Naheed L. Khan

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...

Striatal and cortical pre- and postsynaptic dopaminergic dysfunction in sporadic parkin-linked parkinsonism (2004)

Scherfler, Christoph, Khan, Naheed L., Pavese, Nicola, Eunson, Louise, Graham, Elizabeth, Lees, Andrew J., ...

To investigate striatal and cortical pre- and postsynaptic dopaminergic function in parkin-linked parkinsonism, 13 unrelated patients homozygous or compound heterozygous for parkin mutations were...

Striatal and cortical pre- and postsynaptic dopaminergic dysfunction in sporadic parkin-linked parkinsonism (2004)

Scherfler, Christoph, Khan, Naheed L., Pavese, Nicola, Eunson, Louise, Graham, Elizabeth, Lees, Andrew J., ...

To investigate striatal and cortical pre‐ and postsynaptic dopaminergic function in parkin‐linked parkinsonism, 13 unrelated patients homozygous or compound heterozygous for parkin...

Striatal and cortical pre- and postsynaptic dopaminergic dysfunction in sporadic parkin-linked parkinsonism (2004)

Scherfler, Christoph, Khan, Naheed L., Pavese, Nicola, Eunson, Louise, Graham, Elizabeth, Lees, Andrew J., ...

To investigate striatal and cortical pre- and postsynaptic dopaminergic function in parkin-linked parkinsonism, 13 unrelated patients homozygous or compound heterozygous for parkin mutations were...

Parkin disease: a phenotypic study of a large case series (2003)

Khan, Naheed L., Graham, Elizabeth, Critchley, Peter, Schrag, Anette E, Wood, Nicholas W., Lees, Andrew J., ...

Mutations in the parkin gene, PARK2, are a common cause of parkinsonism in familial as well as isolated cases with an age of onset

Parkin disease: a phenotypic study of a large case series (2003)

Khan, Naheed L., Graham, Elizabeth, Critchley, Peter, Schrag, Anette E, Wood, Nicholas W., Lees, Andrew J., ...

Mutations in the parkin gene, PARK2, are a common cause of parkinsonism in familial as well as isolated cases with an age of onset

Progression of nigrostriatal dysfunction in a parkin kindred: an [18F]dopa PET and clinical study (2002)

Khan, Naheed L., Brooks, David J., Pavese, Nicola, Sweeney, Mary G., Wood, Nicholas W., Lees, Andrew J., ...

Molecular and clinical characterization of parkin‐associated parkinsonism is well described; however, there are no data available on progression of dopamine terminal dysfunction in...