Patrick Abou-Sleiman

Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data (2005)

Khan, Naheed L., Jain, Shushant, Lynch, John M., Pavese, Nicola, Abou-Sleiman, Patrick, Holton, Janice L., ...

We have established that the frequency of LRRK2 mutations in a series of 118 cases of familial Parkinson's disease is 5.1%. In the largest family with autosomal dominant, late-onset Parkinson's...

Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data (2005)

Khan, Naheed L., Jain, Shushant, Lynch, John M., Pavese, Nicola, Abou-Sleiman, Patrick, Holton, Janice L., ...

We have established that the frequency of LRRK2 mutations in a series of 118 cases of familial Parkinson's disease is 5.1%. In the largest family with autosomal dominant, late-onset Parkinson's...

The structure of the tau haplotype in controls and in progressive supranuclear palsy (2004)

Pittman, Alan, Myers, Amanda J., Duckworth, Jaime, Bryden, Leslie, Hanson, Melissa, Abou-Sleiman, Patrick, ...

The group of neurodegenerative diseases collectively known as tauopathies are characterised by hallmark lesions consisting of fibrillar aggregates of the microtubule associated protein, tau....

The structure of the tau haplotype in controls and in progressive supranuclear palsy (2004)

Pittman, Alan, Myers, Amanda J., Duckworth, Jaime, Bryden, Leslie, Hanson, Melissa, Abou-Sleiman, Patrick, ...

The group of neurodegenerative diseases collectively known as tauopathies are characterised by hallmark lesions consisting of fibrillar aggregates of the microtubule associated protein, tau....