HTLV-I-associated leukemia: a model for chronic retroviral diseases.

Abstract:

:Human T-lymphotropic virus type I (HTLV-I) has been associated with adult T-cell leukemia/lymphoma (ATL), a malignancy of mature CD4-positive lymphocytes, and with tropical spastic paraparesis (TSP), a demyelinating neurological syndrome. This article describes the clinical and pathological features of ATL and reviews the epidemiology of this disease and of its putative etiological agent, HTLV-I. From what is known about the molecular biology and epidemiology of HTLV-I, hypotheses on the etiology of TSP are proposed, and strategies for studying the neurological syndrome are suggested.

journal_name

Ann Neurol

journal_title

Annals of neurology

authors

Murphy EL,Blattner WA

doi

10.1002/ana.410230739

subject

Has Abstract

pub_date

1988-01-01 00:00:00

pages

S174-80

eissn

0364-5134

issn

1531-8249

journal_volume

23 Suppl

pub_type

杂志文章,评审
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    abstract:OBJECTIVE:Human immunodeficiency virus (HIV) infection of the central nervous system (CNS) is frequently associated with intrathecal immunoglobulin synthesis and cerebrospinal fluid (CSF) pleocytosis, but little is known about the B-cell response in the CSF of these patients. In this study, we investigated the relation...

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    doi:10.1002/ana.21195

    authors: Cepok S,von Geldern G,Nolting T,Grummel V,Srivastava R,Zhou D,Hartung HP,Adams O,Arendt G,Hemmer B

    更新日期:2007-11-01 00:00:00

  • Role of infection in Guillain-Barré syndrome: laboratory confirmation of herpesviruses in 41 cases.

    abstract::Serological evidence of either acute cytomegalovirus (CMV) or Epstein-Barr virus (EBV) infection was sought in a large series of patients with Guillain-Barré syndrome (GBS) and control subjects. Using an indirect immunofluorescent technique, IgM antibody directed against CMV was found in the serum of 33 of 220 GBS pat...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410090709

    authors: Dowling PC,Cook SD

    更新日期:1981-01-01 00:00:00

  • McArdle's disease: biochemical and molecular genetic studies.

    abstract::We have analyzed muscle biopsy specimens from 48 patients with biochemically proven phosphorylase deficiency (McArdle's disease) by sodium dodecylsulphate polyacrylamide gel electrophoresis (SDS-PAGE), immunoblotting, and immunotitration (enzyme-linked immunosorbent assay [ELISA]). Thirty-five of the 42 patients studi...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410240612

    authors: Servidei S,Shanske S,Zeviani M,Lebo R,Fletterick R,DiMauro S

    更新日期:1988-12-01 00:00:00

  • Kearns-Sayre syndrome with reduced plasma and cerebrospinal fluid folate.

    abstract::A young woman with Kearns-Sayre syndrome and progressive central nervous system deterioration over 15 years had decreased plasma and cerebrospinal fluid folate levels while receiving phenytoin for a seizure disorder. A muscle biopsy showed a "ragged red fiber" myopathy with reduced muscle carnitine and mitochondrial e...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410130620

    authors: Allen RJ,DiMauro S,Coulter DL,Papadimitriou A,Rothenberg SP

    更新日期:1983-06-01 00:00:00

  • Posterior hypothalamic activation in paroxysmal hemicrania.

    abstract:OBJECTIVE:Paroxysmal hemicrania (PH) is a severe, strictly unilateral headache that lasts 2 to 30 minutes, occurs more than five times daily, is associated with trigeminal autonomic symptoms, and is exquisitely responsive to indomethacin. The purpose of the study was to determine the brain structures active in PH. MET...

    journal_title:Annals of neurology

    pub_type: 临床试验,杂志文章

    doi:10.1002/ana.20763

    authors: Matharu MS,Cohen AS,Frackowiak RS,Goadsby PJ

    更新日期:2006-03-01 00:00:00

  • Natural history of multiple sclerosis.

    abstract::Multiple sclerosis (MS) is the most common idiopathic inflammatory disease of the central nervous system. The distinction between MS and other benign or fulminant inflammatory demyelinating disorders is based on quantitative, rather than qualitative, differences in chronicity and severity. Primary progressive MS may d...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.410360704

    authors: Weinshenker BG

    更新日期:1994-01-01 00:00:00

  • Antiepileptic drugs interact with folate and vitamin B12 serum levels.

    abstract:OBJECTIVE:Antiepileptic drugs (AEDs) are important for the treatment of epilepsy, psychiatric diseases, and pain syndromes. Small studies have suggested that AED treatment reduces serum levels of folate and vitamin B12. METHODS:This prospective monocenter study aimed at testing the hypothesis that AED treatment is ass...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.22229

    authors: Linnebank M,Moskau S,Semmler A,Widman G,Stoffel-Wagner B,Weller M,Elger CE

    更新日期:2011-02-01 00:00:00

  • Normal pressure hydrocephalus associated with cauda equina neurinoma.

    abstract::A 65-year-old woman with normal pressure hydrocephalus experienced improved gait and hydrocephalus following surgical resection of a cauda equina neurinoma. Fibrinogen, detected in the cerebrospinal fluid, may be involved in the pathophysiological process of normal pressure hydrocephalus. ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410270414

    authors: Ohta K,Gotoh F,Amano T,Obara K

    更新日期:1990-04-01 00:00:00

  • Alzheimer's disease: a study of epidemiological aspects.

    abstract::A case-control study was performed to determine the possible roles of various environmental factors, prior illnesses, drug use, and personal habits in the development of Alzheimer's disease. Such information was collected from 40 patients with onset of dementia prior to age 70 and from 80 community control subjects ma...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410150406

    authors: Heyman A,Wilkinson WE,Stafford JA,Helms MJ,Sigmon AH,Weinberg T

    更新日期:1984-04-01 00:00:00

  • FK506-induced neurotoxicity in liver transplantation.

    abstract::We report FK506-induced neurotoxicity in 14 of 44 consecutive patients following orthoptic liver transplantation. In 10 of these 14 patients, postural hand tremors were found in the first weeks following surgery, transient apraxia of speech in 3, and generalized tonic-clonic seizures were noted in 2 patients. Other ma...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410350422

    authors: Wijdicks EF,Wiesner RH,Dahlke LJ,Krom RA

    更新日期:1994-04-01 00:00:00

  • Seizures induced by thinking.

    abstract::A patient with generalized convulsions noted that seizures were reliably precipitated by mental arithmetic. The interictal electroencephalogram revealed only a mild, diffuse, nonspecific disturbance, but bursts of generalized epileptiform activity with no obvious clinical expression accompanied efforts at mental arith...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410110609

    authors: Wilkins AJ,Zifkin B,Andermann F,McGovern E

    更新日期:1982-06-01 00:00:00

  • Altered excitatory and inhibitory amino acid receptor binding in hippocampus of patients with temporal lobe epilepsy.

    abstract::We examined binding to excitatory amino acid and inhibitory amino acid receptors in frozen hippocampal sections prepared from surgical specimens resected from 8 individuals with medically refractory temporal lobe epilepsy. The excitatory receptors studied included N-methyl-D-aspartate (NMDA), strychnine-insensitive gl...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410290513

    authors: McDonald JW,Garofalo EA,Hood T,Sackellares JC,Gilman S,McKeever PE,Troncoso JC,Johnston MV

    更新日期:1991-05-01 00:00:00

  • Clinical and genetic spectrum of pyruvate dehydrogenase deficiency: dihydrolipoamide acetyltransferase (E2) deficiency.

    abstract::Pyruvate dehydrogenase deficiency is a major cause of primary lactic acidosis and neurological dysfunction in infancy and early childhood. Most cases are caused by mutations in the X-linked gene for the E1alpha subunit of the complex. Mutations in DLAT, the gene encoding dihydrolipoamide acetyltransferase, the E2 core...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.20550

    authors: Head RA,Brown RM,Zolkipli Z,Shahdadpuri R,King MD,Clayton PT,Brown GK

    更新日期:2005-08-01 00:00:00

  • Can semiology predict psychogenic nonepileptic seizures? A prospective study.

    abstract:OBJECTIVE:Reducing health and economic burdens from diagnostic delay of psychogenic nonepileptic seizures (PNES) requires prompt referral for video electroencephalography (VEEG) monitoring, the diagnostic gold standard. Practitioners make VEEG referrals when semiology suggests PNES, although few semiological signs are ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.22345

    authors: Syed TU,LaFrance WC Jr,Kahriman ES,Hasan SN,Rajasekaran V,Gulati D,Borad S,Shahid A,Fernandez-Baca G,Garcia N,Pawlowski M,Loddenkemper T,Amina S,Koubeissi MZ

    更新日期:2011-06-01 00:00:00

  • Cofactors of mitochondrial enzymes attenuate copper-induced death in vitro and in vivo.

    abstract::Copper toxicity contributes to neuronal death in Wilson's disease and has been speculatively linked to the pathogenesis of Alzheimer's and prion diseases. We examined copper-induced neuronal death with the goal of developing neuroprotective strategies. Copper catalyzed an increase in hydroxyl radical generation in sol...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.10276

    authors: Sheline CT,Choi EH,Kim-Han JS,Dugan LL,Choi DW

    更新日期:2002-08-01 00:00:00

  • Gut Microbiome Signatures of Risk and Prodromal Markers of Parkinson Disease.

    abstract:OBJECTIVE:Alterations of the gut microbiome in Parkinson disease (PD) have been repeatedly demonstrated. However, little is known about whether such alterations precede disease onset and how they relate to risk and prodromal markers of PD. We investigated associations of these features with gut microbiome composition. ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.25788

    authors: Heinzel S,Aho VTE,Suenkel U,von Thaler AK,Schulte C,Deuschle C,Paulin L,Hantunen S,Brockmann K,Eschweiler GW,Maetzler W,Berg D,Auvinen P,Scheperjans F

    更新日期:2020-08-01 00:00:00

  • An evidence-based causative classification system for acute ischemic stroke.

    abstract::Regular, evidence-based assignment of patients to etiologic stroke categories is essential to enable valid comparison among studies. We designed an algorithm (SSS-TOAST) that incorporated recent advances in stroke imaging and epidemiology to identify the most probable TOAST category in the presence of evidence for mul...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.20617

    authors: Ay H,Furie KL,Singhal A,Smith WS,Sorensen AG,Koroshetz WJ

    更新日期:2005-11-01 00:00:00

  • Toward an understanding of the role of glutamate in experimental parkinsonism: agonist-sensitive sites in the basal ganglia.

    abstract::Increased glutamatergic transmission in the basal ganglia is implicated in the pathophysiology of Parkinson's disease. However, the mechanisms by which activation of glutamate receptors produce parkinsonism are unknown. Therefore, we examined whether the glutamate agonists N-methyl-D-aspartate (NMDA), alpha-amino-3-hy...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410340413

    authors: Klockgether T,Turski L

    更新日期:1993-10-01 00:00:00

  • Genome-wide variant by serum urate interaction in Parkinson's disease.

    abstract:OBJECTIVE:Serum urate levels have been associated with risk for and progression of Parkinson's disease (PD). Urate-related compounds are therapeutic candidates in neuroprotective efforts to slow PD progression. A urate-elevating agent is currently under investigation as a potential disease-modifying strategy in people ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.24504

    authors: Nazeri A,Roostaei T,Sadaghiani S,Chakravarty MM,Eberly S,Lang AE,Voineskos AN

    更新日期:2015-11-01 00:00:00

  • Cognitive impairment in lacunar strokes: the SPS3 trial.

    abstract:OBJECTIVE:Lacunar strokes are a leading cause of cognitive impairment and vascular dementia. However, adequate characterization of cognitive impairment is lacking. The aim of this study was to estimate the prevalence and characterize the neuropsychological impairment in lacunar stroke patients. METHODS:All English-spe...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.23733

    authors: Jacova C,Pearce LA,Costello R,McClure LA,Holliday SL,Hart RG,Benavente OR

    更新日期:2012-09-01 00:00:00

  • Abnormal unloading reflex in a patient with infarction of the medial lemniscus.

    abstract::The unloading reflex was measured in the intrinsic muscles of the hand. By removing various fractions of the load on the muscles, we determined the size of the electromyographic response as a function of the change in the external force. This technique was applied to both hands of a patient with a pontine lesion who h...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410130309

    authors: Angel RW,Goldstein M

    更新日期:1983-03-01 00:00:00

  • Propagation of focal motor seizures in the pubescent monkey.

    abstract::The rate of local cerebral glucose utilization was determined for quantification of energy metabolism in macrostructures of the sensorimotor system during propagation of focal motor seizures in 24-month-old monkeys. The rate was measured in 4 control animals and in 4 monkeys each with seizures limited to the contralat...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410070304

    authors: Caveness WF,Kato M,Malamut BL,Hosokawa S,Wakisaka S,O'Neill RR

    更新日期:1980-03-01 00:00:00

  • Potential of gene therapy for pediatric neurotransmitter diseases: lessons from Parkinson's disease.

    abstract::Gene therapy methods have continued to develop rapidly, and many initial limitations that hampered clinical application have been overcome. Thus serious consideration of clinical application of gene therapy is warranted for selected disorders in which the pathogenesis is well defined. Parkinson's disease has been the ...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.10654

    authors: Kang UJ,Nakamura K

    更新日期:2003-01-01 00:00:00

  • Acute conduction block associated with experimental antiserum-mediated demyelination of peripheral nerve.

    abstract::Intraneural injection of antisera from rabbits with high antigalactocerebroside antibody levels into rat sciatic nerve produced acute nerve conduction block. This was first apparent in some motor axons between 30 and 60 minutes after injection and progressed to completion within 2 to 4 hours. Concurrent morphological ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410110506

    authors: Sumner AJ,Saida K,Saida T,Silberberg DH,Asbury AK

    更新日期:1982-05-01 00:00:00

  • Caloric-induced nystagmus with isoelectric electroencephalogram.

    abstract::Caloric vestibular testing induced nystagmus in a patient with an isoelectric electroencephalogram after cardiopulmonary arrest. This has been demonstrated previously in patients in a chronic persistent vegetative state with intact brainstem reflexes, but never in a patient with an isoelectric electroencephalogram. An...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410210118

    authors: Nayyar M,Strobos RJ,Singh BM,Brown-Wagner M,Pucillo A

    更新日期:1987-01-01 00:00:00

  • Role of CD8+ CD25+ Foxp3+ regulatory T cells in multiple sclerosis.

    abstract:OBJECTIVE:The objective of this study was to investigate the role of CD8+ CD25+ FoxP3+ cells during the course of multiple sclerosis (MS). METHODS:Peripheral blood and cerebrospinal fluid (CSF) CD8+ T-cell clones (TCCs) recognizing autoreactive CD4+ T cells were isolated from 20 MS patients during exacerbations, 15 pa...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.21944

    authors: Correale J,Villa A

    更新日期:2010-05-01 00:00:00

  • Rapid clearance of human immunodeficiency virus type 1 from ventricular cerebrospinal fluid during antiretroviral treatment.

    abstract::To understand the pathogenesis of human immunodeficiency virus-induced neuropathology, it is critical to know the dynamics of viral replication in the central nervous system. Viral decay kinetics were mathematically analyzed from multiple serial specimens of ventricular cerebrospinal fluid and plasma during antiretrov...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:

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    更新日期:2000-06-01 00:00:00

  • Short- and long-term survival and function of unilateral intrastriatal dopaminergic grafts in Parkinson's disease.

    abstract::Six patients with Parkinson's disease were followed for 10 to 72 months after human embryonic mesencephalic tissue from four to seven donors was grafted unilaterally into the putamen (4 patients) or putamen plus caudate (2 patients). After 8 to 12 months, positron emission tomography showed a 68% increase of 6-L-[18F]...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410420115

    authors: Wenning GK,Odin P,Morrish P,Rehncrona S,Widner H,Brundin P,Rothwell JC,Brown R,Gustavii B,Hagell P,Jahanshahi M,Sawle G,Björklund A,Brooks DJ,Marsden CD,Quinn NP,Lindvall O

    更新日期:1997-07-01 00:00:00

  • Dravet syndrome patient-derived neurons suggest a novel epilepsy mechanism.

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    pub_type: 杂志文章

    doi:10.1002/ana.23897

    authors: Liu Y,Lopez-Santiago LF,Yuan Y,Jones JM,Zhang H,O'Malley HA,Patino GA,O'Brien JE,Rusconi R,Gupta A,Thompson RC,Natowicz MR,Meisler MH,Isom LL,Parent JM

    更新日期:2013-07-01 00:00:00

  • The influence of nuclear background on the biochemical expression of 3460 Leber's hereditary optic neuropathy.

    abstract::The role of mitochondrial DNA (mtDNA) mutations in the pathogenesis of Leber's hereditary optic neuropathy (LHON) has yet to be characterized. Several clinical features of the disease imply that nuclear genes might also be involved in its expression. We have confirmed the presence of a severe NADH:coenzyme Q1 reductas...

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    pub_type: 杂志文章

    doi:10.1002/ana.410440208

    authors: Cock HR,Tabrizi SJ,Cooper JM,Schapira AH

    更新日期:1998-08-01 00:00:00