Insulin and Proinsulin-Like Molecules in Motor Neurone Disease
نویسندگان
چکیده
منابع مشابه
Familial Motor Neurone Disease.
Motor neurone disease is a relatively common condition with a gross prevalence rate of about 4 per 100,000 (Kurland, 1957). It is fairly uniformly distributed throughout the world, with the exception of the Chamorro population of Guam and Rota in the Mariana Islands and Chamorro emigrants in California. In this ethnic group the prevalence is about 420 per 100,000 (Kurland, 1957) and familial ex...
متن کاملMotor neurone disease.
THE story of motor neurone disease goes back more than a hundred years, to the latter half of the igth century, and the days of the great clinical neurologists of France. Of the many famous names linked to this story three are pre-eminent: Charcot-physician and neuropathologist, and great teacher, who became even more renowned for his studies of hysteria (Fig. i); Duchenne, the one from Boulogn...
متن کاملMotor neurone disease
Motor neurone disease (MND), or amyotrophic lateral sclerosis (ALS), is a neurodegenerative disorder of unknown aetiology. Progressive motor weakness and bulbar dysfunction lead to premature death, usually from respiratory failure. Confirming the diagnosis may initially be difficult until the full clinical features are manifest. For all forms of the disease there is a significant differential d...
متن کاملMotor neurone disease.
Motor neurone disease (MND), or amyotrophic lateral sclerosis (ALS), is a neurodegenerative disorder of unknown aetiology. Progressive motor weakness and bulbar dysfunction lead to premature death, usually from respiratory failure. Confirming the diagnosis may initially be difficult until the full clinical features are manifest. For all forms of the disease there is a significant differential d...
متن کاملManagement of motor neurone disease.
Motor neurone disease is a progressive neurodegenerative disorder leading to severe disability and death. It is clinically characterised by mixed upper and lower motor neurone involvement affecting bulbar, limb, and respiratory musculature. Recent guidelines have established diagnostic criteria and defined management of the condition. In a proportion of familial amyotrophic lateral sclerosis th...
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ژورنال
عنوان ژورنال: Annals of Clinical Biochemistry: International Journal of Laboratory Medicine
سال: 1993
ISSN: 0004-5632,1758-1001
DOI: 10.1177/000456329303000215