Based on approximately eight years of data collection with the nationwide Computer Registry of All Myopathies and Polyneuropathies (CRAMP) in the Netherlands, recent epidemiologic information for thirty neuromuscular disorders is presented. This overview includes age and gender data for a number of neuromuscular disorders that are either relatively frequently seen in the neuromuscular clinic, or have a particular phenotype. Since 2004, over 20,000 individuals with a neuromuscular disorder were registered in CRAMP; 56% men and 44% women. The number per diagnosis varied from nine persons with Emery-Dreifuss muscular dystrophy to 2057 persons with amyotrophic lateral sclerosis. Proportions of men ranged from 38% with post-polio syndrome to 68%...
Epidemiologic data on inclusion body myositis (IBM) are scarce, and possibly biased, because they ar...
The Belgian Neuromuscular Disease Registry, commissioned in 2008, aims to collect data to improve kn...
We determined the prevalence of genetically determined neuromuscular diseases in adult Norwegian pat...
Based on approximately eight years of data collection with the nationwide Computer Registry of All M...
Based on approximately eight years of data collection with the nationwide Computer Registry of All M...
Based on approximately eight years of data collection with the nationwide Computer Registry of All M...
Each of the various neuromuscular diseases is rare. Consequently, solid epidemiological data are not...
Contains fulltext : 51646.pdf (publisher's version ) (Closed access)Each of the va...
Each of the various neuromuscular diseases is rare. Consequently, solid epidemiological data are not...
Each of the various neuromuscular diseases is rare. Consequently, solid epidemiological data are not...
The percentage and cause of neuromuscular (NM) diseases have been analysed during a 15-year period o...
Epidemiologic data on inclusion body myositis (IBM) are scarce, and possibly biased, because they ar...
Epidemiologic data on inclusion body myositis (IBM) are scarce, and possibly biased, because they ar...
Epidemiologic data on inclusion body myositis (IBM) are scarce, and possibly biased, because they ar...
The Belgian Neuromuscular Disease Registry, commissioned in 2008, aims to collect data to improve kn...
We determined the prevalence of genetically determined neuromuscular diseases in adult Norwegian pat...
Based on approximately eight years of data collection with the nationwide Computer Registry of All M...
Based on approximately eight years of data collection with the nationwide Computer Registry of All M...
Based on approximately eight years of data collection with the nationwide Computer Registry of All M...
Each of the various neuromuscular diseases is rare. Consequently, solid epidemiological data are not...
Contains fulltext : 51646.pdf (publisher's version ) (Closed access)Each of the va...
Each of the various neuromuscular diseases is rare. Consequently, solid epidemiological data are not...
Each of the various neuromuscular diseases is rare. Consequently, solid epidemiological data are not...
The percentage and cause of neuromuscular (NM) diseases have been analysed during a 15-year period o...
Epidemiologic data on inclusion body myositis (IBM) are scarce, and possibly biased, because they ar...
Epidemiologic data on inclusion body myositis (IBM) are scarce, and possibly biased, because they ar...
Epidemiologic data on inclusion body myositis (IBM) are scarce, and possibly biased, because they ar...
The Belgian Neuromuscular Disease Registry, commissioned in 2008, aims to collect data to improve kn...
We determined the prevalence of genetically determined neuromuscular diseases in adult Norwegian pat...