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Items: 32

1.

Clinical Findings and Electrodiagnostic Testing in Ulnar Neuropathy at the Elbow and Differences According to Site and Type of Nerve Damage.

Vinciguerra C, Curti S, Aretini A, Sicurelli F, Greco G, Mattioli S, Mondelli M.

Am J Phys Med Rehabil. 2019 Jul 31. doi: 10.1097/PHM.0000000000001286. [Epub ahead of print]

PMID:
31369403
2.

Hydroxychloroquine neuromyotoxicity: a case with rapid course and complete recovery.

Vinciguerra C, Sicurelli F, Fioravanti A, Malandrini A, Battisti C, Federico A.

Neurol Sci. 2015 Dec;36(12):2293-4. doi: 10.1007/s10072-015-2355-2. Epub 2015 Aug 11. No abstract available.

PMID:
26260758
3.

Eye movement changes in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).

Vinciguerra C, Federighi P, Rosini F, Pretegiani E, Cardaioli E, Dotti MT, Sicurelli F, Federico A, Rufa A.

J Neurol Sci. 2015 Mar 15;350(1-2):107-9. doi: 10.1016/j.jns.2015.01.031. Epub 2015 Jan 29. No abstract available.

PMID:
25656101
4.

Clinical findings and electrodiagnostic testing in 108 consecutive cases of lumbosacral radiculopathy due to herniated disc.

Mondelli M, Aretini A, Arrigucci U, Ginanneschi F, Greco G, Sicurelli F.

Neurophysiol Clin. 2013 Oct;43(4):205-15. doi: 10.1016/j.neucli.2013.05.004. Epub 2013 Jun 20.

PMID:
24094906
5.

Tarlov cysts: clinical evaluation of an italian cohort of patients.

Marino D, Carluccio MA, Di Donato I, Sicurelli F, Chini E, Di Toro Mammarella L, Rossi F, Rubegni A, Federico A.

Neurol Sci. 2013 Sep;34(9):1679-82. doi: 10.1007/s10072-013-1321-0. Epub 2013 Feb 12.

PMID:
23400656
6.

Sensory nerve action potential amplitude is rarely reduced in lumbosacral radiculopathy due to herniated disc.

Mondelli M, Aretini A, Arrigucci U, Ginanneschi F, Greco G, Sicurelli F.

Clin Neurophysiol. 2013 Feb;124(2):405-9. doi: 10.1016/j.clinph.2012.07.020. Epub 2012 Sep 18.

PMID:
22995591
7.

Fulminant intravascular lymphomatosis mimicking acute haemorrhagic leukoencephalopathy.

Marino D, Sicurelli F, Cerase A, Tripodi S, Cintorino M, Lazzi S, Federico A.

J Neurol Sci. 2012 Sep 15;320(1-2):141-4. doi: 10.1016/j.jns.2012.05.043. Epub 2012 Jun 21.

PMID:
22726354
8.

The first Italian patient with oculopharyngodistal myopathy: case report and considerations on differential diagnosis.

Mignarri A, Carluccio MA, Malandrini A, Sicurelli F, Galli L, Mazzei MA, Federico A, Orrico A, Dotti MT.

Neuromuscul Disord. 2012 Aug;22(8):759-62. doi: 10.1016/j.nmd.2012.03.010. Epub 2012 May 29.

PMID:
22652077
9.

Clinical and biochemical improvement following HSCT in a patient with MNGIE: 1-year follow-up.

Sicurelli F, Carluccio MA, Toraldo F, Tozzi M, Bucalossi A, Lenoci M, Jacomelli G, Micheli V, Cardaioli E, Mondelli M, Federico A, Marotta G, Dotti MT.

J Neurol. 2012 Sep;259(9):1985-7. doi: 10.1007/s00415-012-6500-z. Epub 2012 Apr 25. No abstract available.

PMID:
22532170
10.

Peripheral neuropathy in late-onset Krabbe disease: report of three cases.

Malandrini A, D'Eramo C, Palmeri S, Gaudiano C, Gambelli S, Sicurelli F, Berti G, Formichi P, Kuqo A, Dotti MT, Federico A.

Neurol Sci. 2013 Jan;34(1):79-83. doi: 10.1007/s10072-012-0956-6. Epub 2012 Jan 25.

PMID:
22274816
11.

Myotonic dystrophy type 2 and autoimmune chronic gastritis: an incidental association?

Sicurelli F, Mignarri A, Cardani R, Mondelli M, Carluccio A, Marino D, Meola G, Federico A, Dotti MT.

Neurol Sci. 2011 Dec;32(6):1249-50. doi: 10.1007/s10072-011-0782-2. Epub 2011 Sep 24. No abstract available.

PMID:
21948056
12.

A new thymidine phosphorylase mutation causing elongation of the protein underlies mitochondrial neurogastrointestinal encephalomyopathy.

Cardaioli E, Sicurelli F, Carluccio MA, Gallus GN, Da Pozzo P, Mondelli M, Margollicci MA, Micheli V, Federico A, Dotti MT.

J Neurol. 2012 Jan;259(1):172-4. doi: 10.1007/s00415-011-6113-y. Epub 2011 Jun 12. No abstract available.

PMID:
21667329
13.

Neuromyotonia as paraneoplastic manifestation of bladder carcinoma.

Forte F, Pretegiani E, Battisti C, Sicurelli F, Federico A.

J Neurol Sci. 2009 May 15;280(1-2):111-2. doi: 10.1016/j.jns.2009.01.022. Epub 2009 Feb 27.

PMID:
19249799
14.

Recurrent venous thrombosis including cerebral venous sinus thrombosis in a patient taking sildenafil for erectile dysfunction.

Rufa A, Cerase A, Monti L, Dotti MT, Giorgio A, Sicurelli F, Federico A.

J Neurol Sci. 2007 Sep 15;260(1-2):293-5. Epub 2007 Jun 18.

PMID:
17572443
15.

Leukoencephalopathy as a rare complication of hepatitis C infection.

Buccoliero R, Gambelli S, Sicurelli F, Malandrini A, Palmeri S, De Santis M, Stromillo ML, De Stefano N, Sperduto A, Musumeci SA, Federico A.

Neurol Sci. 2006 Nov;27(5):360-3.

PMID:
17122948
16.

Peripheral neuropathy in vanishing white matter disease with a novel EIF2B5 mutation.

Federico A, Scali O, Stromillo ML, Di Perri C, Bianchi S, Sicurelli F, De Stefano N, Malandrini A, Dotti MT.

Neurology. 2006 Jul 25;67(2):353-5.

PMID:
16864840
17.

Rapidly progressive neurodegeneration in a case with the 7472insC mutation and the A7472C polymorphism in the mtDNA tRNA ser(UCN) gene.

Cardaioli E, Da Pozzo P, Cerase A, Sicurelli F, Malandrini A, De Stefano N, Stromillo ML, Battisti C, Dotti MT, Federico A.

Neuromuscul Disord. 2006 Jan;16(1):26-31. Epub 2005 Dec 20.

PMID:
16368237
18.

Lung involvement in Niemann-Pick disease type C1: improvement with bronchoalveolar lavage.

Palmeri S, Tarugi P, Sicurelli F, Buccoliero R, Malandrini A, De Santi MM, Marcian├▓ G, Battisti C, Dotti MT, Calandra S, Federico A.

Neurol Sci. 2005 Jul;26(3):171-3.

PMID:
16086131
19.

Peripheral neuropathy in CADASIL.

Sicurelli F, Dotti MT, De Stefano N, Malandrini A, Mondelli M, Bianchi S, Federico A.

J Neurol. 2005 Oct;252(10):1206-9. Epub 2005 Apr 15.

PMID:
15827866
20.

Acute unilateral visual loss as the first symptom of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Rufa A, De Stefano N, Dotti MT, Bianchi S, Sicurelli F, Stromillo ML, D'Aniello B, Federico A.

Arch Neurol. 2004 Apr;61(4):577-80.

PMID:
15096408
21.

MR evidence of structural and metabolic changes in brains of patients with Werner's syndrome.

De Stefano N, Dotti MT, Battisti C, Sicurelli F, Stromillo ML, Mortilla M, Federico A.

J Neurol. 2003 Oct;250(10):1169-73.

PMID:
14586596
22.

Protocol of outcome evaluation for surgical release of carpal tunnel syndrome.

Reale F, Ginanneschi F, Sicurelli F, Mondelli M.

Neurosurgery. 2003 Aug;53(2):343-50; discussion 350-1.

PMID:
12925250
23.

The Primrose syndrome with progressive neurological involvement and cerebral calcification.

Battisti C, Dotti MT, Cerase A, Rufa A, Sicurelli F, Scarpini C, Federico A.

J Neurol. 2002 Oct;249(10):1466-8. No abstract available.

PMID:
12532939
24.

Spinocerebellar ataxia type 2 (SCA2) associated with retinal pigmentary degeneration.

Rufa A, Dotti MT, Galli L, Orrico A, Sicurelli F, Federico A.

Eur Neurol. 2002;47(2):128-9. No abstract available.

PMID:
11844906
25.

A Rett syndrome MECP2 mutation that causes mental retardation in men.

Dotti MT, Orrico A, De Stefano N, Battisti C, Sicurelli F, Severi S, Lam CW, Galli L, Sorrentino V, Federico A.

Neurology. 2002 Jan 22;58(2):226-30.

PMID:
11805248
26.

Genetic leukoencephalopathies with unknown metabolic pathogenesis.

Federico A, Rufa A, Battisti C, Bianchi S, Cardaioli E, Da Pozzo P, De Stefano N, Formichi P, Sicurelli F, Dotti MT.

Neurol Sci. 2001 Nov;22 Suppl 2:S108-12. Review.

PMID:
11794472
27.

Cerebrotendinous xanthomatosis: 11-year treatment with chenodeoxycholic acid in five patients. An electrophysiological study.

Mondelli M, Sicurelli F, Scarpini C, Dotti MT, Federico A.

J Neurol Sci. 2001 Sep 15;190(1-2):29-33.

PMID:
11574103
28.
29.

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.

Brain Dev. 1998 Aug;20(5):290-4.

PMID:
9760997
30.

A syndrome of autosomal recessive pontocerebellar hypoplasia with white matter abnormalities and protracted course in two brothers.

Malandrini A, Palmeri S, Villanova M, Parrotta E, Sicurelli F, Amato D, DeFalco D, Guazzi GC.

Brain Dev. 1997 Apr;19(3):209-11.

PMID:
9134193
31.

An unusual type of primary cerebral hemihypotrophy with signs of dysfunctional neuronal migration.

Malandrini A, Lo Russo F, Villanova M, Salvestroni R, Sicurelli F, Salvadori C, Paolozzi C, Guazzi GC.

Acta Neuropathol. 1996 Dec;92(6):631-4.

PMID:
8960323
32.

Autosomal recessive paraparesis with amyotrophy of hands and feet and white matter lesions.

Malandrini A, Scarpini C, Villanova M, Sicurelli F, Parrotta E, DeFalco D, Guazzi GC.

Acta Neurol Scand. 1996 Jul;94(1):60-2.

PMID:
8874595

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