Thomas Dorn

Thomas Dorn

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Thomas Dorn

Thomas Dorn

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Correction: The landscape of epilepsy-related GATOR1 variants.

Genet Med 2019 Aug;21(8):1896

Sorbonne Université, UPMC Univ Paris 06, UMR S 1127, F-75013 Paris, France.

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http://dx.doi.org/10.1038/s41436-018-0325-9DOI Listing
August 2019

Correction to: The landscape of epilepsy-related GATOR1 variants.

Genet Med 2019 Jul;21(7):1671

Sorbonne Université, UPMC Univ Paris 06, UMR S 1127, F-75013, Paris, France.

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http://dx.doi.org/10.1038/s41436-018-0284-1DOI Listing
July 2019

Clinical spectrum of -related epileptic disorders.

Neurology 2019 Mar 8;92(11):e1238-e1249. Epub 2019 Feb 8.

From the University of Tübingen (S. Wolking, J.M., Y.G.W., H.L., J.S.), Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, Tübingen, Germany; Luxembourg Centre for Systems Biomedicine (P.M.), University of Luxembourg, Esch-sur-Alzette; Pediatric Neurology and Neurogenetics Unit and Laboratories (D.M., R.G., C.M.), Children's Hospital Anna Meyer, University of Florence, Italy; Danish Epilepsy Centre (R.S.M.), Dianalund; Institute for Regional Health Services (R.S.M.), University of Southern Denmark, Odense; Department of Clinical and Experimental Epilepsy (S.B.), UCL Institute of Neurology and Epilepsy Society, UK, London; Division of Neurology (K.L.H., I.H.), Children's Hospital of Philadelphia, PA; Department of Pediatric Neurology (C.D.A.), Centre de Compétences Maladies Rares, CHU Besançon; Service de Génétique (N.C.), Hospices Civils des Lyon, Bron; GENDEV Team (N.C.), Neurosciences Research Center of Lyon, Bron, France; Neuropediatric Clinic and Clinic for Neurorehabilitation (K.S.), Epilepsy Center for Children and Adolescents, Schoen Klinik Vogtareuth, Germany; Beaumont Hospital (P.W.-W.), Dublin, Ireland; Department of Pediatrics, Division of Medical Genetics, Institute of Human Genetics (B.A.M.), Departments of Neurology and Pediatrics (A.N.), and Departments of Neurology and Pediatrics, and Institute of Human Genetics (M.R.C.), University of California, San Francisco; Department of Neurology (W.V.P.), University Hospitals Leuven, Belgium; Department of Pediatrics (L.L.S.), Hvidovre Hospital, Denmark; King's College Hospital (S.O., E.H., S.G., D.K.P.), London; Evelina London Children's Hospital (S.O., E.H., S.G.), London, UK; Section of Genetics (K.B., M.S.S.), Department of Pediatrics, University of Colorado and Children's Hospital Colorado, Aurora; Clinique Bernoise Montana (T.D.), Crans-Montana, Switzerland; Department of Neuropediatrics (H.M.), University Medical Center Schleswig-Holstein, Christian-Albrechts University, Kiel, Germany; National Institute for Health Research Oxford Biomedical Research Centre, Wellcome Centre for Human Genetics (A.T.P., S.J.L.K., J.C.T.) and Department of Oncology (D.V.V.), University of Oxford, UK; Epilepsy Center (M.P.C.), Health Sciences Department, San Paolo Hospital, University of Milan; Child Neuropsychiatry (F.D.), Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, Italy; Departments of Neurology and Clinical Genomics (R.H.G.) and Health Sciences Research and Clinical Genomics (E.W.K., C.K.), Mayo Clinic, Rochester, MN; Ambry Genetics (Z.P.), Aliso Viejo, CA; Department of Clinical Neuroscience (S.T.), King's College London; New Medicines (M.A., D.M.), UCB Pharma, Slough, UK; Neuropediatric Clinic and Clinic for Neurorehabilitation (G.J.K.), Epilepsy Center for Children and Adolescents, Schoen Klinik Vogtareuth, Germany; Research Institute for Rehabilitation, Transition and Palliation (G.J.K.), PMU Salzburg, Austria; Department of Neurology (D.H.L.), University of California, San Francisco; Neurogenetics Group (S. Weckhuysen), Center for Molecular Neurology, VIB, Antwerp; Laboratory of Neurogenetics (S. Weckhuysen), Institute Born-Bunge, University of Antwerp; Department of Neurology (S. Weckhuysen), Antwerp University Hospital, Antwerp, Belgium; Department of Basic & Clinical Neuroscience, Institute of Psychiatry, Psychology & Neuroscience (D.K.P.), MRC Centre for Neurodevelopmental Disorders (D.K.P.), King's College London, UK; Evelina London Children's Hospital (D.K.P.), London, UK; Department of Neuropediatrics (I.H.), University Medical Center Schleswig-Holstein, Christian-Albrechts University, Kiel, Germany; Institute of Neuroscience (R.H.T.), Henry Wellcome Building, Newcastle University; Neurology Research Group (M.I.R.), Institute of Life Science, Swansea University Medical School, Swansea, UK; Service de Génétique (G.L.), Hospices Civils des Lyon, Bron; GENDEV Team (G.L.), Neurosciences Research Center of Lyon, Bron, France; NIHR University College London Hospitals Biomedical Research Centre (S.M.S.), UCL Institute of Neurology, London, UK; Cologne Center for Genomics (D.L.), University of Cologne, Germany; Stanley Center for Psychiatric Research (D.L.) and Program in Medical and Population Genetics (D.L.), Broad Institute of MIT and Harvard, Cambridge; Psychiatric and Neurodevelopmental Genetics Unit (D.L.), Massachusetts General Hospital and Harvard Medical School, Boston.

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http://dx.doi.org/10.1212/WNL.0000000000007089DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6511102PMC
March 2019

The landscape of epilepsy-related GATOR1 variants.

Genet Med 2019 02 10;21(2):398-408. Epub 2018 Aug 10.

Sorbonne Université, UPMC Univ Paris 06, UMR S 1127, F-75013, Paris, France.

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http://www.nature.com/articles/s41436-018-0060-2
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http://dx.doi.org/10.1038/s41436-018-0060-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292495PMC
February 2019

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.

Brain 2017 May;140(5):1316-1336

The Danish Epilepsy Centre, Dianalund, Denmark.

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http://dx.doi.org/10.1093/brain/awx054DOI Listing
May 2017

Towards a Molecular Syndromology of the Epilepsies.

Mol Syndromol 2016 Sep 17;7(4):169-171. Epub 2016 Aug 17.

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http://dx.doi.org/10.1159/000448358DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073502PMC
September 2016

Generalized Epilepsy and Myoclonic Seizures in 22q11.2 Deletion Syndrome.

Mol Syndromol 2016 Sep 24;7(4):239-246. Epub 2016 Aug 24.

Institute of Human Genetics, University Hospital and Clinics, Leipzig, Germany.

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http://dx.doi.org/10.1159/000448445DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073659PMC
September 2016

[Work and epilepsy--facts and phantasies].

Authors:
Thomas Dorn

Praxis (Bern 1994) 2015 Nov;104(23):1279-85

1 Klinik Lengg AG, Schweizerische Epilepsieklinik, Zürich.

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http://dx.doi.org/10.1024/1661-8157/a002188DOI Listing
November 2015

Investigation of GRIN2A in common epilepsy phenotypes.

Epilepsy Res 2015 Sep 2;115:95-9. Epub 2015 Jun 2.

Division of Human Genetics, University Children's Hospital Inselspital, Bern, Switzerland; Institute of Human Genetics, University Medical Center Leipzig, Leipzig, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.eplepsyres.2015.05.010DOI Listing
September 2015

Galanin pathogenic mutations in temporal lobe epilepsy.

Hum Mol Genet 2015 Jun 17;24(11):3082-91. Epub 2015 Feb 17.

Department of Genetic Medicine and Development, University of Geneva Medical School and University Hospitals of Geneva, Geneva, Switzerland Institute of Genetics and Genomics in Geneva (iGE3), Geneva, Switzerland.

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http://dx.doi.org/10.1093/hmg/ddv060DOI Listing
June 2015

Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.

Brain 2013 Oct 6;136(Pt 10):3140-50. Epub 2013 Sep 6.

1 NIHR University College London Hospitals Biomedical Research Centre, Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK.

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https://academic.oup.com/brain/article/136/10/3140/330027
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http://dx.doi.org/10.1093/brain/awt233DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3784283PMC
October 2013

Waste disposal technology transfer matching requirement clusters for waste disposal facilities in China.

Waste Manag 2012 Nov 6;32(11):2177-84. Epub 2012 Jul 6.

University of Rostock, Faculty of Agricultural and Environmental Sciences, Department Waste Management, 18059 Rostock, Germany.

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https://linkinghub.elsevier.com/retrieve/pii/S0956053X120024
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http://dx.doi.org/10.1016/j.wasman.2012.05.038DOI Listing
November 2012

A review of energy recovery from waste in China.

Waste Manag Res 2012 Apr 5;30(4):432-41. Epub 2012 Apr 5.

Universität Rostock, Rostock, Germany.

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http://dx.doi.org/10.1177/0734242X11433530DOI Listing
April 2012

["I believe we've become more vigilant" (interview by Margrit Bachi)].

Krankenpfl Soins Infirm 2011 ;104(9):13-4

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December 2011

Genomic microdeletions associated with epilepsy: not a contraindication to resective surgery.

Epilepsia 2011 Aug 2;52(8):1388-92. Epub 2011 Jun 2.

Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology and National Hospital for Neurology and Neurosurgery, Queen Square, London, United Kingdom.

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http://dx.doi.org/10.1111/j.1528-1167.2011.03087.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399084PMC
August 2011

Juvenile myoclonic epilepsy with photosensitivity in a female with Velocardiofacial syndrome (del(22)(q11.2))--causal relationship or coincidence?

Seizure 2009 Nov 19;18(9):660-3. Epub 2009 Aug 19.

Swiss Epilepsy Center Zurich, Bleulerstrasse 60, CH-8008 Zürich, Switzerland.

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http://dx.doi.org/10.1016/j.seizure.2009.07.008DOI Listing
November 2009

Bilateral frontoparietal polymicrogyria, Lennox-Gastaut syndrome, and GPR56 gene mutations.

Epilepsia 2009 Jun 6;50(6):1344-53. Epub 2008 Oct 6.

Pediatric Neurology and Neurogenetics Unit, Children's Hospital A. Meyer-University of Florence, Florence, Italy.

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http://dx.doi.org/10.1111/j.1528-1167.2008.01787.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4271835PMC
June 2009

Smoking reduces serum levels of lamotrigine.

Seizure 2008 Oct 25;17(7):651-3. Epub 2008 Jun 25.

Swiss Epilepsy Center, Bleulerstr. 60, 8008 Zurich, Switzerland.

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http://dx.doi.org/10.1016/j.seizure.2008.05.009DOI Listing
October 2008

Automatic striatal volumetry allows for identification of patients with chorea-acanthocytosis at single subject level.

J Neural Transm (Vienna) 2008 Oct 22;115(10):1393-400. Epub 2008 Jul 22.

Swiss Epilepsy Center, Bleulerstrasse 60, 8008, Zurich, Switzerland.

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http://dx.doi.org/10.1007/s00702-008-0094-8DOI Listing
October 2008

Mosaic mutations of the FLN1 gene cause a mild phenotype in patients with periventricular heterotopia.

Neurogenetics 2004 Sep 28;5(3):191-6. Epub 2004 Jul 28.

IRCCS Stella Maris Foundation, Scientific Institute for Child and Adolescence Neurology and Psychiatry, Pisa, Italy.

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http://dx.doi.org/10.1007/s10048-004-0187-yDOI Listing
September 2004

Wernicke encephalopathy - a severe neurological complication in a clinically inactive Crohn's disease.

Eur Neurol 2003 ;50(3):184-5

Department of Neurology, University Clinic, Zürich, Switzerland.

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http://dx.doi.org/10.1159/000073064DOI Listing
November 2003

Metastable isonitrosyl structure of the nitroprusside anion confirmed by nuclear inelastic scattering.

J Am Chem Soc 2002 Mar;124(12):3007-11

Institut für Physik, Medizinische Universität zu Lübeck, Ratzeburger Allee 160, D-23538 Lübeck, Germany.

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http://dx.doi.org/10.1021/ja016239cDOI Listing
March 2002