Human immunodeficiency virus-associated myopathy: analysis of 11 patients.

Abstract:

:Neuromuscular disorders reported in association with human immunodeficiency virus (HIV) infection include several forms of peripheral neuropathy and polymyositis. We report 11 patients with HIV-associated myopathy. Five patients with acquired immunodeficiency syndrome (AIDS), 2 with AIDS-related complex, and 4 otherwise asymptomatic HIV-infected patients developed progressive proximal muscle weakness. Serum creatine phosphokinase levels were elevated and electromyography revealed abnormal spontaneous activity and myopathy in most patients. All 8 muscle biopsy specimens showed fiber necrosis. Four had inflammatory infiltrates, and nemaline rod bodies were prominent in 3. Immunosuppressant therapy in 5 patients resulted in improvement. Attempts at viral localization in 4 muscle biopsy specimens were unsuccessful. These findings suggest a distinct association between HIV infection and myopathy with features atypical for polymyositis.

journal_name

Ann Neurol

journal_title

Annals of neurology

authors

Simpson DM,Bender AN

doi

10.1002/ana.410240114

subject

Has Abstract

pub_date

1988-07-01 00:00:00

pages

79-84

issue

1

eissn

0364-5134

issn

1531-8249

journal_volume

24

pub_type

杂志文章
  • Blinded positron emission tomography study of dopamine cell implantation for Parkinson's disease.

    abstract::We assessed nigrostriatal dopaminergic function in Parkinson's disease (PD) patients undergoing a double-blind, placebo-controlled surgical trial of embryonic dopamine cell implantation. Forty PD patients underwent positron emission tomography (PET) imaging with [18F]fluorodopa (FDOPA) prior to randomization to transp...

    journal_title:Annals of neurology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1002/ana.1075

    authors: Nakamura T,Dhawan V,Chaly T,Fukuda M,Ma Y,Breeze R,Greene P,Fahn S,Freed C,Eidelberg D

    更新日期:2001-08-01 00:00:00

  • Multiple sclerosis: activated cells in cerebrospinal fluid in acute exacerbations.

    abstract::Cerebrospinal fluid (CSF) lymphocytes from three young patients undergoing acute exacerbations of multiple sclerosis were studied by flow cytometry. Using a new method that simultaneously measures cell-surface antigens and the cell-cycle phase, we determined that the CSF lymphocytes in these patients were activated. T...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410180617

    authors: Noronha A,Richman DP,Arnason BG

    更新日期:1985-12-01 00:00:00

  • The frequency of multiple sclerosis in Italy: a descriptive study in Ferrara.

    abstract::Results of intensive prevalence surveys on multiple sclerosis carried out in different small regions of Italy have suggested that this country falls into the high-frequency zone for the disease. To verify this hypothesis by studying a large population, we conducted intensive incidence and prevalence survey in the prov...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410170117

    authors: Granieri E,Tola R,Paolino E,Rosati G,Carreras M,Monetti VC

    更新日期:1985-01-01 00:00:00

  • Abnormal B-cell cytokine responses a trigger of T-cell-mediated disease in MS?

    abstract:OBJECTIVE:To study antibody-independent contributions of B cells to inflammatory disease activity, and the immune consequences of B-cell depletion with rituximab, in patients with multiple sclerosis (MS). METHODS:B-Cell effector-cytokine responses were compared between MS patients and matched controls using a 3-signal...

    journal_title:Annals of neurology

    pub_type: 杂志文章,随机对照试验

    doi:10.1002/ana.21939

    authors: Bar-Or A,Fawaz L,Fan B,Darlington PJ,Rieger A,Ghorayeb C,Calabresi PA,Waubant E,Hauser SL,Zhang J,Smith CH

    更新日期:2010-04-01 00:00:00

  • A predictive clinical-genetic model of tissue plasminogen activator response in acute ischemic stroke.

    abstract:OBJECTIVE:Wide interindividual variability exists in response to tissue plasminogen activator (t-PA) treatment in the acute phase of ischemic stroke. We aimed to find genetic variations associated with hemorrhagic transformation (HT) and mortality rates after t-PA. We then generated a clinical-genetic model for predict...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.23664

    authors: del Río-Espínola A,Fernández-Cadenas I,Giralt D,Quiroga A,Gutiérrez-Agulló M,Quintana M,Fernández-Álvarez P,Domingues-Montanari S,Mendióroz M,Delgado P,Turck N,Ruíz A,Ribó M,Castellanos M,Obach V,Martínez S,Freijo MM,Ji

    更新日期:2012-11-01 00:00:00

  • Cerebrovascular abnormalities in pediatric stroke: assessment using parenchymal and angiographic magnetic resonance imaging.

    abstract::Three-dimensional (volume) magnetic resonance angiography is a noninvasive technique that images the intracranial and cervical arterial vasculature without contrast agents. Twenty-four children with strokes had combined parenchymal magnetic resonance imaging and magnetic resonance angiography 1 day to 4 years after ac...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410290603

    authors: Wiznitzer M,Masaryk TJ

    更新日期:1991-06-01 00:00:00

  • Animal models and therapeutic prospects for Charcot-Marie-Tooth disease.

    abstract::Charcot-Marie-Tooth (CMT) neuropathies are inherited neuromuscular disorders caused by a length-dependent neurodegeneration of peripheral nerves. More than 900 mutations in 60 different genes are causative of the neuropathy. Despite significant progress in therapeutic strategies, the disease remains incurable. The inc...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.23987

    authors: Bouhy D,Timmerman V

    更新日期:2013-09-01 00:00:00

  • Dentatorubral-pallidoluysian atrophy: clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat.

    abstract::Dentatorubral-pallidoluysian atrophy is an autosomal dominant neurodegenerative disease characterized by various combinations of ataxia, choreoathetosis, myoclonus, epilepsy, and dementia as well as a wide range of ages at onset. A specific unstable trinucleotide repeat expansion in a gene on the short arm of chromoso...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410370610

    authors: Ikeuchi T,Koide R,Tanaka H,Onodera O,Igarashi S,Takahashi H,Kondo R,Ishikawa A,Tomoda A,Miike T

    更新日期:1995-06-01 00:00:00

  • Enzyme-linked immunosorbent assay for antibody against the nicotinic acetylcholine receptor in human myasthenia gravis.

    abstract::Antibody against acetylcholine receptor (AChR) of human skeletal muscle was measured using enzyme-linked immunosorbent assay and found in 23 (74%) of 31 Japanese patients with generalized myasthenia gravis. In 15 patients with generalized myasthenia gravis who had not undergone thymectomy and who were not receiving ad...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410150214

    authors: Kawanami S,Tsuji R,Oda K

    更新日期:1984-02-01 00:00:00

  • Polymorphonuclear neutral protease activity in multiple sclerosis and other diseases.

    abstract::Polymorphonuclear neutral protease activity (PMN-NPA) was examined in 87 patients with definite multiple sclerosis (MS) (48 active, 39 inactive), 49 patients with other neurological diseases (OND), 24 patients with immune-mediated non-neurological diseases (INND), and 32 normal subjects. PMN-NPA was found to be signif...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410180519

    authors: Guarnieri B,Lolli F,Amaducci L

    更新日期:1985-11-01 00:00:00

  • Does tremor pace repetitive voluntary motor behavior in Parkinson's disease?

    abstract::In patients with Parkinson's disease and in normal subjects, the influence of tremor on repetitive voluntary movement was investigated in the index finger by comparing frequency of isometric force tremor with frequency of voluntary alternating isometric contractions. Tremor frequency, measured over the range from 0 to...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410300208

    authors: Logigian E,Hefter H,Reiners K,Freund HJ

    更新日期:1991-08-01 00:00:00

  • Adrenoleukodystrophy: a correlation between saturated very long-chain fatty acids in mononuclear cells and phenotype.

    abstract::Saturated very long-chain fatty acids in erythrocyte membranes, blood plasma, and mononuclear cells were studied in 4 patients with childhood-adolescent adrenoleukodystrophy and 4 patients with adult adrenoleukodystrophy and 19 normal control subjects by using high-performance liquid chromatography. Ratios of C26:0 to...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410300118

    authors: Antoku Y,Koike F,Ohtsuka Y,Sakai T,Tsukamoto K,Nagara H,Iwashita H,Goto I

    更新日期:1991-07-01 00:00:00

  • Calmodulin systems in neuronal excitability: a molecular approach to epilepsy.

    abstract::Calmodulin is a major Ca2+ -binding protein that may mediate many Ca2+ -regulated processes in neuronal function. Calmodulin is present in the presynaptic nerve terminal in association with synaptic vesicles and in postsynaptic density fractions. Several calmodulin-regulated synaptic biochemical processes have been id...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410160716

    authors: DeLorenzo RJ

    更新日期:1984-01-01 00:00:00

  • Carbamazepine and phenytoin inhibit somatostatin release from dispersed cerebral cells in culture.

    abstract::To elucidate the mechanism by which carbamazepine lowers somatostatin concentration in cerebrospinal fluid of humans, the effect of carbamazepine on secretion of this peptide was studied in rat cerebral cell cultures. Concentrations of carbamazepine within the therapeutic range (4 x 10(-5) M) inhibited spontaneous rel...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410290412

    authors: Reichlin S,Mothon S

    更新日期:1991-04-01 00:00:00

  • Central levodopa metabolism in Parkinson's disease after administration of stable isotope-labeled levodopa.

    abstract::We report the use of a new stable isotope-labeled form of levodopa (LD) to examine in vivo central LD metabolism in Parkinson's disease (PD). Eight patients representing a wide spectrum of disease severity were administered 50 mg of carbidopa orally followed in 1 hour by an intravenous bolus of 150 mg of stable isotop...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410420305

    authors: Durso R,Evans JE,Josephs E,Szabo GK,Evans BA,Handler JS,Jennings D,Browne TR

    更新日期:1997-09-01 00:00:00

  • Mitochondrial abnormalities in Alzheimer brain: mechanistic implications.

    abstract::Reductions in cerebral metabolism sufficient to impair cognition in normal individuals also occur in Alzheimer's disease (AD). The degree of clinical disability in AD correlates closely to the magnitude of the reduction in brain metabolism. Therefore, we tested whether impairments in tricarboxylic acid (TCA) cycle enz...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.20474

    authors: Bubber P,Haroutunian V,Fisch G,Blass JP,Gibson GE

    更新日期:2005-05-01 00:00:00

  • The trends in incidence of primary brain tumors in the population of Rochester, Minnesota.

    abstract::A number of reports have suggested an increasing incidence of primary brain tumors, especially malignant astrocytomas, in the elderly population. To investigate this issue, we analyzed the incidence and temporal trends of primary intracranial neoplasms diagnosed in the population of Rochester, Minnesota, over the 40 y...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410370113

    authors: Radhakrishnan K,Mokri B,Parisi JE,O'Fallon WM,Sunku J,Kurland LT

    更新日期:1995-01-01 00:00:00

  • Limitations of ultrasound in detecting cerebral ischemic lesions in the neonate.

    abstract::Ultrasound scans of three newborn infants with cerebral ischemic lesions demonstrated on computed tomographic scan showed unexpected changes in echogenicity of brain parenchyma in addition to lateralized mass effect. Areas of increased echogenicity were present adjacent to regions of infarction identified on computed ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410140212

    authors: Wilson-Davis SL,Lo W,Filly RA

    更新日期:1983-08-01 00:00:00

  • Magnetoencephalographic localization in pediatric epilepsy surgery: comparison with invasive intracranial electroencephalography.

    abstract::The object of this study was to determine the concordance of the anatomical location of interictal magnetoencephalographic (MEG) spike foci with the location of ictal onset zones identified by invasive ictal intracranial electroencephalographic recordings in children undergoing evaluation for epilepsy surgery. MEG was...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/1531-8249(199910)46:4<627::aid-ana11>3.0.c

    authors: Minassian BA,Otsubo H,Weiss S,Elliott I,Rutka JT,Snead OC 3rd

    更新日期:1999-10-01 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

  • Long-term treatment response and fluorodopa positron emission tomographic scanning of parkinsonism in a family with dopa-responsive dystonia.

    abstract::Dopa-responsive dystonia (DRD) is one form of childhood-onset idiopathic torsion dystonia. Adult-onset parkinsonism has appeared in several previously unaffected members in families with DRD suggesting that this may be an additional phenotypical expression of the disease. We report a family with DRD in which 2 women a...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410320502

    authors: Nygaard TG,Takahashi H,Heiman GA,Snow BJ,Fahn S,Calne DB

    更新日期:1992-11-01 00:00:00

  • Cerebral amyloid angiopathy without and with cerebral hemorrhages: a comparative histological study.

    abstract::To identify those factors associated with cerebral hemorrhage among brains with cerebral amyloid angiopathy (CAA), we undertook a comparative postmortem histopathological study of amyloid-containing vessels in the brains of patients with and without hemorrhage. Those without hemorrhage were represented by the followin...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410300503

    authors: Vonsattel JP,Myers RH,Hedley-Whyte ET,Ropper AH,Bird ED,Richardson EP Jr

    更新日期:1991-11-01 00:00:00

  • Multiple sclerosis: immune mechanism and update on current therapies.

    abstract::Multiple sclerosis (MS) is a demyelinating disease of the central nervous system (CNS) afflicting approximately 250,000 individuals in the United States. This inflammatory disease has variable clinical manifestations, ranging from a relapsing-remitting course to a chronic progressive disease. Approximately one third o...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.410370710

    authors: Bansil S,Cook SD,Rohowsky-Kochan C

    更新日期:1995-05-01 00:00:00

  • Electroconvulsive therapy treatment of depression in a patient with adult GM2 gangliosidosis.

    abstract::Adult GM2 gangliosidosis is a rare disorder that often presents with both neurological and psychiatric syndromes. Effective treatment of the psychotic and affective symptoms associated with this disorder has been complicated by poor treatment response and the concern that many psychotropic agents may worsen the underl...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.410310320

    authors: Renshaw PF,Stern TA,Welch C,Schouten R,Kolodny EH

    更新日期:1992-03-01 00:00:00

  • Cerebrospinal fluid polyamines: biochemical markers of malignant childhood brain tumors.

    abstract::The clinical value of cerebrospinal fluid (CSF) polyamine determinations in childhood medulloblastoma has been suggested. We performed 72 CSF polyamine determinations in 35 children with primary brain tumors. Spermine values were normal and spermidine values were inconsistently elevated. CSF putrescine values, however...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410190409

    authors: Phillips PC,Kremzner LT,De Vivo DC

    更新日期:1986-04-01 00:00:00

  • Leptomeningeal metastases: peripheral nerve and root involvement--clinical and electrophysiological study.

    abstract::Twenty-five patients with recently diagnosed leptomeningeal metastases underwent a prospective clinical and electro-physiological study to assess the mode and extent of peripheral nerve and spinal root involvement. Motor conduction velocities and F wave latencies in the legs were found frequently to be disturbed compa...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410170611

    authors: Argov Z,Siegal T

    更新日期:1985-06-01 00:00:00

  • Electrophysiological correlates of a paroxysmal movement disorder.

    abstract::Averaged electroencephalographic activity related to rhythmic jerking movements was recorded in a patient with a complex neurological symptomatology. The diagnosis of a functional disorder was strongly suggested by his clinical course, inconsistent findings from physical examination, and negative workup. His abnormal ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410200614

    authors: Toro C,Torres F

    更新日期:1986-12-01 00:00:00

  • B lineage cells in the inflammatory central nervous system environment: migration, maintenance, local antibody production, and therapeutic modulation.

    abstract::B cells have long played an enigmatic role in the scenario of multiple sclerosis pathogenesis. This review summarizes recent progress in our understanding of B-cell trafficking, survival, and differentiation in the central nervous system (CNS). We propose four possible routes of intrathecal immunoglobulin-producing ce...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.20890

    authors: Meinl E,Krumbholz M,Hohlfeld R

    更新日期:2006-06-01 00:00:00

  • Acquired perinatal leukoencephalopathy.

    abstract::Between 36 and 44 weeks after conception, telencephalic white matter in the newborn appears to be particularly vulnerable to insults that result in morphological disturbances. Available evidence indicates that this disorder (or group of disorders), named acquired perinatal leukoencephalopathy, reflects a decrease in b...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410160102

    authors: Leviton A,Gilles FH

    更新日期:1984-07-01 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