Literature DB >> 4749680

Chronic generalized spinal muscular atrophy of infancy and childhood. Arrested Werdnig-Hoffman disease.

J H Pearn, J Wilson.   

Abstract

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Year:  1973        PMID: 4749680      PMCID: PMC1648514          DOI: 10.1136/adc.48.10.768

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


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  23 in total

1.  Progressive spinal muscular atrophy in infancy and childhood.

Authors:  I Gamstorp
Journal:  Acta Neurol Scand       Date:  1967       Impact factor: 3.209

2.  A graphic method for the evaluation of motor development in infants.

Authors:  M Zdańska-Brincken; N Wolański
Journal:  Dev Med Child Neurol       Date:  1969-04       Impact factor: 5.449

3.  The genetic relationship of progressive muscular dystrophy (Duchenne type) and mental retardation.

Authors:  H J Cohen; G E Molnar; L T Taft
Journal:  Dev Med Child Neurol       Date:  1968-12       Impact factor: 5.449

4.  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

5.  A distal form of chronic spinal muscular atrophy.

Authors:  J C Meadows; C D Marsden
Journal:  Neurology       Date:  1969-01       Impact factor: 9.910

6.  Scapuloperoneal muscular atrophy.

Authors:  H E Kaeser
Journal:  Brain       Date:  1965-06       Impact factor: 13.501

7.  The Denver developmental screening test.

Authors:  W K Frankenburg; J B Dodds
Journal:  J Pediatr       Date:  1967-08       Impact factor: 4.406

8.  The reliability of paediatric case-history milestones.

Authors:  E C Donoghue; R A Shakespeare
Journal:  Dev Med Child Neurol       Date:  1967-02       Impact factor: 5.449

9.  Benign spinal muscular atrophy arising in childhood and adolescence.

Authors:  D Gardner-Medwin; P Hudgson; J N Walton
Journal:  J Neurol Sci       Date:  1967 Jul-Aug       Impact factor: 3.181

10.  Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations.

Authors:  P J Dyck; E H Lambert
Journal:  Arch Neurol       Date:  1968-06
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  5 in total

1.  Ultrastructural aspects of muscle and nerve in Werdnig-Hoffmann disease.

Authors:  H B Szliwowski; P Drochmans
Journal:  Acta Neuropathol       Date:  1975       Impact factor: 17.088

2.  A predominantly cervical form of spinal muscular atrophy.

Authors:  F Goutières; D Bogicevic; J Aicardi
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-03       Impact factor: 10.154

3.  Monogenic disorders.

Authors:  C O Carter
Journal:  J Med Genet       Date:  1977-10       Impact factor: 6.318

4.  Incidence, prevalence, and gene frequency studies of chronic childhood spinal muscular atrophy.

Authors:  J Pearn
Journal:  J Med Genet       Date:  1978-12       Impact factor: 6.318

Review 5.  Phosphatase and tensin homologue: a therapeutic target for SMA.

Authors:  Vinay K Godena; Ke Ning
Journal:  Signal Transduct Target Ther       Date:  2017-09-08
  5 in total

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