Proximal median neuropathy secondary to humeral neck fracture.

Abstract:

:Median neuropathies proximal to the wrist are uncommon and usually result from penetrating injuries, fracture dislocation of the distal humerus, or compression by fibrous bands. A 66-year-old man suffered a comminuted fracture of the proximal humerus after a fall. Electrodiagnostic studies revealed a severe proximal median neuropathy and a mild distal radial mononeuropathy. Proximal median neuropathy rarely occurs in humeral neck fracture, mostly because the median nerve is not in close contact with the humerus proximally.

journal_name

Muscle Nerve

journal_title

Muscle & nerve

authors

Veilleux M,Richardson P

doi

10.1002/(sici)1097-4598(200003)23:3<426::aid-mus15

subject

Has Abstract

pub_date

2000-03-01 00:00:00

pages

426-9

issue

3

eissn

0148-639X

issn

1097-4598

pii

10.1002/(SICI)1097-4598(200003)23:3<426::AID-MUS15

journal_volume

23

pub_type

杂志文章
  • 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

  • Skeletal muscle involvement in tropical spastic paraparesis/HTLV-1-associated myelopathy.

    abstract::The frequency of muscle involvement in TSP/HAM is not known, nor is the precise role that HTLV-1 and the diverse cytokines play in the genesis of HTLV-1-associated diseases. In order to better define the frequency and characteristics of the skeletal muscle involvement in TSP/HAM, we studied 11 affected patients. EMG w...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880170812

    authors: Gabbai AA,Wiley CA,Oliveira AS,Smith R,Schmidt B,Nóbrega JA,Bordin JO,Román GC

    更新日期:1994-08-01 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

  • 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

  • Validation of diagnostic methods for traumatic sensory neuropathy and neuropathic pain.

    abstract:INTRODUCTION:We evaluated diagnostic value of sensory tests during recovery from iatrogenic sensory neuropathy using intraoperatively verified nerve injury with subjective symptoms as gold standard. METHODS:Inferior alveolar nerves were monitored neurophysiologically throughout mandibular osteotomy in 19 patients. Sen...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26400

    authors: Teerijoki-Oksa T,Forssell H,Jääskeläinen SK

    更新日期:2019-03-01 00:00:00

  • Invited review: peripheral neuropathy in Sjogren's syndrome.

    abstract::Our experience and review of the literature reveal that Sjogren's syndrome (SS) is an important, poorly recognized cause of peripheral neuropathy. Several forms of peripheral nerve dysfunction occur in SS including trigeminal sensory neuropathy, mononeuropathy multiplex, distal sensory neuropathy, distal sensorimotor ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.880130703

    authors: Kaplan JG,Rosenberg R,Reinitz E,Buchbinder S,Schaumburg HH

    更新日期:1990-07-01 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

  • 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

  • Seipin S90L mutation in an Italian family with CMT2/dHMN and pyramidal signs.

    abstract::Heterozygous mutations in the Berardinelli-Seip congenital lipodystrophy (BSCL2) gene have been associated with different clinical phenotypes including Silver syndrome/spastic paraplegia 17, distal hereditary motor neuropathy type V, and Charcot-Marie-Tooth disease type 2 (CMT2) with predominant hand involvement. We s...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21734

    authors: Luigetti M,Fabrizi GM,Madia F,Ferrarini M,Conte A,Delgrande A,Tonali PA,Sabatelli M

    更新日期:2010-09-01 00:00:00

  • Lack of anionic phospholipid calcium binding sites in Duchenne muscular dystrophy.

    abstract::We studied membrane ultrastructural localization of anionic phospholipids (AP) and sialic acid (SA) calcium binding sites in muscle biopsies from Duchenne muscular dystrophy (DMD) and 3 Becker's muscular dystrophy (BMD) patients using polymyxin B (PXB) and limulus polyphemus (LP) as cytochemical markers. We found that...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880150311

    authors: Moggio M,Fagiolari G,Prelle A,Gallanti A,Sciacco M,Scarlato G

    更新日期:1992-03-01 00:00:00

  • Response to therapy in demyelinating motor neuropathy.

    abstract::We reviewed results of immunotherapy in patients with demyelinating motor neuropathy (DMN), and found that patients over 50 years of age at onset responded poorly, and younger patients responded variably to intervention. We suggest that patients with DMN be given a guarded prognosis, particularly if >50 years of age a...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199812)21:12<1769::aid-mus

    authors: Markson L,Janzen D,Bril V

    更新日期:1998-12-01 00:00:00

  • Technology literature review: quantitative sensory testing.

    abstract::The development of the personal computer has simplified the process of quantitating sensory thresholds using various testing algorithms. We reviewed the technical aspects and reproducibility of different methods to determine threshold for light touch-pressure, vibration, thermal, and pain stimuli. Clinical uses and li...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.20053

    authors: Chong PS,Cros DP

    更新日期:2004-05-01 00:00:00

  • Role of autonomic nerve functions in patients with familial amyloidotic polyneuropathy as analyzed by laser Doppler flowmetry, capsule hydrograph, and cardiographic R-R interval.

    abstract::Laser Doppler flowmetry (LDF) was conducted on familial amyloidotic polyneuropathy (FAP) patients and asymptomatic carriers of FAP. Vasoconstrictive responses in the 11 FAP patients tested, induced by deep inspiration, were markedly depressed compared with those of the healthy controls. The responses decreased with th...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880150416

    authors: Ando Y,Araki S,Shimoda O,Kano T

    更新日期:1992-04-01 00:00:00

  • Net excitation of the motor unit pool varies with load type during fatiguing contractions.

    abstract::To identify the underlying physiological mechanisms for the difference in the time to failure for two types of fatiguing contractions, 20 subjects performed force and position tasks with the elbow flexor muscles at a comparable net muscle torque for a similar duration. Prior to terminating each task, blood flow was oc...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20241

    authors: Rudroff T,Poston B,Shin IS,Bojsen-Møller J,Enoka RM

    更新日期:2005-01-01 00:00:00

  • Utility of ultrasound-guided surface electrode placement in lateral femoral cutaneous nerve conduction studies.

    abstract:INTRODUCTION:Meralgia paresthetica is a common clinical complaint for which some patients ultimately undergo surgical treatment. The lateral femoral cutaneous nerve (LFCN) has been difficult to reliably test electrophysiologically, likely due to anatomic variability and lack of responses in asymptomatic obese subjects....

    journal_title:Muscle & nerve

    pub_type: 杂志文章,随机对照试验

    doi:10.1002/mus.22102

    authors: Boon AJ,Bailey PW,Smith J,Sorenson EJ,Harper CM,Hurdle MF

    更新日期:2011-10-01 00:00:00

  • Neurodevelopmental, behavioral, and emotional symptoms common in Duchenne muscular dystrophy.

    abstract:INTRODUCTION:We studied neurodevelopmental and behavioral/emotional symptoms in patients with Duchenne muscular dystrophy (DMD). METHODS:Retrospective case series of neurodevelopmental and behavioral/emotional symptoms obtained through review of systems of 700 DMD patients in relation to dystrophin gene mutations. RE...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26803

    authors: Darmahkasih AJ,Rybalsky I,Tian C,Shellenbarger KC,Horn PS,Lambert JT,Wong BL

    更新日期:2020-04-01 00:00:00

  • Differences between young and older women in maximal force, force fluctuations, and surface EMG during isometric knee extension and elbow flexion.

    abstract::The loss of muscle strength with aging appears to be greater in the lower than upper limbs, but strength and its neural control have never been compared in the same population of individuals in both upper and lower limbs. The aim of this study was to investigate differences between eight young (20-31 years) and eight ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20151

    authors: Bazzucchi I,Felici F,Macaluso A,De Vito G

    更新日期:2004-11-01 00:00:00

  • Peripheral nerve ultrasound in amyotrophic lateral sclerosis phenotypes.

    abstract:INTRODUCTION:In this study we sought to determine the cross-sectional area (CSA) of peripheral nerves in patients with distinct subtypes of amyotrophic lateral sclerosis (ALS). METHODS:Ulnar and median nerve ultrasound was performed in 78 ALS patients [classic, n = 21; upper motor neuron dominant (UMND), n = 14; lower...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24431

    authors: Schreiber S,Abdulla S,Debska-Vielhaber G,Machts J,Dannhardt-Stieger V,Feistner H,Oldag A,Goertler M,Petri S,Kollewe K,Kropf S,Schreiber F,Heinze HJ,Dengler R,Nestor PJ,Vielhaber S

    更新日期:2015-05-01 00:00:00

  • Skin biopsy in assessing meralgia paresthetica.

    abstract:INTRODUCTION:Meralgia paresthetica is a focal neuropathy caused by compression of the lateral femoral cutaneous nerve (LFCN). The disease can be difficult to assess by neurophysiological or imaging studies. METHODS:We studied 5 patients who presented to our neuromuscular clinic from April 2012 to December 2014 with a ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25044

    authors: Wongmek A,Shin S,Zhou L

    更新日期:2016-04-01 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

  • 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

  • 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

  • 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

  • Clinical and genetic description of a family with Charcot-Marie-Tooth disease type 1B from a transmembrane MPZ mutation.

    abstract::Mutations in the myelin protein zero gene (MPZ) are associated with certain demyelinating neuropathies, and in particular with Charcot-Marie-Tooth disease type 1B (CMT1B), Dejerine-Sottas syndrome, and congenital hypomyelination. MPZ mutations affecting the protein's transmembrane domain are generally associated with ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20034

    authors: Eggers SD,Keswani SC,Melli G,Cornblath DR

    更新日期:2004-06-01 00:00:00

  • Impact of expiratory strength training in amyotrophic lateral sclerosis: Results of a randomized, sham-controlled trial.

    abstract:INTRODUCTION:The purpose of this study was to determine the impact of an in-home expiratory muscle strength training (EMST) program on pulmonary, swallow, and cough function in individuals with amyotrophic lateral sclerosis (ALS). METHODS:EMST was tested in a prospective, single-center, double-blind, randomized, contr...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,随机对照试验

    doi:10.1002/mus.26292

    authors: Plowman EK,Tabor-Gray L,Rosado KM,Vasilopoulos T,Robison R,Chapin JL,Gaziano J,Vu T,Gooch C

    更新日期:2019-01-01 00:00:00

  • Effects of cardiotrophin-1 (CT-1) in a mouse motor neuron disease.

    abstract::Cardiotrophin-1 (CT-1) has potent survival-promoting effects on motor neurons in vitro and in vivo and may be effective in treating motor neuron diseases (MND). We investigated the effects of CT-1 treatment in wobbler mouse MND. Wobbler mice were randomly assigned to receive subcutaneously injected CT-1 (1 mg/kg, n = ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.1068

    authors: Mitsumoto H,Klinkosz B,Pioro EP,Tsuzaka K,Ishiyama T,O'Leary RM,Pennica D

    更新日期:2001-06-01 00:00:00

  • Pulmonary function and electromyographic study of respiratory muscles in myotonic dystrophy.

    abstract::Ten adult myotonic dystrophy patients underwent measurements of lung function, maximal dynamic and static ventilatory efforts, and respiratory muscle electromyography (EMG). EMG studies were performed during spontaneous breathing or when subjects breathed through high inspiratory or expiratory resistive loads. Present...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880080708

    authors: Jammes Y,Pouget J,Grimaud C,Serratrice G

    更新日期:1985-09-01 00:00:00

  • Estimated cost of treating myasthenia gravis in an insured U.S. population.

    abstract:INTRODUCTION:In this study we estimated the costs paid by U.S. health plans for treating myasthenia gravis (MG) in 2009 and determined the major cost drivers. METHODS:One hundred thirteen MG patients were matched by propensity scores with 339 non-MG patients from a comprehensive health-care insurance database. The mea...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.22327

    authors: Guptill JT,Sharma BK,Marano A,Soucy A,Krueger A,Sanders DB

    更新日期:2012-03-01 00:00:00

  • Neurectomy preserves fast fibers when combined with tenotomy of infraspinatus muscle via upregulation of myogenesis.

    abstract:INTRODUCTION:We evaluated the contribution of denervation-related molecular processes to rotator cuff muscle degeneration after tendon release. METHODS:We assessed the levels of myogenic (myogenin and myogenic differentiation factor [myoD]) and proadipogenic (peroxisome proliferator-activated receptor γ) transcription...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26316

    authors: Flück M,Valdivieso P,Ruoss S,von Rechenberg B,Benn MC,Meyer DC,Wieser K,Gerber C

    更新日期:2019-01-01 00:00:00

  • Spinal irradiation does not inhibit distal axonal sprouting.

    abstract::In an attempt to determine the relative importance of the nerve cell body and of the axon in initiating and controlling axonal regeneration, nerve cell bodies were irradiated and the ability of the distal axon to sprout was examined. Mice were subjected to either 25 or 50 Gray (Gy) of x-irradiation localized to the lu...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880110513

    authors: Pamphlett RS

    更新日期:1988-05-01 00:00:00