当前位置： SCI文献检索 > JOURNAL OF NEUROLOGY期刊下所有文献 > Relationship between cortex and pulvinar abnormalities on diffusion-weighted imaging in status epilepticus.

Relationship between cortex and pulvinar abnormalities on diffusion-weighted imaging in status epilepticus.

Abstract：

:The aim of this study was to analyze the pattern of magnetic resonance diffusion-weighted imaging (DWI) findings in status epilepticus in terms of clinical characteristics. Participants comprised 106 patients with status epilepticus who were admitted to our hospital and underwent DWI. Forty-five patients (42.5 %) showed abnormal findings on DWI and were divided into two groups, comprising 26 patients (24.5 %) with cortex lesions alone and 19 patients (17.9 %) with cortex and pulvinar lesions in the same hemisphere. A long duration of status epilepticus (>120 min) tended to be more prevalent among patients with cortex and pulvinar lesions (57.9 %) than among patients with cortex lesions alone (30.8 %) by univariate and multivariate analyses. Todd's palsy tended to be more frequent in patients with abnormalities on DWI (24/45, 53.3 %) than in patients with normal DWI (21/61, 34.4 %). Six of the 26 patients with cortex lesions alone (23.1 %) had taken anti-epileptic drugs before the attack compared to none of the 19 patients with both cortex and pulvinar lesions. The trend toward a longer duration of status epilepticus in patients with both cortex and pulvinar lesions favors a spreading pattern of seizure discharge from cortex to pulvinar via cortico-pulvinar pathways, and anti-epileptic drugs might, to some extent, prevent spreading of seizure discharge from cortex to pulvinar. In addition, existence of high-intensity areas on DWI at the onset of epilepsy may be a predictive factor for the occurrence of Todd's palsy.

journal_name

J Neurol

journal_title

Journal of neurology

authors

Nakae Y,Kudo Y,Yamamoto R,Dobashi Y,Kawabata Y,Ikeda S,Yokoyama M,Higashiyama Y,Doi H,Johkura K,Tanaka F

doi

10.1007/s00415-015-7948-4

subject

Has Abstract

pub_date

2016-01-01 00:00:00

pages

127-32

issue

1

eissn

0340-5354

issn

1432-1459

pii

10.1007/s00415-015-7948-4

journal_volume

263

pub_type

杂志文章

相关文献

JOURNAL OF NEUROLOGY文献大全
  • Congenital isolated hemifacial hyperplasia.

    abstract：:We report on a 14-year-old boy with congenital isolated hemifacial hyperplasia. Hemifacial hypertrophy most likely represents a minor form of congenital hemihypertrophy. MRI of the soft tissue is particularly suitable to support the diagnosis and reveal associated bony asymmetries. ...

    journal_title：Journal of neurology

    pub_type： 信件

    doi：10.1007/s00415-009-5148-9

    authors： Urban PP,Bruening R

    更新日期：2009-09-01 00:00:00

  • Retrospectively acquired cohort study to evaluate the long-term impact of two different treatment strategies on disability outcomes in patients with relapsing multiple sclerosis (RE.LO.DI.MS): data from the Italian MS Register.

    abstract：BACKGROUND:The increase in disease-modifying drugs (DMDs) allows individualization of treatment in relapsing multiple sclerosis (RMS); however, the long-term impact of different treatment sequences is not well established. This is particularly relevant for MS patients who may need to postpone more aggressive DMD strate...

    journal_title：Journal of neurology

    pub_type： 杂志文章,多中心研究

    doi：10.1007/s00415-019-09531-6

    authors： Paolicelli D,Lucisano G,Manni A,Avolio C,Bonavita S,Brescia Morra V,Capobianco M,Cocco E,Conte A,De Luca G,De Robertis F,Gasperini C,Gatto M,Gazzola P,Lus G,Iaffaldano A,Iaffaldano P,Maimone D,Mallucci G,Maniscalco

    更新日期：2019-12-01 00:00:00

  • Stroke in younger patients: the heart of the matter.

    abstract：:Stroke in young adults is not a rare entity, and often provides difficult management decisions for neurologists. The knowledge gained from stroke in older adults does not transfer easily to this younger group given the different causes of stroke observed. Cardiac causes of stroke are common in this group, but often co...

    journal_title：Journal of neurology

    pub_type： 杂志文章,评审

    doi：10.1007/s00415-010-5647-8

    authors： Cotter PE,Belham M,Martin PJ

    更新日期：2010-11-01 00:00:00

  • The role of mutations in COL6A3 in isolated dystonia.

    abstract：:Specific mutations in COL6A3 have recently been reported as the cause of isolated recessive dystonia, which is a rare movement disorder. In all patients, at least one mutation was located in Exons 41 and 42. In an attempt to replicate these findings, we assessed by direct sequencing the frequency of rare variants in E...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-016-8046-y

    authors： Lohmann K,Schlicht F,Svetel M,Hinrichs F,Zittel S,Graf J,Lohnau T,Schmidt A,Mir P,Krause P,Lang AE,Jabusch HC,Wolters A,Kamm C,Zeuner KE,Altenmüller E,Naz S,Chung SJ,Kostic VS,Münchau A,Kühn AA,Brüggemann N,Kl

    更新日期：2016-04-01 00:00:00

  • The dynamics of multiple sclerosis. The Charcot Lecture.

    abstract：:The history of our understanding of the pathogenesis and pathophysiology of multiple sclerosis are reviewed in the context of Charcot's contribution. The implications for treatment of the new knowledge gained from studies during life of pathology and pathogenesis (by MRI) and pathophysiology (by evoked potentials) are...

    journal_title：Journal of neurology

    pub_type： 传,历史文章,杂志文章

    doi：10.1007/BF00838443

    authors： McDonald WI

    更新日期：1993-01-01 00:00:00

  • Second opinions and tertiary referrals in neurology: a prospective observational study.

    abstract：BACKGROUND AND OBJECTIVE:The number of neurological second opinions (SO) and tertiary referrals (TR) is increasing. The main purpose of this study was to assess whether a day-care admission made a meaningful contribution to standard neurological outpatient care, for a wide range of second opinions and tertiary referral...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-008-0019-3

    authors： Wieske L,Wijers D,Richard E,Vergouwen MD,Stam J

    更新日期：2008-11-01 00:00:00

  • The frequency of spinocerebellar ataxia type 23 in a UK population.

    abstract：:Spinocerebellar ataxias (SCA) are a genetically heterogeneous group of neurodegenerative diseases characterised by progressive cerebellar ataxia, dysarthria and oculomotor abnormalities. Recently the prodynorphin (PDYN) gene was identified as the cause of SCA23 in four Dutch families displaying progressive gait and li...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-012-6721-1

    authors： Fawcett K,Mehrabian M,Liu YT,Hamed S,Elahi E,Revesz T,Koutsis G,Herscheson J,Schottlaender L,Wardle M,Morrison PJ,Morris HR,Giunti P,Wood N,Houlden H

    更新日期：2013-03-01 00:00:00

  • Rapid distinction of acute demyelinating disorders and central nervous system lymphoma by molecular analysis of cerebrospinal fluid cells.

    abstract：:Polymerase chain reaction (PCR) based automated high-resolution fragment analysis of rearranged immunoglobulin heavy-chain genes is a highly sensitive means for identifying clonal B-cell responses. We used this technique to distinguish polyclonal inflammatory from monoclonal neoplastic B-cell populations in the cerebr...

    journal_title：Journal of neurology

    pub_type： 临床试验,杂志文章

    doi：10.1007/s004150170247

    authors： Wildemann B,Jansen O,Haas J,Vogt-Schaden ME,Storch-Hagenlocher B

    更新日期：2001-02-01 00:00:00

  • The role of global and regional gray matter volume decrease in multiple sclerosis.

    abstract：:Disability in multiple sclerosis (MS) patients is associated with white matter (WM) and gray matter (GM) pathology, and both processes contribute differently over the disease course. Total and regional GM volume loss can be imaged via voxel-based morphometry (VBM). Here, we retrospectively analyzed a group of 213 MS p...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-016-8114-3

    authors： Grothe M,Lotze M,Langner S,Dressel A

    更新日期：2016-06-01 00:00:00

  • Classic ataxia-telangiectasia: the phenotype of long-term survivors.

    abstract：OBJECTIVE:Patients with classic ataxia-telangiectasia (A-T) generally die in the second or third decade of life. Clinical descriptions of A-T tend to focus on the symptoms at presentation. However, during the course of the disease, other symptoms and complications emerge. As long-term survivors with classic A-T develop...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-019-09641-1

    authors： van Os NJH,van Deuren M,Weemaes CMR,van Gaalen J,Hijdra H,Taylor AMR,van de Warrenburg BPC,Willemsen MAAP

    更新日期：2020-03-01 00:00:00

  • Fahr's syndrome: local inflammatory factors in the pathogenesis of calcification.

    abstract：:Three cases of Fahr's syndrome are described. All patients had disturbances of calcium metabolism and had had a meningoencephalitis in childhood. It is suggested that gliovascular changes, induced by cerebral inflammation, can later facilitate the occurrence of calcification of the striopallidodentate system when abno...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/BF00313985

    authors： Morgante L,Vita G,Meduri M,Di Rosa AE,Galatioto S,Coraci MA,Di Perri R

    更新日期：1986-02-01 00:00:00

  • Abolished phosphaturic response to parathormone in adult patients with Fahr disease and its restoration after propranolol administration.

    abstract：:The similar localization of intracranial calcification in hypoparathyroidism and in Fahr disease without parathyroid gland disorder suggests that in these two disorders the pathomechanism of calcium phosphate deposition in the brain may be similar. It may be that in Fahr disease some factors, such as chronic respirato...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/BF00314315

    authors： Pronicka E,Kulczycki J,Rowińska E,Kuran W

    更新日期：1988-01-01 00:00:00

  • Leukoencephalopathy with brainstem and spinal cord involvement caused by a novel mutation in the DARS2 gene.

    abstract：:Leukoencephalopathy with brainstem and spinal cord involvement and elevated lactate (LBSL) is a rare, autosomal recessive disorder caused by mutations in the gene encoding a mitochondrial aspartyl-tRNA synthetase, DARS2. The disease is characterized by progressive spastic ataxia and magnetic resonance imaging (MRI) sh...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-011-6176-9

    authors： Tzoulis C,Tran GT,Gjerde IO,Aasly J,Neckelmann G,Rydland J,Varga V,Wadel-Andersen P,Bindoff LA

    更新日期：2012-02-01 00:00:00

  • Amyloid-P-component-like immunoreactivity in beta/A4-immunoreactive deposits in Alzheimer-type dementia brains.

    abstract：:An immunohistochemical study using the mirror-image technique was performed in order to establish whether amyloid P component is involved in the mechanism of deposition of amyloid fibrils in senile plaques (SPs) in Alzheimer-type dementia (ATD). Ninety percent of beta/A4 protein-immunoreactive SPs were also stained by...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/BF00868345

    authors： Kimura M,Arai H,Takahashi T,Iwamoto N

    更新日期：1994-01-01 00:00:00

  • Predicting fatigue 1 year after aneurysmal subarachnoid hemorrhage.

    abstract：:Fatigue is an important contributor to quality of life in patients who survive aneurysmal subarachnoid hemorrhage (SAH), but the determinants of this fatigue are unclear. We assessed the occurrence of fatigue 1 year after SAH and its relation to physical or cognitive impairment, passive coping, and emotional problems,...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-010-5891-y

    authors： Passier PE,Post MW,van Zandvoort MJ,Rinkel GJ,Lindeman E,Visser-Meily JM

    更新日期：2011-06-01 00:00:00

  • C19orf12 mutations in neurodegeneration with brain iron accumulation mimicking juvenile amyotrophic lateral sclerosis.

    abstract：:Mutations in C19orf12 have been recently identified as the molecular genetic cause of a subtype of neurodegeneration with brain iron accumulation (NBIA). Given the mitochondrial localization of the gene product the new NBIA subtype was designated mitochondrial membrane protein-associated neurodegeneration. Frequent fe...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-012-6521-7

    authors： Deschauer M,Gaul C,Behrmann C,Prokisch H,Zierz S,Haack TB

    更新日期：2012-11-01 00:00:00

  • Cardiovascular autonomic dysfunction in multiple sclerosis: correlation with orthostatic intolerance.

    abstract：:Autonomic dysfunction is frequently observed in patients with multiple sclerosis (MS), but clinical studies disagree on the frequency and type of abnormalities in autonomic function tests. Orthostatic dizziness (OD) has been reported in up to 49% of patients, but the pathophysiological mechanisms are poorly understood...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s004150050407

    authors： Flachenecker P,Wolf A,Krauser M,Hartung HP,Reiners K

    更新日期：1999-07-01 00:00:00

  • Combining short interval MRI in Alzheimer's disease: Implications for therapeutic trials.

    abstract：:Cerebral atrophy calculated from serial MRI is a marker of Alzheimer's disease (AD) progression, and a potential outcome measure for therapeutic trials. Reducing within-subject variability in cerebral atrophy rates by acquiring more than two serial scans could allow for shorter clinical trials requiring smaller patien...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-006-0173-4

    authors： Schott JM,Frost C,Whitwell JL,Macmanus DG,Boyes RG,Rossor MN,Fox NC

    更新日期：2006-09-01 00:00:00

  • Genetic association of sirtuin genes and Parkinson's disease.

    abstract：:Parkinson's disease (PD) is a neurodegenerative disease caused by both genetic and environmental factors. Sirtuins are highly-conserved, NAD-dependent class III deacetylases that regulate a variety of cellular functions. Most of the known sirtuins have been involved in animal models of neurodegenerative disorders, suc...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-013-6970-7

    authors： Jesús S,Gómez-Garre P,Carrillo F,Cáceres-Redondo MT,Huertas-Fernández I,Bernal-Bernal I,Bonilla-Toribio M,Vargas-González L,Carballo M,Mir P

    更新日期：2013-09-01 00:00:00

  • Suppression of immune system genes by methylprednisolone in exacerbations of multiple sclerosis. Preliminary results.

    abstract：:Acute relapses of multiple sclerosis (MS) are treated with intravenous methylprednisolone (IVMP), which speeds recovery from exacerbation. It is known that IVMP suppresses the immunological activation which occurs during an acute attack of MS. However, the specific target genes affected by this therapy remain obscure....

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-004-0516-y

    authors： Airla N,Luomala M,Elovaara I,Kettunen E,Knuutila S,Lehtimäki T

    更新日期：2004-10-01 00:00:00

  • Affinities of human NMDA receptor autoantibodies: implications for disease mechanisms and clinical diagnostics.

    abstract：:Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is a common autoimmune encephalitis presenting with psychosis, dyskinesias, autonomic dysfunction and seizures. The underlying autoantibodies against the NR1 subunit are directly pathogenic by disrupting synaptic NMDAR currents. However, antibody titers correlate...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-018-9042-1

    authors： Ly LT,Kreye J,Jurek B,Leubner J,Scheibe F,Lemcke J,Wenke NK,Reincke SM,Prüss H

    更新日期：2018-11-01 00:00:00

  • Sensory trick phenomenon in cervical dystonia: a functional MRI study.

    abstract：:Sensory trick may relieve dystonic symptoms in patients with idiopathic cervical dystonia (CD). We investigated the patterns of brain functional MRI (fMRI) during resting state, sensory trick simulation and sensory trick imagination in CD patients both with and without an effective sensory trick. We recruited 17 CD pa...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-019-09683-5

    authors： Sarasso E,Agosta F,Piramide N,Bianchi F,Butera C,Gatti R,Amadio S,Del Carro U,Filippi M

    更新日期：2020-04-01 00:00:00

  • Autoimmune cortical encephalitis in two children with anti-myelin oligodendrocyte glycoprotein (MOG) antibody.

    abstract：PURPOSE:Anti-myelin oligodendrocyte glycoprotein antibodies (anti-MOG), directed against a component of the myelin sheath, are sometimes detected in the blood or cerebrospinal fluid (CSF) of patients with acute demyelinating conditions. Cortical encephalitic presentations in anti-MOG-antibody-positive patients are reco...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-020-10260-4

    authors： Doig D,McNamara C,Mewasingh L,Beri S,Jones B,Kachramanoglou C,Jan W

    更新日期：2020-10-14 00:00:00

  • Changes in peripheral blood lymphocyte subset frequencies in myasthenia gravis patients are related to immunosuppression.

    abstract：:Surface antigens on peripheral blood lymphocytes from myasthenia gravis patients were investigated. The expression of DR+ and CD8+/DR+ T lymphocytes was increased and the expression of CD4+ T cells reduced. Neither thymectomy, clinical condition nor anti-acetylcholine receptor antibody titre correlated with any of the...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/BF00863771

    authors： Crosti F,Armanini M,Confalonieri P,Antozzi C,Mantegazza R

    更新日期：1994-02-01 00:00:00

  • Is lumbar spondylosis a cause of urinary retention in elderly women?

    abstract：OBJECTIVES:Lumbar spondylosis (LS) is a common spinal degenerative disorder which causes various types of lower urinary tract dysfunction (LUTD). However, it is not certain whether LS may cause urinary retention in elderly women. METHODS:In a period covering the past 3 years, we retrospectively reviewed: a) urodynamic...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-005-0790-3

    authors： Sakakibara R,Yamamoto T,Uchiyama T,Liu Z,Ito T,Yamazaki M,Awa Y,Yamanishi T,Hattori T

    更新日期：2005-08-01 00:00:00

  • DWI and FLAIR imaging in herpes simplex encephalitis: a comparative and topographical analysis.

    abstract：:DWI has been described in some reports to be superior to FLAIR in early stage herpes simple virus encephalitis (HSE). Few data exist on detailed topographical MRI analysis in HSE. Our aim was to study DWI and FLAIR, and analyse topographically these sequences in non-neonatal HSE patients with MRI performed within 60 d...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-015-7818-0

    authors： Renard D,Nerrant E,Lechiche C

    更新日期：2015-09-01 00:00:00

  • ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype.

    abstract：:Autosomal recessive cerebellar ataxia type 3 (ARCA3) is a rare inherited disorder caused by mutations in the ANO10 gene. The disease is characterized by slowly progressive spastic ataxia variably associated with motor neuron involvement, epilepsy, and cognitive decline. We performed mutational screening in 80 patients...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-018-9141-z

    authors： Nanetti L,Sarto E,Castaldo A,Magri S,Mongelli A,Rossi Sebastiano D,Canafoglia L,Grisoli M,Malaguti C,Rivieri F,D'Amico MC,Di Bella D,Franceschetti S,Mariotti C,Taroni F

    更新日期：2019-02-01 00:00:00

  • Benign multiple sclerosis: cognitive, psychological and social aspects in a clinical cohort.

    abstract：OBJECTIVES:A study of cognitive, psychological and social aspects in benign multiple sclerosis (MS). Methods One hundred and sixty three patients with benign MS (defined as disease duration > or = 15 years and Expanded Disability Status Scale (EDSS) score < or = 3.0 ) underwent neuropsychological testing on the Rao's B...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-006-0161-8

    authors： Amato MP,Zipoli V,Goretti B,Portaccio E,De Caro MF,Ricchiuti L,Siracusa G,Masini M,Sorbi S,Trojano M

    更新日期：2006-08-01 00:00:00

  • Progression of sleep disturbances in Parkinson's disease: a 5-year longitudinal study.

    abstract：BACKGROUND:Sleep disorders can occur in early Parkinson's disease (PD). However, the relationship between different sleep disturbances and their longitudinal evolution has not been fully explored. OBJECTIVE:To describe the frequency, coexistence, and longitudinal change in excessive daytime sleepiness (EDS), insomnia,...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/s00415-020-10140-x

    authors： Xu Z,Anderson KN,Saffari SE,Lawson RA,Chaudhuri KR,Brooks D,Pavese N

    更新日期：2021-01-01 00:00:00

  • Histamine metabolism in cluster headache and migraine. Catabolism of 14C histamine.

    abstract：:Various parameters of histamine metabolism were studied in patients with migraine, cluster headache and chronic paroxysmal hemicrania. These included urinary excretion of radioactivity and of 14C histamine and its metabolites, exhaled 14CO2 and fecal radioactivity after oral as well as subcutaneous administration of r...

    journal_title：Journal of neurology

    pub_type： 杂志文章

    doi：10.1007/BF00312944

    authors： Sjaastad O,Sjaastad OV

    更新日期：1977-09-12 00:00:00