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Parkin disease: a phenotypic study of a large case series

Brain (London, England : 1878), 2003-06, Vol.126 (6), p.1279-1292

2003

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Comparison of phosphodiesterase 10A and dopamine transporter levels as markers of disease burden in early Parkinson's disease

Movement disorders, 2019-10, Vol.34 (10), p.1505-1515

2019

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

Brain (London, England : 1878), 2002-10, Vol.125 (10), p.2248-2256

2002

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Striatal and cortical pre‐ and postsynaptic dopaminergic dysfunction in sporadic parkin‐linked parkinsonism

Brain (London, England : 1878), 2004-06, Vol.127 (6), p.1332-1342

2004

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Motor cortical physiology in patients and asymptomatic carriers of parkin gene mutations

Movement disorders, 2008-10, Vol.23 (13), p.1812-1819

2008

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In vivo assessment of brain monoamine systems in parkin gene carriers: A PET study

Experimental neurology, 2010-03, Vol.222 (1), p.120-124

2010

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Upregulation of dopamine D2 receptors in dopaminergic drug-naive patients with parkin gene mutations

Movement disorders, 2006-06, Vol.21 (6), p.783-788

2006

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Autosomal recessive, DYT2-like primary torsion dystonia: a new family

Neurology, 2003-12, Vol.61 (12), p.1801-1803

2003

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Parkinsonism and nigrostriatal dysfunction are associated with spinocerebellar ataxia type 6 (SCA6)

Movement disorders, 2005-09, Vol.20 (9), p.1115-1119

2005

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Marfan syndrome presenting with headache and coincidental ophthalmic artery aneurysm

BMJ case reports, 2013-03, Vol.2013, p.bcr2012008323

2013

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Parkin disease in a Brazilian kindred: Manifesting heterozygotes and clinical follow-up over 10 years

Movement disorders, 2005-04, Vol.20 (4), p.479-484

2005

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Clinical and subclinical dopaminergic dysfunction in PARK6-linked parkinsonism: An 18F-dopa PET study

Annals of neurology, 2002-12, Vol.52 (6), p.849-853

2002

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Nigral degeneration and striatal dopaminergic dysfunction in idiopathic and parkin-linked Parkinson's disease

Movement disorders, 2006-03, Vol.21 (3), p.299-305

2006

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A Subacute Motor and Sensory Tractopathy. A New Syndrome

Open access journal of neurology & neurosurgery, 2017-07, Vol.5 (1)

L Khan, Naheed

2017

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Nigrostriatal dysfunction in homozygous and heterozygous parkin gene carriers: An 18F-dopa PET progression study

Movement disorders, 2009-11, Vol.24 (15), p.2260-2266

2009

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The genetics of Parkinson's disease

Current Opinion in Genetics & Development, 2000-06, Vol.10 (3), p.292-298

2000

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

Brain (London, England : 1878), 2005-12, Vol.128 (12), p.2786-2796

2005

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Nigrostriatal dysfunction in homozygous and heterozygous parkin gene carriers: An 18 F‐dopa PET progression study

Movement disorders, 2009-11, Vol.24 (15), p.2260-2266

2009

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Upregulation of dopamine D 2 receptors in dopaminergic drug‐naive patients with parkin gene mutations

Movement disorders, 2006-06, Vol.21 (6), p.783-788

2006

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Clinical and subclinical dopaminergic dysfunction in PARK6‐linked parkinsonism: An 18 F‐dopa PET study

Annals of neurology, 2002-12, Vol.52 (6), p.849-853

2002

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Prader-Willi and Angelman syndromes: update on genetic mechanisms and diagnostic complexities

Current opinion in neurology, 1999-04, Vol.12 (2), p.149-154

1999

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Familial parkinsonism [Parkinson's disease and early onset parkinsonism]: A genetic, clinical study and 18F-dopa pet study

Khan, Naheed L

2006

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Marfan syndrome presenting with headache and coincidental ophthalmic artery aneurysm

BMJ Case Reports, 2013, Vol.2013

2013

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SEMEN CHARACTERISTICS OF CROSSBRED (FRIESIAN X SAHIW AL) BULLS AT LIVESTOCK RESEARCH ST A T.lON, NA TIONAL AGRICUL TURAL RESEARCH CENTRE, ISLAMABAD

Pakistan veterinary journal, 2002-04, Vol.22 (4), p.181-187

S. M. H. Andrabi, S. Naheed, L. A. Khan and N. Ullah

2002

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A Community-Based Intervention for Managing Hypertension in Rural South Asia

The New England journal of medicine, 2020-02, Vol.382 (8), p.717-726

2020

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Parkin disease: a phenotypic study of a large case series

Comparison of phosphodiesterase 10A and dopamine transporter levels as markers of disease burden in early Parkinson's disease

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

Striatal and cortical pre‐ and postsynaptic dopaminergic dysfunction in sporadic parkin‐linked parkinsonism

Motor cortical physiology in patients and asymptomatic carriers of parkin gene mutations

In vivo assessment of brain monoamine systems in parkin gene carriers: A PET study

Upregulation of dopamine D2 receptors in dopaminergic drug-naive patients with parkin gene mutations

Autosomal recessive, DYT2-like primary torsion dystonia: a new family

Parkinsonism and nigrostriatal dysfunction are associated with spinocerebellar ataxia type 6 (SCA6)

Marfan syndrome presenting with headache and coincidental ophthalmic artery aneurysm

Parkin disease in a Brazilian kindred: Manifesting heterozygotes and clinical follow-up over 10 years

Clinical and subclinical dopaminergic dysfunction in PARK6-linked parkinsonism: An 18F-dopa PET study

Nigral degeneration and striatal dopaminergic dysfunction in idiopathic and parkin-linked Parkinson's disease

A Subacute Motor and Sensory Tractopathy. A New Syndrome

Nigrostriatal dysfunction in homozygous and heterozygous parkin gene carriers: An 18F-dopa PET progression study

The genetics of Parkinson's disease

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

Nigrostriatal dysfunction in homozygous and heterozygous parkin gene carriers: An 18 F‐dopa PET progression study

Upregulation of dopamine D 2 receptors in dopaminergic drug‐naive patients with parkin gene mutations

Clinical and subclinical dopaminergic dysfunction in PARK6‐linked parkinsonism: An 18 F‐dopa PET study

Prader-Willi and Angelman syndromes: update on genetic mechanisms and diagnostic complexities

Familial parkinsonism [Parkinson's disease and early onset parkinsonism]: A genetic, clinical study and 18F-dopa pet study

Marfan syndrome presenting with headache and coincidental ophthalmic artery aneurysm

SEMEN CHARACTERISTICS OF CROSSBRED (FRIESIAN X SAHIW AL) BULLS AT LIVESTOCK RESEARCH ST A T.lON, NA TIONAL AGRICUL TURAL RESEARCH CENTRE, ISLAMABAD

A Community-Based Intervention for Managing Hypertension in Rural South Asia

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