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2. De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group. Issue 8 (August 1998)

3. Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes. Issue 5 (14th October 2005)

5. No effect of the α1-antichymotrypsin A allele in Alzheimer's disease. Issue 1 (1st July 1997)

6. No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group. Issue 8 (August 1996)