Characteristics of temporal lobe epilepsy with mesial temporal sclerosis, with special reference to psychotic episodes.

Abstract:

:This study investigates the histories and the clinical course of 111 patients who had nonlesional temporal lobe epilepsy. We compared 61 patients with unilateral hippocampal sclerosis (UHS group) and 50 patients with minimal change (MRI negative group) assessed on the basis of MRI. In agreement with previous reports, we confirmed statistically that patients in the UHS group strongly tended to have had febrile convulsive status during early childhood or infancy and that habitual seizures tended to begin at a younger age than the other subset of nonlesional temporal lobe epilepsy. Strikingly, episodes of psychoses, especially postictal psychoses, occurred significantly more often in the UHS group than in the MRI negative group. Additional involvement of temporal neocortex further augmented this association. We stress the role of mesial temporal pathology, and its linkage to the temporal neocortex, in the genesis of postictal psychoses.

journal_name

Neurology

journal_title

Neurology

authors

Kanemoto K,Takeuchi J,Kawasaki J,Kawai I

doi

10.1212/wnl.47.5.1199

subject

Has Abstract

pub_date

1996-11-01 00:00:00

pages

1199-203

issue

5

eissn

0028-3878

issn

1526-632X

journal_volume

47

pub_type

杂志文章
  • Lack of apoptosis in mitochondrial encephalomyopathies.

    abstract:BACKGROUND/OBJECTIVE:Apoptosis, or programmed cell death, is an evolutionary conserved mechanism essential for morphogenesis and tissue homeostasis, but it plays an important role also in pathologic conditions, including neurologic disorders. Its execution pathway is critically regulated at the mitochondrial level. Evi...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.56.8.1070

    authors: Sciacco M,Fagiolari G,Lamperti C,Messina S,Bazzi P,Napoli L,Chiveri L,Prelle A,Comi GP,Bresolin N,Scarlato G,Moggio M

    更新日期:2001-04-24 00:00:00

  • Prognosis of photoparoxysmal response in nonepileptic patients.

    abstract::Photoparoxysmal response (PPR) is sometimes incidentally encountered in EEGs performed for evaluation of nonepileptic symptoms. We conducted the first long-term study of a cohort of nonepileptic patients to determine their risk of having seizures subsequent to incidental recording of PPR. After 6 to 12 years (mean, 9 ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.43.9.1719

    authors: So EL,Ruggles KH,Ahmann PA,Olson KA

    更新日期:1993-09-01 00:00:00

  • Estimating cerebral microinfarct burden from autopsy samples.

    abstract:OBJECTIVE:To estimate whole-brain microinfarct burden from microinfarct counts in routine postmortem examination. METHODS:We developed a simple mathematical method to estimate the total number of cerebral microinfarcts from counts obtained in the small amount of tissue routinely examined in brain autopsies. We derived...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e31828c2f52

    authors: Westover MB,Bianchi MT,Yang C,Schneider JA,Greenberg SM

    更新日期:2013-04-09 00:00:00

  • A multi-institutional study of brainstem gliomas in children with neurofibromatosis type 1.

    abstract:OBJECTIVE:To define the clinical and radiologic features of brainstem gliomas (BSGs) in children with neurofibromatosis type 1 (NF1). METHODS:We performed a retrospective cross-sectional study of 133 children with NF1 and concurrent BSGs cared for at 4 NF1 referral centers. BSG was determined using radiographic criter...

    journal_title:Neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1212/WNL.0000000000003881

    authors: Mahdi J,Shah AC,Sato A,Morris SM,McKinstry RC,Listernick R,Packer RJ,Fisher MJ,Gutmann DH

    更新日期:2017-04-18 00:00:00

  • How early can we diagnose Alzheimer disease (and is it sufficient)? The 2017 Wartenberg lecture.

    abstract::A seismic shift in our understanding of the ability to diagnose Alzheimer disease (AD) is occurring. For the last several decades, AD has been a clinical-pathologic diagnosis, and this conceptualization of the disease has served the field well. Typically, the clinician would identify a syndrome such as mild cognitive ...

    journal_title:Neurology

    pub_type: 历史文章,杂志文章

    doi:10.1212/WNL.0000000000006088

    authors: Petersen RC

    更新日期:2018-08-28 00:00:00

  • Recent advances in the treatment of orthostatic hypotension.

    abstract::Orthostatic hypotension is a fall in blood pressure on standing that causes symptoms of dizziness, visual changes, and discomfort in the head and neck. The goal of treatment is the improvement of the patient's functional capacity, rather than a target blood pressure. For treatment to be successful, it must be individu...

    journal_title:Neurology

    pub_type: 杂志文章,评审

    doi:

    authors: Robertson D,Davis TL

    更新日期:1995-04-01 00:00:00

  • Diagnosis of Creutzfeldt-Jakob disease: effect of clinical criteria on incidence estimates.

    abstract:OBJECTIVE:To assess the effect of usage of three different versions of Creutzfeldt-Jakob disease (CJD) diagnostic criteria on estimates of CJD incidence. METHODS:A total of 428 patients referred for suspected sporadic CJD between 1991 and 1997 were classified according to different criteria to be compared after analys...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.54.5.1095

    authors: Brandel JP,Delasnerie-Lauprêtre N,Laplanche JL,Hauw JJ,Alpérovitch A

    更新日期:2000-03-14 00:00:00

  • Cutaneous innervation in sensory neuropathies: evaluation by skin biopsy.

    abstract:OBJECTIVE:To use punch skin biopsies to evaluate the loss of intra-epidermal nerve fibers in sensory neuropathies. BACKGROUND:Previous assessments of epidermal nerve fibers have been constrained by relatively insensitive staining techniques and variability in quantification. METHODS:Punch skin biopsies were performed...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.45.10.1848

    authors: McCarthy BG,Hsieh ST,Stocks A,Hauer P,Macko C,Cornblath DR,Griffin JW,McArthur JC

    更新日期:1995-10-01 00:00:00

  • Factors influencing osmotic fragility of red blood cells in Duchenne muscular dystrophy.

    abstract::Factors affecting osmotic fragility were studied in red blood cells of patients with Duchenne muscular dystrophy. The mean osmotic fragility (MOF), operationally defined as the NaCl concentration for 50% hemolysis, was found to be higher by 3.63 +/- 0.51 mM in Duchenne cells than in normal cells having an MOF of 60.1 ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.30.7.726

    authors: Kim HD,Luthra MG,Watts RP,Stern LZ

    更新日期:1980-07-01 00:00:00

  • CNS vasculitis in a patient with MS on daclizumab monotherapy.

    abstract:OBJECTIVE:To report the development of CNS vasculitis in a patient with multiple sclerosis (MS) treated with daclizumab. METHODS:This report includes clinical, MRI, immunologic, and pathology data and CSF analysis. RESULTS:After completing a phase II daclizumab monotherapy study with an optimal response as evidenced ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e31827f0f42

    authors: Ohayon J,Oh U,Richert N,Martin J,Vortmeyer A,McFarland H,Bielekova B

    更新日期:2013-01-29 00:00:00

  • Cognitive profiles differ in autopsy-confirmed frontotemporal dementia and AD.

    abstract:BACKGROUND:Frontotemporal dementia (FTD) is currently distinguished from AD primarily on the basis of behavioral features because studies of cognition have shown negligible or inconsistent differences. However, the poor discriminability of cognitive measures may relate to reliance on imprecise clinically diagnosed grou...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.58.12.1801

    authors: Rascovsky K,Salmon DP,Ho GJ,Galasko D,Peavy GM,Hansen LA,Thal LJ

    更新日期:2002-06-25 00:00:00

  • Incidence of stroke in relation to cognitive function and dementia in the Kungsholmen Project.

    abstract:OBJECTIVE:To investigate whether cognitive function is related to incidence of stroke. METHODS:A population-based cohort of 1551 subjects with no clinical history or signs of stroke, age 75 years and over at baseline, were followed up for 3 years. Individuals with a first-ever stroke event that was recorded in the Sto...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.54.11.2103

    authors: Zhu L,Fratiglioni L,Guo Z,Winblad B,Viitanen M

    更新日期:2000-06-13 00:00:00

  • Is late-onset multiple sclerosis associated with a worse outcome?

    abstract:OBJECTIVE:To describe the characteristics of late-onset multiple sclerosis (MS) (LOMS, 50+ years) vs adult-onset MS (AOMS, 16 to <50 years) and examine prognosis and associated risk factors. METHODS:Patients with definite MS, onset prior to July 1988, registered with a BCMS clinic before July 1998, with at least one E...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000237475.01655.9d

    authors: Tremlett H,Devonshire V

    更新日期:2006-09-26 00:00:00

  • Cognitive compensation failure in multiple sclerosis.

    abstract:OBJECTIVES:Compensatory processes involving the recruitment of additional cerebral areas can limit cognitive impairment caused by brain damage as revealed by fMRI. Multiple sclerosis (MS) is characterized by frequent cognitive deficiencies and diffuse brain damage. Understanding the missing or disturbed processes resul...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e3181f612e3

    authors: Bonnet MC,Allard M,Dilharreguy B,Deloire M,Petry KG,Brochet B

    更新日期:2010-10-05 00:00:00

  • Current state of educational compensation in academic neurology: Results of a US national survey.

    abstract::In the current medical climate, medical education is at risk of being de-emphasized, leading to less financial support and compensation for faculty. A rise in compensation plans that reward clinical or research productivity fails to incentivize and threatens to erode the educational missions of our academic institutio...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000007664

    authors: Weber D,Sarva H,Weaver J,Wang F,Chou J,Cornes S,Nickels K,Safdieh JE,Poncelet A,Stern BJ

    更新日期:2019-07-02 00:00:00

  • Retinal thinning associates with nigral dopaminergic loss in de novo Parkinson disease.

    abstract:OBJECTIVE:To analyze the relationship between retinal thinning and nigral dopaminergic loss in de novo Parkinson disease (PD). METHODS:Forty-nine patients with PD and 54 age-matched controls were analyzed. Ophthalmologic examination and macula optical coherence tomography scans were performed with additional microperi...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000006157

    authors: Ahn J,Lee JY,Kim TW,Yoon EJ,Oh S,Kim YK,Kim JM,Woo SJ,Kim KW,Jeon B

    更新日期:2018-09-11 00:00:00

  • Declining incidence of multiple sclerosis in the Orkney Islands.

    abstract::The incidence of MS in the Orkney Islands has been updated from 1941 to September 21, 1983. Since 1965, MS incidence rates have fallen significantly when compared with those for 1941 to 1964. Alterations in age-specific prevalence, mean duration of illness, and mean age of the MS population are consistent with the dec...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.35.4.545

    authors: Cook SD,Cromarty JI,Tapp W,Poskanzer D,Walker JD,Dowling PC

    更新日期:1985-04-01 00:00:00

  • Child neurology: diagnosis of Lambert-Eaton myasthenic syndrome in children.

    abstract:OBJECTIVE:To report a case of Lambert-Eaton myasthenic syndrome (LEMS) in a child and review the existing literature of LEMS in children. METHODS:We report a pediatric case of LEMS with the classic clinical triad of proximal weakness, autonomic dysfunction, and areflexia; the characteristic increment in compound motor...

    journal_title:Neurology

    pub_type: 杂志文章,评审

    doi:10.1212/WNL.0b013e318293e14e

    authors: Morgan-Followell B,de Los Reyes E

    更新日期:2013-05-21 00:00:00

  • Characteristic features and progression of abnormalities on MRI for CARASIL.

    abstract:OBJECTIVES:The objective of this study was to clarify the characteristic brain MRI findings for genetically diagnosed CARASIL (cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy). METHODS:Seven patients with CARASIL carrying HTRA1 mutations (representing 6 Japanese families) we...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000001803

    authors: Nozaki H,Sekine Y,Fukutake T,Nishimoto Y,Shimoe Y,Shirata A,Yanagawa S,Hirayama M,Tamura M,Nishizawa M,Onodera O

    更新日期:2015-08-04 00:00:00

  • Sex difference in prevalence of depression after stroke.

    abstract:OBJECTIVE:This study investigated the sex difference in prevalence of depression at 90 days after first-ever stroke. METHODS:Patients with first-ever stroke (n = 786) were identified from the population-based Brain Attack Surveillance in Corpus Christi project (2011-2016). Poststroke depressive symptoms were assessed ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000009394

    authors: Dong L,Sánchez BN,Skolarus LE,Stulberg E,Morgenstern LB,Lisabeth LD

    更新日期:2020-05-12 00:00:00

  • Assessment of the interaction of age and sex on 90-day outcome after intracerebral hemorrhage.

    abstract:OBJECTIVE:Because age affects hormonal production differently in women compared with men, we sought to define sex and age interactions across a multiracial/ethnic population after intracerebral hemorrhage (ICH) to uncover evidence that loss of gonadal hormone production would result in loss of the known neuroprotective...

    journal_title:Neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1212/WNL.0000000000004255

    authors: James ML,Langefeld CD,Sekar P,Moomaw CJ,Elkind MSV,Worrall BB,Sheth KN,Martini SR,Osborne J,Woo D,ERICH Investigators.

    更新日期:2017-09-05 00:00:00

  • Phase II screening trial of lithium carbonate in amyotrophic lateral sclerosis: examining a more efficient trial design.

    abstract:OBJECTIVE:To use a historical placebo control design to determine whether lithium carbonate slows progression of amyotrophic lateral sclerosis (ALS). METHODS:A phase II trial was conducted at 10 sites in the Western ALS Study Group using similar dosages (300-450 mg/day), target blood levels (0.3-0.8 mEq/L), outcome me...

    journal_title:Neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1212/WNL.0b013e31822dc7a5

    authors: Miller RG,Moore DH,Forshew DA,Katz JS,Barohn RJ,Valan M,Bromberg MB,Goslin KL,Graves MC,McCluskey LF,McVey AL,Mozaffar T,Florence JM,Pestronk A,Ross M,Simpson EP,Appel SH,WALS Study Group.

    更新日期:2011-09-06 00:00:00

  • Ten steps in characterizing and diagnosing patients with peripheral neuropathy.

    abstract::Cost-effective approaches for arriving at correct diagnoses should be used. Herein, we compare three approaches for the differential diagnosis of a common neurologic syndrome, peripheral neuropathy. In the "shotgun" approach, a standard battery of hematologic, biochemical, serologic, antibody, enzyme, molecular geneti...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.47.1.10

    authors: Dyck PJ,Dyck PJ,Grant IA,Fealey RD

    更新日期:1996-07-01 00:00:00

  • Predictive factors of in-hospital CNS complications following liver transplantation.

    abstract::We prospectively evaluated 84 consecutive adult patients with chronic liver disease before and after liver transplantation to define the type and frequency of post-transplant neurologic complications, and to assess possible pretransplant and operative variables associated with in-hospital CNS complications. There were...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.44.7.1226

    authors: Pujol A,Graus F,Rimola A,Beltrán J,Garcia-Valdecasas JC,Navasa M,Grande L,Galofré J,Visa J,Rodés J

    更新日期:1994-07-01 00:00:00

  • Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.

    abstract:BACKGROUND:Frontotemporal dementia associated with motor neuron disease (FTD-MND) is a rare neurodegenerative disorder that may be inherited by autosomal dominant trait. No major gene has been identified but a locus was mapped on chromosome 9 (9p21.3-p13.3). METHODS:Ten French families with FTD-MND were tested for lin...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e3181a55f1c

    authors: Le Ber I,Camuzat A,Berger E,Hannequin D,Laquerrière A,Golfier V,Seilhean D,Viennet G,Couratier P,Verpillat P,Heath S,Camu W,Martinaud O,Lacomblez L,Vercelletto M,Salachas F,Sellal F,Didic M,Thomas-Anterion C,Puel M

    更新日期:2009-05-12 00:00:00

  • Assessment of hand function in a patient with chronic sensory demyelinating neuropathy.

    abstract::A 60-year-old man presented with progressive large fiber sensory loss in the right first three fingers and, to a lesser extent, in both fourth and fifth fingers. Electrophysiologic studies were characteristic of chronic sensory demyelinating polyneuropathy, a variant of chronic inflammatory demyelinating polyneuropath...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.49.1.253

    authors: Thonnard JL,Detrembleur C,Van den Bergh PY

    更新日期:1997-07-01 00:00:00

  • Upholding professionalism: the disciplinary process of the American Academy of Neurology.

    abstract:OBJECTIVE:To review the disciplinary process by which the American Academy of Neurology (AAN) enforces its formalized standards of professional conduct. METHODS:We reviewed the AAN's Disciplinary Action Policy. We tracked the elapsed time from receipt to final decision of all allegations ("complaints") of improper con...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e318202014e

    authors: Hutchins JC,Sagsveen MG,Larriviere D

    更新日期:2010-12-14 00:00:00

  • Neutralizing antibodies against HTLV-I in HTLV-I-associated myelopathy/tropical spastic paraparesis (HAM/TSP) patients and asymptomatic carriers.

    abstract::We tested serum specimens from patients with HAM/TSP and asymptomatic HTLV-I carriers from endemic areas of Japan, Jamaica, Colombia, and Chile for neutralizing antibodies against HTLV-I. The data suggest a trend for neutralizing activity to be found more frequently in the sera from HAM/TSP patients than in sera from ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.42.11.2210

    authors: Minagawa H,Yoshida T,Itoyama Y,Mora CA,Albert P,Mori R

    更新日期:1992-11-01 00:00:00

  • Linking MRI to daily life experience: the example of poststroke depression.

    abstract:OBJECTIVE:The state-of-the-art tools of neurology, in particular modern neuroimaging techniques, have yet to benefit from the revolution in mobile technologies that provide new insights into the mechanisms underlying clinical syndromes. This study demonstrates the manner in which mobile technologies may provide informa...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e31824528b2

    authors: Lassalle-Lagadec S,Allard M,Dilharreguy B,Schweitzer P,Swendsen J,Sibon I

    更新日期:2012-01-31 00:00:00

  • Serial study of gadolinium-DTPA MRI enhancement in multiple sclerosis.

    abstract::We performed serial baseline and gadolinium (Gd)-DTPA-enhanced MRI in 4 patients with definite multiple sclerosis. Studies were performed every month for a total of 4 scans. We obtained short TR/short TE sequences at 10 and 60 minutes after Gd-DTPA injection. All patients had multiple hyperintense lesions seen on base...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.40.4.591

    authors: Bastianello S,Pozzilli C,Bernardi S,Bozzao L,Fantozzi LM,Buttinelli C,Fieschi C

    更新日期:1990-04-01 00:00:00