F. Sicurelli

发表

The Primrose syndrome with progressive neurological involvement and cerebral calcification

C. Scarpini, A. Federico, M. Dotti, 2002, Journal of Neurology.

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

C. Scarpini, A. Federico, M. Dotti, 2001, Journal of the Neurological Sciences.

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

A. Federico, N. Stefano, A. Malandrini, 2006, Neuromuscular Disorders.

A Rett syndrome MECP2 mutation that causes mental retardation in men

A. Federico, M. Dotti, C. Lam, 2002, Neurology.

Leukoencephalopathy as a rare complication of hepatitis C infection

A. Federico, N. Stefano, A. Malandrini, 2006, Neurological Sciences.

Rare phenotype of ALS4 associated with heterozygous missense mutation c.5842A > G/p.M1948V in helicase domain of SETX gene

C. Scarpini, F. Santorelli, C. Battisti, 2020, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Clinical Features and Outcome of the Guillain–Barre Syndrome: A Single-Center 11-Year Experience

F. Ginanneschi, D. Cioncoloni, S. Bartalini, 2022, Frontiers in Neurology.

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

C. Scarpini, G. Guazzi, A. Malandrini, 1996, Acta neurologica Scandinavica.

Genetic leukoencephalopathies with unknown metabolic pathogenesis

A. Federico, M. Dotti, C. Battisti, 2001, Neurological Sciences.

Peripheral neuropathy in CADASIL

A. Federico, N. Stefano, A. Malandrini, 2005, Journal of Neurology.

Hydroxychloroquine neuromyotoxicity: a case with rapid course and complete recovery

A. Federico, A. Malandrini, A. Fioravanti, 2015, Neurological Sciences.

Tarlov cysts: clinical evaluation of an italian cohort of patients

A. Federico, A. Rubegni, I. Di Donato, 2014, Neurological Sciences.

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

S. Curti, S. Mattioli, M. Mondelli, 2019, American journal of physical medicine & rehabilitation.

Risk factors of asymptomatic reduction of motor conduction velocity of the ulnar nerve across the elbow

M. Mondelli, F. Sicurelli, C. Vinciguerra, 2021, Neurological Sciences.

Comorbidities, anthropometric, demographic, and lifestyle risk factors for ulnar neuropathy at the elbow: A case control study

S. Curti, S. Mattioli, M. Mondelli, 2020, Journal of the peripheral nervous system : JPNS.

Neuromyotonia as paraneoplastic manifestation of bladder carcinoma

A. Federico, C. Battisti, E. Pretegiani, 2009, Journal of the Neurological Sciences.

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

A. Federico, M. Dotti, M. Stromillo, 2004, Archives of neurology.

Relationship between the Self-Administered Boston Questionnaire and Electrophysiological Findings in Follow-Up of Surgically-Treated Carpal Tunnel Syndrome

L. Padua, M. Mondelli, F. Reale, 2000, Journal of hand surgery.

Protocol of Outcome Evaluation for Surgical Release of Carpal Tunnel Syndrome

F. Ginanneschi, M. Mondelli, F. Reale, 2003, Neurosurgery.

Fulminant intravascular lymphomatosis mimicking acute haemorrhagic leukoencephalopathy

A. Federico, M. Cintorino, S. Tripodi, 2012, Journal of the Neurological Sciences.

The external elbow measure as surrogate of the anatomical width of cubital groove and possible risk factor of ulnar neuropathy at the elbow

M. Mondelli, A. Aretini, P. Ciaramitaro, 2019, The International journal of neuroscience.

Liver transplantation in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical long-term follow-up and pathogenic implications

L. Fasano, L. Pisani, R. Lodi, 2020, Journal of Neurology.

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

V. Micheli, A. Federico, M. Dotti, 2011, Journal of Neurology.

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

F. Ginanneschi, U. Arrigucci, M. Mondelli, 2013, Clinical Neurophysiology.

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

A. Federico, M. Mazzei, A. Malandrini, 2012, Neuromuscular Disorders.

Neuronal intranuclear inclusion disease: neuropathologic study of a case

G. Guazzi, A. Malandrini, M. Villanova, 1998, Brain and Development.

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

F. Ginanneschi, U. Arrigucci, M. Mondelli, 2013, Neurophysiologie Clinique/Clinical Neurophysiology.

Lumbosacral Plexopathy in Pelvic Radiotherapy: An Association not to be Neglected; A Systematic Review

S. Cappabianca, V. Nardone, F. Sicurelli, 2019, Archives of Neuroscience.

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

C. Di Perri, A. Federico, A. Malandrini, 2006, Neurology.

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

A. Giorgio, A. Federico, M. Dotti, 2007, Journal of the Neurological Sciences.

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

A. Malandrini, A. Federico, M. Dotti, 2005, Neurological Sciences.

A case of spastic paraplegia type 11 mimicking a GM2-gangliosidosis

E. Bertini, A. Federico, A. Malandrini, 2022, Neurological Sciences.

Eye movement changes in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)

A. Federico, M. Dotti, E. Cardaioli, 2015, Journal of the Neurological Sciences.

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

V. Micheli, A. Federico, M. Dotti, 2012, Journal of Neurology.

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

A. Federico, N. Stefano, M. Dotti, 2003, Journal of Neurology.

Spinocerebellar Ataxia Type 2 (Sca2) Associated with Retinal Pigmentary Degeneration

A. Federico, M. Dotti, A. Rufa, 2002, European Neurology.

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

G. Guazzi, A. Malandrini, M. Villanova, 1996, Acta Neuropathologica.

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

A. Federico, A. Malandrini, M. Dotti, 2012, Neurological Sciences.