听力与言语-语言病理学

行为科学

医学伦理学

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  • Is atrial fibrillation associated with poor outcome after thrombolysis?

    abstract::Atrial fibrillation (AF) is considered a predictor for severe stroke and poor outcome. The aim was to evaluate whether AF is associated with poor outcome in acute ischemic stroke (IS) patients treated with intravenous thrombolysis (IVT). In a retrospective study, 157 consecutive IS patients (98 males, mean age 67.3 +/...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-010-5452-4

    authors: Sanák D,Herzig R,Král M,Bártková A,Zapletalová J,Hutyra M,Skoloudík D,Vlachová I,Veverka T,Horák D,Kanovský P

    更新日期:2010-06-01 00:00:00

  • Neurological manifestations of Behçet's disease in Japan: a study of 54 patients.

    abstract::The type and frequency of neurological manifestations of Behçet's disease (BD) vary with ethnicity. We analyzed the neurological manifestations of BD in Japanese patients. All patients undergoing treatment at one of the two Yokohama City University hospitals from July 1991 to December 2007 and who fulfilled the Japane...

    journal_title:Journal of neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1007/s00415-010-5454-2

    authors: Ideguchi H,Suda A,Takeno M,Kirino Y,Ihata A,Ueda A,Ohno S,Baba Y,Kuroiwa Y,Ishigatsubo Y

    更新日期:2010-06-01 00:00:00

  • Copper deficiency myelopathy.

    abstract::Acquired copper deficiency has been recognised as a rare cause of anaemia and neutropenia for over half a century. Copper deficiency myelopathy (CDM) was only described within the last decade, and represents a treatable cause of non-compressive myelopathy which closely mimics subacute combined degeneration due to vita...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-010-5511-x

    authors: Jaiser SR,Winston GP

    更新日期:2010-06-01 00:00:00

  • Neurocognitive dysfunction in adult moyamoya disease.

    abstract::We wanted to determine the neurocognitive profile of adult patients with moyamoya disease prior to neurosurgical intervention. The experience of three United States medical centers, Columbia University, University of Illinois at Chicago, and the University of Texas Southwestern Medical Center at Dallas, were combined....

    journal_title:Journal of neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1007/s00415-009-5424-8

    authors: Festa JR,Schwarz LR,Pliskin N,Cullum CM,Lacritz L,Charbel FT,Mathews D,Starke RM,Connolly ES,Marshall RS,Lazar RM

    更新日期:2010-05-01 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

  • Clinical features of CIS of the brainstem/cerebellum of the kind seen in MS.

    abstract::Recognition of multiple sclerosis (MS) attacks relies mostly on clinical assessment. However, their definition based on McDonald criteria refers mostly to timing and when dealing with clinical features is rather ambiguous: "...of the kind seen in multiple sclerosis." This is heightened in clinically isolated syndromes...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-5403-0

    authors: Sastre-Garriga J,Tintoré M,Nos C,Tur C,Río J,Téllez N,Castilló J,Horga A,Perkal H,Comabella M,Rovira A,Montalban X

    更新日期:2010-05-01 00:00:00

  • Copy number variations are a rare cause of non-CMT1A Charcot-Marie-Tooth disease.

    abstract::Hereditary peripheral neuropathies present a group of clinically and genetically heterogeneous entities. All known forms, including the various forms of Charcot-Marie-Tooth disease (CMT) are characterized as Mendelian traits and over 35 genes have been identified thus far. The mutational mechanism of the most common C...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-5401-2

    authors: Huang J,Wu X,Montenegro G,Price J,Wang G,Vance JM,Shy ME,Züchner S

    更新日期:2010-05-01 00:00:00

  • Antibodies and neuronal autoimmune disorders of the CNS.

    abstract::We review the neuronal antibodies described in CNS disorders in order to clarify their diagnostic value, emphasize potentials pitfalls and limitations in the diagnosis of paraneoplastic neurological syndromes (PNS), and examine the current evidence for a possible pathogenic role. We propose to classify the neuronal an...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-009-5431-9

    authors: Graus F,Saiz A,Dalmau J

    更新日期:2010-04-01 00:00:00

  • The first Italian family with tibial muscular dystrophy caused by a novel titin mutation.

    abstract::Tibial muscular dystrophy (TMD) or Udd myopathy is an autosomal dominant distal myopathy with late onset, at first described in the Finnish population. We report here the first Italian cases of TTN mutated titinopathy. The proband, a 60 year-old female, had the first muscular signs at the age of 59 years, with difficu...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-5372-3

    authors: Pollazzon M,Suominen T,Penttilä S,Malandrini A,Carluccio MA,Mondelli M,Marozza A,Federico A,Renieri A,Hackman P,Dotti MT,Udd B

    更新日期:2010-04-01 00:00:00

  • Gender-specific differences in stroke knowledge, stroke risk perception and the effects of an educational multimedia campaign.

    abstract::This study aimed at identifying gender-specific differences in stroke knowledge, stroke risk perception and the educational effects of a multimodal educational intervention. We performed computer-assisted telephone surveys among an average sample of 500 members of the general public (44.0% male, 56.0% female), before ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-5326-9

    authors: Marx JJ,Klawitter B,Faldum A,Eicke BM,Haertle B,Dieterich M,Nedelmann M

    更新日期:2010-03-01 00:00:00

  • REM sleep behaviour disorder and visuoperceptive dysfunction: a disorder of the ventral visual stream?

    abstract::In idiopathic rapid eye movement sleep behaviour disorder (RBD), an association with visuoperceptive disorders has been described. However, such an association has not been clearly established in RBD secondary to Parkinson's disease (PD). We compared visuoperceptive function in four groups of non-demented patients (pa...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-5328-7

    authors: Marques A,Dujardin K,Boucart M,Pins D,Delliaux M,Defebvre L,Derambure P,Monaca C

    更新日期:2010-03-01 00:00:00

  • Optic neuritis presenting with amaurosis fugax.

    abstract::Optic neuritis usually presents with rapid and gradual loss of vision that is either complete or incomplete, and typically associated with retro-orbital pain. To our knowledge there have been no documented reports of optic neuritis presenting with multiple episodes of amaurosis fugax, the sudden and transient loss of ...

    journal_title:Journal of neurology

    pub_type: 信件

    doi:10.1007/s00415-009-5302-4

    authors: Awad AM,Estephan B,Warnack W,Stüve O

    更新日期:2009-12-01 00:00:00

  • Is there a difference in gastric emptying between Parkinson's disease patients under long-term L-dopa therapy with and without motor fluctuations? An analysis using the 13C-acetate breath test.

    abstract::The mechanism underlying the motor fluctuations that develop after long-term L-dopa therapy is not fully known. It has been speculated that malabsorption of L-dopa from the small intestine occurs. It was reported that gastric retention in Parkinson's disease (PD) patients with motor fluctuations is increased as compar...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-5220-5

    authors: Tanaka Y,Kato T,Nishida H,Araki H,Murase M,Nagaki M,Moriwaki H,Inuzuka T

    更新日期:2009-12-01 00:00:00

  • Recent developments in multiple system atrophy.

    abstract::Multiple system atrophy (MSA) is a rare late onset neurodegenerative disorder which presents with autonomic failure and a complicated motor syndrome including atypical parkinsonism, ataxia and pyramidal signs. MSA is a glial alpha-synucleinopathy with rapid progression and currently poor therapeutic management. This p...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-009-5173-8

    authors: Wenning GK,Stefanova N

    更新日期:2009-11-01 00:00:00

  • Missense exchanges in the TTBK2 gene mutated in SCA11.

    abstract::The spinocerebellar ataxias (SCAs) with autosomal dominant inheritance are a clinically and genetically heterogeneous group of neurological disorders with overlapping as well as highly variable phenotypes primarily affecting the cerebellum. To date, 28 different loci have been identified. Nine SCAs are caused by repea...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-5209-0

    authors: Edener U,Kurth I,Meiner A,Hoffmann F,Hübner CA,Bernard V,Gillessen-Kaesbach G,Zühlke C

    更新日期:2009-11-01 00:00:00

  • New therapeutic maneuver for anterior canal benign paroxysmal positional vertigo.

    abstract::This article describes the clinical features of anterior semicircular canal benign paroxysmal positional vertigo (AC-BPPV) and a new therapeutic maneuver for its management. Our study was a retrospective review of cases from an ambulatory tertiary referral center. Thirteen patients afflicted with positional paroxysmal...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-5208-1

    authors: Yacovino DA,Hain TC,Gualtieri F

    更新日期:2009-11-01 00:00:00

  • Rare association of motor neuron disease and spinocerebellar ataxia type 2 (SCA2): a new case and review of the literature.

    abstract::We report a rare association of spinocerebellar ataxia and motor neuron disease (MND) in a woman with genetically confirmed SCA2 who subsequently developed a rapidly progressive and fatal form of MND. Considering the rarity of these two neurological conditions, it is interesting to note that the concomitant occurrence...

    journal_title:Journal of neurology

    pub_type: 信件,评审

    doi:10.1007/s00415-009-5237-9

    authors: Nanetti L,Fancellu R,Tomasello C,Gellera C,Pareyson D,Mariotti C

    更新日期:2009-11-01 00:00:00

  • Juvenile seropositive myasthenia gravis with anti-MuSK antibody after thymectomy.

    abstract::We report the case of a 17.5-year old girl with generalized myasthenia gravis (MG). When she was 13, she started to complain of episodic diplopia, ptosis and mild fatigability of upper and lower extremity muscles. She was diagnosed with MG 3 years later, after exacerbation of her limb muscle weakness. Acetylcholine re...

    journal_title:Journal of neurology

    pub_type: 信件

    doi:10.1007/s00415-009-5215-2

    authors: Kostera-Pruszczyk A,Kwiecinski H

    更新日期:2009-10-01 00:00:00

  • Efficacy of anti-epileptic drugs in patients with gliomas and seizures.

    abstract::Although seizures in brain tumor patients are common, the knowledge on optimal anti-seizure therapy in this patient group is limited. An observational study was carried out using a database of all patients from the neuro-oncology service during the period 2000-2005, with data on seizure characteristics, therapy with A...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-5156-9

    authors: van Breemen MS,Rijsman RM,Taphoorn MJ,Walchenbach R,Zwinkels H,Vecht CJ

    更新日期:2009-09-01 00:00:00

  • 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

  • Management of non-motor complications in Parkinson's disease.

    abstract::This paper summarizes the methods we devised for the treatment of psychosis, orthostatic hypotension, and mood disorders among the various non-motor complications of Parkinson's disease. Psychosis may not manifest when a patient believes in his/her delusions. If left untreated over a prolonged period, however, the del...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-009-5245-9

    authors: Fujimoto K

    更新日期:2009-08-01 00:00:00

  • Risk factors for tumor occurrence in patients with myasthenia gravis.

    abstract::There is still uncertainty regarding risk factors for cancer occurrence in patients with myasthenia gravis (MG). The objective of this study is to determine the prevalence of extrathymic neoplasms in patients with MG and the factors associated with tumor occurrence. The archives of four tertiary MG centers were consul...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-5091-9

    authors: Citterio A,Beghi E,Millul A,Evoli A,Mantegazza R,Antozzi C,Baggi F,Cornelio F,Durelli L,Clerico M,Piccolo G,Cosi V

    更新日期:2009-08-01 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

  • Reversible acute cognitive dysfunction induced by bilateral STN stimulation.

    abstract::Deep brain stimulation of the subthalamic nucleus (STN) is an effective treatment modality for motor symptoms of advanced Parkinson's disease. Recent studies focus on exploring its possible effects on cognition and behavior. We present a case with acute cognitive dysfunction due to misalignment of the electrodes to th...

    journal_title:Journal of neurology

    pub_type: 信件

    doi:10.1007/s00415-009-5103-9

    authors: Cakmakli GY,Oruckaptan H,Saka E,Elibol B

    更新日期:2009-08-01 00:00:00

  • Rapid-eye-movement sleep behavior disorder secondary to acute aseptic limbic encephalitis.

    abstract::Rapid-eye-movement (REM) sleep behavior disorder (RBD) is a parasomnia characterized by complex motor activity associated with dreaming during REM sleep. RBD may be idiopathic or associated with various neurological diseases involving the brainstem. The association of RBD and limbic system impairment was unclear. We r...

    journal_title:Journal of neurology

    pub_type: 信件

    doi:10.1007/s00415-009-5067-9

    authors: Lin FC,Liu CK,Hsu CY

    更新日期:2009-07-01 00:00:00

  • 1H MR spectroscopy of gray and white matter in carbon monoxide poisoning.

    abstract::Carbon monoxide (CO) intoxication leads to acute and chronic neurological deficits, but little is known about the specific noxious mechanisms. (1)H magnetic resonance spectroscopy (MRS) may allow insight into the pathophysiology of CO poisoning by monitoring neurochemical disturbances, yet only limited information is ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-5057-y

    authors: Kondziella D,Danielsen ER,Hansen K,Thomsen C,Jansen EC,Arlien-Soeborg P

    更新日期:2009-06-01 00:00:00

  • From amaurosis fugax to asymptomatic bithalamic infarct.

    abstract::Bilateral paramedian thalamic infarctions are usually associated with impaired consciousness, oculomotor disturbances and neuropsychological changes. A 44-year-old healthy woman presented with amaurosis fugax of the right eye immediately after a Valsalva maneuver. Neurological examination, in particular visual acuity,...

    journal_title:Journal of neurology

    pub_type: 信件

    doi:10.1007/s00415-009-5030-9

    authors: Emond H,Landis T,Perren F

    更新日期:2009-06-01 00:00:00

  • Eradication of Helicobacter pylori may be beneficial in the management of Alzheimer's disease.

    abstract::Infectious agents have been proposed as potential causes of Alzheimer's disease (AD). Recently, we documented a high prevalence of Helicobacter pylori (Hp) infection in patients with AD. We aim to access the effect of Hp eradication on the AD cognitive (MMSE: Mini Mental State Examination and CAMCOG: Cambridge Cogniti...

    journal_title:Journal of neurology

    pub_type: 临床试验,杂志文章

    doi:10.1007/s00415-009-5011-z

    authors: Kountouras J,Boziki M,Gavalas E,Zavos C,Grigoriadis N,Deretzi G,Tzilves D,Katsinelos P,Tsolaki M,Chatzopoulos D,Venizelos I

    更新日期:2009-05-01 00:00:00

  • Recent advances in the diagnosis, genetics and treatment of restless legs syndrome.

    abstract::Knowledge of restless legs syndrome (RLS) has greatly increased in recent years due to the many advances that have been made in diagnosis, management and genetics. Tools have been developed that facilitate the diagnosis and treatment of RLS, in particular the essential diagnostic criteria for RLS have been refined, se...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-0134-9

    authors: Trenkwalder C,Högl B,Winkelmann J

    更新日期:2009-04-01 00:00:00

  • "Vestibular migraine": effects of prophylactic therapy with various drugs. A retrospective study.

    abstract::Vertigo is frequently associated with migraine, and sometimes it is the cardinal symptom. This type of migraine is called "vestibular migraine", "migrainous vertigo", or "migraine-associated vertigo". Earlier findings on effective prophylactic medication for such migraine attacks and their clinical features are few an...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-0111-3

    authors: Baier B,Winkenwerder E,Dieterich M

    更新日期:2009-03-01 00:00:00

  • The costs and prognostic characteristics of ischaemic neurological deficit due to subarachnoid haemorrhage in the United Kingdom. Evidence from the MRC International Subarachnoid Aneurysm Trial.

    abstract:BACKGROUND:Delayed ischaemic neurological deficit (DID) following subarachnoid haemorrhage from aneurysm rupture (aSAH) is a serious complication and a major cause of mortality and morbidity. No empirical estimates of resource use and costs of patients with delayed ischaemic deficit compared to those without have been ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-0034-z

    authors: Rivero-Arias O,Wolstenholme J,Gray A,Molyneux AJ,Kerr RS,Yarnold JA,Sneade M

    更新日期:2009-03-01 00:00:00

  • Clinical experience with high-dose idebenone in Friedreich ataxia.

    abstract::Several reports in the literature describe the effects of low-dose (5 mg/kg/day) idebenone in significantly reducing cardiac hypertrophy in patients with Friedreich ataxia. However, the effects of idebenone on neurological function have not been reliably determined in these studies; when neurological parameters were r...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-009-1008-x

    authors: Schulz JB,Di Prospero NA,Fischbeck K

    更新日期:2009-03-01 00:00:00

  • An epidemiological study of neuromyelitis optica in Cuba.

    abstract:INTRODUCTION:Two population-based studies of neuromyelitis optica (NMO) in non-white populations provided prevalence rates of 0.32 and 3.1 per 100,000 population. OBJECTIVE:To estimate NMO prevalence in the multiethnic Cuban population by nation-wide case ascertainment. METHODS:The study was conducted from October 1,...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-0009-0

    authors: Cabrera-Gómez JA,Kurtzke JF,González-Quevedo A,Lara-Rodríguez R

    更新日期:2009-01-01 00:00:00

  • Monitoring of multiple sclerosis immunotherapy: from single candidates to biomarker networks.

    abstract::Applying microarray technology to identify new diagnostic and prognostic markers in peripheral blood cells (PBC) after therapeutic intervention opens great perspectives regarding patient subclassification. Three recombinant products of the pleiotropic agent interferon beta (rIFN-beta) are available for disease modifyi...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-008-6010-1

    authors: Goertsches RH,Hecker M,Zettl UK

    更新日期:2008-12-01 00:00:00

  • Cerebral MRI lesions and anti-tumor necrosis factor-alpha therapy.

    abstract::We discuss two cases receiving different anti-tumornecrosis-factor alpha antagonists (anti-TNF-alpha); one for psoriatic arthritis (PA) and the other for ankylosing spondylitis (AS). Due to neurological symptoms cerebral magnetic resonance imaging (MRI) was performed and cerebral lesions were detected. Our interpretat...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-008-6020-z

    authors: Winkelmann A,Patejdl R,Wagner S,Benecke R,Zettl UK

    更新日期:2008-12-01 00:00:00

  • Cognitive impairment in myotonic dystrophy type 1 (DM1): a longitudinal follow-up study.

    abstract:OBJECTIVE:To characterize the progression of the cognitive involvement in patients affected by myotonic dystrophy type 1 (DM1) by a longitudinal neuropsychological follow-up study. METHODS:In a previous study we documented an ageing-related decline of frontal and temporal cognitive functions in juvenile/adult forms of...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-008-0017-5

    authors: Modoni A,Silvestri G,Vita MG,Quaranta D,Tonali PA,Marra C

    更新日期:2008-11-01 00:00:00

  • Basal ganglia volume and clinical correlates in 'preclinical' Huntington's disease.

    abstract:OBJECTIVE:To establish differences in basal ganglia and thalamic volume between preclinical carriers and non-carriers of the Huntington's disease (HD) gene and to link the volume to motor, cognitive and behavioural characteristics in carriers. METHODS:Sixteen HD gene carriers without overt clinical motor signs and 14 ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-008-0050-4

    authors: Jurgens CK,van de Wiel L,van Es AC,Grimbergen YM,Witjes-Ané MN,van der Grond J,Middelkoop HA,Roos RA

    更新日期:2008-11-01 00:00:00

  • Sensory loss, pains, motor deficit and axonal regeneration in length-dependent diabetic polyneuropathy.

    abstract::In order to learn more on the occurrence of pains and motor deficit in severe diabetic polyneuropathy we reviewed the data of a series of 30 diabetic patients with an uncommonly severe length-dependent diabetic polyneuropathy (LDDP). Extensive sensory loss predominated with pains and temperature sensations and affecte...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-008-0999-z

    authors: Said G,Baudoin D,Toyooka K

    更新日期:2008-11-01 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

  • Frequency of nocturnal sudden death in patients with multiple system atrophy.

    abstract::Sudden death has been reported in patients with multiple system atrophy (MSA), although the frequency of this event has not been well delineated. We investigated the frequency and potential causes of sudden death in patients with MSA. During the 5-year observation period, 10 of 45 patients with probable MSA died. The ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-008-0941-4

    authors: Shimohata T,Ozawa T,Nakayama H,Tomita M,Shinoda H,Nishizawa M

    更新日期:2008-10-01 00:00:00

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