Pub Date : 2003-01-01DOI: 10.1177/155005940303400106
John R Hughes
This paper deals with a patient with the Frontal Arousal Rhythm (FAR), a rare rhythmic pattern usually seen in young children awakening from sleep, with a history of seizures. In this patient, subtle clinical changes were observed on the video during the pattern, consisting of a sequence of brief eye lid flutter, chewing, increased inspiration and upper lip quivering. This exact sequence was seen on three successive occasions lasting for 6,9, and 10 sec. The conclusion is the FAR is not just a sign of seizure disorder, but is actually an ictal pattern.
{"title":"The frontal arousal rhythm (FAR) is an ictal pattern: a case report.","authors":"John R Hughes","doi":"10.1177/155005940303400106","DOIUrl":"https://doi.org/10.1177/155005940303400106","url":null,"abstract":"<p><p>This paper deals with a patient with the Frontal Arousal Rhythm (FAR), a rare rhythmic pattern usually seen in young children awakening from sleep, with a history of seizures. In this patient, subtle clinical changes were observed on the video during the pattern, consisting of a sequence of brief eye lid flutter, chewing, increased inspiration and upper lip quivering. This exact sequence was seen on three successive occasions lasting for 6,9, and 10 sec. The conclusion is the FAR is not just a sign of seizure disorder, but is actually an ictal pattern.</p>","PeriodicalId":75713,"journal":{"name":"Clinical EEG (electroencephalography)","volume":"34 1","pages":"13-4"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/155005940303400106","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22184673","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2003-01-01DOI: 10.1177/155005940303400107
M Luigia Vaccario, Maria A Valenti, Anna Carullo, Rossella Di Bartolomeo, Salvatore Mazza
Benign neonatal sleep myoclonus (BNSM), characterized by myoclonic jerks of the extremities only in non-REM sleep, occurs in the first months of life with spontaneous disappearance within 3-4 months. We examined five siblings with typical BNSM, at the 3-10 years follow-up neurological examination. Psychomotor development, cognitive functions and EEG were completely normal. These cases confirm that BNSM is a self limited and nonepileptic disorder.
{"title":"Benign neonatal sleep myoclonus: case report and follow-up of four members of an affected family.","authors":"M Luigia Vaccario, Maria A Valenti, Anna Carullo, Rossella Di Bartolomeo, Salvatore Mazza","doi":"10.1177/155005940303400107","DOIUrl":"https://doi.org/10.1177/155005940303400107","url":null,"abstract":"<p><p>Benign neonatal sleep myoclonus (BNSM), characterized by myoclonic jerks of the extremities only in non-REM sleep, occurs in the first months of life with spontaneous disappearance within 3-4 months. We examined five siblings with typical BNSM, at the 3-10 years follow-up neurological examination. Psychomotor development, cognitive functions and EEG were completely normal. These cases confirm that BNSM is a self limited and nonepileptic disorder.</p>","PeriodicalId":75713,"journal":{"name":"Clinical EEG (electroencephalography)","volume":"34 1","pages":"15-7"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/155005940303400107","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22184674","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2003-01-01DOI: 10.1177/155005940303400108
P Mariotti, G Della Marca, L Iuvone, S Vernacotola, R Ricci, G F Mennuni, S Mazza
Objective: A high prevalence of sleep disorders is reported in patients affected by Mucopolysaccharidosis III (Sanfilippo syndrome). These disorders have never been investigated by prolonged, objective, and instrumental evaluations. The present work is based on sleep duration and structure in Sanfilippo patients. Study design: The features of sleep/wake cycle in 6 Sanfilippo patients and 6 healthy controls were evaluated by means of sleep diaries and 48 hour ambulatory EEG and polygraphic recordings. Statistical analysis was performed by means of the U-test (Mann-Whitney). Results: Four out of six Sanfilippo patients, the oldest patients in our sample, showed an extremely irregular sleep pattern, with several sleep episodes of inconstant duration, irregularly distributed along 24 hours. The two younger patients showed sleep maintenance insomnia with several nocturnal awakenings. Conclusions: These results suggest that sleep disruption in Sanfilippo syndrome consists of an irregular sleep/wake pattern, which at its onset might appear as a disorder of initiating or maintaining sleep. This could explain why some patients do not respond to conventional hypnotics. The present observation might suggest attempting therapies aimed at resynchronization, such as behavioral treatment, light therapy or melatonin.
{"title":"Sleep disorders in Sanfilippo syndrome: a polygraphic study.","authors":"P Mariotti, G Della Marca, L Iuvone, S Vernacotola, R Ricci, G F Mennuni, S Mazza","doi":"10.1177/155005940303400108","DOIUrl":"https://doi.org/10.1177/155005940303400108","url":null,"abstract":"Objective: A high prevalence of sleep disorders is reported in patients affected by Mucopolysaccharidosis III (Sanfilippo syndrome). These disorders have never been investigated by prolonged, objective, and instrumental evaluations. The present work is based on sleep duration and structure in Sanfilippo patients. Study design: The features of sleep/wake cycle in 6 Sanfilippo patients and 6 healthy controls were evaluated by means of sleep diaries and 48 hour ambulatory EEG and polygraphic recordings. Statistical analysis was performed by means of the U-test (Mann-Whitney). Results: Four out of six Sanfilippo patients, the oldest patients in our sample, showed an extremely irregular sleep pattern, with several sleep episodes of inconstant duration, irregularly distributed along 24 hours. The two younger patients showed sleep maintenance insomnia with several nocturnal awakenings. Conclusions: These results suggest that sleep disruption in Sanfilippo syndrome consists of an irregular sleep/wake pattern, which at its onset might appear as a disorder of initiating or maintaining sleep. This could explain why some patients do not respond to conventional hypnotics. The present observation might suggest attempting therapies aimed at resynchronization, such as behavioral treatment, light therapy or melatonin.","PeriodicalId":75713,"journal":{"name":"Clinical EEG (electroencephalography)","volume":"34 1","pages":"18-22"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/155005940303400108","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22184675","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2003-01-01DOI: 10.1177/155005940303400111
John R Hughes, John J Fino
A simultaneous video-EEG on a waking 6-year-old male revealed rapid horizontal and then vertical eye movements and 10 sec later showed ictal rhythms maximal on the occipital areas, quickly spreading to all other areas. A second ictal event during wakefulness was very similar to the first. During sleep interictal discharges were seen from the right frontal-temporal area and one more ictal event was noted. This latter seizure in the NREM sleep record did not show any eye movements, but showed ictal activity on the right frontal-temporal area, which later became generalized. We propose that the interictal discharges on the right frontal-temporal area likely arose from the amygdala, which activated the pontine nuclei responsible for PGO (ponto-geniculo-occipital) spikes and the rapid eye movements seen in our patient. The PGO spikes activated the occipital areas, which then showed clear ictal rhythms to complete the sequence of events. This case demonstrates a sequence of rapid eye movements without ictal patterns, followed by seizure rhythms, but may still be an example of "epileptic nystagmus," assuming that the eye movements arose from an ictal activation of the deep subcortical portion of the PGO system.
{"title":"Epileptic nystagmus and its possible relationship with PGO spikes.","authors":"John R Hughes, John J Fino","doi":"10.1177/155005940303400111","DOIUrl":"https://doi.org/10.1177/155005940303400111","url":null,"abstract":"<p><p>A simultaneous video-EEG on a waking 6-year-old male revealed rapid horizontal and then vertical eye movements and 10 sec later showed ictal rhythms maximal on the occipital areas, quickly spreading to all other areas. A second ictal event during wakefulness was very similar to the first. During sleep interictal discharges were seen from the right frontal-temporal area and one more ictal event was noted. This latter seizure in the NREM sleep record did not show any eye movements, but showed ictal activity on the right frontal-temporal area, which later became generalized. We propose that the interictal discharges on the right frontal-temporal area likely arose from the amygdala, which activated the pontine nuclei responsible for PGO (ponto-geniculo-occipital) spikes and the rapid eye movements seen in our patient. The PGO spikes activated the occipital areas, which then showed clear ictal rhythms to complete the sequence of events. This case demonstrates a sequence of rapid eye movements without ictal patterns, followed by seizure rhythms, but may still be an example of \"epileptic nystagmus,\" assuming that the eye movements arose from an ictal activation of the deep subcortical portion of the PGO system.</p>","PeriodicalId":75713,"journal":{"name":"Clinical EEG (electroencephalography)","volume":"34 1","pages":"32-8"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/155005940303400111","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22184678","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The goal of this study was to assess the spikes systematically and to clarify an epileptc abnormality induced by electroconvulsive therapy (ECT). Our subjects were 20 psychotic patients with no spikes on prior EEGs. ECT was performed by applying electrical current to both sides of the patient's temple every 2 or 3 days for a period of between 1-4 weeks. The first EEG examination was performed either on the day that the ECT course was completed or on the following day. Subsequent EEG examinations were performed at intervals of 2 or 3 days. Thirteen of the 20 patients showed spikes. There were no significant differences in age, gender, diagnosis, or type of ECT. Patients with spikes had significantly more ECT sessions than those without spikes. The spikes were present in the frontal, temporal and central areas, predominantly frontal, anterior temporal and mid-temporal region, and almost disappeared in 1-3 weeks. The occurrence of spikes immediately after ECT was demonstrated. Although this abnormality was transient, it could indicate that in humans ECT causes the early stage of kindling phenomenon as a result of repeated application, and that the temporal lobe seems to play a major role in order to induce the phenomenon.
{"title":"Spikes immediately after electroconvulsive therapy in psychotic patients.","authors":"Fumio Kubota, Nobuyoshi Shibata, Takushiro Akata, Senichiro Kikuchi, Akira Kifune, Naoya Yuuki, Kazuo Takeuchi","doi":"10.1177/155005940303400109","DOIUrl":"https://doi.org/10.1177/155005940303400109","url":null,"abstract":"<p><p>The goal of this study was to assess the spikes systematically and to clarify an epileptc abnormality induced by electroconvulsive therapy (ECT). Our subjects were 20 psychotic patients with no spikes on prior EEGs. ECT was performed by applying electrical current to both sides of the patient's temple every 2 or 3 days for a period of between 1-4 weeks. The first EEG examination was performed either on the day that the ECT course was completed or on the following day. Subsequent EEG examinations were performed at intervals of 2 or 3 days. Thirteen of the 20 patients showed spikes. There were no significant differences in age, gender, diagnosis, or type of ECT. Patients with spikes had significantly more ECT sessions than those without spikes. The spikes were present in the frontal, temporal and central areas, predominantly frontal, anterior temporal and mid-temporal region, and almost disappeared in 1-3 weeks. The occurrence of spikes immediately after ECT was demonstrated. Although this abnormality was transient, it could indicate that in humans ECT causes the early stage of kindling phenomenon as a result of repeated application, and that the temporal lobe seems to play a major role in order to induce the phenomenon.</p>","PeriodicalId":75713,"journal":{"name":"Clinical EEG (electroencephalography)","volume":"34 1","pages":"23-7"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/155005940303400109","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22184676","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2003-01-01DOI: 10.1177/155005940303400110
M Gansaeuer, T M Alsaadi
A 58-year-old patient who was somnolent, distractible and confused is presented. She was previously treated with lithium, and a plasma level was mildly elevated at 1.7 mmol/l (normal 0.5-1.5 mmol/l). The EEG was suggestive of electrographic status epilepticus. Following treatment with i.v. lorazepam, neither mental status nor EEG abnormalities improved. She had a full recovery of mental function and markedly improved EEG findings following discontinuation of lithium. The EEG is an effective tool for diagnosing lithium neurotoxicity in patients with normal or mildly elevated lithium plasma levels. However, caution is needed before making an assumption of status epilepticus.
{"title":"Lithium intoxication mimicking clinical and electrographic features of status epilepticus: a case report and review of the literature.","authors":"M Gansaeuer, T M Alsaadi","doi":"10.1177/155005940303400110","DOIUrl":"https://doi.org/10.1177/155005940303400110","url":null,"abstract":"<p><p>A 58-year-old patient who was somnolent, distractible and confused is presented. She was previously treated with lithium, and a plasma level was mildly elevated at 1.7 mmol/l (normal 0.5-1.5 mmol/l). The EEG was suggestive of electrographic status epilepticus. Following treatment with i.v. lorazepam, neither mental status nor EEG abnormalities improved. She had a full recovery of mental function and markedly improved EEG findings following discontinuation of lithium. The EEG is an effective tool for diagnosing lithium neurotoxicity in patients with normal or mildly elevated lithium plasma levels. However, caution is needed before making an assumption of status epilepticus.</p>","PeriodicalId":75713,"journal":{"name":"Clinical EEG (electroencephalography)","volume":"34 1","pages":"28-31"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/155005940303400110","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22184677","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2002-10-01DOI: 10.1177/155005940203300406
John R Hughes, C C Wang
This study investigated the relationship between slow waves and sharp waves (spikes) and also clinical seizures in 255 patients with 694 EEGs over a 25-yr period. Slow waves were quantified into five groups, sharp waves into three groups and clinical seizures also into three groups. In general, as clinical seizures increased, the number of patients with many discharges increased and the number with only rare discharges decreased. Also, as patients became seizure free, there was a decreasing incidence of many sharp waves and an increasing incidence of only rare sharp waves. No relationships could be found in patients with a typical number of discharges or a steady number of seizures. Thus, a relationship between sharp waves and seizures was found mainly when there were changes in these variables. For sharp and slow waves, rare discharges were most often associated with mild slowing, while many discharges were most often related to a marked degree of slow wave abnormality. The combination of slow and sharp waves together, compared with only one type of EEG abnormality, was associated with more clinical neurological symptoms, especially a mental status change. The EEG groups were divided into four types of findings of slow and sharp waves, appearing in at least a first and/or second record. The results from these four EEG groups allow for a prediction of the findings to be found in a second record, based on the results of the first EEG. In general, there was a relationship between more slow waves, more sharp waves and more seizures. Also minimal slowing and rare discharges on the first record tended to disappear in the next EEG.
{"title":"The relationship between slow and sharp waves (spikes) and also clinical seizures.","authors":"John R Hughes, C C Wang","doi":"10.1177/155005940203300406","DOIUrl":"https://doi.org/10.1177/155005940203300406","url":null,"abstract":"<p><p>This study investigated the relationship between slow waves and sharp waves (spikes) and also clinical seizures in 255 patients with 694 EEGs over a 25-yr period. Slow waves were quantified into five groups, sharp waves into three groups and clinical seizures also into three groups. In general, as clinical seizures increased, the number of patients with many discharges increased and the number with only rare discharges decreased. Also, as patients became seizure free, there was a decreasing incidence of many sharp waves and an increasing incidence of only rare sharp waves. No relationships could be found in patients with a typical number of discharges or a steady number of seizures. Thus, a relationship between sharp waves and seizures was found mainly when there were changes in these variables. For sharp and slow waves, rare discharges were most often associated with mild slowing, while many discharges were most often related to a marked degree of slow wave abnormality. The combination of slow and sharp waves together, compared with only one type of EEG abnormality, was associated with more clinical neurological symptoms, especially a mental status change. The EEG groups were divided into four types of findings of slow and sharp waves, appearing in at least a first and/or second record. The results from these four EEG groups allow for a prediction of the findings to be found in a second record, based on the results of the first EEG. In general, there was a relationship between more slow waves, more sharp waves and more seizures. Also minimal slowing and rare discharges on the first record tended to disappear in the next EEG.</p>","PeriodicalId":75713,"journal":{"name":"Clinical EEG (electroencephalography)","volume":"33 4","pages":"165-70"},"PeriodicalIF":0.0,"publicationDate":"2002-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/155005940203300406","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22128112","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2002-10-01DOI: 10.1177/155005940203300408
M Gansaeuer, T M Alsaadi
Carbamazepine has been reported to exacerbate seizures in children with primary generalized epilepsy and epilepsy with mixed seizure types. Seizure exacerbation has been rarely observed in adults, mainly in the mentally retarded or in those with primary generalized epilepsy. We present an adult patient who had frequent absence seizures and simple partial seizures for 20 years. She was treated with carbamazepine for over 16 years. The patient's EEG showed generalized spike and wave complexes. Her seizures remitted and the EEG normalized after the discontinuation of carbamazepine therapy.
{"title":"Carbamazepine-induced seizures: a case report and review of the literature.","authors":"M Gansaeuer, T M Alsaadi","doi":"10.1177/155005940203300408","DOIUrl":"https://doi.org/10.1177/155005940203300408","url":null,"abstract":"<p><p>Carbamazepine has been reported to exacerbate seizures in children with primary generalized epilepsy and epilepsy with mixed seizure types. Seizure exacerbation has been rarely observed in adults, mainly in the mentally retarded or in those with primary generalized epilepsy. We present an adult patient who had frequent absence seizures and simple partial seizures for 20 years. She was treated with carbamazepine for over 16 years. The patient's EEG showed generalized spike and wave complexes. Her seizures remitted and the EEG normalized after the discontinuation of carbamazepine therapy.</p>","PeriodicalId":75713,"journal":{"name":"Clinical EEG (electroencephalography)","volume":"33 4","pages":"174-7"},"PeriodicalIF":0.0,"publicationDate":"2002-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/155005940203300408","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22128114","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2002-10-01DOI: 10.1177/155005940203300407
Murat Fani Bozkurt, Serap Saygi, Belkis Erbas
The pathophysiological relation between periodic lateralized epileptiform discharges (PLEDs) and epileptic seizures is not known and the exact causative mechanism of PLEDs still remains unclear. In this report, the authors present a case in which the EEG displayed PLEDs after a complex partial seizure. This patient, with a long history of complex partial seizures, had previously undergone right standard anterior temporal lobectomy with hippocampectomy, with a diagnosis of mesial temporal sclerosis. She had one complex partial seizure 72 days after operation and was admitted to hospital. Her brain MRI revealed changes due to temporal lobectomy and small residual posterior hippocampic anomalies. PLEDs over the right temporal lobe were seen in postictal EEGs and persisted for 4 days despite the patient's normal mental status and normal neurologic examination. Brain perfusion scintigraphy with Tc-99m-HMPAO during PLEDs was performed on the second day after the seizure, and right temporal hyperperfusion was detected. EEGs and scintigraphic imaging were repeated after cessation of PLEDs. The repeated brain scan displayed right temporal hypoperfusion. PLEDs during the postictal period may actually be an ictal pattern, and if hyperperfusion in the brain SPECT studies during PLEDs is seen, further aggressive antiepileptic drug therapy may be necessary in some cases.
{"title":"SPECT in a patient with postictal PLEDs: is hyperperfusion evidence of electrical seizure?","authors":"Murat Fani Bozkurt, Serap Saygi, Belkis Erbas","doi":"10.1177/155005940203300407","DOIUrl":"https://doi.org/10.1177/155005940203300407","url":null,"abstract":"<p><p>The pathophysiological relation between periodic lateralized epileptiform discharges (PLEDs) and epileptic seizures is not known and the exact causative mechanism of PLEDs still remains unclear. In this report, the authors present a case in which the EEG displayed PLEDs after a complex partial seizure. This patient, with a long history of complex partial seizures, had previously undergone right standard anterior temporal lobectomy with hippocampectomy, with a diagnosis of mesial temporal sclerosis. She had one complex partial seizure 72 days after operation and was admitted to hospital. Her brain MRI revealed changes due to temporal lobectomy and small residual posterior hippocampic anomalies. PLEDs over the right temporal lobe were seen in postictal EEGs and persisted for 4 days despite the patient's normal mental status and normal neurologic examination. Brain perfusion scintigraphy with Tc-99m-HMPAO during PLEDs was performed on the second day after the seizure, and right temporal hyperperfusion was detected. EEGs and scintigraphic imaging were repeated after cessation of PLEDs. The repeated brain scan displayed right temporal hypoperfusion. PLEDs during the postictal period may actually be an ictal pattern, and if hyperperfusion in the brain SPECT studies during PLEDs is seen, further aggressive antiepileptic drug therapy may be necessary in some cases.</p>","PeriodicalId":75713,"journal":{"name":"Clinical EEG (electroencephalography)","volume":"33 4","pages":"171-3"},"PeriodicalIF":0.0,"publicationDate":"2002-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/155005940203300407","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22128113","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2002-10-01DOI: 10.1177/155005940203300404
S Mazza, A Pavone, E Niedermeyer
The study of the early history of electroencephalography can yield fascinating insights and surprises. A revisit to the work of Mario Gozzano (1898-1986) has proved to be particularly stimulating. His EEG study of 1935 is a classic and should be resurrected from the graveyard of history. Gozzano was an eminent clinical neurologist-epileptologist and chairman of the neurological-psychiatric university departments in Cagliari, Pisa, Bologna and, from 1951 to his retirement, in Rome. He quickly recognized the significance of EEG and produced his major experimental EEG work in the wake of a stay at the Berlin-Buch Brain Institute. His prolonged corticograms of various regions in the rabbit demonstrated striking differences between various cortical areas. Topical cortical strychnine produced spikes (a barely known phenomenon at that time) and the evolution from interictal to ictal spiking. Spikes induced by visual stimuli may be regarded as precursors of evoked potentials. While Hans Berger was a holist ("the brain working as a whole"), Gozzano (influenced by Vogt and Kornmueller) provided EEG support for the localizationists.
{"title":"Mario Gozzano: the work of an EEG pioneer.","authors":"S Mazza, A Pavone, E Niedermeyer","doi":"10.1177/155005940203300404","DOIUrl":"https://doi.org/10.1177/155005940203300404","url":null,"abstract":"<p><p>The study of the early history of electroencephalography can yield fascinating insights and surprises. A revisit to the work of Mario Gozzano (1898-1986) has proved to be particularly stimulating. His EEG study of 1935 is a classic and should be resurrected from the graveyard of history. Gozzano was an eminent clinical neurologist-epileptologist and chairman of the neurological-psychiatric university departments in Cagliari, Pisa, Bologna and, from 1951 to his retirement, in Rome. He quickly recognized the significance of EEG and produced his major experimental EEG work in the wake of a stay at the Berlin-Buch Brain Institute. His prolonged corticograms of various regions in the rabbit demonstrated striking differences between various cortical areas. Topical cortical strychnine produced spikes (a barely known phenomenon at that time) and the evolution from interictal to ictal spiking. Spikes induced by visual stimuli may be regarded as precursors of evoked potentials. While Hans Berger was a holist (\"the brain working as a whole\"), Gozzano (influenced by Vogt and Kornmueller) provided EEG support for the localizationists.</p>","PeriodicalId":75713,"journal":{"name":"Clinical EEG (electroencephalography)","volume":"33 4","pages":"155-9"},"PeriodicalIF":0.0,"publicationDate":"2002-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/155005940203300404","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"22127065","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}