Publications by authors named "Sameer M Zuberi"

80Publications

Infantile spasms: Etiology, lead time and treatment response in a resource limited setting.

Epilepsy Behav Rep 2020 17;14:100397. Epub 2020 Oct 17.

Departments' of Pediatrics, Pediatric Neurology & Radio Diagnosis, Santokba Durlabhji Memorial Hospital, Jaipur, India.

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http://dx.doi.org/10.1016/j.ebr.2020.100397DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7656466PMC
October 2020

NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns.

Genet Med 2020 Nov 4. Epub 2020 Nov 4.

Epilepsy Research Centre, Department of Medicine, Austin Health, University of Melbourne, Melbourne, VIC, Australia.

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http://dx.doi.org/10.1038/s41436-020-00988-9DOI Listing
November 2020

The training & organisation of paediatric neurology in Europe.

Authors:
Sameer M Zuberi

Eur J Paediatr Neurol 2020 09 21;28. Epub 2020 Aug 21.

Royal Hospital for Children, Glasgow, UK. Electronic address:

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http://dx.doi.org/10.1016/j.ejpn.2020.08.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7441983PMC
September 2020

Neuronal antibody prevalence in children with seizures under 3 years: A prospective national cohort.

Neurology 2020 09 20;95(11):e1590-e1598. Epub 2020 Jul 20.

From the Paediatric Neurosciences Research Group (J.D.S., M.E.O., S.M., A.B., L.D., M.W., S.M.Z.), Royal Hospital for Children; College of Medical, Veterinary & Life Sciences (J.D.S., A.B., L.D., S.M.Z.), University of Glasgow; Nuffield Department of Clinical Neurosciences (T.C.M., B.L., A.V., S.T.), John Radcliffe Hospital, Oxford; Department of Paediatric Neurosciences (A.M., J.S.), Royal Hospital for Sick Children, Edinburgh; Paediatric Neurology (A.J., M.K., P.B., E.P.), Tayside Children's Hospital, Dundee; Neuroradiology (K.F.), Queen Elizabeth University Hospitals, Glasgow; Department of Paediatrics (I.A.-A., R.G.), Forth Valley Royal Hospital, Larbert; Department of Paediatrics (J.A., M.C.), University Hospital Wishaw; Department of Paediatrics (J.C.), Victoria Hospital, Kirkcaldy; Department of Paediatrics (C.F., C.A.M.), University Hospital Crosshouse, Kilmarnock; Department of Paediatrics (J. MacDonnell), Borders General Hospital, Melrose; Department of Paediatrics (J. McKnight), Dumfries and Galloway Royal Infirmary; Department of Paediatrics (L.N.), Royal Alexandra Hospital, Paisley; Paediatric Neurology (E.S.), Royal Aberdeen Children's Hospital; and Department of Paediatrics (A.W.), Raigmore Hospital, Inverness, UK.

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http://dx.doi.org/10.1212/WNL.0000000000010318DOI Listing
September 2020

Introduction to the special issue on epilepsy & neurodevelopmental disorders.

Authors:
Sameer M Zuberi

Eur J Paediatr Neurol 2020 01 10;24. Epub 2020 Jan 10.

European Journal of Paediatric Neurology, United Kingdom. Electronic address:

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http://dx.doi.org/10.1016/j.ejpn.2020.01.007DOI Listing
January 2020

Phenotypic spectrum and genetics of SCN2A-related disorders, treatment options, and outcomes in epilepsy and beyond.

Epilepsia 2019 12;60 Suppl 3:S59-S67

Paediatric Neurosciences Research Group, Royal Hospital for Children & School of Medicine, University of Glasgow, Glasgow, UK.

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http://dx.doi.org/10.1111/epi.14935DOI Listing
December 2019

Progressive intellectual impairment in children with Encephalopathy related to Status Epilepticus during slow Sleep.

Epileptic Disord 2019 Jun;21(S1):88-96

Paediatric Neurosciences Research Group, Royal Hospital for Children, Glasgow, UK, School of Medicine, University of Glasgow, Glasgow, UK.

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http://dx.doi.org/10.1684/epd.2019.1063DOI Listing
June 2019

Encephalopathy related to Status Epilepticus during slow Sleep: from concepts to terminology.

Epileptic Disord 2019 Jun;21(S1):5-12

Paediatric Neurosciences Research Group, Royal Hospital for Children & University of Glasgow, Member of the European Reference Network EpiCARE, Glasgow, UK.

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http://dx.doi.org/10.1684/epd.2019.1051DOI Listing
June 2019

Editorial note.

Authors:
Sameer M Zuberi

Eur J Paediatr Neurol 2019 01;23(1)

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http://dx.doi.org/10.1016/j.ejpn.2018.12.007DOI Listing
January 2019

The clinical utility of ambulatory EEG in childhood.

Seizure 2019 Jan 29;64:45-49. Epub 2018 Nov 29.

School of Medicine, College of Medical & Veterinary Life Sciences, University of Glasgow, United Kingdom; Paediatric Neurosciences Research Group & EEG Department, Royal Hospital for Children, Glasgow, United Kingdom. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S10591311183058
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http://dx.doi.org/10.1016/j.seizure.2018.11.020DOI Listing
January 2019

Precious time to respond to infantile spasms.

Authors:
Sameer M Zuberi

Lancet Child Adolesc Health 2018 10 29;2(10):691-693. Epub 2018 Aug 29.

Paediatric Neurosciences Research Group, Royal Hospital for Children & School of Medicine, University of Glasgow, Glasgow G51 4TF, UK. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S23524642183028
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http://dx.doi.org/10.1016/S2352-4642(18)30285-2DOI Listing
October 2018

Heart rate variability in epilepsy: A potential biomarker of sudden unexpected death in epilepsy risk.

Epilepsia 2018 07 6;59(7):1372-1380. Epub 2018 Jun 6.

Department of Medicine, Epilepsy Research Centre, Austin Health, University of Melbourne, Heidelberg, Victoria, Australia.

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http://dx.doi.org/10.1111/epi.14438DOI Listing
July 2018

Effect of Cannabidiol on Drop Seizures in the Lennox-Gastaut Syndrome.

N Engl J Med 2018 May;378(20):1888-1897

From New York University Langone Comprehensive Epilepsy Center, New York (O.D.); Nationwide Children's Hospital and the Ohio State University College of Medicine, Columbus (A.D.P.), and the University of Cincinnati Medical Center, Department of Neurology, Cincinnati (M.P.) - all in Ohio; UCL Great Ormond Street Institute of Child Health, London (J.H.C.), GW Research Ltd., Cambridge (S.M.G., C.R., D.C.), and the Royal Hospital for Children and School of Medicine, University of Glasgow, Glasgow (S.M.Z.) - all in the United Kingdom; Refractory Epilepsy Unit, Neurology Service, Hospital Universitario y Politécnico La Fe, Valencia, Spain (V.V.); the Divisions of Child and Adolescent Neurology and Epilepsy, Department of Neurology, Mayo Clinic, Rochester, MN (E.C.W.); and Greenwich Biosciences, Carlsbad, CA (K.E.V.).

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http://dx.doi.org/10.1056/NEJMoa1714631DOI Listing
May 2018

Epilepsy in 2017: Precision medicine drives epilepsy classification and therapy.

Nat Rev Neurol 2018 Feb 19;14(2):67-68. Epub 2018 Jan 19.

Royal Hospital for Children and School of Medicine, University of Glasgow, 1345 Govan Road, Glasgow G51 4TF, UK.

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http://dx.doi.org/10.1038/nrneurol.2017.190DOI Listing
February 2018

Sleep, oxygen saturation, and seizures in Dravet syndrome.

Authors:
Sameer M Zuberi

Dev Med Child Neurol 2018 02 14;60(2):118. Epub 2017 Dec 14.

Paediatric Neurosciences Research Group, Royal Hospital for Children Glasgow, Glasgow, UK.

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http://dx.doi.org/10.1111/dmcn.13644DOI Listing
February 2018

Genetics update: Monogenetics, polygene disorders and the quest for modifying genes.

Neuropharmacology 2018 04 14;132:3-19. Epub 2017 Oct 14.

The Paediatric Neurosciences Research Group, Royal Hospital for Children, Queen Elizabeth University Hospitals, Glasgow, UK; School of Medicine, University of Glasgow, Glasgow, UK. Electronic address:

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http://dx.doi.org/10.1016/j.neuropharm.2017.10.013DOI Listing
April 2018

Dravet syndrome and its mimics: Beyond SCN1A.

Epilepsia 2017 11 7;58(11):1807-1816. Epub 2017 Sep 7.

The Paediatric Neurosciences Research Group, Royal Hospital for Children, Glasgow, United Kingdom.

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http://dx.doi.org/10.1111/epi.13889DOI Listing
November 2017

The "plus" side of epilepsy phenotyping.

Neurology 2017 09 25;89(12):1202-1203. Epub 2017 Aug 25.

From the Paediatric Neurosciences Research Group (S.M.Z.), Royal Hospital for Children & University of Glasgow, UK; and Pediatric Neurology and Muscular Diseases Unit, Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (P.S.), University of Genoa, "G. Gaslini" Institute, Italy.

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http://dx.doi.org/10.1212/WNL.0000000000004399DOI Listing
September 2017

WITHDRAWN: Genetics update: Monogenetics, polygene disorders and the quest for modifying genes.

Neuropharmacology 2017 Jul 27. Epub 2017 Jul 27.

The Paediatric Neurosciences Research Group, Royal Hospital for Children, Queen Elizabeth University Hospitals, Glasgow, UK; School of Medicine, University of Glasgow, Glasgow, UK.

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http://dx.doi.org/10.1016/j.neuropharm.2017.07.016DOI Listing
July 2017

The humanistic and economic burden of Dravet syndrome on caregivers and families: Implications for future research.

Epilepsy Behav 2017 05 18;70(Pt A):104-109. Epub 2017 Apr 18.

Medical and Scientific Affairs, Zogenix, Inc., Emeryville, CA, USA.

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http://dx.doi.org/10.1016/j.yebeh.2017.02.003DOI Listing
May 2017

A new classification is born.

Epilepsia 2017 04 8;58(4):511. Epub 2017 Mar 8.

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http://dx.doi.org/10.1111/epi.13694DOI Listing
April 2017

Advances in epilepsy gene discovery and implications for epilepsy diagnosis and treatment.

Curr Opin Neurol 2017 04;30(2):193-199

aPaediatric Neurosciences Research Group, Fraser of Allander Neurosciences Unit, Royal Hospital for Children bSchool of Medicine, University of Glasgow, Glasgow cDivision of Brain Sciences, Imperial College London, London, United Kingdom.

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http://dx.doi.org/10.1097/WCO.0000000000000433DOI Listing
April 2017

Editorial note.

Authors:
Sameer M Zuberi

Eur J Paediatr Neurol 2016 09;20(5):689

Royal Hospital for Children, Glasgow, G51 4TF, United Kingdom. Electronic address:

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http://dx.doi.org/10.1016/j.ejpn.2016.07.016DOI Listing
September 2016

Editorial.

Authors:
Sameer M Zuberi

Eur J Paediatr Neurol 2016 Jan;20(1):1-2

Royal Hospital for Children, Glasgow, UK. Electronic address:

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http://dx.doi.org/10.1016/j.ejpn.2015.12.001DOI Listing
January 2016

Update on diagnosis and management of childhood epilepsies.

J Pediatr (Rio J) 2015 Nov-Dec;91(6 Suppl 1):S67-77. Epub 2015 Sep 4.

Pediatric Neurosciences Research Group, Fraser of Allander Neurosciences Unit, Royal Hospital for Sick Children, Glasgow, United Kingdom.

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http://dx.doi.org/10.1016/j.jped.2015.07.003DOI Listing
April 2016

Epileptic activity is a surrogate for an underlying etiology and stopping the activity has a limited impact on developmental outcome.

Epilepsia 2015 Oct 21;56(10):1477-81. Epub 2015 Aug 21.

The Paediatric Neurosciences Research Group, Royal Hospital for Sick Children, Glasgow, United Kingdom.

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http://dx.doi.org/10.1111/epi.13105DOI Listing
October 2015

Editorial note.

Authors:
Sameer M Zuberi

Eur J Paediatr Neurol 2015 Jul;19(4):389

Royal Hospital for Sick Children, Glasgow, UK. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S10903798150009
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http://dx.doi.org/10.1016/j.ejpn.2015.05.003DOI Listing
July 2015

Homozygous mutations in the SCN1A gene associated with genetic epilepsy with febrile seizures plus and Dravet syndrome in 2 families.

Eur J Paediatr Neurol 2015 Jul 21;19(4):484-8. Epub 2015 Feb 21.

The Paediatric Neurosciences Research Group, Royal Hospital for Sick Children, Glasgow, UK; School of Medicine, College of Medical, Veterinary & Life Sciences, University of Glasgow, UK. Electronic address:

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http://dx.doi.org/10.1016/j.ejpn.2015.02.001DOI Listing
July 2015

ICD coding for epilepsy: past, present, and future--a report by the International League Against Epilepsy Task Force on ICD codes in epilepsy.

Epilepsia 2015 Mar 12;56(3):348-55. Epub 2015 Feb 12.

Department of Clinical Neurosciences and Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada; Department of Community Health Sciences and Institute for Public Health, University of Calgary, Calgary, Alberta, Canada.

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http://dx.doi.org/10.1111/epi.12895DOI Listing
March 2015

Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.

Authors:
Yanick J Crow Diana S Chase Johanna Lowenstein Schmidt Marcin Szynkiewicz Gabriella M A Forte Hannah L Gornall Anthony Oojageer Beverley Anderson Amy Pizzino Guy Helman Mohamed S Abdel-Hamid Ghada M Abdel-Salam Sam Ackroyd Alec Aeby Guillermo Agosta Catherine Albin Stavit Allon-Shalev Montse Arellano Giada Ariaudo Vijay Aswani Riyana Babul-Hirji Eileen M Baildam Nadia Bahi-Buisson Kathryn M Bailey Christine Barnerias Magalie Barth Roberta Battini Michael W Beresford Geneviève Bernard Marika Bianchi Thierry Billette de Villemeur Edward M Blair Miriam Bloom Alberto B Burlina Maria Luisa Carpanelli Daniel R Carvalho Manuel Castro-Gago Anna Cavallini Cristina Cereda Kate E Chandler David A Chitayat Abigail E Collins Concepcion Sierra Corcoles Nuno J V Cordeiro Giovanni Crichiutti Lyvia Dabydeen Russell C Dale Stefano D'Arrigo Christian G E L De Goede Corinne De Laet Liesbeth M H De Waele Ines Denzler Isabelle Desguerre Koenraad Devriendt Maja Di Rocco Michael C Fahey Elisa Fazzi Colin D Ferrie António Figueiredo Blanca Gener Cyril Goizet Nirmala R Gowrinathan Kalpana Gowrishankar Donncha Hanrahan Bertrand Isidor Bülent Kara Nasaim Khan Mary D King Edwin P Kirk Ram Kumar Lieven Lagae Pierre Landrieu Heinz Lauffer Vincent Laugel Roberta La Piana Ming J Lim Jean-Pierre S-M Lin Tarja Linnankivi Mark T Mackay Daphna R Marom Charles Marques Lourenço Shane A McKee Isabella Moroni Jenny E V Morton Marie-Laure Moutard Kevin Murray Rima Nabbout Sheela Nampoothiri Noemi Nunez-Enamorado Patrick J Oades Ivana Olivieri John R Ostergaard Belén Pérez-Dueñas Julie S Prendiville Venkateswaran Ramesh Magnhild Rasmussen Luc Régal Federica Ricci Marlène Rio Diana Rodriguez Agathe Roubertie Elisabetta Salvatici Karin A Segers Gyanranjan P Sinha Doriette Soler Ronen Spiegel Tommy I Stödberg Rachel Straussberg Kathryn J Swoboda Mohnish Suri Uta Tacke Tiong Y Tan Johann te Water Naude Keng Wee Teik Maya Mary Thomas Marianne Till Davide Tonduti Enza Maria Valente Rudy Noel Van Coster Marjo S van der Knaap Grace Vassallo Raymon Vijzelaar Julie Vogt Geoffrey B Wallace Evangeline Wassmer Hannah J Webb William P Whitehouse Robyn N Whitney Maha S Zaki Sameer M Zuberi John H Livingston Flore Rozenberg Pierre Lebon Adeline Vanderver Simona Orcesi Gillian I Rice

Am J Med Genet A 2015 Feb 16;167A(2):296-312. Epub 2015 Jan 16.

INSERM UMR 1163, Laboratory of Neurogenetics and Neuroinflammation, Paris Descartes - Sorbonne Paris Cité University, Institut Imagine, Hôpital Necker, Paris, France; Manchester Centre for Genomic Medicine, Institute of Human Development, Faculty of Medical and Human Sciences, Manchester Academic Health Sciences Centre, University of Manchester, Manchester, UK.

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http://dx.doi.org/10.1002/ajmg.a.36887DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382202PMC
February 2015

Chipping away at the channels: Can we fashion a syndrome?

Authors:
Sameer M Zuberi

Neurology 2015 Feb 7;84(5):446-7. Epub 2015 Jan 7.

From the Paediatric Neurosciences Research Group, School of Medicine, University of Glasgow, and Fraser of Allander Neurosciences Unit, Royal Hospital for Sick Children, Glasgow, UK.

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http://dx.doi.org/10.1212/WNL.0000000000001219DOI Listing
February 2015

A White Paper on the medical and social needs of people with epilepsy and intellectual disability: the Task Force on Intellectual Disabilities and Epilepsy of the International League Against Epilepsy.

Epilepsia 2014 Dec 6;55(12):1902-6. Epub 2014 Nov 6.

Institute of Psychiatric Medicine & Clinical Neurosciences, Cardiff University, Cardiff, United Kingdom.

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http://dx.doi.org/10.1111/epi.12848DOI Listing
December 2014

Genotype phenotype associations across the voltage-gated sodium channel family.

J Med Genet 2014 Oct 27;51(10):650-8. Epub 2014 Aug 27.

The Paediatric Neurosciences Research Group, Royal Hospital for Sick Children, Glasgow, UK School of Medicine, College of Medical, Veterinary & Life Sciences, University of Glasgow, UK.

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http://dx.doi.org/10.1136/jmedgenet-2014-102608DOI Listing
October 2014

Dravet syndrome--from epileptic encephalopathy to channelopathy.

Epilepsia 2014 Jul 16;55(7):979-84. Epub 2014 May 16.

The Paediatric Neurosciences Research Group, Royal Hospital for Sick Children, Glasgow, United Kingdom; College of Medicine, Veterinary & Life Sciences, University of Glasgow, Glasgow, United Kingdom.

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http://dx.doi.org/10.1111/epi.12652DOI Listing
July 2014

The impact of methylphenidate on seizure frequency and severity in children with attention-deficit-hyperactivity disorder and difficult-to-treat epilepsies.

Dev Med Child Neurol 2013 Oct 3;55(10):966-7. Epub 2013 Jun 3.

The Paediatric Neurosciences Research Group, Royal Hospital for Sick Children, Glasgow, UK.

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http://dx.doi.org/10.1111/dmcn.12192DOI Listing
October 2013

Chromosome disorders associated with epilepsy.

Authors:
Sameer M Zuberi

Handb Clin Neurol 2013 ;111:543-8

Fraser of Allander Neurosciences Unit, Royal Hospital for Sick Children, Glasgow, UK. Electronic address:

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http://dx.doi.org/10.1016/B978-0-444-52891-9.00057-9DOI Listing
April 2014

Treatment of behavioral problems in intellectually disabled adult patients with epilepsy.

Epilepsia 2013 Mar;54 Suppl 1:34-40

Welsh Centre for Learning Disabilities, Institute of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, United Kingdom.

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http://dx.doi.org/10.1111/epi.12103DOI Listing
March 2013

Outcome and prognostic features in opsoclonus-myoclonus syndrome from infancy to adult life.

Pediatrics 2011 Aug 25;128(2):e388-94. Epub 2011 Jul 25.

Fraser of Allander Neurosciences Unit, Royal Hospital for Sick Children, Glasgow G3 8SJ, UK.

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http://dx.doi.org/10.1542/peds.2010-3114DOI Listing
August 2011

Comorbidities and predictors of health-related quality of life in Dravet syndrome.

Epilepsia 2011 Aug 10;52(8):1476-82. Epub 2011 Jun 10.

The Paediatric Neurosciences Research Group, Royal Hospital for Sick Children, Glasgow, United Kingdom School of Medicine, University of Glasgow, Glasgow, United Kingdom.

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http://dx.doi.org/10.1111/j.1528-1167.2011.03129.xDOI Listing
August 2011

Investigating neuroblastoma in childhood opsoclonus-myoclonus syndrome.

Arch Dis Child 2012 May 3;97(5):461-3. Epub 2011 Apr 3.

Fraser of Allander Neurosciences Unit, Royal Hospital for Sick Children, Glasgow, UK.

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http://adc.bmj.com/lookup/doi/10.1136/adc.2010.204792
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http://dx.doi.org/10.1136/adc.2010.204792DOI Listing
May 2012

Hepatic coma culminating in severe brain damage in a child with a SCN1A mutation.

Eur J Paediatr Neurol 2010 Sep 13;14(5):456-9. Epub 2010 Apr 13.

Pediatric Neurology Unit, Wolfson Medical Center, Holon 58100, affiliated to Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

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http://dx.doi.org/10.1016/j.ejpn.2010.03.002DOI Listing
September 2010

De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin.

J Med Genet 2010 Feb 8;47(2):137-41. Epub 2009 Jul 8.

Epilepsy Program, SA Pathology at Women's and Children's Hospital, North Adelaide , South Australia SA 5006, Australia.

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http://dx.doi.org/10.1136/jmg.2008.065912DOI Listing
February 2010

Psychosocial and intellectual functioning in childhood narcolepsy.

Dev Neurorehabil 2008 Jul;11(3):187-94

Fraser of Allander Neurosciences Unit, Royal Hospital for Sick Children, Glasgow, UK.

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http://dx.doi.org/10.1080/17518420802011493DOI Listing
July 2008

Clinical and molecular phenotype of Aicardi-Goutieres syndrome.

Authors:
Gillian Rice Teresa Patrick Rekha Parmar Claire F Taylor Alec Aeby Jean Aicardi Rafael Artuch Simon Attard Montalto Carlos A Bacino Bruno Barroso Peter Baxter Willam S Benko Carsten Bergmann Enrico Bertini Roberta Biancheri Edward M Blair Nenad Blau David T Bonthron Tracy Briggs Louise A Brueton Han G Brunner Christopher J Burke Ian M Carr Daniel R Carvalho Kate E Chandler Hans-Jurgen Christen Peter C Corry Frances M Cowan Helen Cox Stefano D'Arrigo John Dean Corinne De Laet Claudine De Praeter Catherine Dery Colin D Ferrie Kim Flintoff Suzanna G M Frints Angels Garcia-Cazorla Blanca Gener Cyril Goizet Francoise Goutieres Andrew J Green Agnes Guet Ben C J Hamel Bruce E Hayward Arvid Heiberg Raoul C Hennekam Marie Husson Andrew P Jackson Rasieka Jayatunga Yong-Hui Jiang Sarina G Kant Amy Kao Mary D King Helen M Kingston Joerg Klepper Marjo S van der Knaap Andrew J Kornberg Dieter Kotzot Wilfried Kratzer Didier Lacombe Lieven Lagae Pierre Georges Landrieu Giovanni Lanzi Andrea Leitch Ming J Lim John H Livingston Charles M Lourenco E G Hermione Lyall Sally A Lynch Michael J Lyons Daphna Marom John P McClure Robert McWilliam Serge B Melancon Leena D Mewasingh Marie-Laure Moutard Ken K Nischal John R Ostergaard Julie Prendiville Magnhild Rasmussen R Curtis Rogers Dominique Roland Elisabeth M Rosser Kevin Rostasy Agathe Roubertie Amparo Sanchis Raphael Schiffmann Sabine Scholl-Burgi Sunita Seal Stavit A Shalev C Sierra Corcoles Gyan P Sinha Doriette Soler Ronen Spiegel John B P Stephenson Uta Tacke Tiong Yang Tan Marianne Till John L Tolmie Pam Tomlin Federica Vagnarelli Enza Maria Valente Rudy N A Van Coster Nathalie Van der Aa Adeline Vanderver Johannes S H Vles Thomas Voit Evangeline Wassmer Bernhard Weschke Margo L Whiteford Michel A A Willemsen Andreas Zankl Sameer M Zuberi Simona Orcesi Elisa Fazzi Pierre Lebon Yanick J Crow

Am J Hum Genet 2007 Oct 4;81(4):713-25. Epub 2007 Sep 4.

Leeds Institute of Molecular Medicine, St James's University Hospital, Leeds, LS9 7TF, UK.

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http://dx.doi.org/10.1086/521373DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2227922PMC
October 2007

Memory consolidation and accelerated forgetting in children with idiopathic generalized epilepsy.

Epilepsy Behav 2007 Nov 21;11(3):394-400. Epub 2007 Aug 21.

Section of Psychological Medicine, University of Glasgow, Glasgow, UK.

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http://dx.doi.org/10.1016/j.yebeh.2007.05.004DOI Listing
November 2007

Developmental outcome in benign myoclonic epilepsy in infancy and reflex myoclonic epilepsy in infancy: a literature review and six new cases.

Epilepsy Res 2006 Aug 10;70 Suppl 1:S110-5. Epub 2006 Aug 10.

Fraser of Allander Neurosciences Unit, Royal Hospital for Sick Children, Yorkhill, Glasgow G3 SJ, United Kingdom.

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http://dx.doi.org/10.1016/j.eplepsyres.2006.01.014DOI Listing
August 2006

De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study.

Lancet Neurol 2006 Jun;5(6):488-92

Epilepsy Research Centre and Department of Medicine, University of Melbourne, Austin Health, Heidelberg West, Victoria, Australia.

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http://dx.doi.org/10.1016/S1474-4422(06)70446-XDOI Listing
June 2006

Symptoms of narcolepsy in children misinterpreted as epilepsy.

Epileptic Disord 2005 Mar;7(1):13-7

Fraser of Allander Neurosciences Unit, Royal Hospital for Sick Children, Glasgow, United Kingdom.

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March 2005

Electro-clinical phenotypes of chromosome disorders associated with epilepsy in the absence of dysmorphism.

Brain Dev 2005 Mar;27(2):118-24

Fraser of Allander Neurosciences Unit, Royal Hospital for Sick Children, Yorkhill, Glasgow, UK.

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http://linkinghub.elsevier.com/retrieve/pii/S038776040400110
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http://dx.doi.org/10.1016/j.braindev.2003.10.006DOI Listing
March 2005

The movement disorders of Coffin-Lowry syndrome.

Brain Dev 2005 Mar;27(2):108-13

Fraser of Allander Neurosciences Unit, Royal Hospital for Sick Children, Yorkhill, Glasgow, Scotland G3 8SJ, UK.

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http://dx.doi.org/10.1016/j.braindev.2003.11.010DOI Listing
March 2005

Gene table. Central nervous system/neuromuscular channelopathies.

Authors:
Sameer M Zuberi

Eur J Paediatr Neurol 2003 ;7(4):187-90

Fraser of Allander Neurosciences Unit, Department of Neurology and Child Development, Royal Hospital for Sick Children, Glasgow, UK.

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http://dx.doi.org/10.1016/s1090-3798(03)00053-9DOI Listing
October 2003