Stephan Klebe

Stephan Klebe

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Stephan Klebe

Stephan Klebe

Publications by authors named "Stephan Klebe"

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Management of delirium in Parkinson's disease.

J Neural Transm (Vienna) 2019 Jul 6;126(7):905-912. Epub 2019 Feb 6.

Department of Neurology, Charité-Universitätsmedizin Berlin, Hindenburgdamm 30, 12200, Berlin, Germany.

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http://dx.doi.org/10.1007/s00702-019-01980-7DOI Listing
July 2019

[Genetics of movement disorders-rare but important].

Nervenarzt 2019 Feb;90(2):197-210

Klinik für Neurologie, Universitätsmedizin Essen, Hufelandstr. 55, 45147, Essen, Deutschland.

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http://dx.doi.org/10.1007/s00115-018-0659-1DOI Listing
February 2019

Chorea-Acanthocytosis Presenting as Autosomal Recessive Epilepsy in a Family With a Novel Mutation.

Front Neurol 2018 9;9:1168. Epub 2019 Jan 9.

Department of Neurology, Faculty of Medicine, Medical Center, University of Freiburg, Freiburg, Germany.

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http://dx.doi.org/10.3389/fneur.2018.01168DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6334619PMC
January 2019

Retinal changes in Parkinson's disease and glaucoma.

Parkinsonism Relat Disord 2018 11 21;56:41-46. Epub 2018 Jun 21.

Department of Neurology, University Hospital Würzburg, Josef-Schneider-Str. 11, 97080, Würzburg, Germany; Department of Neurology, University Hospital Essen, Hufelandstr. 55, 45147, Essen, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.parkreldis.2018.06.016DOI Listing
November 2018

Longitudinal analysis of impulse control disorders in Parkinson disease.

Neurology 2018 07 20;91(3):e189-e201. Epub 2018 Jun 20.

From the Assistance Publique Hôpitaux de Paris (J.-C.C., F.C.-D., L.L., C.B., D.G., S.K., G.M., H.Y., A.B., M.V.); Sorbonne Université (J.-C.C., F.C.-D., L.L., C.B., D.G., S.K., G.M., H.Y., A.B., M.V.); INSERM (J.-C.C., F.C.-D., L.L., C.B., D.G., S.K., G.M., H.Y., A.B., M.V.), Institut du cerveau et de la Moelle, Centre d'Investigation Clinique Neurosciences, NS-PARK/FCRIN Network; CNRS (J.-C.C., F.C.-D., L.L., C.B., D.G., S.K., G.M., H.Y., A.B., M.V.); Departments of Neurology and Genetics (J.-C.C., F.C.-D., L.L., C.B., D.G., S.K., G.M., H.Y., A.B., M.V.), Hôpital Pitié-Salpêtrière, Paris; CESP (F.A., A.E.), Faculte de médecine, Université Paris-Sud; Faculte de médecine (F.A., A.E.), UVSQ, Institut National de la Santé et de la Recherche Médicale, Université Paris-Saclay, Villejuif; University of Toulouse 3 (O.R., C.B.-C., F.O.-M), Centre Hospitalo-Universitaire de Toulouse and INSERM; Centre d'Investigation Clinique CIC1436 (O.R., C.B.-C., F.O.-M), NS-PARK/FCRIN Network, Départements de Neurosciences et de Pharmacologie Clinique, NeuroToul COEN Center, Toulouse; Department of Neurology (F.D., A.-R.M.), NS-PARK/FCRIN Network, Centre Hospitalo-Universitaire de Clermont-Ferrand; Department of Neurology (P.D.), NS-PARK/FCRIN Network, Centre Hospitalo-Universitaire de Nantes; Department of Neurology (F.B.), Hôpital Foch, Suresnes; Department of Neurology (J.-P.B.), Fondation Rothschild, Paris; Department of Neurology (F.P.), Centre Hospitalier de Versailles; Université Versailles Saint Quentin en Yvelines et Paris Saclay (F.P.), Versailles; Department of Neurology (V.M.), Centre Hospitalo-Universitaire Saint-Antoine, Paris, France; and Department of Health Care Management (P.-C.L.), College of Health Technology, National Taipei University of Nursing and Health Sciences, Taiwan.

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http://dx.doi.org/10.1212/WNL.0000000000005816DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6059034PMC
July 2018

Atypical Presentation of Rapid-onset Dystonia-parkinsonism (DYT12) Unresponsive to Deep Brain Stimulation of the Subthalamic Nucleus.

Mov Disord Clin Pract 2018 Jul-Aug;5(4):427-429. Epub 2018 Apr 1.

Department of Neurology and Neuroscience, Medical Center - University of Freiburg, Medical Faculty University of Freiburg, Breisacher Straße 64 D-79106, Freiburg Germany.

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http://dx.doi.org/10.1002/mdc3.12605DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336285PMC
April 2018

Severe camptocormia due to myositis of paraspinal muscles as an early manifestation of Parkinson's disease.

Parkinsonism Relat Disord 2018 01 20;46:95-97. Epub 2017 Nov 20.

Department of Neurology and Neuroscience, Medical Center - University of Freiburg, Breisacher Straße 64, D-79106 Freiburg, Germany.

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http://dx.doi.org/10.1016/j.parkreldis.2017.11.008DOI Listing
January 2018

Ataxia and autonomic dysfunction as presenting symptoms in late-onset Alexander disease.

Neurol Clin Pract 2017 Dec;7(6):523-526

Freiburg University Medical Center and Medical Faculty, Freiburg University, Germany.

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http://dx.doi.org/10.1212/CPJ.0000000000000392DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800710PMC
December 2017

Novel compound heterozygous synaptojanin-1 mutation causes l-dopa-responsive dystonia-parkinsonism syndrome.

Mov Disord 2017 03 21;32(3):478-480. Epub 2016 Nov 21.

Department of Neurology, Freiburg University Medical Center and Medical Faculty, Freiburg University, Freiburg, Germany.

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http://dx.doi.org/10.1002/mds.26876DOI Listing
March 2017

Early- and late-onset essential tremor patients represent clinically distinct subgroups.

Mov Disord 2016 10;31(10):1560-1566

Department of Neurology, University Hospital Schleswig Holstein, Kiel, Germany.

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http://dx.doi.org/10.1002/mds.26708DOI Listing
October 2016

PARKIN Inactivation Links Parkinson's Disease to Melanoma.

J Natl Cancer Inst 2016 Mar 17;108(3). Epub 2015 Dec 17.

Affiliations of authors: INSERM, U976, Centre de Recherche sur la Peau, Hôpital Saint Louis , Paris , France (HHH, JA, SM, LM, VD, NBS, MB, AB, CL, ND, NS); AP-HP, Hôpital Bichat Claude Bernard, Département de Génétique , Paris , France (HHH, CK, AT, BG, NS); Université Paris Diderot, Sorbonne Paris Cité , UMRS976, Paris , France (HHH, CK, JA, LM, NBS, MB, AB, LD, AT, BG, ND, NS); Université Paris 6, INSERM UMRS975, Centre de Recherche de l'Institut du Cerveau et de la Moelle Epinière, Hôpital Pitié-Salpêtrière, AP-HP , Paris , France (SL, AB); INSERM, U940, Laboratoire de Pharmacologie, Hôpital Saint Louis Paris , France (SM); AP-HP, Hôpital Bichat Claude Bernard, Service de Dermatologie , Paris , France (VD); AP-HP, Hôpital Saint Louis, Service de Dermatologie , Paris , France (NBS, MB, CL, ND); INSERM, CRB3, Département de Pathologie, Hôpital Bichat, AP-HP , Paris , France (LD); AP-HP, Hôpital Ambroise Paré, Service de Dermatologie , Boulogne Billancourt , France (PS); CHU Grenoble, Service de Dermatologie , Grenoble , France (MTL); Gustave Roussy, Service de Génétique, Département de Biopathologie , Villejuif , France (BBdP); Division of Molecular Genetic Epidemiology, German Cancer Research Center, Im Neuenheimer Feld 580 , Heidelberg , Germany (RK); Department of Neurology, University Hospital of Würzburg , Würzburg , Germany (SK); Inserm UMR1037, Centre de Recherche en Cancérologie de Toulouse , Toulouse , France (NAA); Hôpital de l'Hôtel-Dieu, Service de Dermatologie , Lyon , France (LT); AP-HP, Groupe Pitié-Salpêtrière, Département de Génétique, Cytogénétique et Embryologie , Paris , France (AB).

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http://dx.doi.org/10.1093/jnci/djv340DOI Listing
March 2016

Non-Motor Symptoms of Essential Tremor Are Independent of Tremor Severity and Have an Impact on Quality of Life.

Tremor Other Hyperkinet Mov (N Y) 2016 8;6:361. Epub 2016 Mar 8.

Department of Neurology, University Hospital of Würzburg, Würzburg, Germany; Department of Neurology, University Hospital of Freiburg, Freiburg, Germany.

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http://dx.doi.org/10.7916/D8542NCHDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4790197PMC
March 2016

Distinctive distribution of phospho-alpha-synuclein in dermal nerves in multiple system atrophy.

Mov Disord 2015 Oct 14;30(12):1688-92. Epub 2015 Jul 14.

Department of Neurology, University of Würzburg, Würzburg, Germany.

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http://dx.doi.org/10.1002/mds.26293DOI Listing
October 2015

The cardiomyopathy in Friedreich's ataxia - New biomarker for staging cardiac involvement.

Int J Cardiol 2015 Sep 15;194:50-7. Epub 2015 May 15.

Comprehensive Heart Failure Center, University of Würzburg, Würzburg, Germany; Department of Internal Medicine I, University Hospital Würzburg, Würzburg, Germany.

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http://dx.doi.org/10.1016/j.ijcard.2015.05.074DOI Listing
September 2015

Mutations in HTRA2 are not a common cause of familial classic ET.

Mov Disord 2015 Jul 13;30(8):1149-50. Epub 2015 May 13.

Department of Neurology, University Hospital Schleswig Holstein, Kiel, Germany.

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http://dx.doi.org/10.1002/mds.26252DOI Listing
July 2015

High nigral iron deposition in LRRK2 and Parkin mutation carriers using R2* relaxometry.

Mov Disord 2015 Jul 22;30(8):1077-84. Epub 2015 May 22.

Institut du Cerveau et de la Moelle épinière-ICM, Centre de NeuroImagerie de Recherche-CENIR, Paris, France.

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http://dx.doi.org/10.1002/mds.26218DOI Listing
July 2015

Reply: Parkinson's disease in GTP cyclohydrolase 1 mutation carriers.

Brain 2015 May 14;138(Pt 5):e352. Epub 2014 Nov 14.

1 Department of Molecular Neuroscience, UCL Institute of Neurology, London WC1N 3BG, UK

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http://dx.doi.org/10.1093/brain/awu309DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4407186PMC
May 2015

Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.

Neurology 2014 Jun 7;82(22):1999-2002. Epub 2014 May 7.

From INSERM, U 975, and CNRS 7225-CRICM (A.M., C.D., O.T., D.B., I.L., M.V., A.B., E.R.), Département de Neurologie (A.M., M.V., E.R.), Fédération de Génétique, Département de Génétique et de Cytogénétique (C.D., A.B.), Banque d'ADN et de cellules (I.L.), Department of Biostatistics (J.-L.G.), and Centre d'Investigation Clinique Pitié Neurosciences 1422 (E.R.), Hôpital Pitié-Salpêtrière, AP-HP, Paris; Université Pierre et Marie Curie-Paris-6 (A.M., C.D., M.V., A.B., E.R.), UMR_S 975, Paris; Laboratoire de Génétique (F.R.), Groupe hospitalier Lariboisière-Fernand Widal, AP-HP, Paris; INSERM UMR_S740 (F.R.), Université Paris 7 Denis Diderot, Paris, France; Unit of Neurology (M.C., A.B.), Florence Health Authority, Italy; Génétique Médicale (P.B.), CHU Paris Nord, Hôpital Jean Verdier, Bondy, France; Department of Human Genetics (J.W.), University Medical Center Hamburg-Eppendorf, Hamburg, Germany; Institute of Neurogenetics (A.W.), University of Lübeck, Germany; Service de Neuropédiatrie (D.D.), Hôpital Trousseau, AP-HP, Paris, France; Unit of Neurology (M.R.), Villa Sofia-Cervello Hospital, Palermo; Department of Neuroscience (S.R.), Section of Neurology and Clinical Neurophysiology, Azienda Ospedaliera Universitaria of Siena, Italy; Neurologie et Pathologie du Mouvement (L.D.), Neurologie A, Hopital Salengro, Centre Hospitalier Universitaire, EA 1046, Lille, France; Pediatric Neurology and Metabolism (L.D.M.), Universitair Ziekenhuis Brussel, Belgium; James J. and Joan A. Gardner Family Center for Parkinson's disease and Movement Disorders (A.J.E.), University of Cincinnati Academic Health Center, Cincinnati, OH; IRCCS Fondazione Stella Maris (S.F.), Calambrone, Pisa, Italy; Department of Neurology (S.K.), University Hospital Würzburg, Germany; Service de Génétique Clinique (C.Q.), Hôpital Sud, Rennes, France; Institute for Human Genetics (S.R.-S.), Uniklinik RWTH Aachen, Germany; Service de Génétique (G.P.), CHU Clémenceau, Caen, F

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http://dx.doi.org/10.1212/WNL.0000000000000477DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105259PMC
June 2014

EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?

Neurobiol Aging 2012 Sep 1;33(9):2233.e1-2233.e5. Epub 2012 Jun 1.

Université Pierre et Marie Curie-Paris6, Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière, UMR-S975, Inserm, U975, Cnrs, UMR 7225, Hôpital de la Pitié-Salpêtrière, Paris, France.

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http://dx.doi.org/10.1016/j.neurobiolaging.2012.05.006DOI Listing
September 2012

Axonal integrity of corticospinal projections to the upper limbs in patients with pure hereditary spastic paraplegia.

Clin Neurophysiol 2011 Jul 30;122(7):1417-20. Epub 2010 Dec 30.

Department of Neurology, Christian-Albrechts-University Kiel, Germany.

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http://dx.doi.org/10.1016/j.clinph.2010.12.033DOI Listing
July 2011

LINGO1 is not associated with Parkinson's disease in German patients.

Am J Med Genet B Neuropsychiatr Genet 2010 Sep;153B(6):1173-8

Department of Neurology, University Hospital Schleswig-Holstein, Campus Kiel, Arnold-Heller Strasse 3, Kiel, Germany.

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http://dx.doi.org/10.1002/ajmg.b.31085DOI Listing
September 2010

LINGO1 polymorphisms are associated with essential tremor in Europeans.

Mov Disord 2010 Apr;25(6):717-23

Department of Neurology, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.

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http://dx.doi.org/10.1002/mds.22887DOI Listing
April 2010

Analysis of CYP7B1 in non-consanguineous cases of hereditary spastic paraplegia.

Neurogenetics 2009 Apr 15;10(2):97-104. Epub 2008 Oct 15.

Sektion Klinische Neurogenetik, Hertie Institut für Klinische Hirnforschung, Tübingen, Germany.

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http://dx.doi.org/10.1007/s10048-008-0158-9DOI Listing
April 2009

Screening of hereditary spastic paraplegia patients for alterations at NIPA1 mutational hotspots.

J Neurol Sci 2008 May 14;268(1-2):131-5. Epub 2008 Jan 14.

Institut für Klinische Chemie und Laboratoriumsdiagnostik, Universitätsklinikum, 07747 Jena, Germany.

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http://dx.doi.org/10.1016/j.jns.2007.11.015DOI Listing
May 2008

Evaluation of a screening instrument for essential tremor.

Mov Disord 2008 May;23(7):1006-1012

Department of Neurology, Christian-Albrechts-University Kiel, Germany.

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http://dx.doi.org/10.1002/mds.22010DOI Listing
May 2008

Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description.

Am J Med Genet B Neuropsychiatr Genet 2007 Oct;144B(7):854-61

INSERM U679, Pierre and Marie Curie Paris 6 University, Pitié-Salpêtrière Hospital, 47 Boulevard de l'Hôpital, 75651 Paris Cedex 13, France.

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http://dx.doi.org/10.1002/ajmg.b.30518DOI Listing
October 2007

Methylphenidate fails to improve gait and muscle tone in patients with sporadic and hereditary spastic paraplegia.

Mov Disord 2006 Sep;21(9):1468-71

Department of Neurology, Christian-Albrechts-Universität zu Kiel, Kiel, Germany.

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http://dx.doi.org/10.1002/mds.20973DOI Listing
September 2006

Autosomal recessive spastic paraplegia (SPG30) with mild ataxia and sensory neuropathy maps to chromosome 2q37.3.

Brain 2006 Jun 24;129(Pt 6):1456-62. Epub 2006 Jan 24.

INSERM U679, Federative Institute for Neuroscience Research (IFR70), Salpetriere Hospital, Paris, France.

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http://dx.doi.org/10.1093/brain/awl012DOI Listing
June 2006

New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14.

Ann Neurol 2005 Nov;58(5):720-9

Institut National de la Sante et de la Recherche Médicale U679 (formerly U289) and Institut Fédératif de Recherche en Neurosciences, Paris, France.

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http://dx.doi.org/10.1002/ana.20628DOI Listing
November 2005

Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28).

Ann Neurol 2005 Apr;57(4):567-71

INSERM U679 (former U289), Federative Institute for Neuroscience Research (IFR70), Salpetriere Hospital, Paris, France.

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http://dx.doi.org/10.1002/ana.20416DOI Listing
April 2005

Prevalence of gait disorders in hospitalized neurological patients.

Mov Disord 2005 Jan;20(1):89-94

Department of Neurology, Universitätsklinikum Kiel, Kiel, Germany.

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http://dx.doi.org/10.1002/mds.20266DOI Listing
January 2005

Hand coordination following capsular stroke.

Brain 2005 Jan 7;128(Pt 1):64-74. Epub 2004 Oct 7.

Departments of Neurology, Christian-Albrechts-Universität Kiel, Kiel, Germany.

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http://dx.doi.org/10.1093/brain/awh317DOI Listing
January 2005

Falls in frequent neurological diseases--prevalence, risk factors and aetiology.

J Neurol 2004 Jan;251(1):79-84

Department of Neurology, Universitätsklinikum Kiel, Niemannsweg 147, 24105 Kiel, Germany.

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http://dx.doi.org/10.1007/s00415-004-0276-8DOI Listing
January 2004

Force overflow and levodopa-induced dyskinesias in Parkinson's disease.

Brain 2002 Apr;125(Pt 4):871-9

Department of Neurology of the Christian-Albrechts Universität Kiel, Germany.

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http://dx.doi.org/10.1093/brain/awf084DOI Listing
April 2002