Literature DB >> 14419782

Neurogenic muscular atrophy simulating muscular dystrophy.

K R MAGEE, R N DEJONG.   

Abstract

Entities:  

Keywords:  MUSCULAR ATROPHY/diagnosis; MUSCULAR DYSTROPHY/diagnosis

Mesh：

Year:  1960        PMID： 14419782     DOI： 10.1001/archneur.1960.03840120083009

Source DB:  PubMed          Journal:  Arch Neurol        ISSN： 0003-9942


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  10 in total

1.  [On proximal neurogenic amyotrophias with special reference to electromyography].

Authors:  M WIESENDANGER
Journal:  Dtsch Z Nervenheilkd       Date:  1960

2.  A family of juvenile proximal spinal muscular atrophy with dominant inheritance.

Authors:  A Cao; C Cainchetti; L Calisti; W Tangheroni
Journal:  J Med Genet       Date:  1976-04       Impact factor: 6.318

3.  Asymptomatic benign familial spinal muscular atrophy with hypertrophy of the calves and high creatine kinase levels.

Authors:  M Yamada; M Kano; K Chida; T Furukawa; H Tsukagoshi
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-03       Impact factor: 10.154

4.  [Histological-histochemical studies on muscular changes in pseudomyopathic spinal muscular atrophy (Wohlfart-Kugelberg-Welander)].

Authors:  R Heene
Journal:  Z Neurol       Date:  1970

5.  [Contribution to the "pseudo-dystrophic" nature of muscular atrophy in Wohlfart-Kugelberg-Welander's disease].

Authors:  K Kondo
Journal:  Acta Neuropathol       Date:  1969       Impact factor: 17.088

6.  A clinical, epidemiological and genetic study of hereditary motor neuropathies in Benghazi, Libya.

Authors:  K Radhakrishnan; A K Thacker; J C Maloo
Journal:  J Neurol       Date:  1988-09       Impact factor: 4.849

7.  Genetic investigations on chronic forms of infantile and juvenile spinal muscular atrophy.

Authors:  I Hausmanowa-Petrusewicz; J Zaremba; J Borkowska; J Prot
Journal:  J Neurol       Date:  1976-10-04       Impact factor: 4.849

Review 8.  The nosology of the spinal muscular atrophies.

Authors:  A E Emery
Journal:  J Med Genet       Date:  1971-12       Impact factor: 6.318

9.  Kugelberg-Welander syndrome (hereditary proximal spinal muscular atrophy).

Authors:  J M Garvie; A L Woolf
Journal:  Br Med J       Date:  1966-06-11

10.  Evidence of autosomal dominant mutations in childhood-onset proximal spinal muscular atrophy.

Authors:  S Rudnik-Schöneborn; B Wirth; K Zerres
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025
  10 in total

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