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A real‐world, observational study of erenumab for migraine prevention in Canadian patients

Headache, 2022-04, Vol.62 (4), p.522-529

2022

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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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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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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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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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Unilateral pallidal deep brain stimulation in a patient with dystonia secondary to episodic ataxia type 2

Stereotactic and functional neurosurgery, 2013-01, Vol.91 (4), p.233-235

2013

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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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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 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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Novel CACNB4 Variant Associated with a Case of Progressive Ataxia (P5.391)

Neurology, 2016-04, Vol.86 (16_supplement)

2016

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A Real-World, Observational Study of Erenumab for Migraine Prevention in Canadian Patients With Prior Prophylactic Treatment Failure (P10-2.002)

Neurology, 2022-05, Vol.98 (18_supplement)

2022

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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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Adult onset spinocerebellar ataxia in a Canadian movement disorders clinic

Canadian journal of neurological sciences, 2005-11, Vol.32 (4), p.450-458

2005

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Canadian Headache Society Guideline: Acute Drug Therapy for Migraine Headache

Canadian journal of neurological sciences, 2013-09, Vol.40 (S3), p.S1-S3

2013

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Acute and prophylactic treatment of migraine: 2023 update

Canadian Primary Care Today, 2023-06

2023

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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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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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Migraine with aura as the predominant phenotype in a family with a PRRT2 mutation

Journal of neurology, 2013-02, Vol.260 (2), p.656-660

2013

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EPILEPSY AND MOVEMENT DISORDERS. 2002. Edited by Renzo Guerrini, Jean Aicardi Frederick Andermann and Mark Hallet. Published by Cambridge University Press. 557 pages. C$193.40 approx

Canadian journal of neurological sciences, 2002-08, Vol.29 (3), p.297-298

Spacey, Sian

2002

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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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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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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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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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Brief Communication: 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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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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A real‐world, observational study of erenumab for migraine prevention in Canadian patients

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

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

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

Early Clinical Features Differentiate Cerebellar Variant MSA and Sporadic Ataxia

Unilateral pallidal deep brain stimulation in a patient with dystonia secondary to episodic ataxia type 2

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

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

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

Novel CACNB4 Variant Associated with a Case of Progressive Ataxia (P5.391)

A Real-World, Observational Study of Erenumab for Migraine Prevention in Canadian Patients With Prior Prophylactic Treatment Failure (P10-2.002)

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

Adult onset spinocerebellar ataxia in a Canadian movement disorders clinic

Canadian Headache Society Guideline: Acute Drug Therapy for Migraine Headache

Acute and prophylactic treatment of migraine: 2023 update

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

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

Migraine with aura as the predominant phenotype in a family with a PRRT2 mutation

EPILEPSY AND MOVEMENT DISORDERS. 2002. Edited by Renzo Guerrini, Jean Aicardi Frederick Andermann and Mark Hallet. Published by Cambridge University Press. 557 pages. C$193.40 approx

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

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

Ataxia and the role of antigliadin antibodies

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

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

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

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