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Orphan Drugs in Epilepsy

Genton Pierre, Nikanorova Marina, Johannessen Landmark Cecilie, Johannessen Svein I.
Publication date 22/09/2011
EAN: 9782742008100
Availability Available from publisher
More than half of epilepsies start before the age of 20 years and nearly 25% of them are refractory.A tiny proportion of them are even labelled a "rare illness", i.e. one affecting less than 200,000 people in the United States or less than 5 out of 1... See full description
Attribute nameAttribute value
Common books attribute
PublisherJOHN LIBBEY
Page Count76
Languageen
AuthorGenton Pierre, Nikanorova Marina, Johannessen Landmark Cecilie, Johannessen Svein I.
FormatPaperback / softback
Product typeBook
Publication date22/09/2011
Weight188 g
Dimensions (thickness x width x height)0.50 x 17.00 x 23.90 cm
More than half of epilepsies start before the age of 20 years and nearly 25% of them are refractory.A tiny proportion of them are even labelled a "rare illness", i.e. one affecting less than 200,000 people in the United States or less than 5 out of 10,000 people in the European Union.For these patients, two problems in their management arise:In children, seizures affect an immature brain and can impact its development. It is therefore essential to treat them so that brain development continues as normally as possible.The rarity of these syndromes does not encourage the pharmaceutical industry to invest in research.Therefore, there are few drugs available.However, a few target syndromes with a particularly unfavourable diagnosis. This work outlines 6 molecules in detail that are specifically used in epileptic encephalopathies. Every aspect of these molecules is discussed, including drug development, indication, efficacy, cost, etc.Drafted by international experts in the field of epileptology, it provides all the necessary information on orphan drugs and their clinical use.