Literature DB >> 1015851

Motor nerve conduction velocity in spinal muscular atrophy of childhood.

A Moosa, V Dubowitz.   

Abstract

The ulnar and posterior tibial conduction velocities were measured in 29 children with spinal muscular atrophy, 14 of whom had the servere form of the disease. The ulnar nerve velocity was slow in 12 of the 14 severely affected infants, but normal or fast in 11 of 14 children less severely affected. The corresponding results for the posterior tibial nerve were slow velocities in 11 of 12 infants in the severe group and normal or fast in all 11 infants less severely affected. The difficulty in distinguishing infantile spinal muscular atrophy from peripheral neuropathy is emphasized.

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Year:  1976        PMID: 1015851      PMCID: PMC1546166          DOI: 10.1136/adc.51.12.974

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  9 in total

1.  Infantile polyneuropathy with defective myelination: an autopsy study.

Authors:  S B Karch; H Urich
Journal:  Dev Med Child Neurol       Date:  1975-08       Impact factor: 5.449

2.  [Contribution of electromyography to the diagnosis of Werdnig-Hoffmann infantile spinal amyotrophy].

Authors:  J Raimbault; P Laget
Journal:  Pathol Biol (Paris)       Date:  1972-03

3.  The genetic identity of acute infantile spinal muscular atrophy.

Authors:  J H Pearn; C O Carter; J Wilson
Journal:  Brain       Date:  1973-09       Impact factor: 13.501

4.  Postnatal maturation of peripheral nerves in preterm and full-term infants.

Authors:  A Moosa; V Dubowitz
Journal:  J Pediatr       Date:  1971-12       Impact factor: 4.406

5.  Conduction velocity of motor nerve fibers in progressive spinal atrophy.

Authors:  J Chaco
Journal:  Acta Neurol Scand       Date:  1970       Impact factor: 3.209

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

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

7.  Neurogenic muscular atrophy of infancy with prolonged survival. The variable course of Werdnig-Hoffmann Disease.

Authors:  T L Munsat; R Woods; W Fowler; C M Pearson
Journal:  Brain       Date:  1969-03       Impact factor: 13.501

8.  Progressive spinal muscular atrophy with onset in infancy or early childhood.

Authors:  I Gamstorp
Journal:  Acta Paediatr Scand       Date:  1967-07

9.  Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease).

Authors:  K Fried; A E Emery
Journal:  Clin Genet       Date:  1971       Impact factor: 4.438

  9 in total
  7 in total

1.  Failure of lower motor neuron radial outgrowth precedes retrograde degeneration in a feline model of spinal muscular atrophy.

Authors:  Erin N Wakeling; Béatrice Joussemet; Patrick Costiou; Dominique Fanuel; Philippe Moullier; Martine Barkats; John C Fyfe
Journal:  J Comp Neurol       Date:  2012-06-01       Impact factor: 3.215

2.  Axonal neuropathy in female carriers of the fragile X premutation with fragile x-associated tremor ataxia syndrome.

Authors:  Suresh Ram; Inoka A Devapriya; Grace Fenton; Lindsey Mcvay; Danh V Nguyen; Flora Tassone; Ricardo A Maselli; Randi J Hagerman
Journal:  Muscle Nerve       Date:  2015-08       Impact factor: 3.217

3.  Impaired prenatal motor axon development necessitates early therapeutic intervention in severe SMA.

Authors:  Lingling Kong; David O Valdivia; Christian M Simon; Cera W Hassinan; Nicolas Delestrée; Daniel M Ramos; Jae Hong Park; Celeste M Pilato; Xixi Xu; Melissa Crowder; Chloe C Grzyb; Zachary A King; Marco Petrillo; Kathryn J Swoboda; Crystal Davis; Cathleen M Lutz; Alexander H Stephan; Xin Zhao; Marla Weetall; Nikolai A Naryshkin; Thomas O Crawford; George Z Mentis; Charlotte J Sumner
Journal:  Sci Transl Med       Date:  2021-01-27       Impact factor: 17.956

4.  Diaphragmatic paralysis due to spinal muscular atrophy. An unrecognised cause of respiratory failure in infancy?

Authors:  R C McWilliam; D Gardner-Medwin; D Doyle; J B Stephenson
Journal:  Arch Dis Child       Date:  1985-02       Impact factor: 3.791

5.  Clinical study of proximal spinal muscular atrophy. Report on 89 cases.

Authors:  P Tonali; S Servidei; A Uncini; D Restuccia; G Galluzzi
Journal:  Ital J Neurol Sci       Date:  1984-12

6.  Large scale deletions of the 5q13 region are specific to Werdnig-Hoffmann disease.

Authors:  P Burlet; L Bürglen; O Clermont; S Lefebvre; L Viollet; A Munnich; J Melki
Journal:  J Med Genet       Date:  1996-04       Impact factor: 6.318

Review 7.  Spinal muscular atrophy: from tissue specificity to therapeutic strategies.

Authors:  Daniel M Iascone; Christopher E Henderson; Justin C Lee
Journal:  F1000Prime Rep       Date:  2015-01-05
  7 in total

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