The dropped head syndrome with chronic inflammatory demyelinating polyneuropathy.

Abstract:

:The dropped head syndrome occurs in a variety of neuromuscular disorders. We present a woman with chronic inflammatory demyelinating polyneuropathy who developed this syndrome, likely reflecting severe demyelination of nerves to cervical paraspinal muscles.

journal_name

Muscle Nerve

journal_title

Muscle & nerve

authors

Hoffman D,Gutmann L

doi

10.1002/mus.880170717

subject

Has Abstract

pub_date

1994-07-01 00:00:00

pages

808-10

issue

7

eissn

0148-639X

issn

1097-4598

journal_volume

17

pub_type

杂志文章
  • Evidence for new isoform of fast myosin heavy chain in rat skeletal muscle.

    abstract::The purpose of this study was to investigate whether the previously demonstrated heterogeneity of myosin heavy chain (MHC) in type 2B fibers of the superficial portion of the lateral gastrocnemius (SLG) muscle of the rat may be due to presence of type 2D/X fibers. Immunohistochemical identification of MHC heterogeneit...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880151210

    authors: Sawchak JA,Leung B,Shafiq SA

    更新日期:1992-12-01 00:00:00

  • A multicenter, retrospective medical record review of X-linked myotubular myopathy: The recensus study.

    abstract:INTRODUCTION:X-linked myotubular myopathy (XLMTM), characterized by severe hypotonia, weakness, respiratory distress, and early mortality, is rare and natural history studies are few. METHODS:RECENSUS is a multicenter chart review of male XLMTM patients characterizing disease burden and unmet medical needs. Data were ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,多中心研究

    doi:10.1002/mus.26018

    authors: Beggs AH,Byrne BJ,De Chastonay S,Haselkorn T,Hughes I,James ES,Kuntz NL,Simon J,Swanson LC,Yang ML,Yu ZF,Yum SW,Prasad S

    更新日期:2018-04-01 00:00:00

  • Calmodulin levels in developing muscle tissues and primary cultures of normal and dystrophic (UM-X7.1) hamsters.

    abstract::Calmodulin levels have been assessed in whole muscle and primary culture extracts in order to examine the relationship between calmodulin and the accumulation of calcium in dystrophic hamster muscle tissues. Significant decreases in both normal and dystrophic skeletal muscle, tongue, and heart calmodulin levels were o...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880100113

    authors: Klamut HJ,Kotarba JA,Strickland KP

    更新日期:1987-01-01 00:00:00

  • Clinical, physiological, and histological features in a kindred with the T3271C melas mutation.

    abstract::The majority of patients with MELAS syndrome (mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes) have an A-->G mutation at nucleotide 3243 in mitochondrial transfer (t)RNA. To date there have only been 10 reported cases of MELAS syndrome in patients with a T-->C mutation at position 3271...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199801)21:1<25::aid-mus4>3

    authors: Tarnopolsky MA,Maguire J,Myint T,Applegarth D,Robinson BH

    更新日期:1998-01-01 00:00:00

  • Effects of velocity on maximal torque production in poststroke hemiparesis.

    abstract::Impaired torque production is a major physical impairment following stroke, and has been studied extensively in isometric conditions. However, functional use of a limb requires torque production during movement, and the effects of velocity on maximal torque production may be abnormally enhanced in the paretic limb. Th...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20157

    authors: Lum PS,Patten C,Kothari D,Yap R

    更新日期:2004-12-01 00:00:00

  • Premotor potential study in carpal tunnel syndrome.

    abstract:INTRODUCTION:Premotor potentials (PMPs) precede compound muscle action potentials evoked from the second lumbrical muscle after median nerve stimulation. Although PMP has been identified as a median sensory nerve action potential, few reports have documented the significance of PMP parameters for diagnosing carpal tunn...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.23424

    authors: Kodama M,Sasao Y,Tochikura M,Kasahara T,Koyama Y,Aono K,Fujii C,Hanayama K,Takahashi O,Kobayashi Y,Masakado Y

    更新日期:2012-12-01 00:00:00

  • Probabilistic muscle characterization using QEMG: application to neuropathic muscle.

    abstract::Clinicians who use electromyographic (EMG) signals to help determine the presence or absence of abnormality in a muscle often, with varying degrees of success, evaluate sets of motor unit potentials (MUPs) qualitatively and/or quantitatively to characterize the muscle in a clinically meaningful way. The resulting musc...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21456

    authors: Pino LJ,Stashuk DW,Boe SG,Doherty TJ

    更新日期:2010-01-01 00:00:00

  • Effects of activation pattern on human skeletal muscle fatigue.

    abstract::Variable-frequency stimulation trains (VFTs) that take advantage of the catchlike property of skeletal muscle have been shown to augment the force production of fatigued muscles compared with constant-frequency trains (CFTs). The present study is the first to report the force augmentation produced by VFTs after fatigu...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199809)21:9<1145::aid-mus5

    authors: Binder-Macleod SA,Lee SC,Russ DW,Kucharski LJ

    更新日期:1998-09-01 00:00:00

  • Interaction of monoclonal antibodies to Torpedo acetylcholine receptor with the receptor of skeletal muscle.

    abstract::Several monoclonal antibodies (mcAbs) elicited against the nicotinic acetylcholine receptor (AChR) from Torpedo react also with skeletal muscle AChR. Such mcAbs were used to define antigenic determinants on muscle AChR and to elucidate their effect on muscle AChR functions. Primary chick muscle cultures were used as a...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880060410

    authors: Souroujon MC,Mochly-Rosen D,Gordon AS,Fuchs S

    更新日期:1983-05-01 00:00:00

  • CT muscle imaging and the clinical assessment of neuromuscular disease.

    abstract::Twenty patients with neurogenic disorders, polymyositis, or muscular dystrophies were assessed clinically and by CT imaging of limb, limb girdle, and trunk muscles, using a standard protocol. On each side of these patients 26 movements were graded by the MRC scale, and 20 muscles were assessed by CT imaging. The clini...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880180706

    authors: Swash M,Brown MM,Thakkar C

    更新日期:1995-07-01 00:00:00

  • Clinical-pathologic correlations in voltage-gated Kv1 potassium channel complex-subtyped autoimmune painful polyneuropathy.

    abstract:INTRODUCTION:Voltage-gated Kv1 potassium channel complex (VGKC) autoantibodies subtyped for leucine-rich glioma-inactivated 1 (LGI1), contactin-associated-proteinlike 2 (CASPR2), and Kv IgGs have a spectrum of neurological presentations. Painful polyneuropathy is seen in some patients, but nerve pathology descriptions ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25371

    authors: Lahoria R,Pittock SJ,Gadoth A,Engelstad JK,Lennon VA,Klein CJ

    更新日期:2017-04-01 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

  • Nerve ultrasound reliability of upper limbs: Effects of examiner training.

    abstract:INTRODUCTION:Duration of training to reliably measure nerve cross-sectional area with ultrasound is unknown. METHODS:A retrospective review was performed of ultrasound data, acquired and recorded by 2 examiners-an expert and either a trainee with 2 months (novice) or a trainee with 12 months (experienced) of experienc...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25980

    authors: Garcia-Santibanez R,Dietz AR,Bucelli RC,Zaidman CM

    更新日期:2018-02-01 00:00:00

  • Quantitative muscle ultrasound in upper extremity mononeuropathies.

    abstract:INTRODUCTION:We assessed the potential use of quantitative ultrasound (QUS) in the evaluation hand muscles affected by upper extremity mononeuropathies. METHODS:The gray scale levels (GSLs) of abductor pollicis brevis (APB), abductor digiti minimi (ADM), and first dorsal interosseous (FDI) of 30 healthy and 30 upper e...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26481

    authors: Wang Y,Gutierrez H,Martucci M,Poussaint A,Qi K,Sanchez B,Rutkove SB

    更新日期:2019-07-01 00:00:00

  • Conduction and excitability properties of peripheral nerves in end-stage liver disease.

    abstract::The pathophysiology of hepatic neuropathy is poorly understood, but membrane depolarization due to a toxic inhibition of oxidative metabolism has been proposed. We investigated the relationship between nerve excitability properties, nerve dysfunction, and liver function in 11 pretransplant patients, the majority of wh...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20765

    authors: Ng K,Lin CS,Murray NM,Burroughs AK,Bostock H

    更新日期:2007-06-01 00:00:00

  • Stroke-related effects on maximal dynamic hip flexor fatigability and functional implications.

    abstract:INTRODUCTION:Stroke-related changes in maximal dynamic hip flexor muscle fatigability may be more relevant functionally than isometric hip flexor fatigability. METHODS:Ten chronic stroke survivors performed 5 sets of 30 hip flexion maximal dynamic voluntary contractions (MDVC). A maximal isometric voluntary contractio...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24520

    authors: Kuhnen HR,Rybar MM,Onushko T,Doyel RE,Hunter SK,Schmit BD,Hyngstrom AS

    更新日期:2015-03-01 00:00:00

  • Focal myositis presenting with radial nerve palsy.

    abstract::Focal myositis is a rare inflammatory pseudotumor of skeletal muscle which usually has a benign course. We report a 56-year-old woman with a painful mass in the left arm with a radial nerve palsy. Magnetic resonance imaging (MRI) of the left arm showed a mass in the triceps muscle that was suggestive of a soft-tissue ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199907)22:7<956::aid-mus25

    authors: Alzagatiti BI,Bertorini TE,Horner LH,Maccarino VS,O'Brien T

    更新日期:1999-07-01 00:00:00

  • A novel electrodiagnostic assessment of the laryngeal closure reflex.

    abstract:INTRODUCTION:We describe a novel, clinically applicable conduction study of the laryngeal nerves. METHODS:Seventeen normal volunteer subjects were included. Activation of the sensory territory of the superior laryngeal nerve was performed by administration of low level brief electrical stimuli. The laryngeal closure r...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.23544

    authors: Carey B,Sulica L,Wu A,Branski R

    更新日期:2013-03-01 00:00:00

  • Effects of extracorporeal shock-wave lithotripsy directed at the parotid gland on oxidative stress parameters and some trace element levels in facial nerve of rats.

    abstract:INTRODUCTION:This study was designed to assess the effect of extracorporeal shock-wave lithotripsy (ESWL) exposure of the parotid gland on oxidative stress and some trace element levels in the facial nerves of rats. METHODS:Twelve male Wistar albino rats were divided into two groups, each consisting of 6 animals. The ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.22326

    authors: Kavak S,Garca MF,Gecit I,Meral I,Cengiz N,Demir H

    更新日期:2012-04-01 00:00:00

  • Transcriptional deficits in oxidative phosphorylation with statin myopathy.

    abstract:INTRODUCTION:Hydroxymethylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors, or statins, are widely used drugs for hyperlipidemia and are generally well-tolerated, but the can produce skeletal muscle toxicity. The molecular mechanisms driving statin myopathy are unknown. We investigated the effects of statin treatment...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.22081

    authors: Hubal MJ,Reich KA,De Biase A,Bilbie C,Clarkson PM,Hoffman EP,Thompson PD

    更新日期:2011-09-01 00:00:00

  • Cytokines and the pathogenesis of myasthenia gravis.

    abstract::Myasthenia gravis (MG) and its animal model experimental autoimmune myasthenia gravis (EAMG) are caused by autoantibodies against nicotinic acetylcholine receptor (AChR) in skeletal muscle. The production of anti-AChR antibodies is mediated by cytokines produced by CD4+ and CD8+ T helper (Th) cells. Emerging investiga...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199705)20:5<543::aid-mus2>

    authors: Zhang GX,Navikas V,Link H

    更新日期:1997-05-01 00:00:00

  • Myopathies with abnormal mitochondria: a clinicopathologic classification.

    abstract::Of 185 patients with myopathy, 22 showed abnormal muscle mitochondria. In 12 of the 22 patients, all of whom had ocular myopathy or the ophthalmoplegia-plus syndrome, muscle biopsies contained 5%-25% "ragged red" fibers. In 4 patients with a facioscapulohumeral distribution of weakness, ragged red fibers were less num...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880010513

    authors: Kamieniecka Z,Schmalbruch H

    更新日期:1978-09-01 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

  • Simulation of myopathic motor unit action potentials.

    abstract::Normal motor units (MUs) were simulated and their architecture altered to simulate the changes produced by myopathy. The concentric needle electromyographic recordings of motor unit action potentials (MUAPs) from the MUs were then also simulated. These simulated MUAPs showed features that are seen in myopathy: normal ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880120306

    authors: Nandedkar SD,Sanders DB

    更新日期:1989-03-01 00:00:00

  • Electromyographic and lower extremity short time to inversion recovery magnetic resonance imaging findings in lumbar radiculopathy.

    abstract::To determine if short TI (time to inversion) recovery (STIR) magnetic resonance imaging (MRI) is useful in assessing lower extremity (LE) denervation in subacute lumbar radiculopathy (LR), 25 subjects underwent lumbar spine MRI, LE STIR MRI and needle electromyography (EMG). In 23 (92%) subjects there was a positive c...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199709)20:9<1191::aid-mus1

    authors: Carter GT,Fritz RC

    更新日期:1997-09-01 00:00:00

  • Continuous motor unit activity confined to the upper extremities.

    abstract::We report a patient with clinical vermiform motor activity, muscle cramps, delayed relaxation of grip, and continuous motor unit discharges who developed mild symmetric symptoms in the upper extremities following a viral infection. Treatment with carbamazepine produced considerable symptomatic improvement. Needle elec...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880110310

    authors: Tandan R,Fries TJ

    更新日期:1988-03-01 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

  • Ultrasound imaging of the quadriceps muscle in elderly athletes and untrained men.

    abstract::Ultrasound (US) technique was applied to measure the thickness, cross-sectional area (CSA), and internal structure of the quadriceps muscle in 70- to 80-year-old endurance and power athletes and untrained men. Isometric knee extension strength was higher in the power athletes than in the other groups. The mean values ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880140607

    authors: Sipilä S,Suominen H

    更新日期:1991-06-01 00:00:00

  • Coping strategies in relation to quality of life in amyotrophic lateral sclerosis.

    abstract:INTRODUCTION:The aim of this study was to examine the coping strategies of 49 patients with amyotrophic lateral sclerosis (ALS) and the relationships of these strategies to their perceived health-related quality of life (HRQoL). METHODS:Forty-nine subjects were assessed for collection of demographic and medical data. ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.22270

    authors: Montel S,Albertini L,Spitz E

    更新日期:2012-01-01 00:00:00

  • Red blood cell alterations in muscular dystrophy: the role of lipids.

    abstract::Biochemical, morphologic, and biophysical studies support the concept that the red blood cell (RBC) membrane is altered in both myotonic muscular dystrophy (MyD) and Duchenne muscular dystrophy (DMD). These studies have not identified a primary metabolic defect that would explain the various alterations of membrane pr...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.880030108

    authors: Plishker GA,Appel SH

    更新日期:1980-01-01 00:00:00