Stroke after zoster ophthalmicus in a 12-year-old girl with protein C deficiency.

Abstract:

:A 12-year-old girl who had zoster ophthalmicus 10 months earlier presented with hemiparesis and corresponding basal ganglionic infarction related to middle cerebral artery branch thrombosis ipsilateral to the zoster. Hematologic evaluation disclosed protein C deficiency. This represents the first zoster-associated stroke reported in childhood associated with protein C deficiency, with extension of the latency period between zoster and infarction, previously reported to be 6 months.

journal_name

Neurology

journal_title

Neurology

authors

Cadavid D,Pearl PL,Dubovsky EC,Angiolillo A,Vezina LG

doi

10.1212/wnl.53.5.1128

subject

Has Abstract

pub_date

1999-09-22 00:00:00

pages

1128-9

issue

5

eissn

0028-3878

issn

1526-632X

journal_volume

53

pub_type

杂志文章
  • Attentional bias induced by viewing actual or illusory movements.

    abstract:OBJECTIVE:To learn to which portions of a line normal subjects would attend when watching this line actually moving or when perceiving movement even in the absence of actual movement, an illusory movement. METHODS:Twenty normal subjects watched a computer monitor on which either lines or dots moved to the right or lef...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000120546.14213.c7

    authors: Jeong Y,Lee BH,Ahn HJ,Park KC,Heilman KM,Na DL

    更新日期:2004-04-27 00:00:00

  • Efficacy and tolerability of the new antiepileptic drugs II: treatment of refractory epilepsy: report of the Therapeutics and Technology Assessment Subcommittee and Quality Standards Subcommittee of the American Academy of Neurology and the American Epile

    abstract:OBJECTIVE:To assess the evidence demonstrating efficacy, tolerability, and safety of seven new antiepileptic drugs (AEDs) (gabapentin, lamotrigine, topiramate, tiagabine, oxcarbazepine, levetiracetam, and zonisamide) in the treatment of children and adults with refractory partial and generalized epilepsies. METHODS:A ...

    journal_title:Neurology

    pub_type: 指南,杂志文章,实务指引,评审

    doi:10.1212/01.wnl.0000123695.22623.32

    authors: French JA,Kanner AM,Bautista J,Abou-Khalil B,Browne T,Harden CL,Theodore WH,Bazil C,Stern J,Schachter SC,Bergen D,Hirtz D,Montouris GD,Nespeca M,Gidal B,Marks WJ Jr,Turk WR,Fischer JH,Bourgeois B,Wilner A,Faught R

    更新日期:2004-04-27 00:00:00

  • CCM1 mutation screen of sporadic cases with cerebral cavernous malformations.

    abstract::Cerebral cavernous malformations (CCM) are CNS vascular anomalies associated with seizures, headaches, and hemorrhagic strokes. The CCM1 gene was screened in 35 sporadic cases with either single or multiple CCM. It was found that 29% of the individuals with multiple CCM have a CCM1 mutation, whereas cases with only on...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000118299.55857.bb

    authors: Verlaan DJ,Laurent SB,Sure U,Bertalanffy H,Andermann E,Andermann F,Rouleau GA,Siegel AM

    更新日期:2004-04-13 00:00:00

  • LGI1 mutations in temporal lobe epilepsies.

    abstract:BACKGROUND AND OBJECTIVES:A number of familial temporal lobe epilepsies (TLE) have been recently recognized. Mutations in LGI1 (leucine-rich, glioma-inactivated 1 gene) have been found in a few families with the syndrome of autosomal dominant partial epilepsy with auditory features (ADPEAF). The authors aimed to determ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000118213.94650.81

    authors: Berkovic SF,Izzillo P,McMahon JM,Harkin LA,McIntosh AM,Phillips HA,Briellmann RS,Wallace RH,Mazarib A,Neufeld MY,Korczyn AD,Scheffer IE,Mulley JC

    更新日期:2004-04-13 00:00:00

  • Droxidopa for neurogenic orthostatic hypotension: a randomized, placebo-controlled, phase 3 trial.

    abstract:OBJECTIVE:To determine whether droxidopa, an oral norepinephrine precursor, improves symptomatic neurogenic orthostatic hypotension (nOH). METHODS:Patients with symptomatic nOH due to Parkinson disease, multiple system atrophy, pure autonomic failure, or nondiabetic autonomic neuropathy underwent open-label droxidopa ...

    journal_title:Neurology

    pub_type: 杂志文章,多中心研究,随机对照试验

    doi:10.1212/WNL.0000000000000615

    authors: Kaufmann H,Freeman R,Biaggioni I,Low P,Pedder S,Hewitt LA,Mauney J,Feirtag M,Mathias CJ,NOH301 Investigators.

    更新日期:2014-07-22 00:00:00

  • Short- and long-term outcome of chronic pallidal neurostimulation in monogenic isolated dystonia.

    abstract:OBJECTIVES:Deep brain stimulation of the internal pallidum (GPi-DBS) is an established therapeutic option in treatment-refractory dystonia, and the identification of factors predicting surgical outcome is needed to optimize patient selection. METHODS:In this retrospective multicenter study, GPi-DBS outcome of 8 patien...

    journal_title:Neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1212/WNL.0000000000001312

    authors: Brüggemann N,Kühn A,Schneider SA,Kamm C,Wolters A,Krause P,Moro E,Steigerwald F,Wittstock M,Tronnier V,Lozano AM,Hamani C,Poon YY,Zittel S,Wächter T,Deuschl G,Krüger R,Kupsch A,Münchau A,Lohmann K,Volkmann J,Kle

    更新日期:2015-03-03 00:00:00

  • Acute disseminated encephalomyelitis: a follow-up study of 40 adult patients.

    abstract:OBJECTIVES:To describe the clinical, CSF, and radiologic findings and long-term follow-up in a cohort of patients with acute disseminated encephalomyelitis (ADEM), and to determine possible prognostic factors for progression to MS. METHODS:Forty adults (28 women, mean age 33.5 years) diagnosed with ADEM were analyzed....

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.56.10.1313

    authors: Schwarz S,Mohr A,Knauth M,Wildemann B,Storch-Hagenlocher B

    更新日期:2001-05-22 00:00:00

  • Mevalonate kinase deficiency: Evidence for a phenotypic continuum.

    abstract::Both mevalonic aciduria, characterized by psychomotor retardation, cerebellar ataxia, recurrent fever attacks, and death in early childhood, and hyper-immunoglobulin D (hyper-IgD) syndrome, with recurrent fever attacks without neurologic symptoms, are caused by a functional deficiency of mevalonate kinase. In a system...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000115390.33405.f7

    authors: Simon A,Kremer HP,Wevers RA,Scheffer H,De Jong JG,Van Der Meer JW,Drenth JP

    更新日期:2004-03-23 00:00:00

  • Effect of ApoE isoforms on mitochondria in Alzheimer disease.

    abstract:OBJECTIVE:To test the hypothesis that ApoE isoforms affect mitochondrial structure and function that are related to cognitive impairment in Alzheimer disease (AD), we systematically investigated the effects of ApoE isoforms on mitochondrial biogenesis and dynamics, oxidative stress, synapses, and cognitive performance ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000009582

    authors: Yin J,Reiman EM,Beach TG,Serrano GE,Sabbagh MN,Nielsen M,Caselli RJ,Shi J

    更新日期:2020-06-09 00:00:00

  • Spatial-temporal functional mapping of language at the bedside with electrocorticography.

    abstract:OBJECTIVE:To investigate the feasibility and clinical utility of using passive electrocorticography (ECoG) for online spatial-temporal functional mapping (STFM) of language cortex in patients being monitored for epilepsy surgery. METHODS:We developed and tested an online system that exploits ECoG's temporal resolution...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000002525

    authors: Wang Y,Fifer MS,Flinker A,Korzeniewska A,Cervenka MC,Anderson WS,Boatman-Reich DF,Crone NE

    更新日期:2016-03-29 00:00:00

  • Cerebral ischemia and atrial fibrillation: prospective study.

    abstract::The frequency of recurrent cerebral ischemia and death was determined prospectively in 36 patients who presented with ischemic stroke and had atrial fibrillation. Patients were followed an average of 2.3 months (range, 3 weeks to 9 months). The recurrence rate for cerebral ischemia was 33%, and the mortality rate was ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.34.10.1285

    authors: Kelley RE,Berger JR,Alter M,Kovacs AG

    更新日期:1984-10-01 00:00:00

  • A randomized trial of rizatriptan in migraine attacks in children.

    abstract:OBJECTIVE:To examine the efficacy of rizatriptan and the consistency of treatment response in migraine attacks of children and adolescents. METHODS:We conducted a double-blind, placebo-controlled three-way crossover trial in patients ages 6 to 17 years diagnosed with migraine in two pediatric hospital outpatient clini...

    journal_title:Neurology

    pub_type: 杂志文章,随机对照试验

    doi:10.1212/01.wnl.0000238179.79888.44

    authors: Ahonen K,Hämäläinen ML,Eerola M,Hoppu K

    更新日期:2006-10-10 00:00:00

  • Age of onset, sex, and cardiomyopathy as predictors of disability and survival in Friedreich's disease: a retrospective study on 119 patients.

    abstract::We performed a retrospective study on a series of 119 of our patients who have Friedreich's disease to assess the predictive value of age at onset, gender, and left ventricular hypertrophy in regard to disease progression. Outcome variables were survival, time to loss of independent gait, and time to confinement in a ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.47.5.1260

    authors: De Michele G,Perrone F,Filla A,Mirante E,Giordano M,De Placido S,Campanella G

    更新日期:1996-11-01 00:00:00

  • Neurologic abnormalities in murderers.

    abstract::Thirty-one individuals awaiting trial or sentencing for murder or undergoing an appeal process requested a neurologic examination through legal counsel. We attempted in each instance to obtain EEG, MRI or CT, and neuropsychological testing. Neurologic examination revealed evidence of "frontal" dysfunction in 20 (64.5%...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.45.9.1641

    authors: Blake PY,Pincus JH,Buckner C

    更新日期:1995-09-01 00:00:00

  • Cerebral ischemia and deterioration with lower blood pressure target in intracerebral hemorrhage.

    abstract:OBJECTIVE:To determine the incidence and predictors of acute cerebral ischemia and neurologic deterioration in intracerebral hemorrhage (ICH) patients after an institutional protocol change in systolic blood pressure (SBP) target from <160 to <140 mm Hg. METHODS:We retrospectively compared persons admitted with primar...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000006156

    authors: Buletko AB,Thacker T,Cho SM,Mathew J,Thompson NR,Organek N,Frontera JA,Uchino K

    更新日期:2018-09-11 00:00:00

  • Avoidance of dyskinesia: preclinical evidence for continuous dopaminergic stimulation.

    abstract::Current concepts suggest that avoidance of pulsatile stimulation of dopamine receptors in Parkinson's disease (PD) can prevent the onset of dyskinesia. In MPTP-treated primates, repeated administration of levodopa or other short-acting dopamine agonist drugs leads to the onset of marked involuntary movements. In contr...

    journal_title:Neurology

    pub_type: 杂志文章,评审

    doi:10.1212/wnl.62.1_suppl_1.s47

    authors: Jenner P

    更新日期:2004-01-13 00:00:00

  • Hallucinations and sleep disturbances in Parkinson's disease.

    abstract::Visual hallucinations (VHs) occur frequently in Parkinson's disease (PD). VHs occur more frequently in elderly patients with longer duration of illness, cognitive impairment, and sleep disturbances. The relationship between the use of antiparkinsonian drugs and VHs is complicated, but most drugs used to treat parkinso...

    journal_title:Neurology

    pub_type: 杂志文章,评审

    doi:10.1212/wnl.63.8_suppl_3.s28

    authors: Kulisevsky J,Roldan E

    更新日期:2004-10-26 00:00:00

  • Arm-diaphragm synkinesis: electrodiagnostic studies of aberrant regeneration of phrenic motor neurons.

    abstract::Arm-diaphragm synkinesis may occur after injury to the proximal portion of the brachial plexus or cervical nerve roots. Regenerating axons of phrenic motor neurons are misdirected to supply limb muscles. Electrodiagnostic investigations of three patients with symptoms referable to upper brachial plexus or cervical roo...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.30.4.339

    authors: Swift TR,Leshner RT,Gross JA

    更新日期:1980-04-01 00:00:00

  • Petasites hybridus root (butterbur) is an effective preventive treatment for migraine.

    abstract:OBJECTIVE:To evaluate the clinical efficacy of a standardized special root extract from the plant Petasites hybridus as a preventive therapy for migraine. METHODS:This is a three-arm, parallel-group, randomized trial comparing Petasites extract 75 mg bid, Petasites extract 50 mg bid, or placebo bid in 245 patients wit...

    journal_title:Neurology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1212/01.wnl.0000147290.68260.11

    authors: Lipton RB,Göbel H,Einhäupl KM,Wilks K,Mauskop A

    更新日期:2004-12-28 00:00:00

  • The spectrum of familial inclusion body myopathies in 13 families and a description of a quadriceps-sparing phenotype in non-Iranian Jews.

    abstract::The frequency, patterns of inheritance and clinical phenotypes of inherited myopathies with histologic features of rimmed vacuoles, tubulofilamentous inclusions and absence of inflammation (familial and hereditary inclusion body myopathy [f-IBM]) are poorly defined. Quadriceps sparing is a characteristic of f-IBM seen...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.47.4.977

    authors: Sivakumar K,Dalakas MC

    更新日期:1996-10-01 00:00:00

  • Horner's syndrome after coronary artery bypass surgery.

    abstract::We established the frequency of Horner's syndrome (HS) in 248 elective patients after coronary artery bypass surgery. Patients were evaluated neurologically pre- and post-operatively and 6 months after surgery. Nineteen patients (7.7%) developed unilateral HS postoperatively, 12 involving the left eye. The finding per...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.46.1.181

    authors: Barbut D,Gold JP,Heinemann MH,Hinton RB,Trifiletti RR

    更新日期:1996-01-01 00:00:00

  • Prognosis with stroke in Europe: A collaborative study of population-based cohorts. Neurologic Diseases in the Elderly Research Group.

    abstract::The authors pooled four population-based European studies to determine the risk for institutionalization and death after stroke. Risk for institutionalization was assessed in 13,095 subjects. Survival was calculated for prevalent stroke in 7929 individuals and incident stroke in 8550 individuals. The adjusted risk of ...

    journal_title:Neurology

    pub_type: 杂志文章,多中心研究

    doi:

    authors: Schmidt R,Breteler MM,Inzitari D,Fratiglioni L,Hofman A,Launer LJ

    更新日期:2000-01-01 00:00:00

  • Tuberculous meningitis in the southwest United States: a community-based study.

    abstract::This community-based study analyzed 54 patients with definite or probable tuberculous meningitis (TBM) in New Mexico from 1970 through 1990. Patients ranged in age from 4 months to 86 years. The highest age-specific incidence occurred in the elderly, but 22% of patients were less than 10 years old. Native American pat...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.43.9.1775

    authors: Davis LE,Rastogi KR,Lambert LC,Skipper BJ

    更新日期:1993-09-01 00:00:00

  • Cognitive correlates of 1H MRSI-detected hippocampal abnormalities in temporal lobe epilepsy.

    abstract:OBJECTIVES:To examine associations between 1H magnetic resonance spectroscopic imaging (1H MRSI)-detected hippocampal creatine to N-acetylaspartate (Cr/NAA) ratios and neuropsychological measures sensitive to mesial temporal lobe function. BACKGROUND:The measurement of 1H MRSI-detected hippocampal metabolites has prov...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.53.9.2052

    authors: Martin RC,Sawrie S,Hugg J,Gilliam F,Faught E,Kuzniecky R

    更新日期:1999-12-10 00:00:00

  • Primary Sjögren's syndrome in patients with multiple sclerosis.

    abstract::The relationship between multiple sclerosis (MS) and primary Sjögren's syndrome (PSS) is ambiguous; it was suggested that some patients diagnosed with MS may instead have PSS. In a recent epidemiologic study, the prevalence of PSS was 2.7% in southern Sweden. We randomly selected 30 patients with definite MS from our ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.42.4.845

    authors: Sandberg-Wollheim M,Axéll T,Hansen BU,Henricsson V,Ingesson E,Jacobsson L,Larsson A,Lieberkind K,Manthorpe R

    更新日期:1992-04-01 00:00:00

  • The quicksilver prize: Mercury vapor poisoning aboard HMS Triumph and HMS Phipps.

    abstract::In 1810, two British ships, HMS Triumph and HMS Phipps, salvaged a large load of elemental mercury from a wrecked Spanish vessel near Cadiz, Spain. The bladders containing the mercury soon ruptured. The element spread about the ships in liquid and vapor forms. The sailors presented with neurologic compromises: tremor,...

    journal_title:Neurology

    pub_type: 历史文章,杂志文章

    doi:10.1212/01.wnl.0000118789.33171.47

    authors: Doherty MJ

    更新日期:2004-03-23 00:00:00

  • The one-and-a-half syndrome--a unilateral disorder of the pontine tegmentum: a study of 20 cases and review of the literature.

    abstract::The one-and-a-half syndrome is a clinical disorder of extraocular movements characterized by a conjugate horizontal gaze palsy in one direction plus an internuclear ophthalmoplegia in the other. The syndrome is usually due to a single unilateral lesion of the paramedian pontine reticular formation or the abducens nucl...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.33.8.971

    authors: Wall M,Wray SH

    更新日期:1983-08-01 00:00:00

  • Familial cerebellar ataxia with muscle coenzyme Q10 deficiency.

    abstract:OBJECTIVE:To describe a clinical syndrome of cerebellar ataxia associated with muscle coenzyme Q10 (CoQ10) deficiency. BACKGROUND:Muscle CoQ10 deficiency has been reported only in a few patients with a mitochondrial encephalomyopathy characterized by 1) recurrent myoglobinuria; 2) brain involvement (seizures, ataxia, ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.56.7.849

    authors: Musumeci O,Naini A,Slonim AE,Skavin N,Hadjigeorgiou GL,Krawiecki N,Weissman BM,Tsao CY,Mendell JR,Shanske S,De Vivo DC,Hirano M,DiMauro S

    更新日期:2001-04-10 00:00:00

  • A novel autosomal dominant limb-girdle muscular dystrophy (LGMD 1F) maps to 7q32.1-32.2.

    abstract::In 2001, the authors described the clinical features of a genetically distinct autosomal dominant limb-girdle muscular dystrophy (LGMD; LGMD 1F). Using a genome-wide screen with more than 400 microsatellite markers, the authors identified a novel LGMD disease locus at chromosome 7q32.1-32.2. Within this chromosomal re...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000073984.46546.4f

    authors: Palenzuela L,Andreu AL,Gàmez J,Vilà MR,Kunimatsu T,Meseguer A,Cervera C,Fernandez Cadenas I,van der Ven PF,Nygaard TG,Bonilla E,Hirano M

    更新日期:2003-08-12 00:00:00

  • Absence of genetic linkage of Charcot-Marie-Tooth disease (HMSN Ia) with chromosome 1 gene markers.

    abstract::We previously reported a large Charcot-Marie-Tooth family not linked to the Duffy blood group marker, supporting the existence of genetic heterogeneity in this neuropathy. In order to investigate the possibility of another disease locus on chromosome 1, we analyzed this family further, using DNA polymorphisms of 6 gen...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.39.6.844

    authors: Raeymaekers P,De Jonghe P,Backhovens H,Wehnert A,De Winter G,Swerts L,Gheuens J,Martin JJ,Vandenberghe A,Van Broeckhoven C

    更新日期:1989-06-01 00:00:00