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You searched for: Author/Creator Iba-Zizen, M T

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1. Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7q. Issue 1 (1st July 1997)

4. Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal ganglia. Issue 11 (6th July 2007)

5. Therapeutic effect of mitoxantrone combined with methylprednisolone in multiple sclerosis: a randomised multicentre study of active disease using MRI and clinical criteria. Issue 2 (February 1997)