Mycophenolate mofetil in the therapy of polymyositis associated with a polyautoimmune syndrome.

Abstract:

:Mycophenolate mofetil 1.5 g daily (30 mg/kg body weight) was given to a patient with ankylosing spondylitis, ulcerative colitis, and severe refractory polymyositis after conventional treatment regimes had failed. No severe side effects occurred. Considerable improvement of clinical symptoms and electromyographic findings were seen within 6 months after the initiation of mycophenolate mofetil, allowing for tapering and discontinuation of methylprednisolone. Mycophenolate mofetil may be considered as an useful alternative in the treatment of polymyositis when standard therapeutic regimens fail.

journal_name

Muscle Nerve

journal_title

Muscle & nerve

authors

Schneider C,Gold R,Schäfers M,Toyka KV

doi

10.1002/mus.10026

subject

Has Abstract

pub_date

2002-02-01 00:00:00

pages

286-8

issue

2

eissn

0148-639X

issn

1097-4598

pii

10.1002/mus.10026

journal_volume

25

pub_type

杂志文章
  • Effects of prolonged repetitive stimulation of median, ulnar and peroneal nerves.

    abstract::It is important to know the effects of prolonged repetitive nerve stimulation (RNS) when it is used in neurophysiological studies. RNS with up to 100 supramaximal stimuli was given to the median, ulnar, and peroneal nerves of normal subjects and the ulnar nerves of subjects with early amyotrophic lateral sclerosis (AL...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21604

    authors: Baumann F,Henderson RD,Tremayne F,Hutchinson N,McCombe PA

    更新日期:2010-06-01 00:00:00

  • Inflammatory processes in amyotrophic lateral sclerosis.

    abstract::Neuroinflammation is a characteristic of pathologically affected tissue in several neurodegenerative disorders. These changes can be observed in the brainstem and spinal cord of amyotrophic lateral sclerosis (ALS) cases and in mouse models of the disease. They include an accumulation of large numbers of activated micr...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.10191

    authors: McGeer PL,McGeer EG

    更新日期:2002-10-01 00:00:00

  • The familial occurrence of carpal tunnel syndrome.

    abstract::Epidemiological studies of the carpal tunnel syndrome have generally overlooked the possibility of a familial occurrence. A prospective study was undertaken to determine the prevalence and significance of a positive family history of carpal tunnel syndrome. Seventy-five of 253 women and 40 of 168 men with a confirmed ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880170311

    authors: Radecki P

    更新日期:1994-03-01 00:00:00

  • Differential susceptibility of muscles to myotonia and force impairment in a mouse model of myotonic dystrophy.

    abstract:INTRODUCTION:Myotonic dystrophy, or dystrophia myotonica (DM), is characterized by prominent muscle wasting and weakness as well as delayed muscle relaxation resulting from persistent electrical discharges. METHODS:We hypothesized heterogeneity among muscles in degree of weakness and myotonia in an expanded [(CUG)(250...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21988

    authors: Moyer M,Berger DS,Ladd AN,Van Lunteren E

    更新日期:2011-06-01 00:00:00

  • Cross-sectional and longitudinal analysis of an oxidative stress biomarker for spinal and bulbar muscular atrophy.

    abstract:INTRODUCTION:Spinal and bulbar muscular atrophy (SBMA) is an adult-onset motor neuron disease caused by a CAG repeat expansion in the androgen receptor gene. The aim of this study was to verify whether urinary 8-hydroxydeoxyguanosine (8-OHdG), an oxidative stress marker, is a biomarker for SBMA. METHODS:We measured th...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.23413

    authors: Mano T,Katsuno M,Banno H,Suzuki K,Suga N,Hashizume A,Tanaka F,Sobue G

    更新日期:2012-11-01 00:00:00

  • Relating applied strain to the type and severity of structural damage in the rat median nerve using second harmonic generation microscopy.

    abstract:INTRODUCTION:Stretch injuries in peripheral nerves can cause pain, paralysis, and loss of sensation. Although optimal treatment depends on the degree of injury, it is difficult to determine the severity of induced nerve damage. METHODS:The load-deformation curves of rat median nerves were generated from monotonic load...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.23443

    authors: Sinclair EB,Andarawis-Puri N,Ros SJ,Laudier DM,Jepsen KJ,Hausman MR

    更新日期:2012-12-01 00:00:00

  • Pain location and intensity impacts function in persons with myotonic dystrophy type 1 and facioscapulohumeral dystrophy with chronic pain.

    abstract:INTRODUCTION:We examined the effects of pain site and intensity on function in patients with myotonic dystrophy type 1 (DM1) and facioscapulohumeral muscular dystrophy (FSHD) and chronic pain. METHODS:Questionnaires assessing pain sites, pain extent (number of sites), pain intensity, and pain interference were complet...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24079

    authors: Miró J,Gertz KJ,Carter GT,Jensen MP

    更新日期:2014-06-01 00:00:00

  • Hexosaminidase A activity and amyotrophic lateral sclerosis.

    abstract::Abnormalities of GM2 ganglioside metabolism owing to hexosaminidase A (Hex A) deficiency have been associated with ALS phenotypes. The clinical features described in these ALS patients with Hex A deficiency include early onset, positive family history, and/or long disease duration. In an attempt to determine prospecti...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880110307

    authors: Gudesblatt M,Ludman MD,Cohen JA,Desnick RJ,Chester S,Grabowski GA,Caroscio JT

    更新日期:1988-03-01 00:00:00

  • Skeletal muscle ultrastructure and function in statin-tolerant individuals.

    abstract:INTRODUCTION:Statins have well-known benefits on cardiovascular mortality, though up to 15% of patients experience side effects. With guidelines from the American Heart Association, American College of Cardiology, and American Diabetes Association expected to double the number of statin users, the overall incidence of ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24722

    authors: Rengo JL,Callahan DM,Savage PD,Ades PA,Toth MJ

    更新日期:2016-02-01 00:00:00

  • Single fiber EMG in the frontalis muscle in ocular myasthenia: specificity and sensitivity.

    abstract::Patients (n = 41) with isolated weakness of the eyelids or extraocular muscles, who had been referred for single fiber electromyography (SFEMG), were followed up after 4 to 24 months, At follow-up the patients were classified as "definite ocular myasthenia gravis" (MG), "definite other diagnosis," or "no definite diag...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880150322

    authors: Rouseev R,Ashby P,Basinski A,Sharpe JA

    更新日期:1992-03-01 00:00:00

  • Evaluation of admittance control as an alternative to passive arm supports to increase upper extremity function for individuals with Duchenne muscular dystrophy.

    abstract::The degree of upper extremity active range of motion provided by an admittance control robot compared with a commercially available passive arm support for individuals with DMD who have limited arm function was investigated in this study. The reachable workspace evaluation was used to assess active range of motion pro...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.26848

    authors: Corrigan MC,Foulds RA

    更新日期:2020-06-01 00:00:00

  • Concentric-needle single-fiber electromyography for the diagnosis of myasthenia gravis.

    abstract::The goal of this study was to estimate the accuracy of concentric-needle single-fiber electromyography (CN-SFEMG) for the diagnosis of myasthenia gravis (MG). A consecutive series of patients referred for CN-SFEMG was evaluated by an investigator blinded to the results of CN-SFEMG in order to determine the presence or...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20568

    authors: Benatar M,Hammad M,Doss-Riney H

    更新日期:2006-08-01 00:00:00

  • Neurologic complications after surgery for obesity.

    abstract::Bariatric surgical procedures are increasingly common. In this review, we characterize the neurologic complications of such procedures, including their mechanisms, frequency, and prognosis. Literature review yielded 50 case reports of 96 patients with neurologic symptoms after bariatric procedures. The most common pre...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.20394

    authors: Koffman BM,Greenfield LJ,Ali II,Pirzada NA

    更新日期:2006-02-01 00:00:00

  • Guidelines for ethical behavior relating to clinical practice issues in neuromuscular and electrodiagnostic medicine.

    abstract::The American Association of Neuromuscular & Electrodiagnostic Medicine (AANEM) developed guidelines to formalize the ethical standards that neuromuscular and electrodiagnostic (EDx) physicians should observe in their clinical and scientific activities. Neuromuscular and EDx medicine is a subspecialty of medicine that ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24910

    authors: Abel NA,De Sousa EA,Govindarajan R,Mayer MP,Simpson DA

    更新日期:2015-12-01 00:00:00

  • Burden of hereditary transthyretin amyloidosis on quality of life.

    abstract:INTRODUCTION:Hereditary transthyretin (hATTR) amyloidosis is a progressive, degenerative disease, with peripheral neuropathy, cardiomyopathy, and other clinical manifestations. In this study we examine the impact of hATTR amyloidosis on quality of life (QOL). METHODS:Neuropathy-specific QOL, measured with the Norfolk ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26515

    authors: Yarlas A,Gertz MA,Dasgupta NR,Obici L,Pollock M,Ackermann EJ,Lovley A,Kessler AS,Patel PA,White MK,Guthrie SD

    更新日期:2019-08-01 00:00:00

  • Ultrasound elastography assessment of the median nerve in leprosy patients.

    abstract:INTRODUCTION:We sought to compare median nerve elasticity between leprosy patients (LPs) and healthy volunteers (HVs) using ultrasound elastography (UE). METHODS:Two radiologists independently measured the strain ratio of the median nerve/flexor digitorum superficialis muscle (MN/FDSM) of 18 LP and 18 HV using real-ti...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25510

    authors: Nogueira-Barbosa MH,Lugão HB,Gregio-Júnior E,Crema MD,Kobayashi MTT,Frade MAC,Pavan TZ,Carneiro AAO

    更新日期:2017-09-01 00:00:00

  • Multiple genotypes, multiple phenotypes, and partial defects.

    abstract::In recent years, the following ideas have been expressed: (a) that all cases of a discrete, inherited neuromuscular syndrome should prove to be due to a single biochemical defect, (b) that any single biochemical defect should give rise only to one syndrome, and (c) that an enzymatic defect cannot give rise to a diseas...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.880040107

    authors: Kark RA,Becker DM

    更新日期:1981-01-01 00:00:00

  • Diagnostic yield of stimulation and voluntary single-fiber electromyography in myasthenia gravis.

    abstract::Voluntary and stimulation single-fiber electromyography were performed in the extensor digitorum communis muscle of 15 myasthenic patients. The increase in mean and individual mean consecutive difference as well as the proportion of blocking in the volitional activation were greater than in the stimulation method. The...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199808)21:8<1081::aid-mus1

    authors: Murga L,Sánchez F,Menéndez C,Castilla JM

    更新日期:1998-08-01 00:00:00

  • Provocation tests in doppler ultrasonography for carpal tunnel syndrome.

    abstract:INTRODUCTION:Doppler ultrasonography (DU) has recently been shown to be useful in imaging carpal tunnel syndrome (CTS). In this study, we aim to characterize the changes seen after exercise and electrical stimulation. METHODS:Five patients with CTS were recruited with 5 age-matched subjects. DU was used to visualize t...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.23637

    authors: Ng ES,Ng KW,Wilder-Smith EP

    更新日期:2013-01-01 00:00:00

  • Mechanically evoked sensory and motor responses to dynamic compression of the ulnar nerve.

    abstract::Mechanical deformation of a peripheral nerve can evoke action potentials in sensory and motor axons. The generation of these impulses with brief stimuli (<0.5 s) and their relationship to the deformation conditions have not been systematically studied in human subjects. Controlled compression stimuli over a range of a...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20701

    authors: Clarke EC,McNulty PA,Macefield VG,Bilston LE

    更新日期:2007-03-01 00:00:00

  • Canine inflammatory myopathy: analysis of cellular infiltrates.

    abstract::Inflammatory myopathies (IMs) occur relatively frequently in dogs, and, with the exception of masticatory muscle myositis (MMM), have not been characterized. This study analyzed the distribution and types of cellular infiltrates in 21 cases of generalized IM, 3 cases of focal IM (MMM), and 1 case with features of both...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20043

    authors: Pumarola M,Moore PF,Shelton GD

    更新日期:2004-06-01 00:00:00

  • Marked increase in CD44-highly positive cells in hyperplastic thymuses from patients with Myasthenia gravis.

    abstract::To investigate the role of the thymus in the pathogenesis of myasthenia gravis (MG), immunohistochemical expression of CD44, CD45R0, B7-1, and IL-2 was studied in: (1) hyperplastic thymuses of patients with MG whose symptoms markedly improved after thymectomy, (2) remnant thymuses of patients with MG whose symptoms di...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(200004)23:4<507::aid-mus8>

    authors: Utsugisawa K,Nagane Y,Tohgi H

    更新日期:2000-04-01 00:00:00

  • Prolonged erythropoietin treatment does not impact gene expression in human skeletal muscle.

    abstract:INTRODUCTION:We tested for the presence of erythropoietin receptor (Epo-R) in human skeletal muscle and alterations in gene expression after prolonged use of an erythropoiesis-stimulating agent (ESA). METHODS:Nine healthy men were treated with ESA for 10 weeks (darbepoietin alfa). Muscle biopsies were collected before...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24355

    authors: Christensen B,Nellemann B,Thorsen K,Nielsen MM,Pedersen SB,Ornstrup MJ,JØrgensen JO,Jessen N

    更新日期:2015-04-01 00:00:00

  • The risk of iatrogenic pneumothorax after electromyography.

    abstract:INTRODUCTION:Pneumothorax is a potentially serious complication of electromyography (EMG). Data on the frequency of pneumothorax after EMG are lacking. The purpose of this study was to determine the frequency, timing, and risk factors for iatrogenic pneumothorax after EMG. METHODS:Cases of pneumothorax after EMG were ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24883

    authors: Kassardjian CD,O'gorman CM,Sorenson EJ

    更新日期:2016-04-01 00:00:00

  • Chronic inflammatory demyelinating polyradiculoneuropathy in children: II. Long-term follow-up, with comparison to adults.

    abstract::We previously reviewed the presentation, initial clinical course, and electrodiagnostic features of children with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). We now report the long-term follow-up of 12 children with idiopathic CIDP, and compare these to 62 adults with idiopathic CIDP. Children of...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199712)20:12<1569::aid-mus

    authors: Simmons Z,Wald JJ,Albers JW

    更新日期:1997-12-01 00:00:00

  • Modeling fiber type grouping by a binary Markov random field.

    abstract::A new approach to the quantification of fiber type grouping is presented, in which the distribution of histochemical type in a muscle cross section is regarded as a realization of a binary Markov random field (BMRF). Methods for the estimation of the parameters of this model are discussed. The first order BMRF, which ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880150617

    authors: Venema HW

    更新日期:1992-06-01 00:00:00

  • Isolated necrotizing myopathy associated with ANTI-PL12 antibody.

    abstract:INTRODUCTION:Immune-mediated myopathies are a heterogeneous group of chronic autoimmune disorders. Autoantibodies associated with this disease complex are classified into myositis-associated and myositis-specific. Anti-tRNA synthetase antibodies are the most well known of the myositis-specific antibodies. Previous repo...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.23383

    authors: Mehndiratta P,Mehta S,Manjila SV,Kammer GM,Cohen ML,Preston DC

    更新日期:2012-08-01 00:00:00

  • The utility of a point-of-care sural nerve conduction device for detection of diabetic polyneuropathy: A cross-sectional study.

    abstract:INTRODUCTION:Rapid and accessible methods for diagnosing diabetic polyneuropathy (DPN) have been developed, but not validated, in large cohorts of people with diabetes. METHODS:The performance of a point-of-care device (POCD) was studied in 168 patients with type 2 diabetes, estimating the sensitivity, specificity, po...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26361

    authors: Kural MA,Andersen ST,Andersen NT,Andersen H,Charles M,Finnerup NB,Jensen TS,Tankisi H

    更新日期:2019-02-01 00:00:00

  • An 8-generation family with X-linked Charcot-Marie-Tooth: Confirmation Of the pathogenicity Of a 3' untranslated region mutation in GJB1 and its clinical features.

    abstract:INTRODUCTION:Mutations in gap junction protein beta 1 (GJB1) on the X chromosome represent one of the most common causes of hereditary neuropathy. We assessed manifestations associated with a rare 3' untranslated region mutation (UTR) of GJB1 in a large family with X-linked Charcot-Marie-Tooth disease (CMTX). METHODS:...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26037

    authors: Chen DH,Ma M,Scavina M,Blue E,Wolff J,Karna P,Dorschner MO,Raskind WH,Bird TD

    更新日期:2018-05-01 00:00:00

  • A mechanistic approach to the myotonic syndromes.

    abstract::The electrical characteristics of myotonia in skeletal muscle appear remarkably similar in a variety of natural disorders and animal models. Recent experimental work has made it clear, however, that the pathophysiologic mechanisms underlying these myotonic discharges can be quite different. A mechanistic classificatio...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:

    authors: Barchi RL

    更新日期:1982-01-01 00:00:00