Literature DB >> 14349945

A genetic study of progressive spinal muscular atrophy.

N C MYRIANTHOPOULOS, I A BROWN.   

Abstract

Entities:  

Keywords:  HEREDITY; PROGRESSIVE MUSCULAR ATROPHY/heredity

Mesh:

Year:  1954        PMID: 14349945      PMCID: PMC1716574     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


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  3 in total

1.  Progressive bulbar paralysis showing heredofamilial incidence and intellectual impairment.

Authors:  E E ROBERTSON
Journal:  AMA Arch Neurol Psychiatry       Date:  1953-02

2.  "Wetherbee Ail"; the inheritance of progressive muscular atrophy as a dominant trait in two New England families.

Authors:  M R BROWN
Journal:  N Engl J Med       Date:  1951-10-25       Impact factor: 91.245

3.  Ophthalmoplegia Exterior, with Report of Cases.

Authors:  H Friedenwald
Journal:  Trans Am Ophthalmol Soc       Date:  1922
  3 in total
  5 in total

1.  FAMILIAL MOTOR NEURONE DISEASE.

Authors:  P F ROE
Journal:  J Neurol Neurosurg Psychiatry       Date:  1964-04       Impact factor: 10.154

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.  Oculopharyngeal dystrophy diagnostic problems and possibilities.

Authors:  L A Bastiaensen; B P Schulte
Journal:  Doc Ophthalmol       Date:  1979-03-15       Impact factor: 2.379

4.  Oculopharyngeal involvement in familial neurogenic muscular atrophy.

Authors:  M Matsunaga; T Inokuchi; A Onishi; Y Kuroiwa
Journal:  J Neurol Neurosurg Psychiatry       Date:  1973-02       Impact factor: 10.154

5.  Manometric characteristics of the pharynx, upper esophageal sphincter, esophagus, and lower esophageal sphincter in patients with oculopharyngeal muscular dystrophy.

Authors:  J A Castell; D O Castell; C A Duranceau; P Topart
Journal:  Dysphagia       Date:  1995       Impact factor: 3.438

  5 in total

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