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Human Molecular Genetics|September 16, 1998
Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonismC Dumanchin, A Camuzat, D Campion, et al.European Journal of Human Genetics : EJHG|April 10, 1999
No evidence for involvement of KCNN3 (hSKCa3) potassium channel gene in familial and isolated cases of schizophreniaF Bonnet-Brilhault, C Laurent, D Campion, et al.Psychiatry Research|June 1, 1996
Association study between schizophrenia and monoamine oxidase A and B DNA polymorphismsB Coron, D Campion, F Thibaut, et al.Journal of Medical Genetics|August 1, 1996
No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study GroupD Campion, A Brice, D Hannequin, et al.Journal of Neurology|May 28, 2023
A randomized double-blind placebo-controlled trial of low-dose interleukin-2 in relapsing-remitting multiple sclerosisC Louapre, M Rosenzwajg, M Golse, et al.British Journal of Cancer|April 16, 2009
TP53 mutations predict disease control in metastatic colorectal cancer treated with cetuximab-based chemotherapyA Oden-Gangloff, F Di Fiore, F Bibeau, et al.American Journal of Human Genetics|August 12, 1999
Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrumD Campion, C Dumanchin, D Hannequin, et al.British Journal of Cancer|March 22, 2007
Clinical relevance of KRAS mutation detection in metastatic colorectal cancer treated by Cetuximab plus chemotherapyF Di Fiore, F Blanchard, F Charbonnier, et al.Pageof 5