about
SUNCT and high nocturnal prolactin levels: some new unusual characteristicsTwo novel SCN1A missense mutations in generalized epilepsy with febrile seizures plusGeneralized versus partial reflex seizures: a review.Epilepsy in cerebrovascular diseases: Review of experimental and clinical data with meta-analysis of risk factors.Positivity to p-ANCA in patients with status epilepticus.Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizuresMutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy.Anti-NMDA receptor encephalitis: a video case report.Rosacea-like facial rash related to metformin administration in a young woman.White matter abnormalities differentiate severe from benign temporal lobe epilepsy.Familial mesial temporal lobe epilepsies: clinical and genetic features.Usefulness of rectal biopsy for the diagnosis of Kufs disease: a controlled study and review of the literature.A possible case of natalizumab-dependent suicide attempt: A brief review about drugs and suicide.The role of calcium channel mutations in human epilepsy.Epilepsy and sleep disorders improve in adolescents and adults with Angelman syndrome: A multicenter study on 46 patients.Pharmacological modulation in mesial temporal lobe epilepsy: Current status and future perspectives.Topiramate and temporal lobe epilepsy: an open-label study.An SNP site in pri-miR-124, a brain expressed miRNA gene, no contribution to mesial temporal lobe epilepsy in an Italian sample.Long-term outcome of mild mesial temporal lobe epilepsy: A prospective longitudinal cohort study.Epilepsy associated with Leukoaraiosis mainly affects temporal lobe: a casual or causal relationship?Unilateral basal ganglia atrophy in a patient with tuberous sclerosis complex and hemichorea.Association between the M129V variant allele of PRNP gene and mild temporal lobe epilepsy in women.Electroclinical features of a family with simple febrile seizures and temporal lobe epilepsy associated with SCN1A loss-of-function mutation.Unexpected detection of melanoma brain metastasis by PET with iodine-124 betaCIT.Benign mesial temporal lobe epilepsy.Comment on Brázdil (2012) "unveiling the mystery of dèjà-vù: the structural anatomy of dèjà-vù".Advanced MRI morphologic study shows no atrophy in healthy individuals with hippocampal hyperintensity.Failure to confirm association of a polymorphism in KCNMB4 gene with mesial temporal lobe epilepsy.Autosomal dominant lateral temporal epilepsy (ADLTE): absence of chromosomal rearrangements in LGI1 gene.Startle epilepsy complicating aspartylglucosaminuria.A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy.No evidence for a role of the coding variant of the Toll-like receptor 4 gene in temporal lobe epilepsy.Juvenile Huntington's disease presenting as progressive myoclonic epilepsy.The DRD2 TaqIA polymorphism associated with changed midbrain volumes in healthy individuals.Orolingual tremor as unusual presentation of anti-Hu paraneoplastic syndrome.MAO A VNTR polymorphism and variation in human morphology: a VBM study.Impact of catechol-O-methyltransferase Val(108/158) Met genotype on hippocampal and prefrontal gray matter volume.Levetiracetam in patients with generalised epilepsy and myoclonic seizures: an open label study.Psychopathological constellation in patients with PNES: A new hypothesis.Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study.
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Angelo Labate
@ast
Angelo Labate
@en
Angelo Labate
@es
Angelo Labate
@nl
Angelo Labate
@sl
type
label
Angelo Labate
@ast
Angelo Labate
@en
Angelo Labate
@es
Angelo Labate
@nl
Angelo Labate
@sl
prefLabel
Angelo Labate
@ast
Angelo Labate
@en
Angelo Labate
@es
Angelo Labate
@nl
Angelo Labate
@sl
P106
P1153
7004100448
P21
P31
P496
0000-0002-8827-7324
P569
2000-01-01T00:00:00Z