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Genetic heterogeneity in paroxysmal nonkinesigenic dyskinesia

Neurology, 2006-05, Vol.66 (10), p.1588-1590

2006

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A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16

Brain (London, England : 1878), 2000-10, Vol.123 (10), p.2040-2045

2000

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Ataxia and the role of antigliadin antibodies

Canadian journal of neurological sciences, 2007-05, Vol.34 (2), p.193-196

2007

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The molecular basis and clinical management of ataxia telangiectasia

Canadian journal of neurological sciences, 2000-08, Vol.27 (3), p.184-191

2000

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Mutation analysis of the sodium/hydrogen exchanger gene (NHE5) in familial paroxysmal kinesigenic dyskinesia

Journal of Neural Transmission, 2002-09, Vol.109 (9), p.1189-1194

2002

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Neuroimaging features of heroin inhalation toxicity: "chasing the dragon"

American journal of roentgenology (1976), 2003-03, Vol.180 (3), p.847-850

2003

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PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine

Neurology, 2012-11, Vol.79 (21), p.2115-2121

2012

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Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: Evidence for a third EKD gene

Movement disorders, 2002-07, Vol.17 (4), p.717-725

2002

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The genetics of Parkinson's disease

Current opinion in neurology, 1999-08, Vol.12 (4), p.427-432

1999

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Fatal familial insomnia: the first account in a family of Chinese descent

Archives of neurology (Chicago), 2004-01, Vol.61 (1), p.122

2004

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Functional implications of a novel EA2 mutation in the P/Q-type calcium channel

Annals of neurology, 2004-08, Vol.56 (2), p.213-220

2004

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Pseudomigraine With Lymphocytic Pleocytosis: A Calcium Channelopathy? Clinical Description of 10 Cases and Genetic Analysis of the Familial Hemiplegic Migraine Gene CACNA1A

Headache, 2003-09, Vol.43 (8), p.892-895

2003

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A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16

Brain (London, England : 1878), 2000-10, Vol.123 (10), p.2040

2000

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Familial Hemiplegic Migraine Presenting as Recurrent Encephalopathy in a Native Indian Family

Headache, 2005-10, Vol.45 (9), p.1244-1249

2005

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Malaysian siblings with friedreich ataxia and chorea: a novel deletion in the frataxin gene

Canadian journal of neurological sciences, 2004-08, Vol.31 (3), p.383-386

2004

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Ca(V)2.1 P/Q-type calcium channel alternative splicing affects the functional impact of familial hemiplegic migraine mutations: implications for calcium channelopathies

Channels (Austin, Tex.), 2009-03, Vol.3 (2), p.110-121

2009

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Paroxysmal Exertion-induced Dyskinesia

Encyclopedia of Movement Disorders, 2009, Vol.2, p.430-432

Spacey, S.D.

2009

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Two novel CACNA1A gene mutations associated with episodic ataxia type 2 and interictal dystonia

Archives of neurology (Chicago), 2005-02, Vol.62 (2), p.314

2005

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352 Did the Discontinuation of Pulse-Lavage Have A Detrimental Effect on The Quality of Hip Hemiarthroplasties Performed During the First COVID-19 Wave?

British journal of surgery, 2021-10, Vol.108 (Suppl 6)

2021

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To P or not to P? FSSA classification provides only fair to moderate agreement in hip arthroplasty

Bone & joint 360, 2021-12, Vol.10 (6), p.8-10

2021

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Synthesis and Biological Evaluation of Novel Pyrazoles and Indazoles as Activators of the Nitric Oxide Receptor, Soluble Guanylate Cyclase

Journal of medicinal chemistry, 2001-01, Vol.44 (1), p.78-93

2001

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Chasing the dragon - characterizing cases of leukoencephalopathy associated with heroin inhalation in British Columbia

Harm reduction journal, 2011-01, Vol.8 (1), p.3-3

2011

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Randomized Trial of a Lay Health Advisor and Computer Intervention to Increase Mammography Screening in African American Women

Cancer epidemiology, biomarkers & prevention, 2010-01, Vol.19 (1), p.201-210

2010

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Early Clinical Features Differentiate Cerebellar Variant MSA and Sporadic Ataxia

Canadian journal of neurological sciences, 2013-03, Vol.40 (2), p.252-254

2013

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CaV2.1 P/Q-type calcium channel alternative splicing affects the functional impact of familial hemiplegic migraine mutations: Implications for calcium channelopathies

Channels (Austin, Tex.), 2009-03, Vol.3 (2), p.110-121

2009

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Genetic heterogeneity in paroxysmal nonkinesigenic dyskinesia

A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16

Ataxia and the role of antigliadin antibodies

The molecular basis and clinical management of ataxia telangiectasia

Mutation analysis of the sodium/hydrogen exchanger gene (NHE5) in familial paroxysmal kinesigenic dyskinesia

Neuroimaging features of heroin inhalation toxicity: "chasing the dragon"

PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine

Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: Evidence for a third EKD gene

The genetics of Parkinson's disease

Fatal familial insomnia: the first account in a family of Chinese descent

Functional implications of a novel EA2 mutation in the P/Q-type calcium channel

Pseudomigraine With Lymphocytic Pleocytosis: A Calcium Channelopathy? Clinical Description of 10 Cases and Genetic Analysis of the Familial Hemiplegic Migraine Gene CACNA1A

A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16

Familial Hemiplegic Migraine Presenting as Recurrent Encephalopathy in a Native Indian Family

Malaysian siblings with friedreich ataxia and chorea: a novel deletion in the frataxin gene

Ca(V)2.1 P/Q-type calcium channel alternative splicing affects the functional impact of familial hemiplegic migraine mutations: implications for calcium channelopathies

Paroxysmal Exertion-induced Dyskinesia

Two novel CACNA1A gene mutations associated with episodic ataxia type 2 and interictal dystonia

352 Did the Discontinuation of Pulse-Lavage Have A Detrimental Effect on The Quality of Hip Hemiarthroplasties Performed During the First COVID-19 Wave?

To P or not to P? FSSA classification provides only fair to moderate agreement in hip arthroplasty

Synthesis and Biological Evaluation of Novel Pyrazoles and Indazoles as Activators of the Nitric Oxide Receptor, Soluble Guanylate Cyclase

Chasing the dragon - characterizing cases of leukoencephalopathy associated with heroin inhalation in British Columbia

Randomized Trial of a Lay Health Advisor and Computer Intervention to Increase Mammography Screening in African American Women

Early Clinical Features Differentiate Cerebellar Variant MSA and Sporadic Ataxia

CaV2.1 P/Q-type calcium channel alternative splicing affects the functional impact of familial hemiplegic migraine mutations: Implications for calcium channelopathies

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