F Kristmundsdottir
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    Explore the profile of F Kristmundsdottir including associated specialties, affiliations and a list of published articles.
           
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              15
            
            
              Citations
              68
            
            
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  Recent Articles
          1.
        
    
    Carter A, Kristmundsdottir F, Gilmour J, Glasby M
  
  
    J Hand Surg Br
    . 1998 Jul;
          23(3):365-9.
    
    PMID: 9665527
  
  
          The aim of this study was to assess the changes which occurred in the rat in target muscles after the injury and repair of a specific peripheral nerve, using several...
      
2.
        
    
    Kristmundsdottir F, Mahon M, Froes M, CUMMING W
  
  
    Neuropathol Appl Neurobiol
    . 1990 Dec;
          16(6):461-75.
    
    PMID: 2096316
  
  
          Abnormalities in muscle histology have been reported frequently for the cricopharyngeus muscle of patients with oculopharyngeal muscular dystrophy, motor neuron disease and other neurological disorders in which dysphagia is a...
      
3.
        
    
    CUMMING W, Kristmundsdottir F, Mahon M
  
  
    J Neurol Neurosurg Psychiatry
    . 1989 Feb;
          52(2):266-9.
    
    PMID: 2703844
  
  
          Autosomal dominant inheritance of an unusual muscle disease is reported in a family. The pathological appearance, of regularly arranged markedly atrophic muscle fibres without other evidence of disturbed innervation, are...
      
4.
        
    Sequential studies of a childhood myopathy: a clinical, histochemical and morphometric investigation
  
  
    
    Mahon M, Kristmundsdottir F, CUMMING W, Noronha M
  
  
    Neuropathol Appl Neurobiol
    . 1989 Jan;
          15(1):3-12.
    
    PMID: 2725830
  
  
          An unusual inherited progressive distal myopathy of early childhood onset is described in two sisters from a consanguineous Asian family. Motor milestones were normal but gait deteriorated slowly thereafter with...
      
5.
        
    
    Carrington P, Evans D, CUMMING W, Mahon M, Kristmundsdottir F
  
  
    Clin Lab Haematol
    . 1989 Jan;
          11(4):323-9.
    
    PMID: 2605873
  
  
          We report a family in which a combination of myopathy and thrombocytopenia is transmitted as an autosomal dominant characteristic through three generations. The myopathy has unusual histological features with type...
      
6.
        
    
    Mahon M, CUMMING W, Kristmundsdottir F, Evans D, Carrington P
  
  
    J Neurol Sci
    . 1988 Dec;
          88(1-3):55-67.
    
    PMID: 3225629
  
  
          We describe an unusual vacuolar myopathy with tubular aggregates in a mother and son from a family presenting with a slowly progressive, predominantly limb girdle, weakness and distal upper limb...
      
7.
        
    
    Froes M, Kristmundsdottir F, Mahon M, CUMMING W
  
  
    Neuropathol Appl Neurobiol
    . 1987 Nov;
          13(6):405-19.
    
    PMID: 3447070
  
  
          It has previously been suggested that the pathological abnormalities seen in muscle biopsies from patients with motor neuron disease (MND) are of predictive value in relation to the rate of...
      
8.
        
    
    Kristmundsdottir F, Burwell R, Harrison M
  
  
    Acta Orthop Scand
    . 1987 Jun;
          58(3):277-9.
    
    PMID: 3630662
  
  
          We have studied skeletal maturation and carpal bone development in 27 girls with Perthes' disease by assessing consecutive radiographs during an observation time of 5 years. At the time of...
      
9.
        
    
    Kristmundsdottir F, David T
  
  
    J R Soc Med
    . 1987 Jan;
          80(1):9-12.
    
    PMID: 3560137
  
  
          Growth was studied in 89 children with atopic eczema aged 1-16 years. Nine (10%) had a standing height below the 3rd centile. Both boys and girls had significantly reduced sitting...
      
10.
        
    
    Burwell R, Vernon C, Dangerfield P, Hall D, Kristmundsdottir F
  
  
    Clin Orthop Relat Res
    . 1986 Aug;
          (209):129-38.
    
    PMID: 3731586
  
  
          This paper reports a study of the serum somatomedin activity in 67 boys with Perthes' disease and in 43 control boys aged three to 11 years. It was undertaken to...