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1.
Early-onset motor polyneuropathy associated with a novel dominant NAGLU mutation.
Neurol Sci
; 44(4): 1415-1418, 2023 Apr.
Article
in English
| MEDLINE | ID: mdl-36648562
2.
A case of spastic paraplegia type 11 mimicking a GM2-gangliosidosis.
Neurol Sci
; 43(4): 2849-2852, 2022 Apr.
Article
in English
| MEDLINE | ID: mdl-35066644
3.
Diagnosis, treatment, and follow-up of patients with cerebral amyloid angiopathy-related inflammation.
Neurol Sci
; 43(11): 6381-6387, 2022 Nov.
Article
in English
| MEDLINE | ID: mdl-35930182
4.
Changes in corticomotor pathway excitability after exercise training in Parkinson's disease.
Neurol Sci
; 42(8): 3375-3381, 2021 Aug.
Article
in English
| MEDLINE | ID: mdl-33411200
5.
NGS in Hereditary Ataxia: When Rare Becomes Frequent.
Int J Mol Sci
; 22(16)2021 Aug 06.
Article
in English
| MEDLINE | ID: mdl-34445196
6.
HTRA1 expression profile and activity on TGF-ß signaling in HTRA1 mutation carriers.
J Cell Physiol
; 235(10): 7120-7127, 2020 10.
Article
in English
| MEDLINE | ID: mdl-32017060
7.
Eye movement changes in autosomal dominant spinocerebellar ataxias.
Neurol Sci
; 41(7): 1719-1734, 2020 Jul.
Article
in English
| MEDLINE | ID: mdl-32130555
8.
Primary familial brain calcification with a novel SLC20A2 mutation: Analysis of PiT-2 expression and localization.
J Cell Physiol
; 233(3): 2324-2331, 2018 Mar.
Article
in English
| MEDLINE | ID: mdl-28722801
9.
Primary cilium alterations and expression changes of Patched1 proteins in niemann-pick type C disease.
J Cell Physiol
; 233(1): 663-672, 2018 Jan.
Article
in English
| MEDLINE | ID: mdl-28332184
10.
A case report of FAVA syndrome in a young woman carrying a mutation in the PIK3CA gene.
Neurol Sci
; 44(11): 4147-4150, 2023 Nov.
Article
in English
| MEDLINE | ID: mdl-37438545
11.
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients.
Neurol Sci
; 38(4): 563-570, 2017 Apr.
Article
in English
| MEDLINE | ID: mdl-28130605
12.
Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): update on molecular genetics.
Neurol Sci
; 37(9): 1565-9, 2016 Sep.
Article
in English
| MEDLINE | ID: mdl-27338940
13.
A case series of two post-infectious acute cerebellitis an insidious path to the diagnosis and therapy.
Neurol Sci
; 42(11): 4843-4846, 2021 Nov.
Article
in English
| MEDLINE | ID: mdl-34515890
14.
Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease.
Am J Hum Genet
; 90(3): 467-77, 2012 Mar 09.
Article
in English
| MEDLINE | ID: mdl-22341971
15.
A case of painless neuralgic amyotrophy responsive to immunotherapy.
Neurol Sci
; 41(8): 2297-2298, 2020 Aug.
Article
in English
| MEDLINE | ID: mdl-32189092
16.
A case of pneumocephalus as complication of ozone therapy: diagnosis and treatment.
Neurol Sci
; 41(2): 481-483, 2020 02.
Article
in English
| MEDLINE | ID: mdl-31478149
17.
A case of reversible cerebral vasoconstriction syndrome and cavernous hemangioma: just a coincidence?
Neurol Sci
; 39(11): 1989-1990, 2018 Nov.
Article
in English
| MEDLINE | ID: mdl-30062645
18.
Effects of cerebrolysin administration on oxidative stress-induced apoptosis in lymphocytes from CADASIL patients.
Neurol Sci
; 34(4): 553-6, 2013 Apr.
Article
in English
| MEDLINE | ID: mdl-22878905
19.
FOLR1 Gene Variation With Adult-Onset Cerebral Folate Deficiency and Stable Clinical and MRI Features up to 2 Years.
Neurol Genet
; 9(6): e200104, 2023 Dec.
Article
in English
| MEDLINE | ID: mdl-38239817
20.
Altered apoptosis regulation in Kufor-Rakeb syndrome patients with mutations in the ATP13A2 gene.
J Cell Mol Med
; 16(8): 1916-23, 2012 Aug.
Article
in English
| MEDLINE | ID: mdl-22117566