about
TBC1D24, an ARF6-interacting protein, is mutated in familial infantile myoclonic epilepsyStroke in neurological services in ItalyThe role of emergency neurology in Italy: outcome of a consensus meeting for a Intersociety position.Familial benign nonprogressive myoclonic epilepsies.Otoneurological findings in Friedreich's ataxia and other inherited neuropathies.[Proposed clinical rating scale for spino-cerebellar ataxia][Clinical efficacy of picotamide]Bioptically demonstrated Lafora disease without EPM2A mutation: a clinical and neurophysiological study of two sisters.Correlation between hyperglycemia and cerebral infarct size in patients with stroke. A clinical and X-ray computed tomography study in 104 patients.Calcium antagonist nimodipine in intractable epilepsy.Specific impairment of BAER's in Friedreich's ataxia. Auditory evoked responses in clinical evaluation and differential diagnosis.Atrial fibrillation and infarct area extent in ischemic stroke. A clinical and neuroradiological study in 104 patients.An unusual EEG pattern in elderly subjects: subclinical rhythmic EEG discharge of adults ("SREDA"). Electroclinical study of six cases.The neurologist in the emergency department. An Italian nationwide epidemiological survey.Bilateral thalamic damage, cortical hypometabolism and behavioural disturbances.[Effect of the chronic treatment with L-acetylcarnitine in Down's syndrome]Primary generalized epilepsy with photosensitivity and seizures on awakening. Report of a familyBenign partial epilepsy with multiple foci. Its characterization among primary partial epilepsies[Kugelberg-Welander type spinal amyotrophy. Familial study of 2 cases]Photoparoxysmal response on eye closure in photosensitive patientsEEG findings in West syndrome a follow-up of 20 patientsHypoglossal-sympathetic-carotid syndrome produced by internal carotid arteritis. Case reportEEG and spectral analysis in HIV immunocompetent patients free from clinical CNS impairment. A follow-up study in 20 casesParoxysmal lateralized epileptiform discharges (PLEDS). Clinical-EEG correlations in twenty casesCreutzfeldt-Jakob disease. Electro-clinical evaluation in five casesProgressive supranuclear palsy. Part I. Clinical study of 10 casesProgressive supranuclear palsy. Part 2. Electro-oculographic and neuro-otological study[A multidisciplinary approach to the study of cerebrovascular diseases]Pancreatic encephalopathy. A case report with multifocal neurological signsUsefulness and limits of a new method for biochemical screening of lysosomal storage diseasesCardiac abnormalities in Friedreich's ataxia patients and first-degree relatives. Evidence of hypertrophic cadiomyopathy in obligate heterozygotesAlexander's disease. A clinical study with computerized tomographic scans of the first two Italian casesContribution to the problem of the adrenoleukomyeloneuropathy complex. Study of two Italian brothers with adrenoleukodystrophy and their mother with myeloneuropathy[Electromyographic and neurographic study of a family with HMSN (hereditary motor and sensory neuropathy) "plus"]Autosomal recessive benign myoclonic epilepsy of infancyNeed for neurology specialists to be dedicated to hospital care in ItalyRecurrent Intraventricular Hemorrhages Caused by an AVM Detected by Angiography with Initially Normal Angiogram
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Fabrizio De Falco
@ast
Fabrizio De Falco
@en
Fabrizio De Falco
@es
Fabrizio De Falco
@nl
Fabrizio De Falco
@sl
type
label
Fabrizio De Falco
@ast
Fabrizio De Falco
@en
Fabrizio De Falco
@es
Fabrizio De Falco
@nl
Fabrizio De Falco
@sl
prefLabel
Fabrizio De Falco
@ast
Fabrizio De Falco
@en
Fabrizio De Falco
@es
Fabrizio De Falco
@nl
Fabrizio De Falco
@sl
P106
P21
P31
P496
0000-0001-5065-1678