Conduction block in neuralgic amyotrophy.

Abstract:

:We describe two cases of neuralgic amyotrophy with electrophysiological evidence of conduction block across the lower trunk of the brachial plexus. Low-output impedance stimulation of the cervical spinal roots in combination with collision was used to accurately demonstrate the conduction block. Complete electrophysiological recovery of the conduction block occurred within 3 months. Early clinical and electrophysiological recovery in both patients suggests that, in some cases, demyelination may predominate early in the course of neuralgic amyotrophy.

journal_name

Muscle Nerve

journal_title

Muscle & nerve

authors

Watson BV,Nicolle MW,Brown JD

doi

10.1002/mus.1041

subject

Has Abstract

pub_date

2001-04-01 00:00:00

pages

559-63

issue

4

eissn

0148-639X

issn

1097-4598

pii

10.1002/mus.1041

journal_volume

24

pub_type

杂志文章
  • Comparison of neuromuscular blockade and recovery with botulinum toxins A and F.

    abstract::Intramuscular injection of botulinum toxin A is used to treat focal dystonias. Because immunoresistance has been documented in some patients, other molecular forms of the toxin have been evaluated clinically. The present investigation compared the time course and extent of neuromuscular blockade and recovery of botuli...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.10213

    authors: Billante CR,Zealear DL,Billante M,Reyes JH,Sant'Anna G,Rodriguez R,Stone RE Jr

    更新日期:2002-09-01 00:00:00

  • Using complementary DNA from MyoD-transduced fibroblasts to sequence large muscle genes.

    abstract::Large muscle genes are often sequenced using complementary DNA (cDNA) made from muscle messenger RNA (mRNA) to reduce the cost and workload associated with sequencing from genomic DNA. Two potential barriers are the availability of a frozen muscle biopsy, and difficulties in detecting nonsense mutations due to nonsens...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.22118

    authors: Waddell LB,Monnier N,Cooper ST,North KN,Clarke NF

    更新日期:2011-08-01 00:00:00

  • Sensory ganglionopathy with livedoid vasculopathy controlled by immunotherapy.

    abstract:INTRODUCTION:Livedoid vasculopathy is a rare dermatological condition characterized by painful ulceration, atrophic scarring, and persistent livedo reticularis. The pathogenesis is unclear. METHODS:We report a patient with biopsy-proven livedoid vasculopathy who developed a progressive sensory ganglionopathy with prof...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24452

    authors: Alix JJ,Hadjivassiliou M,Ali R,Slater D,Messenger AG,Rao DG

    更新日期:2015-02-01 00:00:00

  • Multiple mitochondrial DNA deletions in a patient with mitochondrial myopathy and cardiomyopathy but no ophthalmoplegia.

    abstract::Deletions of muscle mitochondrial DNA are known in mitochondrial myopathy patients who have chronic progressive external ophthalmoplegia (CPEO). A 41-year-old patient with no apparent family history of this condition suffers from hypertrophic cardiomyopathy, slight muscle atrophy, and weakness of the extremities, but ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880181115

    authors: Takei Y,Ikeda S,Yanagisawa N,Takahashi W,Sekiguchi M,Hayashi T

    更新日期:1995-11-01 00:00:00

  • Muscle precursor cells injected into irradiated mdx mouse muscle persist after serial injury.

    abstract::Muscle of donor origin was formed after implantation of H-2Kb-tsA58 muscle precursor cells (mpc) into irradiated mdx nu/nu mouse muscles. A series of injections of the myotoxin, notexin, which destroys mature muscle fibers but spares muscle precursor cells and other tissues, was made into the mpc-injected muscles, lea...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199902)22:2<174::aid-mus5>

    authors: Gross JG,Morgan JE

    更新日期:1999-02-01 00:00:00

  • Adolescent spinal muscular atrophy with calf hypertrophy and a deletion in the SMN gene.

    abstract::Spinal muscular atrophy (SMA) is generally associated with proximal weakness and muscle wasting. An X-linked variant with calf hypertrophy has been reported. We describe a young man with SMA type 4 with prominent calf hypertrophy in whom DNA analysis showed a homozygous deletion of exons 7 and 8 in the telomeric copy ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21013

    authors: Yiu EM,Ravat S,Ryan MM,Shield LK,Smith LJ,Kornberg AJ

    更新日期:2008-07-01 00:00:00

  • Dysmorphic neuromuscular junctions associated with motor ability in cerebral palsy.

    abstract::Cerebral palsy (CP) is the most prevalent neurologic disease in children and a leading cause of severe physical disability. Research and clinical experience indicate that children with CP have abnormal neuromuscular junctions (NMJs), and we present evidence that nonapposition of neuromuscular junction components is as...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20401

    authors: Theroux MC,Oberman KG,Lahaye J,Boyce BA,Duhadaway D,Miller F,Akins RE

    更新日期:2005-11-01 00:00:00

  • Inaccurate projection of rat soleus motoneurons: a comparison of nerve repair techniques.

    abstract::The objectives of this study were 1) to determine the degree to which soleus motoneurons find their appropriate target following crush and transection injuries to the sciatic nerve, and 2) to determine whether repair of a transected nerve with a silicone tube leads to greater specificity of reinnervation and recovery ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199701)20:1<29::aid-mus4>3

    authors: Bodine-Fowler SC,Meyer RS,Moskovitz A,Abrams R,Botte MJ

    更新日期:1997-01-01 00:00:00

  • Failure to detect HTLV-I by in situ hybridization in the biopsied muscles of viral carriers with polymyositis.

    abstract::Direct infection of muscle fibers by human T-lymphotropic virus type I (HTLV-I) has recently been reported in a patient with polymyositis infected with both HTLV-I and human immunodeficiency virus (HIV). Coinfections of these viruses are frequently found in the United States. In Kagoshima, Japan, patients with polymyo...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880150108

    authors: Higuchi I,Nerenberg M,Yoshimine K,Yoshida M,Fukunaga H,Tajima K,Osame M

    更新日期:1992-01-01 00:00:00

  • Association between pulmonary function and left ventricular volume and function in duchenne muscular dystrophy.

    abstract:INTRODUCTION:Duchenne muscular dystrophy (DMD) is characterized by absence of the subsarcolemmal protein dystrophin, present in skeletal muscles and cardiomyocytes. We hypothesized that progressive respiratory and left ventricular (LV) insufficiencies in DMD could be parallel and interrelated phenomena. METHODS:We con...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26623

    authors: Khokhar A,Nair A,Midya V,Kumar A,Sinharoy A,Ahmad TA,Abu-Hasan M,Mondal P

    更新日期:2019-09-01 00:00:00

  • Poisson distribution to analyze near-threshold motor evoked potentials.

    abstract::Motor unit action potentials (MUAPs) evoked by repetitive, low-intensity transcranial magnetic stimulation can be modeled as a Poisson process. A mathematical consequence of such a model is that the ratio of the variance to the mean of the amplitudes of motor evoked potentials (MEPs) should provide an estimate of the ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21818

    authors: Kaelin-Lang A,Conforto AB,Z'Graggen W,Hess CW

    更新日期:2010-11-01 00:00:00

  • Chronic bilateral T1 denervation in women with macromastia.

    abstract:INTRODUCTION:The objective of this study was to identify the pattern of neurological deficits and document electrophysiological changes in women with macromastia. METHODS:Patients with macromastia and neurological complaints underwent clinical evaluation and electrodiagnostic (EDx) studies of the upper limbs. RESULTS...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.23501

    authors: Ansell JR,Buchholz MC

    更新日期:2013-02-01 00:00:00

  • Slower conduction velocity and motor unit discharge frequency are associated with muscle fatigue during isometric exercise in type 1 diabetes mellitus.

    abstract::Type 1 diabetes mellitus (T1DM) is associated with a peripheral neuropathy that reduces nerve conduction velocity. This may impair high motor-unit discharge frequencies (MUDF), decrease muscle activation, and curtail the ability to sustain repetitive contractile tasks. We examined (1) whether MUDF, the contractile pro...

    journal_title:Muscle & nerve

    pub_type: 临床试验,杂志文章

    doi:10.1002/mus.20919

    authors: Almeida S,Riddell MC,Cafarelli E

    更新日期:2008-02-01 00:00:00

  • Transient focal conduction block following experimental occlusion of the vasa nervorum.

    abstract::Injection of low-dose arachidonic acid into the rat femoral artery occludes the vasa nervorum of the tibial nerve and produces focal and generalized ischemia with transient effects on nerve conduction. Across a severely ischemic segment of the proximal tibial nerve there is a marked fall in amplitude of the compound m...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880090411

    authors: Parry GJ,Linn DJ

    更新日期:1986-05-01 00:00:00

  • Preparation of cell-free extracellular matrix from human peripheral nerve.

    abstract::The extracellular matrix of human peripheral nerve, which is mainly basement membrane and fibrillar collagen, has been prepared by a procedure involving extensive detergent extraction of isolated endoneurium and perineurium obtained from various nerves. The ultrastructure of the isolated nerve extracellular matrix was...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880050410

    authors: Johnson PC,Duhamel RC,Meezan E,Brendel K

    更新日期:1982-04-01 00:00:00

  • Autophagy markers LC3 and p62 accumulate in immune-mediated necrotizing myopathy.

    abstract:INTRODUCTION:The molecular mechanism of immune-mediated necrotizing myopathy (IMNM) remains unknown. Autophagy impairment, described in autoimmune diseases, is a key process in myofiber protein degradation flux and muscle integrity and has not been studied in IMNM. METHODS:Muscle biopsies from patients with IMNM (n = ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26608

    authors: Girolamo F,Lia A,Annese T,Giannini M,Amati A,D'Abbicco D,Tampoia M,Virgintino D,Ribatti D,Serlenga L,Iannone F,Trojano M

    更新日期:2019-09-01 00:00:00

  • Early changes of muscle insulin-like growth factor-1 and myostatin gene expression in gastric cancer patients.

    abstract:INTRODUCTION:Cachexia increases morbidity and mortality of cancer patients. The progressive loss of muscle mass negatively affects physical function and quality of life. We previously showed reduced muscle insulin-like growth factor-1 (IGF-1) expression and enhanced myostatin signaling in tumor-bearing animals. This st...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.23798

    authors: Bonetto A,Penna F,Aversa Z,Mercantini P,Baccino FM,Costelli P,Ziparo V,Lucia S,Rossi Fanelli F,Muscaritoli M

    更新日期:2013-09-01 00:00:00

  • VCP myopathy: A family with unusual clinical manifestations.

    abstract:INTRODUCTION:Valosin-containing protein (VCP) variants that affect muscle, bone, and the nervous system are termed multisystem proteinopathy. VCP myopathy is manifested as limb-girdle weakness, distal weakness and scapuloperoneal weakness. METHODS:We reviewed clinical, genetic, and muscle biopsy data from 6 members of...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26389

    authors: Guo X,Zhao Z,Shen H,Qi B,Li N,Hu J

    更新日期:2019-03-01 00:00:00

  • Predictors of response to immunomodulation in patients with myasthenia gravis.

    abstract:INTRODUCTION:Factors determining response to intravenous immunoglobulin (IVIg) and plasmapheresis in myasthenia gravis (MG) have not been evaluated systematically. METHODS:This study included patients treated with IVIg (n = 63) or plasmapheresis (n = 42) from two trials evaluating IVIg vs. placebo or plasmapheresis in...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.23236

    authors: Katzberg HD,Barnett C,Bril V

    更新日期:2012-05-01 00:00:00

  • Thrombocytosis distinguishes POEMS syndrome from chronic inflammatory demyelinating polyneuropathy.

    abstract:INTRODUCTION:POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal plasma cell disorder, and skin changes) syndrome may be mistaken for chronic inflammatory demyelinating polyneuropathy (CIDP). Differentiating the 2 entities is crucial, as there are major treatment implications. METHODS:We compared platelet ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24768

    authors: Naddaf E,Dispenzieri A,Mandrekar J,Mauermann ML

    更新日期:2015-10-01 00:00:00

  • TrkB expression at the neuromuscular junction is reduced during aging.

    abstract:INTRODUCTION:Full-length tyrosine kinase B (TrkB.FL) and truncated TrkB (TrkB.t1) receptors are colocalized with acetylcholine receptors (AChRs) at the neuromuscular junction. We have recently shown that reduced TrkB expression leads to age-related alterations in AChR structure, neurotransmission failure, and muscle we...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.23616

    authors: Personius KE,Parker SD

    更新日期:2013-04-01 00:00:00

  • Effect of spinal cord TRH deficiency on lower motorneuron function in the rat.

    abstract::Thyrotropin-releasing hormone (TRH), present in high concentrations in the mammalian spinal cord, exerts excitatory effects on the alpha-motorneuron (AMN) via axodendritic contacts. We used the neurotoxin 5,7-dihydroxytryptamine (5,7-DHT) to deplete TRH from the ventral horn of the spinal cord of adult rats to determi...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880100504

    authors: Van den Bergh P,Kelly JJ Jr,Adelman L,Munsat TL,Jackson IM,Lechan RM

    更新日期:1987-06-01 00:00:00

  • Vibration injury damages arterial endothelial cells.

    abstract::Prolonged exposure to hand-transmitted vibration can cause debilitating neural and vascular dysfunction in humans. It is unclear whether the pathophysiology involves simultaneous or sequential injury of arteries and nerves. The mechanism of vibration injury was investigated in a rat tail model, containing arteries and...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.10058

    authors: Curry BD,Bain JL,Yan JG,Zhang LL,Yamaguchi M,Matloub HS,Riley DA

    更新日期:2002-04-01 00:00:00

  • Muscle computed tomography in adult-onset acid maltase deficiency.

    abstract::Nine patients with adult-onset acid maltase deficiency (Pompe's disease) were examined clinically and with computed tomography (CT). The CT scan showed early and severe involvement of the muscles of trunk and thighs, with selective sparing of the tensor fasciae latae, short head of biceps femoris, gracilis, and sartor...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199803)21:3<398::aid-mus15

    authors: de Jager AE,van der Vliet TM,van der Ree TC,Oosterink BJ,Loonen MC

    更新日期:1998-03-01 00:00:00

  • Dystrophin gene transcripts skipping the mdx mutation.

    abstract::The mdx mouse, an animal model used to study Duchenne muscular dystrophy, has a nonsense mutation in exon 23 of the dystrophin gene which should result in a truncated protein that cannot be correctly localized at the sarcolemma of the muscle fibers. Immunohistochemical staining with antidystrophin antibodies has shown...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199706)20:6<728::aid-mus10

    authors: Wilton SD,Dye DE,Laing NG

    更新日期:1997-06-01 00:00:00

  • Application of futility analysis to refine jitter recordings in myasthenia gravis.

    abstract:INTRODUCTION:The current practice of single-fiber electromyography (SFEMG) requires that 20 fiber pairs with normal jitter be collected to exclude myasthenia gravis (MG). We applied principles of futility analysis from clinical trials in an attempt to reduce that requirement. METHODS:We utilized conditional power futi...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.22340

    authors: Narayanaswami P,Pantoja-Galicia N,Betensky RA,Rutkove SB

    更新日期:2012-04-01 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

  • A novel points system to predict the prognosis of ulnar neuropathy at the elbow.

    abstract:INTRODUCTION:In this study we aimed to identify prognostic factors of ulnar neuropathy at the elbow (UNE) and developed a scoring system to establish the prognosis. METHODS:We collected baseline clinical, electrophysiologic, and ultrasonographic data from 2 cohorts. The outcomes for all patients were determined on fol...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25406

    authors: Beekman R,Zijlstra W,Visser LH

    更新日期:2017-05-01 00:00:00

  • Effects of hemodialysis on intraneural blood flow in end-stage kidney disease.

    abstract:INTRODUCTION:We quantified intraneural blood flow (INBF) in 18 patients with end-stage kidney disease (ESKD) and examined its relationship with nerve size, neuropathy severity, and nerve excitability parameters. METHODS:Sonographic measurements of the median nerve were performed at the same site before and after hemod...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25704

    authors: Borire AA,Arnold R,Pussell BA,Kwai NC,Visser LH,Simon NG,Kiernan MC,Krishnan AV

    更新日期:2018-02-01 00:00:00

  • Multifocal motor neuropathy: current concepts and controversies.

    abstract::Multifocal motor neuropathy (MMN) is now a well-defined purely motor multineuropathy characterized by the presence of multifocal partial motor conduction blocks (CB), frequent association with anti-GM1 IgM antibodies, and usually a good response to high-dose intravenous immunoglobulin (IVIg) therapy. However, several ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.20296

    authors: Nobile-Orazio E,Cappellari A,Priori A

    更新日期:2005-06-01 00:00:00