, Lombardi R, Penza P, Cavaletti G, Piatti ML, Frigeni B, Filipponi M, Rubis N, Noris G, Motterlini N, Ene-Iordache B, Gaspari F, Perna A, Zaletel J, Bossi A, Dodesini AR, Trevisan R, Remuzzi G; DEMAND Study Investigators.

Hypertension. 2011 Nov;58(5):776-83. doi: 10.1161/HYPERTENSIONAHA.111.174474. Epub 2011 Sep 19.

PMID:
21931073
3.

Clinical and radiological features of brain neurotoxicity caused by antitumor and immunosuppressant treatments.

Erbetta A, Salmaggi A, Sghirlanzoni A, Silvani A, Potepan P, Botturi A, Ciceri E, Bruzzone MG.

Neurol Sci. 2008 Jun;29(3):131-7. doi: 10.1007/s10072-008-0924-3. Epub 2008 Jul 9.

PMID:
18612759
4.

Normal expression of myelin protein zero with frame-shift mutation correlates with mild phenotype.

Steck AJ, Erne B, Pareyson D, Sghirlanzoni A, Taroni F, Schaeren-Wiemers N.

J Peripher Nerv Syst. 2006 Mar;11(1):61-6.

PMID:
16519783
5.

Sensory neuron diseases.

Sghirlanzoni A, Pareyson D, Lauria G.

Lancet Neurol. 2005 Jun;4(6):349-61. Review.

PMID:
15907739
6.

Tubule and neurofilament immunoreactivity in human hairy skin: markers for intraepidermal nerve fibers.

Lauria G, Borgna M, Morbin M, Lombardi R, Mazzoleni G, Sghirlanzoni A, Pareyson D.

Muscle Nerve. 2004 Sep;30(3):310-6.

PMID:
15318342
7.

Neurophysiological diagnosis of acquired sensory ganglionopathies.

Lauria G, Pareyson D, Sghirlanzoni A.

Eur Neurol. 2003;50(3):146-52.

PMID:
14530620
8.

Axonal swellings predict the degeneration of epidermal nerve fibers in painful neuropathies.

Lauria G, Morbin M, Lombardi R, Borgna M, Mazzoleni G, Sghirlanzoni A, Pareyson D.

Neurology. 2003 Sep 9;61(5):631-6.

9.

Case 38-2001: paraneoplastic encephalomyelitis and sensory ganglioneuropathy.

Lauria G, Pareyson D, Sghirlanzoni A.

N Engl J Med. 2002 Mar 28;346(13):1029-30; author reply 1029-30. No abstract available.

10.

Parenchymatous neurosyphilis.

Lauria G, Erbetta A, Pareyson D, Sghirlanzoni A.

Neurol Sci. 2001 Jun;22(3):281-2. No abstract available.

PMID:
11731886
11.

Spinal cord lesion due to epidural anesthesia.

Lauria G, Chiapparini L, Pareyson D, Sghirlanzoni A.

Neurol Sci. 2000 Dec;21(6):411-2. No abstract available.

PMID:
11441580
12.

Epidermal nerve fiber density in sensory ganglionopathies: clinical and neurophysiologic correlations.

Lauria G, Sghirlanzoni A, Lombardi R, Pareyson D.

Muscle Nerve. 2001 Aug;24(8):1034-9.

PMID:
11439378
13.

The insomnia plague: a Gabriel García Márquez story.

Sghirlanzoni A, Carella F.

Neurol Sci. 2000 Aug;21(4):251-3.

PMID:
11214666
14.

Deletion of exons 11-17 and novel mutations of the galactocerebrosidase gene in adult- and early-onset patients with Krabbe disease.

Selleri S, Torchiana E, Pareyson D, Lulli L, Bertagnolio B, Savoiardo M, Farina L, Carrara F, Filocamo M, Gatti R, Sghirlanzoni A, Uziel G, Finocchiaro G.

J Neurol. 2000 Nov;247(11):875-7. No abstract available.

PMID:
11151421
15.

MR imaging and proton MR spectroscopy in adult Krabbe disease.

Farina L, Bizzi A, Finocchiaro G, Pareyson D, Sghirlanzoni A, Bertagnolio B, Savoiardo M, Naidu S, Singhal BS, Wenger DA.

AJNR Am J Neuroradiol. 2000 Sep;21(8):1478-82.

16.

Imaging and outcome in severe complications of lumbar epidural anaesthesia: report of 16 cases.

Chiapparini L, Sghirlanzoni A, Pareyson D, Savoiardo M.

Neuroradiology. 2000 Aug;42(8):564-71.

PMID:
10997561
17.

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

Sghirlanzoni A, Solari A, Ciano C, Mariotti C, Fallica E, Pareyson D.

Neurol Sci. 2000 Feb;21(1):31-7.

PMID:
10938200
18.

Partial laminin alpha2 chain deficiency in a patient with myopathy resembling inclusion body myositis.

Di Blasi C, Mora M, Pareyson D, Farina L, Sghirlanzoni A, Vignier N, Blasevich F, Cornelio F, Guicheney P, Morandi L.

Ann Neurol. 2000 Jun;47(6):811-6.

PMID:
10852549
19.

Chronic cryptogenic sensory polyneuropathy.

Lauria G, Pareyson D, Sghirlanzoni A.

Arch Neurol. 2000 May;57(5):759-60. No abstract available.

20.

Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation.

Pareyson D, Taroni F, Botti S, Morbin M, Baratta S, Lauria G, Ciano C, Sghirlanzoni A.

Neurology. 2000 Apr 25;54(8):1696-8.

21.

Clinical and magnetic resonance imaging findings in chronic sensory ganglionopathies.

Lauria G, Pareyson D, Grisoli M, Sghirlanzoni A.

Ann Neurol. 2000 Jan;47(1):104-9.

PMID:
10632108
22.

Heterozygous null mutation in the P0 gene associated with mild Charcot-Marie-Tooth disease.

Pareyson D, Menichella D, Botti S, Sghirlanzoni A, Fallica E, Mora M, Ciano C, Shy ME, Taroni F.

Ann N Y Acad Sci. 1999 Sep 14;883:477-80. No abstract available.

PMID:
10586278
23.

Heterozygous Null Mutation in the P0 Gene Associated with Mild Charcot-Marie-Tooth Disease.

Pareyson D, Menichella D, Botti S, Sghirlanzoni A, Fallica E, Mora M, Ciano C, Shy ME, Taroni F.

Ann N Y Acad Sci. 1999 Oct;883(1):477-480. doi: 10.1111/j.1749-6632.1999.tb08615.x. No abstract available.

PMID:
29086956
24.

Charcot-Marie-Tooth disease type 2 and P0 gene mutations.

Pareyson D, Sghirlanzoni A, Bolti S, Ciano C, Fallica E, Mora M, Taroni F.

Neurology. 1999 Mar 23;52(5):1110-1. No abstract available.

PMID:
10102454
25.

Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathy.

Pareyson D, Solari A, Taroni F, Botti S, Fallica E, Scaioli V, Ciano C, Sghirlanzoni A.

Muscle Nerve. 1998 Dec;21(12):1686-91.

PMID:
9843070
27.

PMP22 frameshift mutation and hereditary neuropathy with liability to pressure palsies.

Pareyson D, Botti S, Sghirlanzoni A, Taroni F.

Neurology. 1997 Nov;49(5):1478-9. No abstract available.

PMID:
9371959
28.

Neurologic complications of epidural anesthesia.

Sghirlanzoni A, Pareyson D.

Ital J Neurol Sci. 1997 Feb;18(1):63. No abstract available.

PMID:
9115050
29.

"La toccatina": polyglottal aphasia in Pirandello.

Sghirlanzoni A, Pareyson D.

Ital J Neurol Sci. 1997 Feb;18(1):55-7.

PMID:
9115046
30.

Epidural anesthesia.

Sghirlanzoni A, Pareyson D.

Neurology. 1997 Jan;48(1):293-4; author reply 294-5. No abstract available.

PMID:
9008548
31.

Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion.

Pareyson D, Scaioli V, Taroni F, Botti S, Lorenzetti D, Solari A, Ciano C, Sghirlanzoni A.

Neurology. 1996 Apr;46(4):1133-7.

PMID:
8780105
32.

Acoustic nerve in peripheral neuropathy: a BAEP study. Brainstem Auditory Evoked Potentials.

Pareyson D, Scaioli V, Berta E, Sghirlanzoni A.

Electromyogr Clin Neurophysiol. 1995 Oct;35(6):359-64.

PMID:
8785933
33.

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.

Ital J Neurol Sci. 1995 Oct;16(7):467-71.

PMID:
8749704
34.

Unrecognized Charcot-Marie-Tooth disease: diagnostic difficulties in the assessment of recovery from paralysis.

Fiacchino F, Grandi L, Ciano C, Sghirlanzoni A.

Anesth Analg. 1995 Jul;81(1):199-201. No abstract available.

PMID:
7598259
35.

Spinal epidural abscess complicating tuberculous spondylitis.

Pareyson D, Savoiardo M, D'Incerti L, Sghirlanzoni A.

Ital J Neurol Sci. 1995 Jun;16(5):321-5.

PMID:
8537221
36.

The last days of Alessandro Manzoni.

Sghirlanzoni A.

Ital J Neurol Sci. 1995 Apr;16(3):199-202.

PMID:
7558775
37.

A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies.

Lorenzetti D, Pareyson D, Sghirlanzoni A, Roa BB, Abbas NE, Pandolfo M, Di Donato S, Lupski JR.

Am J Hum Genet. 1995 Jan;56(1):91-8.

38.

Conduction velocities in Charcot-Marie-Tooth polyneuropathy type 1.

Pareyson D, Sghirlanzoni A.

Neurology. 1994 Nov;44(11):2216. No abstract available.

PMID:
7969998
39.

Neurologic symptoms after epidural anaesthesia. Report of three cases.

Gemma M, Bricchi M, Grisoli M, Visintini S, Pareyson D, Sghirlanzoni A.

Acta Anaesthesiol Scand. 1994 Oct;38(7):742-3.

PMID:
7839788
40.

The POEMS syndrome: report of six cases.

Pareyson D, Marazzi R, Confalonieri P, Mancardi GL, Schenone A, Sghirlanzoni A.

Ital J Neurol Sci. 1994 Oct;15(7):353-8.

PMID:
7698893
41.

Homozygous hypertrophic hereditary motor and sensory neuropathies.

Sghirlanzoni A, Pareyson D, Marazzi R, Cavaletti G, Bellone E, Mandich P, Balestrini MR, Riva D.

Ital J Neurol Sci. 1994 Feb;15(1):5-14.

PMID:
8206746
42.

17p11.2 duplication is a common finding in sporadic cases of Charcot-Marie-Tooth type 1.

Mancardi GL, Uccelli A, Bellone E, Sghirlanzoni A, Mandich P, Pareyson D, Schenone A, Abbruzzese M, Ajmar F.

Eur Neurol. 1994;34(3):135-9.

PMID:
8033938
43.

Immunosuppressive treatments. Their efficacy on myasthenia gravis patients' outcome and on the natural course of the disease.

Cornelio F, Antozzi C, Mantegazza R, Confalonieri P, Berta E, Peluchetti D, Sghirlanzoni A, Fiacchino F.

Ann N Y Acad Sci. 1993 Jun 21;681:594-602. No abstract available.

PMID:
8357208
44.

Carbamazepine for paroxysmal dystonia due to spinal cord lesions.

Sghirlanzoni A, Pareyson D.

Ital J Neurol Sci. 1993 Mar;14(2):187. No abstract available.

PMID:
8369053
45.

Combined central and peripheral acute demyelination.

Pareyson D, Ciano C, Fiacchino F, Gemma M, Savoiardo M, Sghirlanzoni A.

Ital J Neurol Sci. 1993 Jan;14(1):83-6.

PMID:
8386146
46.

Neurological examination in patients recovering from general anesthesia.

Fiacchino F, Gemma M, Bricchi M, Sghirlanzoni A.

Ital J Neurol Sci. 1992 Dec;13(9):749-53.

PMID:
1483857
47.

F response and somatosensory and brainstem auditory evoked potential studies in HMSN type I and II.

Scaioli V, Pareyson D, Avanzini G, Sghirlanzoni A.

J Neurol Neurosurg Psychiatry. 1992 Nov;55(11):1027-31.

48.

HMSN III phenotype due to homozygous expression of a dominant HMSN II gene.

Sghirlanzoni A, Pareyson D, Balestrini MR, Bellone E, Berta E, Ciano C, Mandich P, Marazzi R.

Neurology. 1992 Nov;42(11):2201-4.

PMID:
1436537
49.

Charcot-Marie-Tooth (CMT) 1a duplication at 17p11.2 in Italian families.

Bellone E, Mandich P, Mancardi GL, Schenone A, Uccelli A, Abbruzzese M, Sghirlanzoni A, Pareyson D, Ajmar F.

J Med Genet. 1992 Jul;29(7):492-3. No abstract available.

50.

Peripheral nerve involvement in Churg-Strauss syndrome.

Marazzi R, Pareyson D, Boiardi A, Corbo M, Scaioli V, Sghirlanzoni A.

J Neurol. 1992 Jul;239(6):317-21.

PMID:
1324984

Supplemental Content

Loading ...
Support Center