Hardev Pall

Hardev Pall

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Hardev Pall

Publications by authors named "Hardev Pall"

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Subthalamic deep brain stimulation under general anesthesia and neurophysiological guidance while on dopaminergic medication: comparative cohort study.

Authors:
Mohammed Jamil Asha Benjamin Fisher Jamilla Kausar Hayley Garratt Hari Krovvidi Colin Shirley Anwen White Ramesh Chelvarajah Ismail Ughratdar James A Hodson Hardev Pall Rosalind D Mitchell

Acta Neurochir (Wien) 2018 04 2;160(4):823-829. Epub 2018 Feb 2.

Department of Neurosurgery, Queen Elizabeth Hospital, University of Birmingham, Mindelson Way, Birmingham, B15 2TH, UK.

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http://dx.doi.org/10.1007/s00701-018-3473-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5859686PMC
April 2018

-glycosylation and expression in human tissues of the orphan GPR61 receptor.

Authors:
Paweł Kozielewicz Hatun Alomar Syaratul Yusof Gillian Grafton Alison J Cooper S John Curnow James W Ironside Hardev Pall Nicholas M Barnes

FEBS Open Bio 2017 12 20;7(12):1982-1993. Epub 2017 Nov 20.

Institute of Clinical Sciences College of Medical and Dental Sciences University of Birmingham UK.

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http://dx.doi.org/10.1002/2211-5463.12339DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715243PMC
December 2017

Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis.

Authors:
Bradley N Smith Simon D Topp Claudia Fallini Hideki Shibata Han-Jou Chen Claire Troakes Andrew King Nicola Ticozzi Kevin P Kenna Athina Soragia-Gkazi Jack W Miller Akane Sato Diana Marques Dias Maryangel Jeon Caroline Vance Chun Hao Wong Martina de Majo Wejdan Kattuah Jacqueline C Mitchell Emma L Scotter Nicholas W Parkin Peter C Sapp Matthew Nolan Peter J Nestor Michael Simpson Michael Weale Monkel Lek Frank Baas J M Vianney de Jong Anneloor L M A Ten Asbroek Alberto Garcia Redondo Jesús Esteban-Pérez Cinzia Tiloca Federico Verde Stefano Duga Nigel Leigh Hardev Pall Karen E Morrison Ammar Al-Chalabi Pamela J Shaw Janine Kirby Martin R Turner Kevin Talbot Orla Hardiman Jonathan D Glass Jacqueline De Belleroche Masatoshi Maki Stephen E Moss Christopher Miller Cinzia Gellera Antonia Ratti Safa Al-Sarraj Robert H Brown Vincenzo Silani John E Landers Christopher E Shaw

Sci Transl Med 2017 05;9(388)

United Kingdom Dementia Research Institute Centre, Maurice Wohl Clinical Neuroscience Institute, Institute of Psychiatry, Psychology and Neuroscience, King's College London, 125 Coldharbour Lane, Camberwell, SE5 9NU London, UK.

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http://dx.doi.org/10.1126/scitranslmed.aad9157DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6599403PMC
May 2017

Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.

Authors:
Esther Meyer Keren J Carss Julia Rankin John M E Nichols Detelina Grozeva Agnel P Joseph Niccolo E Mencacci Apostolos Papandreou Joanne Ng Serena Barral Adeline Ngoh Hilla Ben-Pazi Michel A Willemsen David Arkadir Angela Barnicoat Hagai Bergman Sanjay Bhate Amber Boys Niklas Darin Nicola Foulds Nicholas Gutowski Alison Hills Henry Houlden Jane A Hurst Zvi Israel Margaret Kaminska Patricia Limousin Daniel Lumsden Shane McKee Shibalik Misra Shekeeb S Mohammed Vasiliki Nakou Joost Nicolai Magnus Nilsson Hardev Pall Kathryn J Peall Gregory B Peters Prab Prabhakar Miriam S Reuter Patrick Rump Reeval Segel Margje Sinnema Martin Smith Peter Turnpenny Susan M White Dagmar Wieczorek Sarah Wiethoff Brian T Wilson Gidon Winter Christopher Wragg Simon Pope Simon J H Heales Deborah Morrogh Alan Pittman Lucinda J Carr Belen Perez-Dueñas Jean-Pierre Lin Andre Reis William A Gahl Camilo Toro Kailash P Bhatia Nicholas W Wood Erik-Jan Kamsteeg Wui K Chong Paul Gissen Maya Topf Russell C Dale Jonathan R Chubb F Lucy Raymond Manju A Kurian

Nat Genet 2017 05;49(6):969

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http://dx.doi.org/10.1038/ng0617-969bDOI Listing
May 2017

Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.

Authors:
Esther Meyer Keren J Carss Julia Rankin John M E Nichols Detelina Grozeva Agnel P Joseph Niccolo E Mencacci Apostolos Papandreou Joanne Ng Serena Barral Adeline Ngoh Hilla Ben-Pazi Michel A Willemsen David Arkadir Angela Barnicoat Hagai Bergman Sanjay Bhate Amber Boys Niklas Darin Nicola Foulds Nicholas Gutowski Alison Hills Henry Houlden Jane A Hurst Zvi Israel Margaret Kaminska Patricia Limousin Daniel Lumsden Shane McKee Shibalik Misra Shekeeb S Mohammed Vasiliki Nakou Joost Nicolai Magnus Nilsson Hardev Pall Kathryn J Peall Gregory B Peters Prab Prabhakar Miriam S Reuter Patrick Rump Reeval Segel Margje Sinnema Martin Smith Peter Turnpenny Susan M White Dagmar Wieczorek Sarah Wiethoff Brian T Wilson Gidon Winter Christopher Wragg Simon Pope Simon J H Heales Deborah Morrogh Alan Pittman Lucinda J Carr Belen Perez-Dueñas Jean-Pierre Lin Andre Reis William A Gahl Camilo Toro Kailash P Bhatia Nicholas W Wood Erik-Jan Kamsteeg Wui K Chong Paul Gissen Maya Topf Russell C Dale Jonathan R Chubb F Lucy Raymond Manju A Kurian

Nat Genet 2017 Feb 19;49(2):223-237. Epub 2016 Dec 19.

Molecular Neurosciences, Developmental Neurosciences, UCL Institute of Child Health, London, UK.

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http://dx.doi.org/10.1038/ng.3740DOI Listing
February 2017

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis.

Authors:
Kevin P Kenna Perry T C van Doormaal Annelot M Dekker Nicola Ticozzi Brendan J Kenna Frank P Diekstra Wouter van Rheenen Kristel R van Eijk Ashley R Jones Pamela Keagle Aleksey Shatunov William Sproviero Bradley N Smith Michael A van Es Simon D Topp Aoife Kenna Jack W Miller Claudia Fallini Cinzia Tiloca Russell L McLaughlin Caroline Vance Claire Troakes Claudia Colombrita Gabriele Mora Andrea Calvo Federico Verde Safa Al-Sarraj Andrew King Daniela Calini Jacqueline de Belleroche Frank Baas Anneke J van der Kooi Marianne de Visser Anneloor L M A Ten Asbroek Peter C Sapp Diane McKenna-Yasek Meraida Polak Seneshaw Asress José Luis Muñoz-Blanco Tim M Strom Thomas Meitinger Karen E Morrison Giuseppe Lauria Kelly L Williams P Nigel Leigh Garth A Nicholson Ian P Blair Claire S Leblond Patrick A Dion Guy A Rouleau Hardev Pall Pamela J Shaw Martin R Turner Kevin Talbot Franco Taroni Kevin B Boylan Marka Van Blitterswijk Rosa Rademakers Jesús Esteban-Pérez Alberto García-Redondo Phillip Van Damme Wim Robberecht Adriano Chio Cinzia Gellera Carsten Drepper Michael Sendtner Antonia Ratti Jonathan D Glass Jesús S Mora Nazli A Basak Orla Hardiman Albert C Ludolph Peter M Andersen Jochen H Weishaupt Robert H Brown Ammar Al-Chalabi Vincenzo Silani Christopher E Shaw Leonard H van den Berg Jan H Veldink John E Landers

Nat Genet 2016 09 25;48(9):1037-42. Epub 2016 Jul 25.

Department of Neurology, University of Massachusetts Medical School, Worcester, Massachusetts, USA.

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http://dx.doi.org/10.1038/ng.3626DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5560030PMC
September 2016

Cost-utility analysis of deep brain stimulation surgery plus best medical therapy versus best medical therapy in patients with Parkinson's: Economic evaluation alongside the PD SURG trial.

Authors:
Emma McIntosh Alastair Gray Jane Daniels Steven Gill Natalie Ives Crispin Jenkinson Rosalind Mitchell Hardev Pall Smitaa Patel Niall Quinn Caroline Rick Keith Wheatley Adrian Williams

Mov Disord 2016 08 5;31(8):1173-82. Epub 2016 Feb 5.

Queen Elizabeth Hospital, Birmingham, United Kingdom.

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http://dx.doi.org/10.1002/mds.26423DOI Listing
August 2016

Phenotypic insights into ADCY5-associated disease.

Authors:
Florence C F Chang Ana Westenberger Russell C Dale Martin Smith Hardev S Pall Belen Perez-Dueñas Padraic Grattan-Smith Robert A Ouvrier Neil Mahant Bernadette C Hanna Matthew Hunter John A Lawson Christoph Max Rani Sachdev Esther Meyer Dennis Crimmins Donald Pryor John G L Morris Alex Münchau Detelina Grozeva Keren J Carss Lucy Raymond Manju A Kurian Christine Klein Victor S C Fung

Mov Disord 2016 07 8;31(7):1033-40. Epub 2016 Apr 8.

Movement Disorders Unit, Department of Neurology, Westmead Hospital, Sydney, Australia.

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http://dx.doi.org/10.1002/mds.26598DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4950003PMC
July 2016

Apathy in patients with Parkinson's disease following deep brain stimulation of the subthalamic nucleus.

Authors:
Isabel Hindle Fisher Hardev S Pall Rosalind D Mitchell Jamilla Kausar Andrea E Cavanna

CNS Spectr 2016 Jun 6;21(3):258-64. Epub 2016 May 6.

2School of Clinical and Experimental Medicine,College of Medicine,University of Birmingham,Birmingham,UK.

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http://dx.doi.org/10.1017/S1092852916000171DOI Listing
June 2016

Subthalamic nucleus microelectrode recordings (MER) can be reliably detected despite general anaesthesia and dopaminergic treatment.

Authors:
Mohammed Asha Jamilla Kausar Hari Krovvidi Colin Shirely Anwen White Ramesh Chelvarajah Hardev Pall Rosalind Mitchell

Acta Neurochir (Wien) 2016 05 4;158(5):1015-6. Epub 2016 Mar 4.

University of Birmingham, Birmingham, UK.

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http://link.springer.com/10.1007/s00701-016-2758-8
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http://dx.doi.org/10.1007/s00701-016-2758-8DOI Listing
May 2016

The effect of dopaminergic therapy on intraoperative microelectrode recordings for subthalamic deep brain stimulation under GA: can we operate on patients 'on medications'?

Authors:
Mohammed J Asha Jamilla Kausar Hari Krovvidi Colin Shirley Anwen White Ramesh Chelvarajah James A Hodson Hardev Pall Rosalind D Mitchell

Acta Neurochir (Wien) 2016 Feb 25;158(2):387-93. Epub 2015 Nov 25.

Divisions of Neurosurgery, University Hospital Birmingham, Birmingham, UK.

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http://dx.doi.org/10.1007/s00701-015-2631-1DOI Listing
February 2016

SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype.

Authors:
Kathryn J Peall Manju A Kurian Mark Wardle Adrian J Waite Tammy Hedderly Jean-Pierre Lin Martin Smith Alan Whone Hardev Pall Cathy White Andrew Lux Philip E Jardine Bryan Lynch George Kirov Sean O'Riordan Michael Samuel Timothy Lynch Mary D King Patrick F Chinnery Thomas T Warner Derek J Blake Michael J Owen Huw R Morris

J Neurol 2014 Dec 11;261(12):2296-304. Epub 2014 Sep 11.

MRC Centre for Neuropsychiatric Genetics and Genomics, Institute of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, UK,

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http://dx.doi.org/10.1007/s00415-014-7488-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495322PMC
December 2014

Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.

Authors:
Bradley N Smith Nicola Ticozzi Claudia Fallini Athina Soragia Gkazi Simon Topp Kevin P Kenna Emma L Scotter Jason Kost Pamela Keagle Jack W Miller Daniela Calini Caroline Vance Eric W Danielson Claire Troakes Cinzia Tiloca Safa Al-Sarraj Elizabeth A Lewis Andrew King Claudia Colombrita Viviana Pensato Barbara Castellotti Jacqueline de Belleroche Frank Baas Anneloor L M A ten Asbroek Peter C Sapp Diane McKenna-Yasek Russell L McLaughlin Meraida Polak Seneshaw Asress Jesús Esteban-Pérez José Luis Muñoz-Blanco Michael Simpson Wouter van Rheenen Frank P Diekstra Giuseppe Lauria Stefano Duga Stefania Corti Cristina Cereda Lucia Corrado Gianni Sorarù Karen E Morrison Kelly L Williams Garth A Nicholson Ian P Blair Patrick A Dion Claire S Leblond Guy A Rouleau Orla Hardiman Jan H Veldink Leonard H van den Berg Ammar Al-Chalabi Hardev Pall Pamela J Shaw Martin R Turner Kevin Talbot Franco Taroni Alberto García-Redondo Zheyang Wu Jonathan D Glass Cinzia Gellera Antonia Ratti Robert H Brown Vincenzo Silani Christopher E Shaw John E Landers

Neuron 2014 Oct 22;84(2):324-31. Epub 2014 Oct 22.

Department of Neurology, University of Massachusetts Medical School, Worcester, MA 01605, USA. Electronic address:

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http://dx.doi.org/10.1016/j.neuron.2014.09.027DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4521390PMC
October 2014

The role of dopamine replacement on the behavioural phenotype of Parkinson's disease.

Authors:
Hajar Alobaidi Hardev Pall

Behav Neurol 2013 ;26(4):225-35

Michael Trimble Neuropsychiatry Research Group, Department of Neuropsychiatry, BSMHFT and University of Birmingham, Birmingham, UK.

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http://dx.doi.org/10.3233/BEN-2012-120265DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5214930PMC
June 2014

Deep brain stimulation improves survival in severe Parkinson's disease.

Authors:
Desire Ngoga Rosalind Mitchell Jamilla Kausar James Hodson Anwen Harries Hardev Pall

J Neurol Neurosurg Psychiatry 2014 Jan 10;85(1):17-22. Epub 2013 Jul 10.

School of Cancer Sciences, The University of Birmingham, , Birmingham, UK.

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http://dx.doi.org/10.1136/jnnp-2012-304715DOI Listing
January 2014

Management of sialorrhoea in motor neuron disease: a survey of current UK practice.

Authors:
Esther V Hobson Alexander McGeachan Ammar Al-Chalabi Siddharthan Chandran Francesca Crawley David Dick Colette Donaghy John Ealing Cathy M Ellis George Gorrie C Oliver Hanemann Timothy Harrower Agam Jung Tahir Majeed Andrea Malaspina Karen Morrison Richard W Orrell Hardev Pall Ashwin Pinto Kevin Talbot Martin R Turner Timothy L Williams Carolyn A Young Pamela J Shaw Christopher J McDermott

Amyotroph Lateral Scler Frontotemporal Degener 2013 Dec 7;14(7-8):521-7. Epub 2013 May 7.

Sheffield Institute for Translational Neuroscience, University of Sheffield, Sheffield, & Academic Directorate of Neurosciences, Royal Hallamshire Hospital , Sheffield Teaching Hospitals NHS Foundation Trust , Sheffield.

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http://dx.doi.org/10.3109/21678421.2013.790452DOI Listing
December 2013

Health-related quality of life and supportive care in patients with rare long-term neurological conditions.

Authors:
Melanie Calvert Hardev Pall Thomas Hoppitt Benjamin Eaton Edward Savill Catherine Sackley

Qual Life Res 2013 Aug 23;22(6):1231-8. Epub 2012 Sep 23.

School of Health and Population Sciences, University of Birmingham, Birmingham, UK.

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http://dx.doi.org/10.1007/s11136-012-0269-5DOI Listing
August 2013

The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder.

Authors:
Bradley N Smith Stephen Newhouse Aleksey Shatunov Caroline Vance Simon Topp Lauren Johnson Jack Miller Younbok Lee Claire Troakes Kirsten M Scott Ashley Jones Ian Gray Jamie Wright Tibor Hortobágyi Safa Al-Sarraj Boris Rogelj John Powell Michelle Lupton Simon Lovestone Peter C Sapp Markus Weber Peter J Nestor Helenius J Schelhaas Anneloor Alm Ten Asbroek Vincenzo Silani Cinzia Gellera Franco Taroni Nicola Ticozzi Leonard Van den Berg Jan Veldink Phillip Van Damme Wim Robberecht Pamela J Shaw Janine Kirby Hardev Pall Karen E Morrison Alex Morris Jacqueline de Belleroche J M B Vianney de Jong Frank Baas Peter M Andersen John Landers Robert H Brown Michael E Weale Ammar Al-Chalabi Christopher E Shaw

Eur J Hum Genet 2013 Jan 13;21(1):102-8. Epub 2012 Jun 13.

Department of Clinical Neurosciences, MRC Centre for Neurodegeneration Research, Institute of Psychiatry, Kings College London, London, UK.

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http://dx.doi.org/10.1038/ejhg.2012.98DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522204PMC
January 2013

Theory of mind deficits in Parkinson's disease: a product of executive dysfunction?

Authors:
Clare M Eddy Sarah R Beck Ian J Mitchell Peter Praamstra Hardev S Pall

Neuropsychology 2013 Jan;27(1):37-47

Birmingham and Solihull Mental Health NHS Foundation Trust, Department of Neuropsychiatry, The Barberry, National Centre for Mental Health, Birmingham, United Kingdom.

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http://dx.doi.org/10.1037/a0031302DOI Listing
January 2013

SGCE mutations cause psychiatric disorders: clinical and genetic characterization.

Authors:
Kathryn J Peall Daniel J Smith Manju A Kurian Mark Wardle Adrian J Waite Tammy Hedderly Jean-Pierre Lin Martin Smith Alan Whone Hardev Pall Cathy White Andrew Lux Philip Jardine Narinder Bajaj Bryan Lynch George Kirov Sean O'Riordan Michael Samuel Timothy Lynch Mary D King Patrick F Chinnery Thomas T Warner Derek J Blake Michael J Owen Huw R Morris

Brain 2013 Jan;136(Pt 1):294-303

MRC Centre for Neuropsychiatric Genetics and Genomics, Institute of Psychological Medicine and Clinical Neurosciences, Henry Wellcome Building, Heath Park, Cardiff, UK.

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http://dx.doi.org/10.1093/brain/aws308DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4052887PMC
January 2013

Analysis of European case-control studies suggests that common inherited variation in mitochondrial DNA is not involved in susceptibility to amyotrophic lateral sclerosis.

Authors:
Catherine J E Ingram Michael E Weale Christopher A Plaster Karen E Morrison Emily F Goodall Hardev S Pall Marcus Beck Sibylle Jablonka Michael Sendtner Elizabeth M C Fisher Neil Bradman Dalia Kasperavičiūtė

Amyotroph Lateral Scler 2012 Jun 13;13(4):341-6. Epub 2012 Mar 13.

The Centre for Genetic Anthropology, University College London Genetics Institute, Research Department of Genetics, Evolution and Environment, University College London, London WC1E 6BT, UK.

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http://www.tandfonline.com/doi/full/10.3109/17482968.2012.65
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http://dx.doi.org/10.3109/17482968.2012.654394DOI Listing
June 2012

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study.

Authors:
Elisa Majounie Alan E Renton Kin Mok Elise G P Dopper Adrian Waite Sara Rollinson Adriano Chiò Gabriella Restagno Nayia Nicolaou Javier Simon-Sanchez John C van Swieten Yevgeniya Abramzon Janel O Johnson Michael Sendtner Roger Pamphlett Richard W Orrell Simon Mead Katie C Sidle Henry Houlden Jonathan D Rohrer Karen E Morrison Hardev Pall Kevin Talbot Olaf Ansorge Dena G Hernandez Sampath Arepalli Mario Sabatelli Gabriele Mora Massimo Corbo Fabio Giannini Andrea Calvo Elisabet Englund Giuseppe Borghero Gian Luca Floris Anne M Remes Hannu Laaksovirta Leo McCluskey John Q Trojanowski Vivianna M Van Deerlin Gerard D Schellenberg Michael A Nalls Vivian E Drory Chin-Song Lu Tu-Hsueh Yeh Hiroyuki Ishiura Yuji Takahashi Shoji Tsuji Isabelle Le Ber Alexis Brice Carsten Drepper Nigel Williams Janine Kirby Pamela Shaw John Hardy Pentti J Tienari Peter Heutink Huw R Morris Stuart Pickering-Brown Bryan J Traynor

Lancet Neurol 2012 Apr 9;11(4):323-30. Epub 2012 Mar 9.

Molecular Genetics Unit, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.

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http://dx.doi.org/10.1016/S1474-4422(12)70043-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3322422PMC
April 2012

Huntington's disease: current epidemiology and pharmacological management in UK primary care.

Authors:
Catherine Sackley Thomas J Hoppitt Melanie Calvert Paramjit Gill Benjamin Eaton Guiqing Yao Hardev Pall

Neuroepidemiology 2011 1;37(3-4):216-21. Epub 2011 Dec 1.

School of Health and Population Sciences, University of Birmingham, Birmingham, UK.

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http://dx.doi.org/10.1159/000331912DOI Listing
March 2012

Deep brain stimulation of the subthalamic nucleus for advanced Parkinson disease using general anesthesia: long-term results.

Authors:
Anwen M Harries Jamilla Kausar Stuart A G Roberts A Paul Mocroft James A Hodson Hardev S Pall Rosalind D Mitchell

J Neurosurg 2012 Jan 14;116(1):107-13. Epub 2011 Oct 14.

Department of Neurosurgery, University Hospital Birmingham, Edgbaston, Birmingham B15 2TH, United Kingdom.

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http://dx.doi.org/10.3171/2011.7.JNS11319DOI Listing
January 2012

A systematic review of the incidence and prevalence of long-term neurological conditions in the UK.

Authors:
Thomas Hoppitt Hardev Pall Mel Calvert Paramjit Gill Guiqing Yao Jill Ramsay Gill James Jacky Conduit Cath Sackley

Neuroepidemiology 2011 17;36(1):19-28. Epub 2010 Nov 17.

School of Health and Population Sciences, University of Birmingham, Birmingham, UK.

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http://dx.doi.org/10.1159/000321712DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2997442PMC
May 2011

An approach to deep brain stimulation for severe treatment-refractory Tourette syndrome: the UK perspective.

Authors:
Andrea E Cavanna Clare M Eddy Rosalind Mitchell Hardev Pall Ian Mitchell Ludvic Zrinzo Tom Foltynie Marjan Jahanshahi Patricia Limousin Marwan I Hariz Hugh Rickards

Br J Neurosurg 2011 Feb 15;25(1):38-44. Epub 2010 Dec 15.

Department of Neuropsychiatry, University of Birmingham and BSMHFT, Birmingham, UK.

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http://www.tandfonline.com/doi/full/10.3109/02688697.2010.53
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http://dx.doi.org/10.3109/02688697.2010.534200DOI Listing
February 2011

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.

Authors:
Aleksey Shatunov Kin Mok Stephen Newhouse Michael E Weale Bradley Smith Caroline Vance Lauren Johnson Jan H Veldink Michael A van Es Leonard H van den Berg Wim Robberecht Philip Van Damme Orla Hardiman Anne E Farmer Cathryn M Lewis Amy W Butler Olubunmi Abel Peter M Andersen Isabella Fogh Vincenzo Silani Adriano Chiò Bryan J Traynor Judith Melki Vincent Meininger John E Landers Peter McGuffin Jonathan D Glass Hardev Pall P Nigel Leigh John Hardy Robert H Brown John F Powell Richard W Orrell Karen E Morrison Pamela J Shaw Christopher E Shaw Ammar Al-Chalabi

Lancet Neurol 2010 Oct;9(10):986-94

King's College London, Medical Research Council Centre for Neurodegeneration Research, Department of Clinical Neuroscience, Institute of Psychiatry, London, UK.

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http://dx.doi.org/10.1016/S1474-4422(10)70197-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3257853PMC
October 2010

Genetic studies of GRN and IFT74 in amyotrophic lateral sclerosis.

Authors:
Shangxi Xiao Christine Sato Toshitaka Kawarai Emily F Goodall Hardev S Pall Lorne H Zinman Janice Robertson Karen Morrison Ekaterina Rogaeva

Neurobiol Aging 2008 Aug 23;29(8):1279-82. Epub 2007 Mar 23.

Centre for Research in Neurodegenerative Diseases, Tanz Neuroscience Building, University of Toronto, 6 Queen's Park Crescent West, Toronto, Ontario, Canada M5S 3H2.

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http://dx.doi.org/10.1016/j.neurobiolaging.2007.02.022DOI Listing
August 2008

Large-scale pathways-based association study in amyotrophic lateral sclerosis.

Authors:
Dalia Kasperaviciute Mike E Weale Kevin V Shianna Gareth T Banks Claire L Simpson Valerie K Hansen Martin R Turner Christopher E Shaw Ammar Al-Chalabi Hardev S Pall Emily F Goodall Karen E Morrison Richard W Orrell Marcus Beck Sibylle Jablonka Michael Sendtner Alice Brockington Paul G Ince Judith Hartley Hannah Nixon Pamela J Shaw Giampietro Schiavo Nicholas W Wood David B Goldstein Elizabeth M C Fisher

Brain 2007 Sep 17;130(Pt 9):2292-301. Epub 2007 Apr 17.

Department of Neurodegenerative Disease, Institute of Neurology, University College London, London, UK.

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http://dx.doi.org/10.1093/brain/awm055DOI Listing
September 2007

VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death.

Authors:
Diether Lambrechts Erik Storkebaum Masafumi Morimoto Jurgen Del-Favero Frederik Desmet Stefan L Marklund Sabine Wyns Vincent Thijs Jörgen Andersson Ingrid van Marion Ammar Al-Chalabi Stephanie Bornes Rhiannon Musson Valerie Hansen Lars Beckman Rolf Adolfsson Hardev Singh Pall Hervé Prats Severine Vermeire Paul Rutgeerts Shigehiro Katayama Takuya Awata Nigel Leigh Loïc Lang-Lazdunski Mieke Dewerchin Christopher Shaw Lieve Moons Robert Vlietinck Karen E Morrison Wim Robberecht Christine Van Broeckhoven Désiré Collen Peter M Andersen Peter Carmeliet

Nat Genet 2003 Aug;34(4):383-94

The Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology and Department of Neurology, University Hospital Gasthuisberg, KU Leuven, Leuven, B-3000, Belgium.

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http://www.nature.com/articles/ng1211
Publisher Site
http://dx.doi.org/10.1038/ng1211DOI Listing
August 2003