Lista de obras - Fabrizio De Falco - Dominio Público Uruguay

A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy

artículo científico publicado en 2008

ADAM23, a Gene Related to LGI1, Is Not Linked to Autosomal Dominant Lateral Temporal Epilepsy

artículo científico publicado en 2010

Alexander's disease. A clinical study with computerized tomographic scans of the first two Italian cases

artículo científico publicado en 1980

An unusual EEG pattern in elderly subjects: subclinical rhythmic EEG discharge of adults ("SREDA"). Electroclinical study of six cases.

artículo científico publicado en 1983

Aspirin and extended-release dipyridamole versus clopidogrel for recurrent stroke

artículo científico publicado en 2008

Atrial fibrillation and infarct area extent in ischemic stroke. A clinical and neuroradiological study in 104 patients.

artículo científico publicado en 1991

Autosomal recessive benign myoclonic epilepsy of infancy

scientific article published on 01 January 2005

Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families

artículo científico publicado en 2008

Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCME

artículo científico publicado en 2003

Benign partial epilepsy with multiple foci. Its characterization among primary partial epilepsies

scientific article published on 01 April 1987

Bilateral thalamic damage, cortical hypometabolism and behavioural disturbances.

artículo científico publicado en 1994

Bioptically demonstrated Lafora disease without EPM2A mutation: a clinical and neurophysiological study of two sisters

artículo científico publicado en 2003

Burden of acute stroke and hospital resources in the Campania region of Italy

artículo científico publicado en 2002

Calcium antagonist nimodipine in intractable epilepsy

artículo científico publicado en 1992

Cardiac abnormalities in Friedreich's ataxia patients and first-degree relatives. Evidence of hypertrophic cadiomyopathy in obligate heterozygotes

artículo científico publicado en 1980

Clinical efficacy of picotamide

artículo científico publicado en 1991

Contribution to the problem of the adrenoleukomyeloneuropathy complex. Study of two Italian brothers with adrenoleukodystrophy and their mother with myeloneuropathy

artículo científico publicado en 1982

Correlation between hyperglycemia and cerebral infarct size in patients with stroke. A clinical and X-ray computed tomography study in 104 patients

artículo científico publicado en 1993

Creutzfeldt-Jakob disease. Electro-clinical evaluation in five cases

scientific article published on 01 April 1984

EEG and spectral analysis in HIV immunocompetent patients free from clinical CNS impairment. A follow-up study in 20 cases

artículo científico publicado en 1989

EEG findings in West syndrome a follow-up of 20 patients

artículo científico publicado en 1992

Effects of aspirin plus extended-release dipyridamole versus clopidogrel and telmisartan on disability and cognitive function after recurrent stroke in patients with ischaemic stroke in the Prevention Regimen for Effectively Avoiding Second [...]

artículo científico publicado en 2008

Electroclinical evolution in ring chromosome 20 epilepsy syndrome: a case with severe phenotypic features followed for 25 years.

artículo científico publicado en 2006

Familial benign nonprogressive myoclonic epilepsies.

scientific article published on May 2009

Familial infantile myoclonic epilepsy: clinical features in a large kindred with autosomal recessive inheritance

artículo científico publicado en 2001

Hypoglossal-sympathetic-carotid syndrome produced by internal carotid arteritis. Case report

artículo científico publicado en 1988

Incidence and predictors of acute symptomatic seizures after stroke

artículo científico publicado en 2011

LGI1 microdeletion in autosomal dominant lateral temporal epilepsy.

artículo científico publicado en 2012

Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.

artículo científico publicado en 2013

Mapping of a locus for a familial autosomal recessive idiopathic myoclonic epilepsy of infancy to chromosome 16p13.

artículo científico publicado en 2000

Metals in the metabolism of cerebral neurotransmitters. Physiological importance and metal-enzyme topographic relationships

artículo científico publicado en 1975

Migraine with aura: which patients are most at risk of stroke?

artículo científico

Multiple cerebral aneurysms associated with atrial myxoma. A case report

artículo científico publicado en 2010

Need for neurology specialists to be dedicated to hospital care in Italy

artículo científico publicado en 2013

Non-motor symptoms in atypical and secondary parkinsonism: the PRIAMO study

artículo científico publicado en 2009

Otoneurological findings in Friedreich's ataxia and other inherited neuropathies.

artículo científico publicado en 1986

Pancreatic encephalopathy. A case report with multifocal neurological signs

artículo científico publicado en 1980

Paroxysmal lateralized epileptiform discharges (PLEDS). Clinical-EEG correlations in twenty cases

artículo científico publicado en 1986

Photoparoxysmal response on eye closure in photosensitive patients

artículo científico publicado en 1992

Primary generalized epilepsy with photosensitivity and seizures on awakening. Report of a family

scientific article published on 01 August 1988

Progressive supranuclear palsy. Part 2. Electro-oculographic and neuro-otological study

artículo científico publicado en 1982

Progressive supranuclear palsy. Part I. Clinical study of 10 cases

scientific article published on 01 February 1982

Proposed clinical rating scale for spino-cerebellar ataxia

artículo científico publicado en 1979

Radiation myelopathy. Report of three cases

artículo científico publicado en 1979

Rationale and design of a randomized, double-blind, parallel-group study of terutroban 30 mg/day versus aspirin 100 mg/day in stroke patients: the prevention of cerebrovascular and cardiovascular events of ischemic origin with terutroban in patients

artículo científico publicado en 2009

Recurrent Intraventricular Hemorrhages Caused by an AVM Detected by Angiography with Initially Normal Angiogram

artículo científico publicado en 2008

Residual reading capability in a patient with alexia without agraphia

artículo científico publicado en 1984

Sentinel headache

artículo científico publicado en 2004

Specific impairment of BAER's in Friedreich's ataxia. Auditory evoked responses in clinical evaluation and differential diagnosis

artículo científico publicado en 1984

Stroke in neurological services in Italy

artículo científico publicado en 2009

TBC1D24, an ARF6-interacting protein, is mutated in familial infantile myoclonic epilepsy

artículo científico publicado en 2010

Telmisartan to prevent recurrent stroke and cardiovascular events

artículo científico publicado en 2008

Terutroban versus aspirin in patients with cerebral ischaemic events (PERFORM): a randomised, double-blind, parallel-group trial

scientific article published in The Lancet

The neurologist in the emergency department. An Italian nationwide epidemiological survey

artículo científico publicado en 2008

The role of emergency neurology in Italy: outcome of a consensus meeting for a Intersociety position

artículo científico publicado en 2011

Unawareness of "illnesses": a case of right-sided hemiballism

artículo científico publicado en 2008

Usefulness and limits of a new method for biochemical screening of lysosomal storage diseases

scientific article published on 01 December 1981

[A multidisciplinary approach to the study of cerebrovascular diseases]

artículo científico publicado en 1980

[Effect of the chronic treatment with L-acetylcarnitine in Down's syndrome]

artículo científico publicado en 1994

[Electromyographic and neurographic study of a family with HMSN (hereditary motor and sensory neuropathy) "plus"]

scientific article published on 01 April 1984

[Kugelberg-Welander type spinal amyotrophy. Familial study of 2 cases]

artículo científico publicado en 1978

Lista de obras de Fabrizio De Falco

A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy

ADAM23, a Gene Related to LGI1, Is Not Linked to Autosomal Dominant Lateral Temporal Epilepsy

Alexander's disease. A clinical study with computerized tomographic scans of the first two Italian cases

An unusual EEG pattern in elderly subjects: subclinical rhythmic EEG discharge of adults ("SREDA"). Electroclinical study of six cases.

Aspirin and extended-release dipyridamole versus clopidogrel for recurrent stroke

Atrial fibrillation and infarct area extent in ischemic stroke. A clinical and neuroradiological study in 104 patients.

Autosomal recessive benign myoclonic epilepsy of infancy

Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families

Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCME

Benign partial epilepsy with multiple foci. Its characterization among primary partial epilepsies

Bilateral thalamic damage, cortical hypometabolism and behavioural disturbances.

Bioptically demonstrated Lafora disease without EPM2A mutation: a clinical and neurophysiological study of two sisters

Burden of acute stroke and hospital resources in the Campania region of Italy

Calcium antagonist nimodipine in intractable epilepsy

Cardiac abnormalities in Friedreich's ataxia patients and first-degree relatives. Evidence of hypertrophic cadiomyopathy in obligate heterozygotes

Clinical efficacy of picotamide

Contribution to the problem of the adrenoleukomyeloneuropathy complex. Study of two Italian brothers with adrenoleukodystrophy and their mother with myeloneuropathy

Correlation between hyperglycemia and cerebral infarct size in patients with stroke. A clinical and X-ray computed tomography study in 104 patients

Creutzfeldt-Jakob disease. Electro-clinical evaluation in five cases

EEG and spectral analysis in HIV immunocompetent patients free from clinical CNS impairment. A follow-up study in 20 cases

EEG findings in West syndrome a follow-up of 20 patients

Effects of aspirin plus extended-release dipyridamole versus clopidogrel and telmisartan on disability and cognitive function after recurrent stroke in patients with ischaemic stroke in the Prevention Regimen for Effectively Avoiding Second [...]

Electroclinical evolution in ring chromosome 20 epilepsy syndrome: a case with severe phenotypic features followed for 25 years.

Familial benign nonprogressive myoclonic epilepsies.

Familial infantile myoclonic epilepsy: clinical features in a large kindred with autosomal recessive inheritance

Hypoglossal-sympathetic-carotid syndrome produced by internal carotid arteritis. Case report

Incidence and predictors of acute symptomatic seizures after stroke

LGI1 microdeletion in autosomal dominant lateral temporal epilepsy.

Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.

Mapping of a locus for a familial autosomal recessive idiopathic myoclonic epilepsy of infancy to chromosome 16p13.

Metals in the metabolism of cerebral neurotransmitters. Physiological importance and metal-enzyme topographic relationships

Migraine with aura: which patients are most at risk of stroke?

Multiple cerebral aneurysms associated with atrial myxoma. A case report

Need for neurology specialists to be dedicated to hospital care in Italy

Non-motor symptoms in atypical and secondary parkinsonism: the PRIAMO study

Otoneurological findings in Friedreich's ataxia and other inherited neuropathies.

Pancreatic encephalopathy. A case report with multifocal neurological signs

Paroxysmal lateralized epileptiform discharges (PLEDS). Clinical-EEG correlations in twenty cases

Photoparoxysmal response on eye closure in photosensitive patients

Primary generalized epilepsy with photosensitivity and seizures on awakening. Report of a family

Progressive supranuclear palsy. Part 2. Electro-oculographic and neuro-otological study

Progressive supranuclear palsy. Part I. Clinical study of 10 cases

Proposed clinical rating scale for spino-cerebellar ataxia

Radiation myelopathy. Report of three cases

Rationale and design of a randomized, double-blind, parallel-group study of terutroban 30 mg/day versus aspirin 100 mg/day in stroke patients: the prevention of cerebrovascular and cardiovascular events of ischemic origin with terutroban in patients

Recurrent Intraventricular Hemorrhages Caused by an AVM Detected by Angiography with Initially Normal Angiogram

Residual reading capability in a patient with alexia without agraphia

Sentinel headache

Specific impairment of BAER's in Friedreich's ataxia. Auditory evoked responses in clinical evaluation and differential diagnosis

Stroke in neurological services in Italy

TBC1D24, an ARF6-interacting protein, is mutated in familial infantile myoclonic epilepsy

Telmisartan to prevent recurrent stroke and cardiovascular events

Terutroban versus aspirin in patients with cerebral ischaemic events (PERFORM): a randomised, double-blind, parallel-group trial

The neurologist in the emergency department. An Italian nationwide epidemiological survey

The role of emergency neurology in Italy: outcome of a consensus meeting for a Intersociety position

Unawareness of "illnesses": a case of right-sided hemiballism

Usefulness and limits of a new method for biochemical screening of lysosomal storage diseases

[A multidisciplinary approach to the study of cerebrovascular diseases]

[Effect of the chronic treatment with L-acetylcarnitine in Down's syndrome]

[Electromyographic and neurographic study of a family with HMSN (hereditary motor and sensory neuropathy) "plus"]

[Kugelberg-Welander type spinal amyotrophy. Familial study of 2 cases]