Zobrazeno 1 - 10
of 127
pro vyhledávání: '"M. Bartolotta"'
Autor:
Paolo Bongiovanni, Tommaso Bocci, Cristina Dolciotti, M. Santin, Andrea Di Rollo, M. Bartolotta, Alessio Pelagatti, Ferdinando Sartucci
Publikováno v:
Clinical Neurophysiology. 130:e90-e91
Background Several methods have been proposed to diagnose and score disease severity in Amyotrophic Lateral Sclerosis (ALS) patients (pt.). Traditionally neurophysiological tests have been employed. The development of neuromuscular ultrasound (US) ha
Autor:
Diego Franciotta, Anna De Rosa, M. Bartolotta, Roberta Ricciardi, Chiara Pizzanelli, Ubaldo Bonuccelli, Melania Guida, Tommaso Bocci, Michelangelo Maestri
Publikováno v:
Clinical Neurophysiology. 129:e164-e165
Introduction Although Myasthenia gravis (MG) is the most common autoimmune disease associated with thymoma, a small proportion of thymomatous patients can suffer from limbic autoimmune encephalitis (LE). LE is usually characterized by rapid progressi
Autor:
D. Barloscio, L. Parenti, M. Bartolotta, M. Vergari, R. Ferrucci, A. Priori, E. Santarcangelo, A. Di Rollo, G. Carli, F. Sartucci, T. Bocci
Publikováno v:
Clinical Neurophysiology. 127:e340-e341
We evaluated the role of cerebellum in defensive responses, by recording the Hand Blink Reflex (HBR) and modulating cerebellar activity with transcranial Direct Current Stimulation (tDCS). The active electrode was centered on the median line 2 cm bel
Publikováno v:
Clinical Neurophysiology. 128:e425
Functional tremor (FT) still remains a challenge for clinicians; here, we propose a simple and fast test battery for an early diagnosis of FT. We enrolled ten patients with probable FT and compared them with patients with essential tremor (ET) or tre
Autor:
L. Parenti, M. Bartolotta, D. Barloscio, Massimiliano Valeriani, Ferdinando Sartucci, Tommaso Bocci
Publikováno v:
Clinical Neurophysiology. 128:e434
Laser-evoked potentials (LEPs) represent the most reliable method to diagnose and follow over time painful small fiber neuropathies. Here, we investigated LEPs in patients with pain of non-organic origin. LEPs were recorded with a Nd:Yag Laser in 4 s
Autor:
M. Bartolotta, C. Del Gamba, Ferdinando Sartucci, L. Parenti, M. Santin, A. Di Rollo, Tommaso Bocci, D. Barloscio
Publikováno v:
Clinical Neurophysiology. 128:e428
Hereditary Motor and Sensory Neuropathies (HMSN) often present a set of challenges on the electrophysiological diagnosis. Even if genetic tests are now available for most of the subtypes, electromyography (EMG) still plays an irreplaceable role in di
Autor:
M. Santin, M. Bartolotta, D. Barloscio, C. De Luca, Tommaso Bocci, L. Parenti, Ferdinando Sartucci, A. Di Rollo
Publikováno v:
Clinical Neurophysiology. 128:e429
Myasthenia Gravis (MG) is an autoimmune neuromuscular disease characterized by abnormal weakness and fatigability of some or all skeletal muscles. Among them, external ocular muscles are often affected resulting in diplopia and ptosis. Our aim was to
Publikováno v:
Clinical Neurophysiology. 127:e339
Transcutaneous spinal Direct Current Stimulation (tsDCS) is a new and safe technique for modulating spinal cord excitability. We evaluated the effects of supraspinal and cortical stimulation in healthy subjects before (T0) and at different intervals
Autor:
Tommaso Bocci, D. Barloscio, A. Di Rollo, Ferdinando Sartucci, Elisa Giorli, L. Parenti, M. Santin, M. Bartolotta, C. Del Gamba
Publikováno v:
Clinical Neurophysiology. 127:e337
Hereditary motor and sensory neuropathies (HMSN) often present a set of challenges on the electrophysiological diagnosis. Genetic tests are available for most of the subtypes, but electromyography (EMG) still plays a fundamental role in diagnosis. De
Publikováno v:
Clinical Neurophysiology. 127:e339
Transcutaneous Direct Current Stimulation (tDCS) is a safe technique for modulating central nervous system excitability. We assessed clinical changes in early Huntington’s Disease (HD) following tDCS by evaluating Unified Huntington Disease Rating