Literature DB >> 11870724

Motor unit number estimation in infants and children with spinal muscular atrophy.

Mark B Bromberg1, Kathryn J Swoboda.   

Abstract

Spinal muscular atrophy (SMA) is a disease of lower motor neurons. Motor unit number estimation (MUNE) is an electrophysiologic method to estimate the number of motor neurons innervating a muscle group. We applied the multiple point stimulation technique to the ulnar nerve--hypothenar muscle group to study lower motor neuron loss in 14 SMA subjects, including those presymptomatic, and varying from newborn through 45 years of age. Preliminary data support the value of MUNE to help understand the time course of motor neuron loss in SMA. Copyright 2002 Wiley Periodicals, Inc.

Entities:  

Mesh:

Year:  2002        PMID: 11870724      PMCID: PMC4334581          DOI: 10.1002/mus.10050

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  13 in total

Review 1.  A review of techniques employed to estimate the number of motor units in a muscle.

Authors:  M P Slawnych; C A Laszlo; C Hershler
Journal:  Muscle Nerve       Date:  1990-11       Impact factor: 3.217

Review 2.  Invited review: motor unit estimation: methods, results, and present status.

Authors:  A J McComas
Journal:  Muscle Nerve       Date:  1991-07       Impact factor: 3.217

3.  Some electrical properties of motor units and their effects on the methods of estimating motor unit numbers.

Authors:  W F Brown; H S Milner-Brown
Journal:  J Neurol Neurosurg Psychiatry       Date:  1976-03       Impact factor: 10.154

4.  Electromyography and muscle biopsy in infantile spinal muscular atrophy.

Authors:  F Buchthal; P Z Olsen
Journal:  Brain       Date:  1970       Impact factor: 13.501

5.  The estimated numbers and relative sizes of thenar motor units as selected by multiple point stimulation in young and older adults.

Authors:  T J Doherty; W F Brown
Journal:  Muscle Nerve       Date:  1993-04       Impact factor: 3.217

Review 6.  From enigmatic to problematic: the new molecular genetics of childhood spinal muscular atrophy.

Authors:  T O Crawford
Journal:  Neurology       Date:  1996-02       Impact factor: 9.910

7.  Motor unit estimation: reproducibility of the spike-triggered averaging technique in normal and ALS subjects.

Authors:  M B Bromberg
Journal:  Muscle Nerve       Date:  1993-05       Impact factor: 3.217

8.  Prospective analysis of strength in spinal muscular atrophy. DCN/Spinal Muscular Atrophy Group.

Authors:  S T Iannaccone; B S Russman; R H Browne; C R Buncher; M White; F J Samaha
Journal:  J Child Neurol       Date:  2000-02       Impact factor: 1.987

9.  Spinal muscular atrophy: the natural course of disease.

Authors:  B S Russman; R Melchreit; J C Drennan
Journal:  Muscle Nerve       Date:  1983 Mar-Apr       Impact factor: 3.217

10.  Natural history in proximal spinal muscular atrophy. Clinical analysis of 445 patients and suggestions for a modification of existing classifications.

Authors:  K Zerres; S Rudnik-Schöneborn
Journal:  Arch Neurol       Date:  1995-05
View more
  25 in total

Review 1.  Spinal muscular atrophy: new and emerging insights from model mice.

Authors:  Gyu-Hwan Park; Shingo Kariya; Umrao R Monani
Journal:  Curr Neurol Neurosci Rep       Date:  2010-03       Impact factor: 5.081

2.  Issues in SMA clinical trial design. The International Coordinating Committee (ICC) for SMA Subcommittee on SMA Clinical Trial Design.

Authors:  P Kaufmann; F Muntoni
Journal:  Neuromuscul Disord       Date:  2007-02-14       Impact factor: 4.296

3.  Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended Family.

Authors:  Kristen Zukosky; Katherine Meilleur; Bryan J Traynor; Jahannaz Dastgir; Livija Medne; Marcella Devoto; James Collins; Jachinta Rooney; Yaqun Zou; Michele L Yang; J Raphael Gibbs; Markus Meier; Joerg Stetefeld; Richard S Finkel; Joachim Schessl; Lauren Elman; Kevin Felice; Toby A Ferguson; Ozge Ceyhan-Birsoy; Alan H Beggs; Gihan Tennekoon; Janel O Johnson; Carsten G Bönnemann
Journal:  JAMA Neurol       Date:  2015-06       Impact factor: 18.302

Review 4.  Spinal muscular atrophy: diagnosis and management in a new therapeutic era.

Authors:  W David Arnold; Darine Kassar; John T Kissel
Journal:  Muscle Nerve       Date:  2014-12-16       Impact factor: 3.217

Review 5.  Spinal muscular atrophy.

Authors:  Susan T Iannaccone; Stephen A Smith; Louise R Simard
Journal:  Curr Neurol Neurosci Rep       Date:  2004-01       Impact factor: 5.081

6.  Temporal requirement for SMN in motoneuron development.

Authors:  Le T Hao; Phan Q Duy; James D Jontes; Marc Wolman; Michael Granato; Christine E Beattie
Journal:  Hum Mol Genet       Date:  2013-03-03       Impact factor: 6.150

7.  Requirement of enhanced Survival Motoneuron protein imposed during neuromuscular junction maturation.

Authors:  Shingo Kariya; Teresa Obis; Caterina Garone; Turgay Akay; Fusako Sera; Shinichi Iwata; Shunichi Homma; Umrao R Monani
Journal:  J Clin Invest       Date:  2014-01-27       Impact factor: 14.808

8.  Treatment of spinal muscolar atrophy with intrathecal mesenchymal cells.

Authors:  Marino Andolina
Journal:  Int J Stem Cells       Date:  2012-05       Impact factor: 2.500

Review 9.  Assessment of Motor Units in Neuromuscular Disease.

Authors:  Robert D Henderson; Pamela A McCombe
Journal:  Neurotherapeutics       Date:  2017-01       Impact factor: 7.620

10.  Motor unit number estimation in the rat tail using a modified multipoint stimulation technique.

Authors:  Lora J Kasselman; Jeremy M Shefner; Seward B Rutkove
Journal:  Muscle Nerve       Date:  2009-07       Impact factor: 3.217

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.