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Correlation or Limits of Agreement? Applying the Bland-Altman Approach to the Comparison of Cognitive Screening Instruments

Dementia and geriatric cognitive disorders, 2016-12, Vol.42 (5-6), p.247-254

Larner, A J

2016

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Presenilin-1 mutation Alzheimer's disease: A genetic epilepsy syndrome?

Epilepsy & behavior, 2011-05, Vol.21 (1), p.20-22

Larner, A.J

2011

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Charles Dickens (1812–1870) and epilepsy

Epilepsy & behavior, 2012-08, Vol.24 (4), p.422-425

Larner, A.J

2012

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Intrafamilial clinical phenotypic heterogeneity with progranulin gene p.Glu498fs mutation

Journal of the neurological sciences, 2012-05, Vol.316 (1), p.189-190

Larner, A.J

2012

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Perry syndrome: A disorder to consider in the differential diagnosis of Parkinsonism

Journal of the neurological sciences, 2013-07, Vol.330 (1), p.117-118

2013

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Prevalence and causes of seizures at the time of diagnosis of probable Alzheimer's disease

Dementia and geriatric cognitive disorders, 2006-01, Vol.22 (2), p.121-124

2006

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Myoclonus-dystonia (DYT11) with novel SGCE mutation misdiagnosed as a primary psychiatric disorder

Journal of the neurological sciences, 2014-11, Vol.346 (1), p.356-357

2014

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Senile myoclonic epilepsy in Down syndrome

Seizure (London, England), 2011-07, Vol.20 (6), p.512-512

Larner, A.J

2011

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Addenbrooke's Cognitive Examination (ACE) for the diagnosis and differential diagnosis of dementia

Clinical neurology and neurosurgery, 2007-07, Vol.109 (6), p.491-494

Larner, A.J

2007

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FTDP-17: 2-Year Follow-Up of Motor and Cognitive Features After Autologous Stem-Cell Transplantation

The Journal of Neuropsychiatry and Clinical Neurosciences, 2012-04, Vol.24 (2), p.E1-E2

Larner, A.J

2012

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Intrafamilial clinical phenotypic heterogeneity with MAPT gene splice site IVS10+16C>T mutation

Journal of the neurological sciences, 2009-12, Vol.287 (1), p.253-256

Larner, A.J

2009

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Margiad Evans (1909–1958): A history of epilepsy in a creative writer

Epilepsy & behavior, 2009-12, Vol.16 (4), p.596-598

Larner, A.J

2009

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Referrals to the neurology clinic from oral and maxillofacial surgery clinics

British journal of oral & maxillofacial surgery, 2011-10, Vol.49 (7), p.576-577

Larner, A.J

2011

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Presenilin-1 mutations in Alzheimer's disease: an update on genotype-phenotype relationships

Journal of Alzheimer's disease, 2013-01, Vol.37 (4), p.653-659

Larner, A J

2013

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MACE versus MoCA: equivalence or superiority? Pragmatic diagnostic test accuracy study

International psychogeriatrics, 2017-06, Vol.29 (6), p.931-937

Larner, A.J.

2017

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The R269H mutation in presenilin-1 presenting as late-onset autosomal dominant Alzheimer's disease

Journal of the neurological sciences, 2007-01, Vol.252 (2), p.173-176

2007

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Pathological heterogeneity of clinically diagnosed corticobasal degeneration

Journal of the neurological sciences, 2003-12, Vol.216 (1), p.127-134

2003

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Late-onset temporal lobe epilepsy with unilateral mesial temporal sclerosis and cognitive decline: A diagnostic dilemma

Seizure (London, England), 2008-07, Vol.17 (5), p.473-476

2008

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Phenotypic similarities causing clinical misdiagnosis of pathologically-confirmed sporadic Creutzfeldt-Jakob disease as dementia with Lewy bodies

Clinical neurology and neurosurgery, 2008-02, Vol.110 (2), p.194-197

2008

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Central Nervous System/Brain Tumour 2-week Referral Guidelines: Prospective 3-year Audit

Clinical oncology (Royal College of Radiologists (Great Britain)), 2008-03, Vol.20 (2), p.201-202

2008

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“Dementia unmasked”: Atypical, acute aphasic, presentations of neurodegenerative dementing disease

Clinical neurology and neurosurgery, 2005-12, Vol.108 (1), p.8-10

Larner, A.J.

2005

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Pseudostatus epilepticus in pregnancy

International journal of gynecology and obstetrics, 2007-04, Vol.97 (1), p.47-47

2007

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Disseminated enteropathy-type T-cell lymphoma: cauda equina syndrome complicating coeliac disease

Clinical neurology and neurosurgery, 2005-10, Vol.107 (6), p.517-520

2005

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Clinical–anatomical correlation in a selective phonemic speech production impairment

Journal of the neurological sciences, 2004-04, Vol.219 (1), p.23-29

2004

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The diagnosis of dementia: diagnostic accuracy of an instrument measuring activities of daily living in a clinic-based population

Dementia and geriatric cognitive disorders, 2007-01, Vol.23 (3), p.133-139

2007

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Correlation or Limits of Agreement? Applying the Bland-Altman Approach to the Comparison of Cognitive Screening Instruments

Presenilin-1 mutation Alzheimer's disease: A genetic epilepsy syndrome?

Charles Dickens (1812–1870) and epilepsy

Intrafamilial clinical phenotypic heterogeneity with progranulin gene p.Glu498fs mutation

Perry syndrome: A disorder to consider in the differential diagnosis of Parkinsonism

Prevalence and causes of seizures at the time of diagnosis of probable Alzheimer's disease

Myoclonus-dystonia (DYT11) with novel SGCE mutation misdiagnosed as a primary psychiatric disorder

Senile myoclonic epilepsy in Down syndrome

Addenbrooke's Cognitive Examination (ACE) for the diagnosis and differential diagnosis of dementia

FTDP-17: 2-Year Follow-Up of Motor and Cognitive Features After Autologous Stem-Cell Transplantation

Intrafamilial clinical phenotypic heterogeneity with MAPT gene splice site IVS10+16C>T mutation

Margiad Evans (1909–1958): A history of epilepsy in a creative writer

Referrals to the neurology clinic from oral and maxillofacial surgery clinics

Presenilin-1 mutations in Alzheimer's disease: an update on genotype-phenotype relationships

MACE versus MoCA: equivalence or superiority? Pragmatic diagnostic test accuracy study

The R269H mutation in presenilin-1 presenting as late-onset autosomal dominant Alzheimer's disease

Pathological heterogeneity of clinically diagnosed corticobasal degeneration

Late-onset temporal lobe epilepsy with unilateral mesial temporal sclerosis and cognitive decline: A diagnostic dilemma

Phenotypic similarities causing clinical misdiagnosis of pathologically-confirmed sporadic Creutzfeldt-Jakob disease as dementia with Lewy bodies

Central Nervous System/Brain Tumour 2-week Referral Guidelines: Prospective 3-year Audit

“Dementia unmasked”: Atypical, acute aphasic, presentations of neurodegenerative dementing disease

Pseudostatus epilepticus in pregnancy

Disseminated enteropathy-type T-cell lymphoma: cauda equina syndrome complicating coeliac disease

Clinical–anatomical correlation in a selective phonemic speech production impairment

The diagnosis of dementia: diagnostic accuracy of an instrument measuring activities of daily living in a clinic-based population

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