Fasciculation potentials in healthy people.

Abstract:

:The aim of this study was to investigate the fasciculation potentials (FPs) in the small-peripheral muscles of the foot and hand and the possible associated factors, in a healthy population. One hundred-twenty-two normal individuals (65 men and 57 women), aged 17-67 years (mean 39.96, SD=12.76) participated in the study. A special questionnaire consisting of 47 questions was devised as the basic instrument of the interview, which included the Hamilton anxiety rating scale. The extensor digitorum brevis (EDB), the flexor hallucis brevis (FHB) and the first dorsal interosseous (FDI) muscles were studied bilaterally using surface electrodes. In 94 (58 men and 36 women) from 122 participants (65 men and 57 women) FPs were recorded (men 89.2%, women 63.1%, all 77%). The mean FPs per minute and muscle, in all three muscles, was 8.0 (SD=4.6). More FPs were recorded in the muscles of foot than in FDI (p<0.01) and in FHB than in EDB (p<0.001). FPs were correlated to gender, body height and weight and to the score of the Hamilton scale (r2>0.1, p<0.01). The syndrome of benign FPs was observed in 2 men (1.6% of men). These results suggest that FPs are a very common phenomenon in the peripheral muscles of healthy persons.

journal_name

Muscle Nerve

journal_title

Muscle & nerve

authors

Mitsikostas DD,Karandreas N,Coutsopetras P,Piperos P,Lygidakis C,Papageorgiou C

doi

10.1002/(sici)1097-4598(199804)21:4<533::aid-mus14

subject

Has Abstract

pub_date

1998-04-01 00:00:00

pages

533-5

issue

4

eissn

0148-639X

issn

1097-4598

pii

10.1002/(SICI)1097-4598(199804)21:4<533::AID-MUS14

journal_volume

21

pub_type

杂志文章
  • Polysaccharide storage myopathy.

    abstract::In a woman with a slowly progressive adult onset proximal myopathy, muscle biopsy showed storage of PAS positive material in type 1 fibers. This material consisted of a branched chain polysaccharide associated with a mucoprotein. No abnormality of glycogen-pathway enzymes was detected. This suggested that this polysac...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880110411

    authors: Thompson AJ,Swash M,Cox EL,Ingram DA,Gray A,Schwartz MS

    更新日期:1988-04-01 00:00:00

  • Enrichment of the R77C alpha-sarcoglycan gene mutation in Finnish LGMD2D patients.

    abstract::Limb-girdle muscular dystrophy 2D (LGMD2D) is caused by mutations in the alpha-sarcoglycan gene (SGCA). The most frequently reported mutation, 229CGC>TGC (R77C) in exon 3 of SGCA, results in the substitution of arginine by cysteine. We present here the clinical, immunohistochemical, and genetic data of 11 Finnish pati...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20267

    authors: Hackman P,Juvonen V,Sarparanta J,Penttinen M,Aärimaa T,Uusitalo M,Auranen M,Pihko H,Alén R,Junes M,Lönnqvist T,Kalimo H,Udd B

    更新日期:2005-02-01 00:00:00

  • The role of cranial and thoracic electromyography within diagnostic criteria for amyotrophic lateral sclerosis.

    abstract:INTRODUCTION:The contribution of cranial and thoracic region electromyography (EMG) to diagnostic criteria for amyotrophic lateral sclerosis (ALS) has not been evaluated. METHODS:Clinical and EMG data from each craniospinal region were retrospectively assessed in 470 patients; 214 had ALS. Changes to diagnostic classi...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25062

    authors: Jenkins TM,Alix JJ,Kandler RH,Shaw PJ,McDermott CJ

    更新日期:2016-09-01 00:00:00

  • Location-dependent change of median nerve mobility in the carpal tunnel of patients with carpal tunnel syndrome.

    abstract:INTRODUCTION:The purpose of this study was to investigate in vivo median nerve longitudinal mobility in different segments of the carpal tunnel associated with active finger motion in carpal tunnel syndrome (CTS) patients in a comparison with healthy controls. METHODS:Eleven healthy volunteers and 11 CTS patients part...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.27017

    authors: Yao Y,Grandy E,Evans PJ,Seitz WH Jr,Li ZM

    更新日期:2020-10-01 00:00:00

  • Addressing heterogeneity in amyotrophic lateral sclerosis CLINICAL TRIALS.

    abstract::Amyotrophic lateral sclerosis (ALS) is a debilitating neurodegenerative disorder with complex biology and significant clinical heterogeneity. Many preclinical and early phase ALS clinical trials have yielded promising results that could not be replicated in larger phase 3 confirmatory trials. One reason for the lack o...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.26801

    authors: Goyal NA,Berry JD,Windebank A,Staff NP,Maragakis NJ,van den Berg LH,Genge A,Miller R,Baloh RH,Kern R,Gothelf Y,Lebovits C,Cudkowicz M

    更新日期:2020-08-01 00:00:00

  • Task-dependent facilitation of motor evoked potentials during dynamic and steady muscle contractions.

    abstract::Task-dependent differences in the facilitation of motor evoked potentials (MEPs) following cortex stimulation were studied in a proximal (deltoid) and a distal muscle (abductor digiti minimi; ADM) in 23 healthy subjects during both dynamic and steady contractions of the target muscle under isometric and under nonisome...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199810)21:10<1309::aid-mus

    authors: Arányi Z,Mathis J,Hess CW,Rösler KM

    更新日期:1998-10-01 00:00:00

  • Transgenic overexpression of laminin alpha1 chain in laminin alpha2 chain-deficient mice rescues the disease throughout the lifespan.

    abstract::Several approaches to treat laminin alpha2 chain-deficient congenital muscular dystrophy (MDC1A) in mouse models have been undertaken. Most have shown promising results in young animals. However, older animals have only been characterized to some extent. Herein we analyze the lifespan of laminin alpha2 chain-deficient...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21616

    authors: Gawlik KI,Durbeej M

    更新日期:2010-07-01 00:00:00

  • Ocular neuropathy in peripheral neuropathies.

    abstract::Ocular movements and coordination require complex and integrated functions of somatic and autonomic nervous systems. Neurological disorders affecting these nervous systems may cause ocular dysfunction involving extraocular muscles and pupils. In this article, the prevalence, clinical presentations, and management of o...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.23414

    authors: Evliyaoglu F,Karadag R,Burakgazi AZ

    更新日期:2012-11-01 00:00:00

  • Growth and denervation response of skeletal muscle fibers of newborn rats.

    abstract::The cross-sectional area of the fibers of hindlimb muscles of rats increased 10-40 times during the first 6 weeks after birth. Denervation at birth stopped the growth of the muscle fibers. The number of satellite cells decreased, and eventually all fibers vanished. Reinnervation, if any, was poor. Partial denervation ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880130509

    authors: Schmalbruch H

    更新日期:1990-05-01 00:00:00

  • What is Normal? Neuromuscular junction reinnervation after nerve injury.

    abstract:INTRODUCTION:In this study we present a reproducible technique to assess motor recovery after nerve injury via neuromuscular junction (NMJ) immunostaining and electrodiagnostic testing. METHODS:Wild-type mice underwent sciatic nerve transection with repair. Hindlimb muscles were collected for microscopy up to 30 weeks...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26654

    authors: Vannucci B,Santosa KB,Keane AM,Jablonka-Shariff A,Lu CY,Yan Y,MacEwan M,Snyder-Warwick AK

    更新日期:2019-11-01 00:00:00

  • Critical review of gangliosides and thyrotropin-releasing hormone in peripheral neuromuscular diseases.

    abstract::The lack of effective therapy for many of the chronic neuromuscular diseases such as amyotrophic lateral sclerosis, hereditary motor sensory neuropathy (Charcot-Marie-Tooth disease), spinocerebellar degenerations and idiopathic polyneuropathy has led to a search for substances that may stimulate peripheral nerve regen...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.880130910

    authors: Bradley WG

    更新日期:1990-09-01 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

  • Systematic test of neurotoxin dose and volume on muscle function in a rat model.

    abstract:INTRODUCTION:Onabotulinum toxin serotype A (BT-A) is used for a variety of motor and sensory disorders related to abnormal muscle activity. METHODS:We developed a high-resolution rodent model to allow precise determination of the effect of BT-A dose (measured in units) and injectate volume (measured in μl) on the effi...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.23983

    authors: Hulst JB,Minamoto VB,Lim MB,Bremner SN,Ward SR,Lieber RL

    更新日期:2014-05-01 00:00:00

  • Ulnar neuropathy and dystonic flexion of the fourth and fifth digits: clinical correlation in musicians.

    abstract::Peripheral nerve lesions are sometimes associated with focal dystonia. We diagnosed ulnar neuropathy in 28 of 73 (40%) cases of occupational cramp in musicians. Focal slowing of ulnar conduction across the elbow was identified in 15 of 19 (79%) patients using the near nerve technique and in 5 of 17 (29%) patients usin...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880190403

    authors: Charness ME,Ross MH,Shefner JM

    更新日期:1996-04-01 00:00:00

  • Risk of thrombotic events after inpatient intravenous immunoglobulin or plasma exchange for neurologic disease: A case-crossover study.

    abstract:INTRODUCTION:Our aim in this study was to determine whether intravenous immunoglobulin (IVIg) or plasma exchange (PLEx) for treatment of neurologic disease is a trigger for thrombotic events. METHODS:Using administrative data from 2005 to 2014, we identified index admissions for thrombotic events. We performed case-cr...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26884

    authors: Jin PH,Shin SC,Dhamoon MS

    更新日期:2020-09-01 00:00:00

  • Diagnostic usefulness of denervation edema in the multifidus muscles using 3-Tesla magnetic resonance imaging in cervical radiculopathy.

    abstract:BACKGROUND:Diagnosing cervical radiculopathy (CR) can be difficult because of symptomatic overlap with peripheral neuropathies. In this retrospective observational study, we aimed to determine whether short-tau inversion recovery (STIR) magnetic resonance imaging (MRI) sequences are useful for detecting signs of denerv...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.27142

    authors: Yoshida T,Suwazono S,Sueyoshi T,Izumi Y,Nodera H

    更新日期:2020-12-13 00:00:00

  • The utility of various sensory nerve conduction responses in assessing brachial plexopathies.

    abstract::To determine which sensory nerve conduction studies (S-NCS) are helpful in detecting supraclavicular axon loss brachial plexopathies, we selected 53 cases (of 417 reviewed) in whom complicating factors were absent and which, by needle electrode examination findings, involved only a single "truncal" element (upper, mid...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880180813

    authors: Ferrante MA,Wilbourn AJ

    更新日期:1995-08-01 00:00:00

  • Contractile properties of human thenar muscles paralyzed by spinal cord injury.

    abstract::The electrical and mechanical properties of paralyzed human thenar muscles were measured in response to supramaximal stimulation of the median nerve in individuals with chronic cervical spinal cord injury. These data were compared to those recorded from control muscles. Spontaneous motor unit activity was common in pa...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199707)20:7<788::aid-mus2>

    authors: Thomas CK

    更新日期:1997-07-01 00:00:00

  • Sural nerve biopsy studies in Leigh's subacute necrotizing encephalomyelopathy.

    abstract::Peripheral neuropathy marked by reduced nerve conduction velocities was found in four unrelated children, between the ages of 15 months and 9 years, whose autopsies revealed Leigh's subacute necrotizing encephalomyelopathy. Sural nerve biopsies disclosed primary demyelination and remyelination, as well as loss of myel...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880090210

    authors: Goebel HH,Bardosi A,Friede RL,Kohlschütter A,Albani M,Siemes H

    更新日期:1986-02-01 00:00:00

  • Real-time visualization of muscle stiffness distribution with ultrasound shear wave imaging during muscle contraction.

    abstract::A stand-alone ultrasound shear wave imaging technology has been developed to quantify and visualize Young's modulus distribution by remotely applying ultrasound radiation force and tracking the resulting microvibrations in soft tissues with ultrafast ultrasound imaging. We report the first preliminary data that detect...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21723

    authors: Shinohara M,Sabra K,Gennisson JL,Fink M,Tanter M

    更新日期:2010-09-01 00:00:00

  • Diabetic neuropathies.

    abstract::Diabetic neuropathies are the most common type of neuropathies seen in clinical practice. These neuropathies can range clinically from asymptomatic to manifesting symptoms caused by motor, sensory, and autonomic nerve dysfunction. These neuropathies can affect the peripheral nervous system, pain receptors, cardiovascu...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.27014

    authors: Patel K,Horak H,Tiryaki E

    更新日期:2021-01-01 00:00:00

  • Anconeus motor unit number estimates using decomposition-based quantitative electromyography.

    abstract:INTRODUCTION:Motor unit number estimates (MUNEs) provide important information in health, aging, and disease, and can be determined using decomposition-enhanced spike-triggered averaging (DE-STA). Discrimination of surface-detected motor unit potentials (S-MUPs) has been limited to contractile forces of ∽30% maximum vo...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24092

    authors: Stevens DE,Harwood B,Power GA,Doherty TJ,Rice CL

    更新日期:2014-07-01 00:00:00

  • Electromyography of the anal sphincter: which muscle to examine?

    abstract::Electromyographic examination of the deeper external anal sphincter (EAS) muscle is far more uncomfortable than of the subcutaneous muscle, so we tested the need for its examination. We compared the findings in 85 paired examinations of ipsilateral subcutaneous and deeper EAS muscles in 67 patients with a cauda equina...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.10417

    authors: Podnar S

    更新日期:2003-09-01 00:00:00

  • Assessment of upper and lower motor neurons in Kennedy's disease: implications for corticomotoneuronal PSTH studies.

    abstract::We used peristimulus time histograms (PSTHs) to estimate characteristics of the composite excitatory postsynaptic potentials (EPSPs) generated at the anterior horn cell by a descending cortical volley induced by subthreshold transcranial magnetic stimuli in 11 normal subjects, 9 patients with DNA-confirmed Kennedy's d...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199903)22:3<299::aid-mus2>

    authors: Weber M,Eisen A

    更新日期:1999-03-01 00:00:00

  • A population-based survey of risk for cancer in individuals diagnosed with myotonic dystrophy.

    abstract:INTRODUCTION:The risk of cancer in patients diagnosed with myotonic dystrophy (DM) is reported for the homogeneous Utah population. METHODS:Clinical data accessed from the largest Utah healthcare providers have been record-linked to the Utah Population Database, a population-based resource also linked to the Utah Canc...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25145

    authors: Abbott D,Johnson NE,Cannon-Albright LA

    更新日期:2016-10-01 00:00:00

  • Toxoplasmic myositis as a presenting manifestation of idiopathic CD4 lymphocytopenia.

    abstract::Toxoplasma gondii encysts in skeletal muscle. Although only rarely found at muscle biopsy, this parasite has previously been regarded as a possible cause of polymyositis. We report a case of biopsy-proven toxoplasmic myositis in a non-HIV-infected patient that led to recognition of idiopathic CD4 lymphocytopenia (ICL)...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.10376

    authors: Plonquet A,Bassez G,Authier FJ,Dray JM,Farcet JP,Gherardi RK

    更新日期:2003-06-01 00:00:00

  • Obturator neuropathy: causes and outcome.

    abstract::To study causes of obturator neuropathy and to correlate them with outcome, we retrospectively studied patients seen at the Mayo Clinic electromyography (EMG) laboratory from 1975 through 1999 with a diagnosis of obturator neuropathy. Twenty-two patients with obturator neuropathy were identified. The clinical outcome ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.10065

    authors: Sorenson EJ,Chen JJ,Daube JR

    更新日期:2002-04-01 00:00:00

  • SMA valiant trial: a prospective, double-blind, placebo-controlled trial of valproic acid in ambulatory adults with spinal muscular atrophy.

    abstract:INTRODUCTION:An open-label trial suggested that valproic acid (VPA) improved strength in adults with spinal muscular atrophy (SMA). We report a 12-month, double-blind, cross-over study of VPA in ambulatory SMA adults. METHODS:There were 33 subjects, aged 20–55 years, included in this investigation. After baseline asse...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,随机对照试验

    doi:10.1002/mus.23904

    authors: Kissel JT,Elsheikh B,King WM,Freimer M,Scott CB,Kolb SJ,Reyna SP,Crawford TO,Simard LR,Krosschell KJ,Acsadi G,Schroth MK,D'Anjou G,LaSalle B,Prior TW,Sorenson S,Maczulski JA,Swoboda KJ,Project Cure Spinal Muscular Atr

    更新日期:2014-02-01 00:00:00

  • Focal inflammatory myopathy.

    abstract::We report three patients with inflammatory myopathy who presented clinically with weakness and wasting of only one limb. The myopathy progressed over 6 months and 5 years, respectively, in two patients and was stable after 8 years in the third patient. One patient had a skin rash. Serum CK was elevated in the two pati...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880070210

    authors: Lederman RJ,Salanga VD,Wilbourn AJ,Hanson MR,Dudley AW Jr

    更新日期:1984-02-01 00:00:00

  • Beta-oxidation enzymes in normal human muscle and in muscle from a patient with an unusual form of myopathic carnitine deficiency.

    abstract::In a reported patient with myopathic carnitine deficiency, addition of exogenous carnitine to muscle homogenates failed to correct palmitate oxidation, and oral carnitine was of no clinical benefit. In a muscle biopsy from this patient, we found that, in contrast to the marked deficiency of free carnitine (3% of norma...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880080809

    authors: Trevisan CP,Reichmann H,DeVivo DC,DiMauro S

    更新日期:1985-10-01 00:00:00