Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy.

Abstract:

:We analyzed the prion protein gene (PRNP) region in patients with transmissible spongiform encephalopathy associated with the PRNP D178N mutation. The results suggest that the D178N chromosomes had independent origins in each affected pedigree or apparently sporadic case. A de novo spontaneous PRNP mutation was observed. We provide evidence that hereditary and apparently sporadic transmissible spongiform encephalopathy cases associated with the D178N mutation result from multiple recurrent mutational events.

journal_name

Ann Neurol

journal_title

Annals of neurology

authors

Dagvadorj A,Petersen RB,Lee HS,Cervenakova L,Shatunov A,Budka H,Brown P,Gambetti P,Goldfarb LG

doi

10.1002/ana.10267

keywords:

subject

Has Abstract

pub_date

2002-09-01 00:00:00

pages

355-9

issue

3

eissn

0364-5134

issn

1531-8249

journal_volume

52

pub_type

杂志文章
  • Interleukin-6 genotype and risk for cerebral palsy in term and near-term infants.

    abstract:OBJECTIVE:Chorioamnionitis is associated with increased risk for cerebral palsy (CP) in term infants. A functional polymorphism in the interleukin-6 (IL-6) gene has been implicated in newborn brain injury. We studied whether the IL-6 -174 G/C polymorphism confers increased risk for CP in term infants. METHODS:This pop...

    journal_title:Annals of neurology

    pub_type: 杂志文章,随机对照试验

    doi:10.1002/ana.21766

    authors: Wu YW,Croen LA,Torres AR,Van De Water J,Grether JK,Hsu NN

    更新日期:2009-11-01 00:00:00

  • A new mitochondrial DNA mutation associated with progressive dementia and chorea: a clinical, pathological, and molecular genetic study.

    abstract::A novel mitochondrial DNA transfer RNA mutation at position 5549 was identified in a patient with dementia, chorea, cerebellar ataxia, deafness, and peripheral neuropathy in the absence of clinical myopathy. Muscle biopsy specimens showed ragged red and cytochrome oxidase-negative fibers, and reduced complex I activit...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410370317

    authors: Nelson I,Hanna MG,Alsanjari N,Scaravilli F,Morgan-Hughes JA,Harding AE

    更新日期:1995-03-01 00:00:00

  • Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene.

    abstract::We report the first molecular defect in an NADH-dehydrogenase gene presenting as isolated myopathy. The proband had lifelong exercise intolerance but no weakness. A muscle biopsy showed cytochrome c oxidase (COX)-positive ragged-red fibers (RRFs), and analysis of the mitochondrial enzymes revealed complex I deficiency...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/1531-8249(199906)45:6<820::aid-ana22>3.0.c

    authors: Andreu AL,Tanji K,Bruno C,Hadjigeorgiou GM,Sue CM,Jay C,Ohnishi T,Shanske S,Bonilla E,DiMauro S

    更新日期:1999-06-01 00:00:00

  • Changes in excitability of motor cortical circuitry in patients with Parkinson's disease.

    abstract::Using the technique of transcranial magnetic stimulation over the motor areas of cortex and recording electromyographic (EMG) responses from the first dorsal interosseous muscle, we measured the excitability of corticocortical inhibitory circuits at rest using a double pulse paradigm, in 11 patients with Parkinson's d...

    journal_title:Annals of neurology

    pub_type: 临床试验,杂志文章

    doi:10.1002/ana.410370208

    authors: Ridding MC,Inzelberg R,Rothwell JC

    更新日期:1995-02-01 00:00:00

  • Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants.

    abstract:OBJECTIVE:The relationship between genetic variation in the T-type calcium channel gene CACNA1H and childhood absence epilepsy is well established. The purpose of this study was to investigate the range of epilepsy syndromes for which CACNA1H variants may contribute to the genetic susceptibility architecture and determ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.21169

    authors: Heron SE,Khosravani H,Varela D,Bladen C,Williams TC,Newman MR,Scheffer IE,Berkovic SF,Mulley JC,Zamponi GW

    更新日期:2007-12-01 00:00:00

  • Gene delivery of neurturin to putamen and substantia nigra in Parkinson disease: A double-blind, randomized, controlled trial.

    abstract:OBJECTIVE:A 12-month double-blind sham-surgery-controlled trial assessing adeno-associated virus type 2 (AAV2)-neurturin injected into the putamen bilaterally failed to meet its primary endpoint, but showed positive results for the primary endpoint in the subgroup of subjects followed for 18 months and for several seco...

    journal_title:Annals of neurology

    pub_type: 杂志文章,多中心研究,随机对照试验

    doi:10.1002/ana.24436

    authors: Warren Olanow C,Bartus RT,Baumann TL,Factor S,Boulis N,Stacy M,Turner DA,Marks W,Larson P,Starr PA,Jankovic J,Simpson R,Watts R,Guthrie B,Poston K,Henderson JM,Stern M,Baltuch G,Goetz CG,Herzog C,Kordower JH,Alt

    更新日期:2015-08-01 00:00:00

  • Cerebellar blood flow and metabolism in cerebral hemisphere infarction.

    abstract::Positron emission tomography was used to study the effect of supratentorial infarction on cerebellar metabolic rate for oxygen and cerebellar blood flow. In a control group of patients, the mean cerebellar metabolic rate for oxygen was 2.97 +/- 0.11 (standard error of the mean [SEM] ) ml-1 . min-1 . hg-1 and mean cere...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410140203

    authors: Martin WR,Raichle ME

    更新日期:1983-08-01 00:00:00

  • Absence of REM and altered NREM sleep in patients with spinocerebellar degeneration and slow saccades.

    abstract::The pontine tegmentum contains the neurons responsible for generation of saccadic eye movements and certain phases of sleep. We studied two genetically unrelated patients with spinocerebellar degeneration and slow saccadic eye movements. Multiple all-night sleep studies in both patients disclosed absence of REM and st...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410070312

    authors: Osorio I,Daroff RB

    更新日期:1980-03-01 00:00:00

  • Isoflurane prevents acquired epilepsy in rat models of temporal lobe epilepsy.

    abstract:OBJECTIVE:Acquired epilepsy is a devastating long-term risk of various brain insults, including trauma, stroke, infections, and status epilepticus (SE). There is no preventive treatment for patients at risk. Attributable to the complex alterations involved in epileptogenesis, it is likely that multitargeted approaches ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.24804

    authors: Bar-Klein G,Klee R,Brandt C,Bankstahl M,Bascuñana P,Töllner K,Dalipaj H,Bankstahl JP,Friedman A,Löscher W

    更新日期:2016-12-01 00:00:00

  • Increased sodium plus potassium adenosine triphosphatase activity in erythrocyte membranes in Huntington's disease.

    abstract::Dopa-decarboxylase, acetylcholinesterase, sodium plus potassium stimulated adenosine triphosphatase (Na+ + K+-ATPase), and membrane-bound protein kinase were compared in the erythrocytes of patients with Huntington's disease and normal controls. All these enzymes also exist in the basal ganglia. The Na+ +K+-ATPase lev...

    journal_title:Annals of neurology

    pub_type: 临床试验,杂志文章

    doi:10.1002/ana.410040111

    authors: Butterfield DA,Oeswein JQ,Prunty ME,Hisle KC,Markesbery WR

    更新日期:1978-07-01 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

  • Peripheral nerve function and metabolic control in diabetes mellitus.

    abstract::Measurement of conduction velocity along the H reflex arc was used to study sensorimotor peripheral nerve function in diabetic patients during short- and long-term improvement of hyperglycemia. In ten type I diabetics a slight (p less than 0.05) conduction increase occurred after 6 hours of normal glycemia induced by ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410160204

    authors: Troni W,Carta Q,Cantello R,Caselle MT,Rainero I

    更新日期:1984-08-01 00:00:00

  • Tourette's syndrome: a neurochemical analysis of postmortem cortical brain tissue.

    abstract::Postmortem frontal, temporal, and occipital regions of the brain from adult patients who had a diagnosis of Tourette's syndrome were analyzed for neurochemical alterations. In 3 of 4 TS-affected brains, the concentration of adenosine 3',5'-monophosphate (cyclic AMP) was reduced in all brain regions evaluated. This dim...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410270415

    authors: Singer HS,Hahn IH,Krowiak E,Nelson E,Moran T

    更新日期:1990-04-01 00:00:00

  • The localizing value of depth electroencephalography in 32 patients with refractory epilepsy.

    abstract::Clinical seizure manifestations, physical examination, radiological studies, neuropsychological tests, and scalp and depth electroencephalographic (EEG) studies were done to localize seizure foci in 32 patients, 23 of whom have undergone surgery with more than one year of follow-up. Of 16 patients with unlocalized sca...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410120306

    authors: Spencer SS,Spencer DD,Williamson PD,Mattson RH

    更新日期:1982-09-01 00:00:00

  • Pediatric Leigh Syndrome: Neuroimaging Features and Genetic Correlations.

    abstract::The neurodiagnostic criteria of Leigh syndrome have not yet been clearly redefined based on the expanding of molecular etiologies. We aimed to analyze 20 years of clinical, genetic, and magnetic resonance studies from our Leigh syndrome cohort to provide a detailed description of central nervous system lesions in Leig...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.25789

    authors: Alves CAPF,Teixeira SR,Martin-Saavedra JS,Guimarães Gonçalves F,Lo Russo F,Muraresku C,McCormick EM,Falk MJ,Zolkipli-Cunningham Z,Ganetzky R,Vossough A,Goldstein A,Zuccoli G

    更新日期:2020-08-01 00:00:00

  • Unusual presentation of traumatic extracranial internal carotid artery aneurysm.

    abstract::A young man presented with apparent transient ischemic attacks following a motorcycle accident in which he sustained minor injuries only. Computerized axial tomography demonstrated a small right frontal infarct, and angiography revealed an aneurysm of the right internal carotid artery in its extracranial course. This ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410040118

    authors: Bradbury PG,Lambert CD

    更新日期:1978-07-01 00:00:00

  • Neuroimaging and clinical outcomes of oral anticoagulant-associated intracerebral hemorrhage.

    abstract:OBJECTIVE:Whether intracerebral hemorrhage (ICH) associated with non-vitamin K antagonist oral anticoagulants (NOAC-ICH) has a better outcome compared to ICH associated with vitamin K antagonists (VKA-ICH) is uncertain. METHODS:We performed a systematic review and individual patient data meta-analysis of cohort studie...

    journal_title:Annals of neurology

    pub_type: 杂志文章,meta分析

    doi:10.1002/ana.25342

    authors: Tsivgoulis G,Wilson D,Katsanos AH,Sargento-Freitas J,Marques-Matos C,Azevedo E,Adachi T,von der Brelie C,Aizawa Y,Abe H,Tomita H,Okumura K,Hagii J,Seiffge DJ,Lioutas VA,Traenka C,Varelas P,Basir G,Krogias C,Purrucke

    更新日期:2018-11-01 00:00:00

  • Abnormal breathing patterns during sleep in diabetes.

    abstract::Nineteen diabetic patients, 12 type I (insulin-dependent) and 7 type II (late-onset, non-insulin-dependent), underwent nocturnal polygraphic monitoring after a daytime medical evaluation that included tests of vagal responses and, in 6 patients, pulmonary function and hypercapnic and hypoxic responses. Five lean type ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410170415

    authors: Mondini S,Guilleminault C

    更新日期:1985-04-01 00:00:00

  • The pathophysiology of myotonia produced by aromatic carboxylic acids.

    abstract::A series of nine related aromatic monocarboxylic acids (ACAs) previously shown to inhibit muscle membrane chloride conductance (GCl) selectively in the rat were studied for their ability to produce myotonia. All nine induced characteristic repetitive electrical activity and delayed relaxation in isolated muscle, altho...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410040411

    authors: Furman RE,Barchi RL

    更新日期:1978-10-01 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...

    journal_title:Annals of neurology

    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

  • Brain neurotransmitters in glycine encephalopathy.

    abstract::We measured neurotransmitter markers in autopsied brain of infants with glycine encephalopathy (GE). Because patients with GE develop intractable seizures, special attention was devoted to those neurotransmitter systems implicated in human epilepsy. Mean levels of glycine in the frontal cortex of GE patients were thre...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410240319

    authors: Kish SJ,Dixon LM,Burnham WM,Perry TL,Becker L,Cheng J,Chang LJ,Rebbetoy M

    更新日期:1988-09-01 00:00:00

  • Residual tumor cells are unique cellular targets in glioblastoma.

    abstract::Residual tumor cells remain beyond the margins of every glioblastoma (GBM) resection. Their resistance to postsurgical therapy is considered a major driving force of mortality, but their biology remains largely uncharacterized. In this study, residual tumor cells were derived via experimental biopsy of the resection m...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.22036

    authors: Glas M,Rath BH,Simon M,Reinartz R,Schramme A,Trageser D,Eisenreich R,Leinhaas A,Keller M,Schildhaus HU,Garbe S,Steinfarz B,Pietsch T,Steindler DA,Schramm J,Herrlinger U,Brüstle O,Scheffler B

    更新日期:2010-08-01 00:00:00

  • Magnetic resonance cerebral metabolic rate of oxygen utilization in hyperacute stroke patients.

    abstract::The purpose of this study was to explore the feasibility of obtaining magnetic resonance-measured cerebral metabolic rate of oxygen utilization (MR-CMRO(2)) in acute ischemic stroke patients. Seven stroke patients were serially imaged: 4.5 +/- 0.9 hours (tp1), 3 to 5 days (tp2), and 1 to 3 months (tp3) after symptom o...

    journal_title:Annals of neurology

    pub_type: 临床试验,杂志文章

    doi:10.1002/ana.10433

    authors: Lee JM,Vo KD,An H,Celik A,Lee Y,Hsu CY,Lin W

    更新日期:2003-02-01 00:00:00

  • Alzheimer's disease and Parkinson's disease: distinct entities or extremes of a spectrum of neurodegeneration?

    abstract::Alzheimer's disease (AD) and Parkinson's disease (PD) are generally considered to be separate and distinct disease entities. However, a considerable amount of evidence demonstrates that these disorders share common clinical and neuropathologic features and that overlap between the two conditions is extensive. For exam...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.410440705

    authors: Perl DP,Olanow CW,Calne D

    更新日期:1998-09-01 00:00:00

  • The hypothalamus in Parkinson disease.

    abstract::The hypothalamus was systematically examined in 30 patients with pathologically documented idiopathic parkinsonism. Using Lewy body formation as a marker for nerve cell degeneration, we observed abnormalities in every hypothalamus examined. Of the thirteen hypothalamic nuclei that could be individually identified, non...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410030207

    authors: Langston JW,Forno LS

    更新日期:1978-02-01 00:00:00

  • A Novel Autoantibody against Plexin D1 in Patients with Neuropathic Pain.

    abstract:OBJECTIVE:To identify novel autoantibodies for neuropathic pain (NeP). METHODS:We screened autoantibodies that selectively bind to mouse unmyelinated C-fiber type dorsal root ganglion (DRG) neurons using tissue-based indirect immunofluorescence assays (IFA) with sera from 110 NeP patients with various inflammatory and...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.25279

    authors: Fujii T,Yamasaki R,Iinuma K,Tsuchimoto D,Hayashi Y,Saitoh BY,Matsushita T,Kido MA,Aishima S,Nakanishi H,Nakabeppu Y,Kira JI

    更新日期:2018-08-01 00:00:00

  • Morphometry, histopathology, and tomography of cerebral atrophy in the acquired immunodeficiency syndrome.

    abstract::Patients with the acquired immunodeficiency syndrome (AIDS) commonly display evidence of gross cerebral atrophy, but its true incidence and pathophysiology in the general AIDS population are unknown. In this study, we measured cerebrospinal fluid (CSF) spaces in 64 consecutively autopsied patients with AIDS, compared ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410320107

    authors: Gelman BB,Guinto FC Jr

    更新日期:1992-07-01 00:00:00

  • Novel amyloid precursor protein mutation in an Iowa family with dementia and severe cerebral amyloid angiopathy.

    abstract::Several mutations in the amyloid precursor protein (APP) gene have been found to associate with pathologic deposition of the beta-amyloid peptide (Abeta) in neuritic plaques or in the walls of cerebral vessels. We report a mutation at a novel site in APP in a three-generation Iowa family with autosomal dominant dement...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.1009

    authors: Grabowski TJ,Cho HS,Vonsattel JP,Rebeck GW,Greenberg SM

    更新日期:2001-06-01 00:00:00

  • Sequence variants in human neurofilament proteins: absence of linkage to familial amyotrophic lateral sclerosis.

    abstract::Neurofilaments, assembled from NF-L (68 kd), NF-M (95 kd), and NF-H (115 kd), are the most abundant structural components in large myelinated axons, particularly those of motor neurons. Aberrant neurofilament accumulation in cell bodies and axons of motor neurons is a prominent pathological feature of several motor ne...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410400410

    authors: Vechio JD,Bruijn LI,Xu Z,Brown RH Jr,Cleveland DW

    更新日期:1996-10-01 00:00:00

  • Amyotrophic lateral sclerosis: Problems and prospects.

    abstract::Amyotrophic lateral sclerosis (ALS) is a lethal degenerative disorder of motoneurons, which may occur concurrently with frontotemporal dementia. Genetic analyses of the ∼10% of ALS cases that are dominantly inherited provide insight into ALS pathobiology. Two broad themes are evident. One, prompted by investigations o...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.24012

    authors: Sreedharan J,Brown RH Jr

    更新日期:2013-09-01 00:00:00