Clinical and electrophysiological studies of carbon disulphide polyneuropathy.

Abstract:

:A clinical and electrophological study was performed on 30 patients with chronic carbon disulphide poisoning. Although the measurements of motor conduction velocity and of terminal latency were within the normal range in the subclinical stage, estimation of nerve excitability threshold showed distal motor hypoexcitability, thus proving a very effective means for the early detection of carbon disulphide polyneuropathy. The distal muscle fatigue found in 35% of patients was confirmed by the decrement (more than 10%) in the amplitude of muscle evoked potentials in the abductor digiti minimi muscle in response to repetitive stimulation of the ulnar nerve. Association of the above findings with the significant electrophysiological changes, viz., decrease in the amplitude of sensory evoked potentials on stimulation of the digital fibres, mild slowing of sensory conduction velocity in the peripheral nerves, and decrease in the amplitude of evoked potentials in the distal muscles, suggest that the carbon disulphide polyneuropathy would be underlain by a primary distal axonopathy.

journal_name

J Neurol

journal_title

Journal of neurology

authors

Vasilescu C,Florescu A

doi

10.1007/BF00313208

subject

Has Abstract

pub_date

1980-01-01 00:00:00

pages

59-70

issue

1

eissn

0340-5354

issn

1432-1459

journal_volume

224

pub_type

杂志文章
  • An unusual association of dentato-rubral degeneration with spinal ataxia, ophthalmoplegia and multiple cranial nerve palsies.

    abstract::Clinical and neuropathological data of a 50-year-old woman with an unusual multisystem degeneration are presented. Clinically the illness was characterized by progressive ataxia with ophthalmoplegia and multiple cranial nerve palsies. Neuropathological investigation showed a severe and selective degeneration of the de...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00313709

    authors: Janzer RC,Barontini F

    更新日期:1985-01-01 00:00:00

  • Decompressive hemicraniectomy in severe cerebral venous thrombosis: a prospective case series.

    abstract::Small retrospective case series suggest that decompressive hemicraniectomy can be life saving in patients with cerebral venous thrombosis (CVT) and impending brain herniation. Prospective studies of consecutive cases are lacking. Thus, a single centre, prospective study was performed. In 2006 we adapted our protocol f...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-011-6307-3

    authors: Zuurbier SM,Coutinho JM,Majoie CB,Coert BA,van den Munckhof P,Stam J

    更新日期:2012-06-01 00:00:00

  • Clinical and biochemical evidence of skeletal muscle involvement in galactose-1-phosphate uridyl transferase deficiency.

    abstract::An 8-year-old boy with galactose-1-phosphate uridyl transferase (GALT) deficiency presented with hypotonia, muscle hypotrophy, hepatomegaly, bilateral cataract and mild mental retardation. Two brothers showed a GALT activity consistent with a homozygotic condition and both parents were found to be heterozygotes for th...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00838160

    authors: Bresolin N,Comi GP,Fortunato F,Meola G,Gallanti A,Tajana A,Velicogna M,Gonano EF,Ninfali P,Pifferi S

    更新日期:1993-05-01 00:00:00

  • Amyotrophic lateral sclerosis: early predictors of prolonged survival.

    abstract:OBJECTIVE:In order to define the predictors of prolonged survival available at the time of first examination we performed a historical cohort study of amyotrophis sclerosis (ALS) patients referred to our ALS Clinic over the last 20 years. METHODS:In a group of 1034 patients with the diagnosis of definite or probable A...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-006-0226-8

    authors: Czaplinski A,Yen AA,Appel SH

    更新日期:2006-11-01 00:00:00

  • Oxidative stress biomarkers in mitochondrial myopathies, basally and after cysteine donor supplementation.

    abstract::Mitochondrial diseases are due to impairment of the mitochondrial respiratory chain. A plausible pathogenic mechanism leading to cellular dysfunction and phenotypic expression is oxidative stress, but there are surprisingly few clinical studies on this subject. Glutathione (GSH) deficiency has been reported in mitocho...

    journal_title:Journal of neurology

    pub_type: 杂志文章,随机对照试验

    doi:10.1007/s00415-009-5409-7

    authors: Mancuso M,Orsucci D,Logerfo A,Rocchi A,Petrozzi L,Nesti C,Galetta F,Santoro G,Murri L,Siciliano G

    更新日期:2010-05-01 00:00:00

  • Behçet's disease and the nervous system.

    abstract::Behçet's disease is a multisystem inflammatory disorder with unknown aetiology. It is a disease of young adults with a more severe course in males subjects. Its prevalence is high in the Mediterranean basin and Japan and has been linked with human leucocyte antigen B5 (HLA-B5) in those countries. According to the diag...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s004150050205

    authors: Serdaroğlu P

    更新日期:1998-04-01 00:00:00

  • Electrophysiological exploration of the sacral conus.

    abstract::Evoked urethral and anal responses are produced by electrical stimulation of penis, bladder neck and anus. Latency and duration of the responses after bladder neck and anal stimulation are greatly dependent on stimulus parameters, suggesting a polysynaptic reflex; penile stimulation probably involves an oligosynaptic ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00313567

    authors: Vereecken RL,De Meirsman J,Puers B,Van Mulders J

    更新日期:1982-01-01 00:00:00

  • SOD2 as a potential modifier of X-linked adrenoleukodystrophy clinical phenotypes.

    abstract::X-linked adrenoleukodystrophy (XALD), a neurological disorder caused by mutations in the peroxisomal membrane protein gene ABCD1, presents as a rapidly progressing, inflammatory cerebral demyelination (cerebral cases) or a slowly progressing, distal axonopathy (non-cerebral cases). Specific ABCD1 defects do not explai...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-011-6371-8

    authors: Brose RD,Avramopoulos D,Smith KD

    更新日期:2012-07-01 00:00:00

  • Global functional connectivity reveals highly significant differences between the vegetative and the minimally conscious state.

    abstract::A major challenge in the diagnosis of disorders of consciousness is the differential diagnosis between the vegetative state (VS) and the minimally conscious state (MCS). Clinically, VS is defined by complete unawareness, whereas MCS is defined by the presence of inconsistent but clearly discernible behavioural signs o...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-012-6734-9

    authors: Kotchoubey B,Merz S,Lang S,Markl A,Müller F,Yu T,Schwarzbauer C

    更新日期:2013-04-01 00:00:00

  • A short scale for evaluation of neuropsychiatric disorders in Parkinson's disease: first psychometric approach.

    abstract::The neuropsychiatric symptoms and behavioral disorders affecting Parkinson's disease (PD) patients are common and disabling. A PD-specific interview-based 12-item scale, the Scale for Evaluation of Neuropsychiatric Disorders in Parkinson's Disease (SEND-PD), has been developed to assess the severity of neuropsychiatri...

    journal_title:Journal of neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1007/s00415-012-6490-x

    authors: Martinez-Martin P,Frades-Payo B,Agüera-Ortiz L,Ayuga-Martinez A

    更新日期:2012-11-01 00:00:00

  • Neuroprotection with glatiramer acetate: evidence from the PreCISe trial.

    abstract::The phase III, multicenter, randomized, placebo-controlled PreCISe trial assessed glatiramer acetate (GA) effects in patients with clinically isolated syndromes (CIS) suggestive of multiple sclerosis (MS). To assess the neuroprotective effect of GA in a subset of patients in the PreCISe trial, we used proton magnetic ...

    journal_title:Journal of neurology

    pub_type: 杂志文章,多中心研究,随机对照试验

    doi:10.1007/s00415-013-6903-5

    authors: Arnold DL,Narayanan S,Antel S

    更新日期:2013-07-01 00:00:00

  • The sleep and circadian problems of Huntington's disease: when, why and their importance.

    abstract:INTRODUCTION:Mounting evidence supports the existence of an important feedforward cycle between sleep and neurodegeneration, wherein neurodegenerative diseases cause sleep and circadian abnormalities, which in turn exacerbate and accelerate neurodegeneration. If so, sleep therapies bear important potential to slow prog...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-020-10334-3

    authors: Voysey Z,Fazal SV,Lazar AS,Barker RA

    更新日期:2020-12-23 00:00:00

  • Quantification of post-concussion symptoms 3 months after minor head injury in 100 consecutive patients.

    abstract::Post-concussion symptoms (PCS) (such as headaches, irritability, anxiety, dizziness, fatigue and impaired concentration) are frequently experienced by patients who have sustained a minor head injury (MHI). The post-concussion syndrome has been defined as a clinical state where 3 or more symptoms persist for more than ...

    journal_title:Journal of neurology

    pub_type: 临床试验,杂志文章

    doi:10.1007/s004150050254

    authors: Ingebrigtsen T,Waterloo K,Marup-Jensen S,Attner E,Romner B

    更新日期:1998-09-01 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

  • Accuracy and inter-observer variation in the classification of dysarthria from speech recordings.

    abstract:BACKGROUND:Dysarthria may be classified as flaccid, spastic, ataxic, hypokinetic, choreatic, dystonic, or mixed. We hypothesized that in routine neurological practice the reliability and accuracy of perceptual analysis alone in the classification of dysarthria is low and that this classification is mainly based on the ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-008-0978-4

    authors: Fonville S,van der Worp HB,Maat P,Aldenhoven M,Algra A,van Gijn J

    更新日期:2008-10-01 00:00:00

  • [Global aphasia. The clinical picture and a consideration of the neurolinguistic structure (author's transl)].

    abstract::Global aphasia is described as a unitary syndrome which is characterized by a severe impairment of all linguistic capabilities. Speech production is extremely limited and consists of stereotyped phrases, recurring utterances or a few isolated words which are usually neologistically distorted. The patients are unable t...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF02430346

    authors: Stachowiak FJ,Huber W,Kerschensteiner M,Poeck K,Weniger D

    更新日期:1977-01-13 00:00:00

  • Intrafamilial heterogeneity of movement disorders: report of three cases in one family.

    abstract::We report three members of a single family with an apparently autosomal dominant, nonparoxysmal, hyperkinetic movement disorder with onset in adolescence. The proband, a 56-year-old woman, manifested dystonia, tremor and myoclonus; one of her daughters exhibited myoclonus with tremor, and the other demonstrated myoclo...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s004150050116

    authors: Lossos A,Cohen O,Meiner V,Blumenfeld A,Reches A

    更新日期:1997-07-01 00:00:00

  • Glatiramer acetate induces pro-apoptotic mechanisms involving Bcl-2, Bax and Cyt-c in peripheral lymphocytes from multiple sclerosis patients.

    abstract::Apoptotic deletion of autoreactive T-cells is defective in patients with multiple sclerosis (MS). Glatiramer acetate (GA) treatment seems to restore apoptosis of detrimental T-cells. We analyzed the mitochondria membrane pro- (Bax) and anti-apoptotic (Bcl- 2) and cytosolic pro-apoptotic (Cyt-c, APAF-1) proteins expres...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-005-0965-y

    authors: Ruggieri M,Avolio C,Scacco S,Pica C,Lia A,Zimatore GB,Papa S,Livrea P,Trojano M

    更新日期:2006-02-01 00:00:00

  • Intrathecal levels of IL-6, IL-11 and LIF in Alzheimer's disease and frontotemporal lobar degeneration.

    abstract::Cerebrospinal fluid (CSF) levels of interleukin (IL)-6, IL-11 and leukaemia inhibitory factor (LIF) were evaluated in 43 patients with Alzheimer's disease (AD) and 24 patients with frontotemporal lobar degeneration (FTLD) as compared with 30 agematched controls (CON), and correlated with clinical and demographic data ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-008-0737-6

    authors: Galimberti D,Venturelli E,Fenoglio C,Guidi I,Villa C,Bergamaschini L,Cortini F,Scalabrini D,Baron P,Vergani C,Bresolin N,Scarpini E

    更新日期:2008-04-01 00:00:00

  • Blink reflex in patients with an ischaemic lesion of the brain-stem verified by MRI.

    abstract::The electrically elicited blink reflex was investigated in 25 patients with ischaemic lesions of the pons or the medulla oblongata. Only patients with a lesion on MRI appropriate to the clinical syndrome were included. Twenty patients had an infarction of the pons, bilateral in 5. Additional 5 patients had an infarcti...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00870670

    authors: Meincke U,Ferbert A

    更新日期:1993-11-01 00:00:00

  • 18F-FDG PET in neurodegenerative Langerhans cell histiocytosis : results and potential interest for an early diagnosis of the disease.

    abstract:INTRODUCTION:The so called "neurodegenerative Langerhans cell histiocytosis" (ND-LCH) is a rare and severe complication of LCH presenting as a progressive cerebellar ataxia associated with pyramidal tract signs, and cognitive impairment. MRI is the gold standard to investigate CNS lesions of ND-LCH but little is known ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-008-0751-8

    authors: Ribeiro MJ,Idbaih A,Thomas C,Remy P,Martin-Duverneuil N,Samson Y,Donadieu J,Hoang-Xuan K

    更新日期:2008-04-01 00:00:00

  • Utility of measuring vitamin B12 and its active fraction, holotranscobalamin, in neurological vitamin B12 deficiency syndromes.

    abstract::Vitamin B(12) (VitB(12), cobalamin) deficiency has been associated with various neuropsychiatric conditions, such as peripheral neuropathy, subacute combined degeneration, affective disorders, and cognitive impairment. Current assays analyze vitamin B(12), of which only a small percentage is metabolically active. Meas...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-010-5764-4

    authors: Schrempf W,Eulitz M,Neumeister V,Siegert G,Koch R,Reichmann H,Storch A

    更新日期:2011-03-01 00:00:00

  • Strategies for optimizing MRI techniques aimed at monitoring disease activity in multiple sclerosis treatment trials.

    abstract::Serial magnetic resonance imaging (MRI) detects substantial subclinical disease activity in multiple sclerosis (MS) and is presently included in most treatment trials as an objective outcome measure. Our current knowledge of the role of MRI in MS treatment trials is derived from very limited patient studies, and the a...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s004150050053

    authors: Barkhof F,Filippi M,Miller DH,Tofts P,Kappos L,Thompson AJ

    更新日期:1997-02-01 00:00:00

  • Forced vital capacity and cross-domain late-onset Pompe disease outcomes: an individual patient-level data meta-analysis.

    abstract:BACKGROUND:Late-onset Pompe disease (LOPD) is a rare, metabolic disease primarily affecting the musculoskeletal and respiratory systems. Forced vital capacity (FVC) is commonly used to measure pulmonary function; however, associations between FVC and other LOPD outcomes remain unclear. METHODS:A systematic literature ...

    journal_title:Journal of neurology

    pub_type: 杂志文章,meta分析

    doi:10.1007/s00415-019-09401-1

    authors: Berger KI,Kanters S,Jansen JP,Stewart A,Sparks S,Haack KA,Bolzani A,Siliman G,Hamed A

    更新日期:2019-09-01 00:00:00

  • The value of leukocyte adhesion molecules in patients after ischemic stroke.

    abstract::Leukocyte recruitment and inflammatory response play an important patho-physiologic role after cerebral ischemia. This study aimed to evaluate whether leukocyte adhesion molecules can predict clinical outcome in patients after ischemic stroke. We prospectively examined serial changes in p-selectin glycoprotein ligand-...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-5117-3

    authors: Tsai NW,Chang WN,Shaw CF,Jan CR,Huang CR,Chen SD,Chuang YC,Lee LH,Lu CH

    更新日期:2009-08-01 00:00:00

  • Neuro-ophthalmology and neuro-otology update.

    abstract::This review summarizes topical papers from the fields of neuro-ophthalmology and neuro-otology published from August 2013 to February 2015. The main findings are: (1) diagnostic criteria for pseudotumor cerebri have been updated, and the Idiopathic Intracranial Hypertension Treatment Trial evaluated the efficacy of ac...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-015-7825-1

    authors: Gold DR,Zee DS

    更新日期:2015-12-01 00:00:00

  • Spontaneous cervical artery dissection is accompanied by a hypercoagulable state and simultaneous inflammatory condition.

    abstract:BACKGROUND:Spontaneous cervical artery dissections (sCAD) are often preceded by infections. However, existing data about inflammatory parameters remained inconsistent. Remarkably, concurrent information about the coagulation system, whose affection seems also reasonable to cause ischaemic events, are still lacking in s...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-017-8696-4

    authors: Pelz JO,Harms K,Metze M,Michalski D

    更新日期:2018-02-01 00:00:00

  • Resting-state functional connectivity of dentate nucleus is associated with tremor in Parkinson's disease.

    abstract::Cerebello-thalamo-cortical circuit has been indicated important for tremor in Parkinson's disease (PD), but the role of dentate nucleus (DN) in parkinsonian tremor remains unclear. To investigate whether DN plays a role in PD tremor, we recruited 50 PD and 29 age-matched health controls (HC). The patients were divided...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-015-7835-z

    authors: Ma H,Chen H,Fang J,Gao L,Ma L,Wu T,Hou Y,Zhang J,Feng T

    更新日期:2015-10-01 00:00:00

  • Myasthenia gravis: a clinical-immunological update.

    abstract::Myasthenia gravis (MG) is the archetypic disorder of both the neuromuscular junction and autoantibody-mediated disease. In most patients, IgG1-dominant antibodies to acetylcholine receptors cause fatigable weakness of skeletal muscles. In the rest, a variable proportion possesses antibodies to muscle-specific tyrosine...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-015-7963-5

    authors: Binks S,Vincent A,Palace J

    更新日期:2016-04-01 00:00:00

  • Cerebrospinal fluid concentrations of the complement MAC inhibitor CD59 in multiple sclerosis and patients with other neurological disorders.

    abstract::Rodent oligodendrocytes have a unique susceptibility among glia to the lytic effects of complement, due in part to a deficiency in CD59 (protectin), a key surface inhibitor of the complement membrane attack complex (MAC). The possibility that shedding of CD59 by human oligodendrocytes contributes to complement-mediate...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00873519

    authors: Roddy J,Clark I,Hazleman BL,Compston DA,Scolding NJ

    更新日期:1994-08-01 00:00:00