Acute urinary retention due to benign inflammatory nervous diseases.

Abstract:

:Both neurologists and urologists might encounter patients with acute urinary retention due to benign inflammatory nervous diseases. Based on the mechanism of urinary retention, these disorders can be divided into two subgroups: disorders of the peripheral nervous system (e.g., sacral herpes) or the central nervous system (e.g., meningitis-retention syndrome [MRS]). Laboratory abnormalities include increased herpes virus titers in sacral herpes, and increased myelin basic protein in the cerebrospinal fluid (CSF) in some cases with MRS. Urodynamic abnormality in both conditions is detrusor areflexia; the putative mechanism of it is direct involvement of the pelvic nerves in sacral herpes; and acute spinal shock in MRS. There are few cases with CSF abnormality alone. Although these cases have a benign course, management of the acute urinary retention is necessary to avoid bladder injury due to overdistension. Clinical features of sacral herpes or MRS differ markedly from those of the original "Elsberg syndrome" cases.

journal_name

J Neurol

journal_title

Journal of neurology

authors

Sakakibara R,Yamanishi T,Uchiyama T,Hattori T

doi

10.1007/s00415-006-0189-9

subject

Has Abstract

pub_date

2006-08-01 00:00:00

pages

1103-10

issue

8

eissn

0340-5354

issn

1432-1459

journal_volume

253

pub_type

杂志文章
  • Malignant diseases among patients with multiple sclerosis.

    abstract::The frequency of malignant diseases among 1866 living and 340 deceased multiple sclerosis (MS) patients was investigated in Finland. The study revealed a low prevalence (0.64%) and mortality (0.07%) rate of cancer among MS patients. The difference between MS patients and general population was significant. The highest...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00313623

    authors: Palo J,Duchesne J,Wikström J

    更新日期:1977-10-07 00:00:00

  • Gluten neuropathy: electrophysiological progression and HLA associations.

    abstract:OBJECTIVE:Gluten neuropathy (GN) is the term used to describe peripheral neuropathy that occurs in patients with gluten sensitivity (GS) or coeliac disease (CD) in the absence of other risk factors. We aimed to describe the neurophysiological progression rate of GN across time and look into the potential role of geneti...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-020-10137-6

    authors: Zis P,Sarrigiannis P,Artemiadis A,Sanders DS,Hadjivassiliou M

    更新日期:2021-01-01 00:00:00

  • Practically applicable nerve ultrasound models for the diagnosis of axonal and demyelinating hereditary motor and sensory neuropathies (HMSN).

    abstract:PURPOSE:To develop specific diagnostic ultrasound (US) models for hereditary motor and sensory neuropathies (HMSN) in patients with primarily demyelinating or axonal polyneuropathies (PNP) according to standard nerve conduction studies (NCS) criteria. METHODS:Single-centre, examiner-blinded cross-sectional study in ac...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-017-8687-5

    authors: Loewenbrück KF,Dittrich M,Böhm J,Klingelhöfer J,Baum P,Schäfer J,Reichmann H,Hermann A,Storch A

    更新日期:2018-01-01 00:00:00

  • Predictors of survival after severe dysphagic stroke.

    abstract:BACKGROUND AND PURPOSE:Dysphagia is estimated to occur in up to 50% of the stroke neurorehabilitation population. Those patients with severe neurogenic oropharyngeal dysphagia (NOD) may receive feeding gastrostomy tubes (FGT) if noninvasive therapies prove ineffective in eliminating aspiration or sustaining adequate nu...

    journal_title:Journal of neurology

    pub_type: 临床试验,杂志文章

    doi:10.1007/s00415-005-0906-9

    authors: Ickenstein GW,Stein J,Ambrosi D,Goldstein R,Horn M,Bogdahn U

    更新日期:2005-12-01 00:00:00

  • Familial Sneddon's syndrome.

    abstract::We report the familial occurrence and apparent autosomal dominant inheritance of Sneddon's syndrome with variable clinical expression. The proband, a 40-year-old woman, presented with livedo reticularis and progressive neurological deterioration following a stroke. The diagnosis was confirmed by cerebral angiogram and...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00936890

    authors: Lossos A,Ben-Hur T,Ben-Nariah Z,Enk C,Gomori M,Soffer D

    更新日期:1995-02-01 00:00:00

  • Botulinum toxin in multiple sclerosis.

    abstract::Local administration of botulinum toxin (BoTx) inhibits presynaptic acetylcholine release. All cholinergically innervated muscles and glands can be paralyzed accordingly. Studies on the application of BoTx in multiple sclerosis have shown good results for focal spasticity, in particular, of the extremities. The first ...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-006-1104-0

    authors: Jost WH

    更新日期:2006-02-01 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

  • Neuro-ophthalmology update.

    abstract::This review summarizes the most relevant articles from the field of neuro-ophthalmology published in the Journal of Neurology from January 2012 to July 2013. With the advent of video-oculography, several articles describe new applications for eye movement recordings as a diagnostic tool for a wide range of disorders. ...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-013-7105-x

    authors: Weber KP,Straumann D

    更新日期:2014-07-01 00:00:00

  • Dopamine D2 receptor binding and cerebral glucose metabolism recover after D-penicillamine-therapy in Wilson's disease.

    abstract::Regional cerebral glucose metabolism (rCMRGlc) and dopamine D2 receptor binding were measured in a 31-year-old, severely affected, untreated patient with Wilson's disease of 3 years' duration using positron emission tomography and 18F-deoxyglucose and 18F-methylspiperone ([18F]MSP), respectively. There was a severe re...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00920620

    authors: Schlaug G,Hefter H,Nebeling B,Engelbrecht V,Weiss P,Stöcklin G,Seitz RJ

    更新日期:1994-10-01 00:00:00

  • Cerebral amyloid angiopathy in the aged.

    abstract::Cerebral amyloid angiopathy (CAA) was found in 57% of 123 autopsy brains removed from patients aged 59-101 years. The incidence of CAA increased with age. CAA was seen most frequently in the occipital cortex. Immunohistochemically, amyloid of CAA was positive for amyloid P component and negative for human AA protein a...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00314080

    authors: Yamada M,Tsukagoshi H,Otomo E,Hayakawa M

    更新日期:1987-08-01 00:00:00

  • [Pseudodystrophic muscle glycogenosis in adults. (Acid maltase deficiency syndrome) (author's transl)].

    abstract::A 40-year-old man suffered for 5 years from a progressive proximal myopathy mimicking an atypical limb-girdle dystrophy. A "myopathic" pattern with myotonic and pseudomyotonic discharges was determined by electromyography. Enzyme histochemical and ultrastructural investigations of muscle and liver biopsies pointed to ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00312870

    authors: Gullotta F,Stefan H,Mattern H

    更新日期:1976-01-01 00:00:00

  • Double-blind crossover study with dolasetron mesilate, a 5-HT3 receptor antagonist in cerebellar syndrome secondary to multiple sclerosis.

    abstract::Cerebellar syndrome is one of the most disabling developments in multiple sclerosis (MS). In neurodegenerative disorders, cerebellar syndrome is thought to be related to a neurochemical deficit of 5-hydroxytryptamine (5-HT). Previous studies found that a levorotatory form of 5-hydroxytryptophan, a 5-HT precursor, and ...

    journal_title:Journal of neurology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1007/s00415-003-0176-3

    authors: Monaca-Charley C,Stojkovic T,Duhamel A,De Seze J,Ferriby D,Vermersch P

    更新日期:2003-10-01 00:00:00

  • The relationship among restless legs syndrome (Willis-Ekbom Disease), hypertension, cardiovascular disease, and cerebrovascular disease.

    abstract::Untreated sleep disorders may contribute to secondary causes of uncontrolled hypertension, cardiovascular disease (CVD), and stroke. Restless legs syndrome, or Willis-Ekbom Disease (RLS/WED), is a common sensorimotor disorder with a circadian rhythmicity defined by an uncontrollable urge to move the legs that worsens ...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-013-7065-1

    authors: Ferini-Strambi L,Walters AS,Sica D

    更新日期:2014-06-01 00:00:00

  • Factors influencing work retention for people with multiple sclerosis: cross-sectional studies using qualitative and quantitative methods.

    abstract:OBJECTIVE:To identify factors that impact on the ability of patients with multiple sclerosis (MS) to remain in work in order to make recommendations for future clinical management. METHODS:Cross-sectional studies using qualitative (phase one) and quantitative (phase two) methods. In phase one, 62 patients were intervi...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-005-0765-4

    authors: O'Connor RJ,Cano SJ,Ramió i Torrentà L,Thompson AJ,Playford ED

    更新日期:2005-08-01 00:00:00

  • An update on idiopathic intracranial hypertension in adults: a look at pathophysiology, diagnostic approach and management.

    abstract::Idiopathic intracranial hypertension is a neurological syndrome determined by a rise in intracranial pressure without a detectable cause. Course and prognosis may be changeable, requiring a multidisciplinary approach for its diagnosis and management. Although its precise pathogenesis is still unknown, many studies hav...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-020-09943-9

    authors: Toscano S,Lo Fermo S,Reggio E,Chisari CG,Patti F,Zappia M

    更新日期:2020-05-27 00:00:00

  • Lumbar spinal stenosis: assessment of cauda equina involvement by electrophysiological recordings.

    abstract:UNLABELLED:The objective of this study was to investigate the relationship between electrophysiological recordings and clinical as well as radiological findings in patients suggestive to suffer from a lumbar spinal stenosis (LSS). We hypothesise that the electrophysiological recordings, especially SSEP, indicate a lumb...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-006-0427-1

    authors: Egli D,Hausmann O,Schmid M,Boos N,Dietz V,Curt A

    更新日期:2007-06-01 00:00:00

  • Cerebellar theta burst stimulation does not improve freezing of gait in patients with Parkinson's disease.

    abstract::Freezing of gait (FOG) in Parkinson's disease (PD) likely results from dysfunction within a complex neural gait circuitry involving multiple brain regions. Herein, cerebellar activity is increased in patients compared to healthy subjects. This cerebellar involvement has been proposed to be compensatory. We hypothesize...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-017-8479-y

    authors: Janssen AM,Munneke MAM,Nonnekes J,van der Kraan T,Nieuwboer A,Toni I,Snijders AH,Bloem BR,Stegeman DF

    更新日期:2017-05-01 00:00:00

  • Lipoic (thioctic) acid increases brain energy availability and skeletal muscle performance as shown by in vivo 31P-MRS in a patient with mitochondrial cytopathy.

    abstract::A woman affected by chronic progressive external ophthalmoplegia and muscle mitochondrial DNA deletion was studied by phosphorus magnetic resonance spectroscopy (31P-MRS) prior to and after 1 and 7 months of treatment with oral lipoic acid. Before treatment a decreased phosphocreatine (PCr) content was found in the oc...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00873552

    authors: Barbiroli B,Medori R,Tritschler HJ,Klopstock T,Seibel P,Reichmann H,Iotti S,Lodi R,Zaniol P

    更新日期:1995-07-01 00:00:00

  • Muscle pathology in the neuroleptic malignant syndrome.

    abstract::In a fatal case of neuroleptic malignant syndrome, a muscle sample taken within 1 h of death showed acute myopathic features with absence of muscle glycogen and neutral lipid. These features suggest that hyperpyrexia in this syndrome may be caused by heat production from uncoupled phosphorylation in muscle and imply t...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00718024

    authors: Martin DT,Swash M

    更新日期:1987-12-01 00:00:00

  • Disease management: the example of amyotrophic lateral sclerosis.

    abstract::Disease management is defined as any medical or pharmaceutical intervention designed to improve both outcomes for the patient and overall cost-effectiveness of the health plan. Disease management focuses on the patient throughout the entire course of the disease, involving both health providers and third-party payers....

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/pl00014806

    authors: Matheron L,Barrau K,Blin O

    更新日期:1998-08-01 00:00:00

  • Release of brain-type and heart-type fatty acid-binding proteins in serum after acute ischaemic stroke.

    abstract::This study aimed at an analysis of the release of Braintype and Heart-type Fatty Acid- Binding Proteins (B-FABP and HFABP) in acute ischaemic stroke and their potential value as neurobiochemical markers of brain damage. We investigated 42 consecutive patients admitted within 6 hours after ischaemic stroke. Serial veno...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-005-0725-z

    authors: Wunderlich MT,Hanhoff T,Goertler M,Spener F,Glatz JF,Wallesch CW,Pelsers MM

    更新日期:2005-06-01 00:00:00

  • The 129 codon polymorphism of the prion protein gene influences earlier cognitive performance in Down syndrome subjects.

    abstract::Recently, a frequent prion protein gene (PRNP) polymorphism consisting of a methionine (M) for valine (V) substitution at codon 129 has been associated with cognitive impairment in elderly individuals. Down syndrome (DS) is associated with mental retardation and development of Alzheimer-like brain abnormalities. In th...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-003-1057-5

    authors: Del Bo R,Comi GP,Giorda R,Crimi M,Locatelli F,Martinelli-Boneschi F,Pozzoli U,Castelli E,Bresolin N,Scarlato G

    更新日期:2003-06-01 00:00:00

  • Treatment of multiple sclerosis: current concepts and future perspectives.

    abstract::Currently, several disease-modifying therapies for the treatment of multiple sclerosis are established and more are likely to be introduced. These treatment options differ with respect to their application profile, mechanism of action, efficacy, safety, and tolerance. Here, we review current concepts of MS therapies, ...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-011-6101-2

    authors: Buck D,Hemmer B

    更新日期:2011-10-01 00:00:00

  • Neutralising antibodies to interferon beta in multiple sclerosis : expert panel report.

    abstract::Interferon beta (IFNbeta) therapy for multiple sclerosis (MS) is associated with a potential for the development of neutralising antibodies (NAbs) that negatively affect therapy. Several factors influence the development of NAbs, such as lack of complete sequence homology with the endogenous IFNbeta sequence, frequenc...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-006-0486-3

    authors: Hartung HP,Polman C,Bertolotto A,Deisenhammer F,Giovannoni G,Havrdova E,Hemmer B,Hillert J,Kappos L,Kieseier B,Killestein J,Malcus C,Comabella M,Pachner A,Schellekens H,Sellebjerg F,Selmaj K,Sorensen PS

    更新日期:2007-07-01 00:00:00

  • Neopterin concentrations in serum and cerebrospinal fluid in HTLV-I infected individuals.

    abstract::The concentration of neopterin was measured in serum samples taken from individuals infected with HTLV-I: 5 from asymptomatic individuals, 1 from a patient with adult T-cell leukaemia and 30 from patients with tropical spastic paraparesis (TSP). In addition, cerebrospinal fluid (CSF) was available from 22 of the TSP p...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00810351

    authors: Ali A,Rudge P,Dalgleish AG

    更新日期:1992-05-01 00:00:00

  • Visually-induced dizziness is associated with sensitivity and avoidance across all senses.

    abstract:BACKGROUND:Persistent postural perceptual dizziness (PPPD) is a common chronic condition presenting in neurology and neuro-otology clinics. Symptoms lie on a spectrum in the general population. The cause is unknown and thought to involve interactions between visual and vestibular systems, but symptoms also correlate wi...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-020-09817-0

    authors: Powell G,Derry-Sumner H,Shelton K,Rushton S,Hedge C,Rajenderkumar D,Sumner P

    更新日期:2020-08-01 00:00:00

  • Magnesium deficiency as a cause of acute intractable seizures.

    abstract::Clinical and experimental investigations have shown that magnesium depletion causes a marked irritability of the nervous system, eventually resulting in epileptic seizures. Although magnesium deficiency as a cause of epilepsy is uncommon, its recognition and correction may prove life-saving. Two case reports are prese...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00319737

    authors: Nuytten D,Van Hees J,Meulemans A,Carton H

    更新日期:1991-08-01 00:00:00

  • Dissections after childbirth.

    abstract::The occurrence of spontaneous internal carotid or vertebral artery dissection after childbirth remains rare. To our knowledge, seven cases of arterial dissection in the postpartum period have been described in the literature as single case reports. We report four additional cases of internal carotid and vertebral arte...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s004150050437

    authors: Gasecki AP,Kwiecinski H,Lyrer PA,Lynch TG,Baxter T

    更新日期:1999-08-01 00:00:00

  • Lactate production upon short-term non-ischemic forearm exercise in mitochondrial disorders and other myopathies.

    abstract:BACKGROUND:The nonischemic forearm exercise test (NIFET) has been shown to be as effective as the classic ischemic forearm exercise test (IFET) in the diagnosis of patients with McArdle disease. Recently, the lactate increase normalized to the mechanical energy production in NIFET was suggested to have a intermediate s...

    journal_title:Journal of neurology

    pub_type: 临床试验,杂志文章

    doi:10.1007/s00415-006-0101-7

    authors: Hanisch F,Eger K,Bork S,Lehnich H,Deschauer M,Zierz S

    更新日期:2006-06-01 00:00:00

  • Detection of anterior horn lesions by MRI in central European tick-borne encephalomyelitis.

    abstract::We report a case of central European tick-borne encephalitis with cervical myelitis presenting clinically as a lower motor neuron syndrome of the upper limbs with proximal asymmetrical pareses and atrophies. There were no sensory deficits nor signs of lesions of the spinal pathways or signs of encephalitis or meningit...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s004150050537

    authors: Beer S,Brune N,Kesselring J

    更新日期:1999-12-01 00:00:00