Author pages are created from data sourced from our academic publisher partnerships and public sources.
Share This Author
Case-control studies of motor neuron disease: association with mechanical injuries.
Two case-control studies of motor neuron disease showed that mechanical injuries were two to three times more frequent in both sexes, heralding amyotrophic lateral sclerosis, progressive bulbar paralysis, and progressive muscular atrophy and that the head, neck, spine, and the extremities were more often traumatized. Expand
A case control study of Creutzfeldt‐Jakob disease: Association with physical injuries
Physical injuries including operations including operations may be a predisposing factor to the development of Creutzfeldt‐Jakob disease. Expand
Epidemiology of Motor Neuron Disease
- K. Kondo
Epidemiology can give fundamental information about the frequency and other determinants of disease, including biological, geographical, and sociological risk factors. These data may give clues… Expand
Phylogeny of the Graphium butterflies inferred from nuclear 28S rDNA and mitochondrial ND5 gene sequences
Congenital Minamata Disease: Warnings From Japan's Experience
- K. Kondo
- Journal of child neurology
- 1 July 2000
This report reviews the history, clinical features, pathology, epidemiology, metal analysis, experiments, and sociolegal aspects of congenital Minamata disease. Expand
HEREDITARY PROXIMAL NEUROGENIC MUSCULAR ATROPHY IN ADULT.
Five patients with muscular atrophy resembling this syndrome are seen, except for the following two points: onset of the disorder in adults; and presence of the syndrome of bulbar palsy in three of the five cases. Expand
No sex difference in mutations rates of Duchenne muscular dystrophy.
Segregation analysis was performed to evaluate possible differences in mutation rates in man. It was based on 514 males with Duchenne type muscular dystrophy (DMD) from five of nineteen hospitals for… Expand
Changing mortality patterns of motor neuron disease in Japan
A rising trend of deaths from motor neuron disease was identified in European countries, but the rate has been stationary in the United States, and the need for extensive epidemiological studies to identify the extrinsic factors which induced such a trend. Expand
Life spans of Duchenne muscular dystrophy patients in the hospital care program in Japan
- M. Mukoyama, K. Kondo, K. Hizawa, H. Nishitani
- Journal of the Neurological Sciences
- 1 November 1987
Analysis of 176 autopsy cases of Duchenne muscular dystrophy demonstrated that hospitalized patients showed longer life spans than their non-hospitalized affected maternal uncles, and pulmonary infection has become a less frequent cause of death in recent years. Expand
Tourette syndrome in Japan: etiologic considerations based on associated factors and familial clustering.