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PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine

Neurology, 2012-11, Vol.79 (21), p.2097-2103

2012

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Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia

Neurology, 2007-05, Vol.68 (21), p.1782-1789

2007

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Correlating phenotype and genotype in the periodic paralyses

Neurology, 2004-11, Vol.63 (9), p.1647-1655

2004

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Long-term Effects of Cholinesterase Inhibitors on Cognitive Decline and Mortality

Neurology, 2021-04, Vol.96 (17), p.e2220

2021

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Impact of Sleep and Circadian Disruption on Energy Balance and Diabetes: A Summary of Workshop Discussions

Sleep (New York, N.Y.), 2015-12, Vol.38 (12), p.1849-1860

2015

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Familial cortical myoclonus with a mutation in NOL3

Annals of neurology, 2012-08, Vol.72 (2), p.175-183

2012

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Risk of epilepsy diagnosis after a first unprovoked seizure in dementia

Seizure (London, England), 2020-11, Vol.82, p.118-124

2020

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Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies

Neurology, 2000-07, Vol.55 (2), p.224-230

2000

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HIV, HSV, SARS-CoV-2 and Ebola Share Long-Term Neuropsychiatric Sequelae

Neuropsychiatric disease and treatment, 2022-01, Vol.18, p.2229-2237

2022

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Deep brain stimulation for Huntington's disease: long-term results of a prospective open-label study

Journal of neurosurgery, 2014-07, Vol.121 (1), p.114-122

2014

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Effects of the COVID-19 Pandemic on the Number of New Dementia Diagnoses and the Quality of Dementia Diagnostics and Treatment

The Journal of Prevention of Alzheimer's Disease, 2024

2024

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ADHD and Present Hedonism: time perspective as a potential diagnostic and therapeutic tool

Neuropsychiatric disease and treatment, 2016-01, Vol.12, p.2963-2971

2016

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A new locus for hemiplegic migraine maps to chromosome 1q31

Neurology, 1997-11, Vol.49 (5), p.1231-1238

1997

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Stroke as a Cause of Death in Death Certificates of Patients with Dementia: A Cohort Study from the Swedish Dementia Registry

Current Alzheimer research, 2018-01, Vol.15 (14), p.1322-1330

2018

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Progressive Dystonia in Mohr-Tranebjaerg Syndrome With Cochlear Implant and Deep Brain Stimulation

Movement disorders, 2013-06, Vol.28 (6), p.737-738

2013

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PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome

Neurology, 2003-06, Vol.60 (11), p.1811

2003

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Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis

Neurology, 1994-08, Vol.44 (8), p.1500-1500

1994

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Dynamic balance in children with attention-deficit hyperactivity disorder and its relationship with cognitive functions and cerebellum

Neuropsychiatric disease and treatment, 2017-01, Vol.13, p.873-880

2017

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Randomized trials of dichlorphenamide in the periodic paralyses

Annals of neurology, 2000-01, Vol.47 (1), p.46-53

2000

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FAME 3: a novel form of progressive myoclonus and epilepsy

Neurology, 2007-04, Vol.68 (17), p.1382-1389

2007

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Novel familial cases of ICCA (infantile convulsions with paroxysmal choreoathetosis) syndrome

Epileptic disorders, 2010-09, Vol.12 (3), p.199-204

2010

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Atypical PLA2G6‐Associated Neurodegeneration: Social Communication Impairment, Dystonia and Response to Deep Brain Stimulation

Movement disorders clinical practice (Hoboken, N.J.), 2014-06, Vol.1 (2), p.128-131

2014

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Episodic movement disorders as channelopathies

Movement disorders, 2000-05, Vol.15 (3), p.429

2000

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Autosomal dominant cerebellar ataxia with retinal degeneration: clinical, neuropathologic, and genetic analysis of a large kindred

Neurology, 1994-08, Vol.44 (8), p.1441-1441

1994

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Localization of the giant axonal neuropathy gene to chromosome 16q24

Annals of neurology, 1998-01, Vol.43 (1), p.143-148

1998

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PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine

Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia

Correlating phenotype and genotype in the periodic paralyses

Long-term Effects of Cholinesterase Inhibitors on Cognitive Decline and Mortality

Impact of Sleep and Circadian Disruption on Energy Balance and Diabetes: A Summary of Workshop Discussions

Familial cortical myoclonus with a mutation in NOL3

Risk of epilepsy diagnosis after a first unprovoked seizure in dementia

Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies

HIV, HSV, SARS-CoV-2 and Ebola Share Long-Term Neuropsychiatric Sequelae

Deep brain stimulation for Huntington's disease: long-term results of a prospective open-label study

Effects of the COVID-19 Pandemic on the Number of New Dementia Diagnoses and the Quality of Dementia Diagnostics and Treatment

ADHD and Present Hedonism: time perspective as a potential diagnostic and therapeutic tool

A new locus for hemiplegic migraine maps to chromosome 1q31

Stroke as a Cause of Death in Death Certificates of Patients with Dementia: A Cohort Study from the Swedish Dementia Registry

Progressive Dystonia in Mohr-Tranebjaerg Syndrome With Cochlear Implant and Deep Brain Stimulation

PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome

Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis

Dynamic balance in children with attention-deficit hyperactivity disorder and its relationship with cognitive functions and cerebellum

Randomized trials of dichlorphenamide in the periodic paralyses

FAME 3: a novel form of progressive myoclonus and epilepsy

Novel familial cases of ICCA (infantile convulsions with paroxysmal choreoathetosis) syndrome

Atypical PLA2G6‐Associated Neurodegeneration: Social Communication Impairment, Dystonia and Response to Deep Brain Stimulation

Episodic movement disorders as channelopathies

Autosomal dominant cerebellar ataxia with retinal degeneration: clinical, neuropathologic, and genetic analysis of a large kindred

Localization of the giant axonal neuropathy gene to chromosome 16q24

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