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1
Ethnic variation in the incidence of ALS : A systematic review
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Artigo
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Ethnic variation in the incidence of ALS : A systematic review

CRONIN, Simon ; HARDIMAN, Orla ; TRAYNOR, Bryan J

Neurology, 2007-03, Vol.68 (13), p.1002-1007 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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2
Genetics of sporadic amyotrophic lateral sclerosis
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Artigo
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Genetics of sporadic amyotrophic lateral sclerosis

Schymick, J.C. ; Talbot, K. ; Traynor, B.J.

Human molecular genetics, 2007-10, Vol.16 (R2), p.R233-R242 [Periódico revisado por pares]

Oxford: Oxford University Press

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3
Incidence of amyotrophic lateral sclerosis in Europe
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Artigo
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Incidence of amyotrophic lateral sclerosis in Europe

Logroscino, Giancarlo ; Traynor, Bryan J ; Hardiman, Orla ; Chiò, Adriano ; Mitchell, Douglas ; Swingler, Robert J ; Millul, Andrea ; Benn, Emma ; Beghi, Ettore

Journal of neurology, neurosurgery and psychiatry, 2010-04, Vol.81 (4), p.385-390 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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4
Effect of a multidisciplinary amyotrophic lateral sclerosis (ALS) clinic on ALS survival: a population based study, 1996–2000
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Effect of a multidisciplinary amyotrophic lateral sclerosis (ALS) clinic on ALS survival: a population based study, 1996–2000

Traynor, B J ; Alexander, M ; Corr, B ; Frost, E ; Hardiman, O

Journal of neurology, neurosurgery and psychiatry, 2003-09, Vol.74 (9), p.1258-1261 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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5
Road to the chromosome 9p-linked ALS/FTD locus
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Artigo
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Road to the chromosome 9p-linked ALS/FTD locus

Traynor, Bryan J

Journal of neurology, neurosurgery and psychiatry, 2012-04, Vol.83 (4), p.356-357 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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6
A novel candidate region for ALS on chromosome 14q11.2
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A novel candidate region for ALS on chromosome 14q11.2

GREENWAY, M. J ; ALEXANDER, M. D ; ENNIS, S ; TRAYNOR, B. J ; CORR, B ; FROST, E ; GREEN, A ; HARDIMAN, O

Neurology, 2004-11, Vol.63 (10), p.1936-1938 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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7
Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues
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Artigo
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Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues

Logroscino, G ; Traynor, B J ; Hardiman, O ; Chio’, A ; Couratier, P ; Mitchell, J D ; Swingler, R J ; Beghi, E

Journal of neurology, neurosurgery and psychiatry, 2008-01, Vol.79 (1), p.6-11 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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8
Epidemiology and clinical features of amyotrophic lateral sclerosis in Ireland between 1995 and 2004
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Artigo
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Epidemiology and clinical features of amyotrophic lateral sclerosis in Ireland between 1995 and 2004

O’Toole, O ; Traynor, B J ; Brennan, P ; Sheehan, C ; Frost, E ; Corr, B ; Hardiman, O

Journal of neurology, neurosurgery and psychiatry, 2008-01, Vol.79 (1), p.30-32 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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9
Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis–frontotemporal dementia phenotypes
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Artigo
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Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis–frontotemporal dementia phenotypes

Schymick, J C ; Yang, Y ; Andersen, P M ; Vonsattel, J P ; Greenway, M ; Momeni, P ; Elder, J ; Chiò, A ; Restagno, G ; Robberecht, W ; Dahlberg, C ; Mukherjee, O ; Goate, A ; Graff-Radford, N ; Caselli, R J ; Hutton, M ; Gass, J ; Cannon, A ; Rademakers, R ; Singleton, A B ; Hardiman, O ; Rothstein, J ; Hardy, J ; Traynor, B J

Journal of neurology, neurosurgery and psychiatry, 2007-07, Vol.78 (7), p.754-756 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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10
A genome-wide association study of sporadic ALS in a homogenous Irish population
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Artigo
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A genome-wide association study of sporadic ALS in a homogenous Irish population

Cronin, Simon ; Berger, Stephen ; Ding, Jinhui ; Schymick, Jennifer C ; Washecka, Nicole ; Hernandez, Dena G. ; Greenway, Matthew J. ; Bradley, Daniel G. ; Traynor, Bryan J. ; Hardiman, Orla

Human molecular genetics, 2008-03, Vol.17 (5), p.768-774 [Periódico revisado por pares]

Oxford: Oxford University Press

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