Pearls and oy-sters: carotid dissection with normal arterial lumen.

Abstract:

:Clinical presentation of carotid artery dissection (CAD) is variable, including acute or subacute headache, cervical pain, or focal neurologic deficit that occurs spontaneously, after a high-speed neck manipulation, or trauma. Isolated lower cranial nerve palsy in carotid dissection is uncommon.

journal_name

Neurology

journal_title

Neurology

authors

Pongmoragot J,Bharatha A,Saposnik G

doi

10.1212/WNL.0b013e31828727e8

subject

Has Abstract

pub_date

2013-03-12 00:00:00

pages

e115-7

issue

11

eissn

0028-3878

issn

1526-632X

pii

80/11/e115

journal_volume

80

pub_type

杂志文章
  • Relationship between Meige syndrome and alpha-methyldopa-induced parkinsonism.

    abstract::We studied two patients with Meige syndrome who developed alpha-methyldopa-induced parkinsonism. Opposite responses of parkinsonian and dystonic symptoms to antiparkinson drugs in some cases suggest a functionally reciprocal relationship between these disorders. ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.35.11.1668

    authors: Sechi GP,Demontis G,Rosati G

    更新日期:1985-11-01 00:00:00

  • Epilepsy after brain infection in adults: A register-based population-wide study.

    abstract:OBJECTIVE:To describe risk and risk factors of epilepsy after hospitalization for brain infection in adults in Sweden. METHODS:This was a matched retrospective cohort study based on the comprehensive National Patient and Cause of Death Registers. All individuals age >18 without prior epilepsy who received inpatient ca...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000010954

    authors: Zelano J,Westman G

    更新日期:2020-12-15 00:00:00

  • Clinical manifestations of chronic thiamine deficiency in rhesus monkey.

    abstract::In the course of multiple episodes of thiamine deficiency in the rhesus monkey, the triad of anorexia, apathy, and hind limb weakness is the earliest clinical manifestation. In later episodes, nystagmus, abducens paresis, midline ataxia, dysmetria, and congestive heart failure are also seen. With the exception of dysm...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.27.3.239

    authors: Mesulam MM,Van Hoesen GW,Butters N

    更新日期:1977-03-01 00:00:00

  • The cerebrospinal fluid production rate is reduced in dementia of the Alzheimer's type.

    abstract:OBJECTIVE:To evaluate the production rate of CSF in patients with differing disease states. METHODS:The authors measured the production rate of CSF in three groups of patients: five patients with PD below age 60 (aged 51 +/- 4 years, mean +/- SD), nine with PD over age 60 (aged 69 +/- 6 years, mean +/- SD), and seven ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.57.10.1763

    authors: Silverberg GD,Heit G,Huhn S,Jaffe RA,Chang SD,Bronte-Stewart H,Rubenstein E,Possin K,Saul TA

    更新日期:2001-11-27 00:00:00

  • Time course of frontal somatosensory evoked potentials. Relation to L-dopa plasma levels and motor performance in PD.

    abstract:OBJECTIVE:To verify whether the change in L-dopa plasma levels after a single dose of carbidopa/L-dopa 50/200 (controlled-release) transiently modifies frontal components of somatosensory evoked potentials (SEPs) in patients with PD in parallel with improvement of motor performance. BACKGROUND:Apomorphine, a potent do...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.53.7.1451

    authors: Ulivelli M,Rossi S,Pasqualetti P,Rossini PM,Ghiglieri O,Passero S,Battistini N

    更新日期:1999-10-22 00:00:00

  • The treatment of postprandial hypotension in autonomic failure with 3,4-DL-threo-dihydroxyphenylserine.

    abstract::Postprandial hypotension occurs commonly in patients with autonomic failure and may be due to attenuation of the normal sympathetic nervous system activation in response to meal ingestion. In a randomized, double-blind, placebo-controlled study, we investigated the therapeutic effect of the norepinephrine precursor 3,...

    journal_title:Neurology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1212/wnl.47.6.1414

    authors: Freeman R,Young J,Landsberg L,Lipsitz L

    更新日期:1996-12-01 00:00:00

  • Multiple cerebral hemorrhages in HTLV-I-associated myelopathy.

    abstract::We describe a 66-year-old woman with long-standing HTLV-I-associated myelopathy who developed multiple parenchymal hemorrhages and whose angiogram suggested cerebral vasculitis. After cyclophosphamide and glucocorticoid therapy, both her acute deficits and chronic paraparesis improved. HTLV-I may be an etiologic agent...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.43.2.412

    authors: Smith D,Lucas S,Jacewicz M

    更新日期:1993-02-01 00:00:00

  • Non-neoplastic pineal cysts.

    abstract::We identified 53 patients with non-neoplastic cysts of the pineal gland. In contrast to patients with pineal neoplasms, pineal cysts are usually asymptomatic. They infrequently obstruct the aqueduct to cause hydrocephalus or compress the tectum to produce the neuro-ophthalmologic signs of dorsal midbrain dysfunction. ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.41.7.1034

    authors: Fetell MR,Bruce JN,Burke AM,Cross DT,Torres RA,Powers JM,Stein BM

    更新日期:1991-07-01 00:00:00

  • Magnetic resonance imaging at the demyelinative foci in chronic inflammatory demyelinating polyneuropathy.

    abstract::Using MRI, we investigated the morphology and blood-nerve barrier function of the peripheral nerve trunk in 10 patients with chronic inflammatory demyelinating polyneuropathy (CIDP). Eight patients had a focal demyelinative segment in the median or ulnar nerve trunk that was defined by conduction block or abnormal tem...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.48.4.874

    authors: Kuwabara S,Nakajima M,Matsuda S,Hattori T

    更新日期:1997-04-01 00:00:00

  • Applying the ATN scheme in a memory clinic population: The ABIDE project.

    abstract:OBJECTIVE:To apply the ATN scheme to memory clinic patients, to assess whether it discriminates patient populations with specific features. METHODS:We included 305 memory clinic patients (33% subjective cognitive decline [SCD]: 60 ± 9 years, 61% M; 19% mild cognitive impairment [MCI]: 68 ± 9 years, 68% M; 48% dementia...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000008361

    authors: Altomare D,de Wilde A,Ossenkoppele R,Pelkmans W,Bouwman F,Groot C,van Maurik I,Zwan M,Yaqub M,Barkhof F,van Berckel BN,Teunissen CE,Frisoni GB,Scheltens P,van der Flier WM

    更新日期:2019-10-22 00:00:00

  • Atherosclerotic carotid artery disease in patients with retinal ischemic syndromes.

    abstract::The extracranial carotid systems of 105 patients with retinal ischemia were examined using B-mode ultrasonography with integrated pulsed Doppler. Sixty-four patients had amaurosis fugax (AF), 17 central retinal artery occlusions (CRAO), and 21 branch retinal artery occlusions (BRAO). The prevalence of carotid stenosis...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.38.6.858

    authors: Chawluk JB,Kushner MJ,Bank WJ,Silver FL,Jamieson DG,Bosley TM,Conway DJ,Cohen D,Savino PJ

    更新日期:1988-06-01 00:00:00

  • Diagnostic accuracy of confrontation visual field tests.

    abstract:OBJECTIVE:To determine the diagnostic accuracy of confrontation visual field testing and to compare the accuracy of confrontation tests both individually and in combination. METHODS:Patients were prospectively recruited from ophthalmology clinics over a 6-month period. All patients underwent SITA-standard 24-2 Humphre...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e3181d90017

    authors: Kerr NM,Chew SS,Eady EK,Gamble GD,Danesh-Meyer HV

    更新日期:2010-04-13 00:00:00

  • Survival and outcome after endotracheal intubation for acute stroke.

    abstract:OBJECTIVE:To assess survival and functional outcome in patients endotracheally intubated after ischemic stroke (IS) or spontaneous intracerebral hemorrhage (ICH). BACKGROUND:Endotracheal intubation is both a necessary life support intervention and a measure of severity in IS or ICH. Knowledge of associated clinical va...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.52.7.1374

    authors: Bushnell CD,Phillips-Bute BG,Laskowitz DT,Lynch JR,Chilukuri V,Borel CO

    更新日期:1999-04-22 00:00:00

  • Paraparesis in hereditary multiple exostoses: case report.

    abstract::The authors report a case of hereditary multiple exostoses (HME) with neurologic complications, and review the literature. A 23-year-old man exhibited a worsening spastic paraparesis with sphincter dysfunction. The cranial nerves and the exteroceptive and deep sensations were apparently undamaged. The family history, ...

    journal_title:Neurology

    pub_type: 杂志文章,评审

    doi:10.1212/wnl.29.7.973

    authors: Ferrari G,Taddei L,Vivenza C,Rossi G

    更新日期:1979-07-01 00:00:00

  • 3-Methylglutaconic aciduria type I redefined: a syndrome with late-onset leukoencephalopathy.

    abstract:OBJECTIVE:3-Methylglutaconic aciduria type I is a rare inborn error of leucine catabolism. It is thought to present in childhood with nonspecific symptoms; it was even speculated to be a nondisease. The natural course of disease is unknown. METHODS:This is a study on 10 patients with 3-methylglutaconic aciduria type I...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e3181f39a8a

    authors: Wortmann SB,Kremer BH,Graham A,Willemsen MA,Loupatty FJ,Hogg SL,Engelke UF,Kluijtmans LA,Wanders RJ,Illsinger S,Wilcken B,Cruysberg JR,Das AM,Morava E,Wevers RA

    更新日期:2010-09-21 00:00:00

  • Serum and CSF vitamin A concentrations in idiopathic intracranial hypertension.

    abstract:BACKGROUND:Elevated serum retinol, CSF retinol, and serum retinol binding protein (RBP) levels have been found in some patients with idiopathic intracranial hypertension (IIH), but serum and CSF retinol levels have not been studied in matched serum and CSF samples in patients with IIH. OBJECTIVE:To determine whether s...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.WNL.0000163556.31080.98

    authors: Tabassi A,Salmasi AH,Jalali M

    更新日期:2005-06-14 00:00:00

  • Body mass index and the risk of Parkinson disease.

    abstract:OBJECTIVE:To examine the association between body mass index (BMI) and the risk of Parkinson disease (PD). METHODS:Study cohorts included 22,367 Finnish men and 23,439 women 25 to 59 years of age without a history of PD at baseline. Hazards ratios (HRs) of incident PD were estimated for different levels of BMI. RESUL...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000247052.18422.e5

    authors: Hu G,Jousilahti P,Nissinen A,Antikainen R,Kivipelto M,Tuomilehto J

    更新日期:2006-12-12 00:00:00

  • A prion protein missense variant is integrated in kuru plaque cores in patients with Gerstmann-Sträussler syndrome.

    abstract::Kuru plaques are the pathologic hallmark in Gerstmann-Sträussler syndrome (GSS). To demonstrate that prion protein (PrP) is a component of kuru plaque cores, we fractionated and sequenced kuru plaque core derived peptides, following digestion with Achromobacter lyticus protease I. We identified 3 PrP-derived peptides ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.41.2_part_1.306

    authors: Kitamoto T,Yamaguchi K,Doh-ura K,Tateishi J

    更新日期:1991-02-01 00:00:00

  • Mitochondrial DNA haplogroups and mutations in children with acquired central demyelination.

    abstract:OBJECTIVE:We investigated mitochondrial DNA (mtDNA) variants in children with a first episode of acquired demyelinating syndromes (PD-ADS) of the CNS and their relationship to disease phenotype, including subsequent diagnosis of multiple sclerosis (MS). METHODS:This exploratory analysis included the initial 213 childr...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e31820ee1bb

    authors: Venkateswaran S,Zheng K,Sacchetti M,Gagne D,Arnold DL,Sadovnick AD,Scherer SW,Banwell B,Bar-Or A,Simon DK,Canadian Pediatric Demyelinating Disease Network.

    更新日期:2011-03-01 00:00:00

  • Methyl bromide intoxication: neurologic features, including simulation of Reye syndrome.

    abstract::Three family members intoxicated with methyl bromide presented with a variety of neuropsychiatric manifestations including coma, severe status epilepticus, hyporeflexia, and acute psychosis. The simulation of Reye syndrome in the child emphasizes the need for careful toxicologic screening of all children presenting wi...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.27.10.959

    authors: Shield LK,Coleman TL,Markesbery WR

    更新日期:1977-10-01 00:00:00

  • Specificity of the fivefold increase in AD in mothers of adults with Down syndrome.

    abstract:BACKGROUND:In a previous study, the authors found that the risk of AD among mothers who were 35 years or younger when their children with Down syndrome (DS) were born was five times that of mothers of children with other forms of mental retardation. The current study investigated the specificity of the familial aggrega...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.57.6.979

    authors: Schupf N,Kapell D,Nightingale B,Lee JH,Mohlenhoff J,Bewley S,Ottman R,Mayeux R

    更新日期:2001-09-25 00:00:00

  • Genetic susceptibility to Parkinson's disease.

    abstract::Genetic factors clearly cause Lewy-body Parkinson's disease (PD) in a subset of autosomal-dominant families. However, most cases of PD are sporadic. The two most likely models of four discussed for sporadic PD are the reduced penetrance model and the multifactorial model. Sporadic PD is likely to be caused by the comb...

    journal_title:Neurology

    pub_type: 杂志文章,评审

    doi:10.1212/wnl.41.5_suppl_2.82

    authors: Johnson WG

    更新日期:1991-05-01 00:00:00

  • Acute hydrocephalus in nonketotic hyperglycinemia.

    abstract::We present four patients with typical neonatal onset non-ketotic hyperglycinemia (NKH) who developed hydrocephalus requiring shunting in early infancy. Brain imaging revealed acute hydrocephalus, a megacisterna magna or posterior fossa cyst, pronounced atrophy of the white matter, and an extremely thin corpus callosum...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.54.3.754

    authors: Van Hove JL,Kishnani PS,Demaerel P,Kahler SG,Miller C,Jaeken J,Rutledge SL

    更新日期:2000-02-08 00:00:00

  • A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiency.

    abstract::The authors describe a novel pathogenic G5540A transition in the mitochondrial transfer RNA (tRNA)Trp gene of a sporadic encephalomyopathy characterized by spinocerebellar ataxia. Clinical features also included neurosensorial deafness, peripheral neuropathy, and dementia. Biochemistry revealed a severe reduction of c...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.54.8.1693

    authors: Silvestri G,Mongini T,Odoardi F,Modoni A,deRosa G,Doriguzzi C,Palmucci L,Tonali P,Servidei S

    更新日期:2000-04-25 00:00:00

  • Upholding professionalism: the disciplinary process of the American Academy of Neurology.

    abstract:OBJECTIVE:To review the disciplinary process by which the American Academy of Neurology (AAN) enforces its formalized standards of professional conduct. METHODS:We reviewed the AAN's Disciplinary Action Policy. We tracked the elapsed time from receipt to final decision of all allegations ("complaints") of improper con...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e318202014e

    authors: Hutchins JC,Sagsveen MG,Larriviere D

    更新日期:2010-12-14 00:00:00

  • A novel mitochondrial tRNAPhe mutation causes MERRF syndrome.

    abstract::A woman with typical features of myoclonic epilepsy with ragged red fibers (MERRF) had a novel heteroplasmic mutation (G611A) in the mitochondrial DNA tRNA phenylalanine gene. The mutation was heteroplasmic (91%) in muscle but undetectable in accessible tissues from the patient and her maternal relatives. Single-fiber...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000127608.48406.f1

    authors: Mancuso M,Filosto M,Mootha VK,Rocchi A,Pistolesi S,Murri L,DiMauro S,Siciliano G

    更新日期:2004-06-08 00:00:00

  • Detection of cortical neuron loss in motor neuron disease by proton magnetic resonance spectroscopic imaging in vivo.

    abstract::We performed proton magnetic resonance spectroscopic imaging (1H-MRSI) in patients with motor neuron disease (MND) to evaluate the distribution and extent of cortical neuron damage or loss as reflected by decreased N-acetyl (NA) to creatine (Cr) resonance intensity ratios. We examined premotor (superior frontal gyrus)...

    journal_title:Neurology

    pub_type: 临床试验,杂志文章

    doi:10.1212/wnl.44.10.1933

    authors: Pioro EP,Antel JP,Cashman NR,Arnold DL

    更新日期:1994-10-01 00:00:00

  • B and T lymphocytes in man. III. B, t, and "null" lymphocytes in multiple sclerosis.

    abstract::T, B, and "null" lymphocytes were determined in peripheral blood obtained from 24 control subjects and 15 multiple sclerosis patients. The total number of lymphocytes and T lymphocytes were reduced significantly in multiple sclerosis patients as compared with those of controls. Although the percentage of B lymphocytes...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.26.10.997

    authors: Reddy MM,Goh KO

    更新日期:1976-10-01 00:00:00

  • Differential effects of beta and gamma interferons on expression of major histocompatibility complex antigens and intercellular adhesion molecule-1 in cultured fetal human astrocytes.

    abstract::We investigated the modulatory effects of human interferon beta (IFN-beta) and gamma (IFN-gamma) on expression of class I and II major histocompatibility complex (MHC) antigens and intercellular adhesion molecule-1 (ICAM-1) in fetal human astrocytes in culture using flow cytometry and immunocytochemistry. Under the ba...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.45.2.367

    authors: Satoh J,Paty DW,Kim SU

    更新日期:1995-02-01 00:00:00

  • Childhood absence epilepsy: poor attention is more than seizures.

    abstract::Dr. Masur and colleagues(1) from the Childhood Absence Epilepsy Study Group tried to answer a few important questions regarding childhood absence epilepsy (CAE) in their article "Pretreatment cognitive deficits and treatment effects on attention in childhood absence epilepsy." First, they wanted to know whether childr...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000436060.67147.25

    authors: Thio LL

    更新日期:2013-10-29 00:00:00