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| ninds.nih.gov/ The NINDS offers news, coordinates events, and conducts research into disorders of the brain and nervous system. Also provides information about specific conditions such as Alzheimer's disease, autism, cerebral palsy, epilepsy, and Parkinson's, together w | |
| neuro-www2.mgh.harvard.edu/gaucher/clinicalperspectives/April1996/labdiagnosis.html Includes information such as phenotypes of gaucher disease, genotype/phenotype correlations, enzymatic diagnosis, molecular diagnosis and genetic counselling. | ||
| neuro-www2.mgh.harvard.edu/gaucher/living.html History, typicalities, diagnosis, and treatments are considered. A guide for patients, parents, relatives, and friends. | ||
| gaucherdisease.org/ Includes details of symptoms, prevalence, transmission, and therapy. Information about Gaucher disease, a lipid-storage disorder. | ||
| ntsad.org/ntsad/gaucher.htm The major disease manifestations are due to the progressive storage of glucocerebroside in Gaucher cells in the bone marrow, spleen and liver. Gaucher cells in the bo Range of information about Gaucher Disease, first described by Phillipe Gaucher in 1882. | ||
| text.nlm.nih.gov/nih/ta/www/16.html Report on a Technology Assessment Conference evaluating the diagnosis and treatment of Gaucher disease. Screening, genetic counselling, and management are covered, as is the natural history of the disease, roles of current molecular and enzymatic assays, | ||
| addenbrookes.org.uk/serv/clin/med/gaucher1.html The service includes full clinical assessment of Gaucher's patients, advice on general medical and specialist needs e.g. pregnancy, surgical procedures, and patient review. An advisory service for patients and families with Gaucher's disease. | ||
| gaucher.org.uk/ Includes news, articles, and a list of regional associations. Information and support for doctors and patients with Gaucher disease (an inherited, enzyme deficiency disorder). | ||
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