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Prognosis of Neurological Diseases Angelo Sghirlanzoni
Publisher: Springer Milan

Knowledge is sometimes the only power there is against the vagaries of neurological ailments. The National Institute of Neurological Disorders and Stroke offers details of diagnosis and treatment. Therefore, to diagnose a congenital myopathy, a neurologist will perform a Currently, only central core disease has an effective treatment (see above). Facts and information including research news and treatment options for Neurological Disorders affecting the human nervous system. Gaucher's Disease information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS). Neurology articles covering symptoms, diagnosis, staging, treatment, Behavioral Neurology and Dementia Inflammatory and Demyelinating Diseases. Huntington's Disease information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS). [Delirium in patients with neurological diseases: diagnosis, management and prognosis]. Symptoms vary according to the specific type of leukodystrophy, and may be difficult to recognize in the early stages of the disease. Neurological Sequelae of Lupus information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS). Guillain-Barré syndrome is a disorder in which the body's immune system attacks part of the peripheral nervous system. ALS, Amyotrophic Lateral Sclerosis or Lou Gehrig's disease information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS). Alzheimer's Disease (AD) information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS). The disease can be difficult to diagnose accurately. Type III is the most serious form of CM, and causes severe neurological defects. Therefore the diagnosis is based on medical history and a neurological examination. National Institute of Neurological Disorders and Stroke Logo. By the National Institute of Neurological Disorders and Stroke (NINDS). Doi: 10.1007/s00115-013-3934-1.