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Spastische Spinalparalyse | Universitätsklinikum Tübingen
www.medizin.uni-tuebingen.de
Prof. Dr. Ludger Schöls. Leiter der Sektion Klinische Neurogenetik. frontend.sr-only_:. PD Dr. Rebecca Schüle. Leitende Oberärztin. frontend.sr-only_: ... › ...
Faculty - CISSN 2022
www.biometec.unict.it
Rebecca Schüle-Freyer - PD. Dr., Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research (HIH), Center of Neurology, ... › events › CISSN2022 › F...
Symposium Bewegungsstörungen | MRI TUM
www.mri.tum.de
PD Dr. Rebecca Schüle Hertie Institut für klinische Hirnforschung, Tübingen. Prof. Dr. Tobias Warnecke Klinik für Neurologie, Klinikum Osnabrück. › symposium...
Rebecca Schüle und Lukas Laumann holen den Pokal - Stühlingen -...
www.badische-zeitung.de
Tolle Atmosphäre beim Pfingstturnier des Tennisclubs Stühlingen.
Telephone & Addresses
WhitePages: Rebecca Schule in Chula Vista, CA | WhitePages
There is 1 person in Chula Vista, CA named Rebecca Schule. Get contact info including address and phone. Find and connect with Rebecca Schule at ...
Network Profiles
Rebecca Schüle - Backnang (Grund- und Hauptschule mit Werkrealschule...
www.stayfriends.de
Rebecca Schüle ist Mitglied bei StayFriends und hat bis diese Schule besucht: Grund- und Hauptschule mit Werkrealschule in der Taus.
Interests
Generation of induced pluripotent stem cells (iPSCs) from a ...
agris.fao.org
by P Höflinger · — ... Tuebingen, Germany); Rebecca Schüle (Department of Neurology and Hertie Institute for Clinical Brain Research, University of Tuebingen, Tuebingen, ... › agris-search › search
Gene linked with early epilepsy discovered -- ScienceDaily
www.sciencedaily.com
Certain types of early-onset epilepsy are caused by previously unknown mutations of a potassium channel gene, KCNA2. The mutations disrupt the electrical...
SERAC1 deficiency causes complicated HSP: evidence from ...jmg.bmj.com › › jmedgenet
jmg.bmj.com
... Tübingen, Germany PubMed articlesGoogle scholar articles; Rebecca Schüle Department of Neurodegeneration, Hertie Institute for Clinical ...
Genetic defect underlying a rare disease identified -- ScienceDaily
www.sciencedaily.com
Wolfgang M. Schmidt, S. Lane Rutledge, Rebecca Schüle, Benjamin Mayerhofer, Stephan Züchner, Eugen Boltshauser, Reginald E. Bittner.
Business Profiles
Researchgate: Rebecca Schüle
Tübingen, Germany
Rebecca Schüle University of Tuebingen | EKU Tübingen
www.researchgate.net
› University of Tuebingen
Education
Enrichment of sarm1 alleles encoding variants with ...
kclpure.kcl.ac.uk
by J Gilley · · Cited by 22 — ... John Ravits, Guy A. Rouleau, Rebecca Schüle, Jishu Xu, Stephan Züchner, Johnathan Cooper-Knock & 3 more Ziv Gan-Or, Mary M. Reilly, ... › portal › publications
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic...
kclpure.kcl.ac.uk
... Saskia Biskup and Markus Wolff and Snezana Maljevic and Rebecca Schüle and Sisodiya, {Sanjay M} and Sarah Weckhuysen and Holger Lerche and Lemke ...
Books & Literature
ParkinsonCanadaV1, Ncbi, Curation, indexItem, Author.i, Rebecca ...
lorexplor.istex.fr
La maladie de Parkinson au Canada (serveur d'exploration) - Curation (Ncbi) Index « » - entrée « Rebecca Schüle ». Attention, ce site est en cours de ... › explor › Site
Encyclopedia of Molecular Mechanisms of Disease
books.google.co.uk
... NY USA REBECCA SCHÜLE Department for Neurodegenerative Diseases Hertie-Institute for Clinical Brain Research and Centre for Neurology Tuebingen Germany ...
Movement Disorder Genetics - Page x - Google Books result
books.google.co.uk
... and Juliane Winkelmann Genetics of Hereditary Spastic Paraplegias (HSP) Rebecca Schüle and Ludger Schöls Genetics of ALS.
Networks in Movement Disorders - Page 4 - Google Books result
books.google.co.uk
... Stefan Vielhaber, Michael Wallner, Bart P. van de Warrenburg, Ginevra Zanni, Stephan Zuchner, Thomas Klockgether, Rebecca Schüle, Ludger Schöls, ...
Related Documents
Real‐Life Turning Movements Capture Subtle Longitudinal ...
movementdisorders.onlinelibrary.wiley.com
by A Thierfelder · Cited by 3 — Rebecca Schüle MD,. Rebecca Schüle MD. . Department of Neurodegeneration, Hertie Institute for ... › mds
Effect of spastic paraplegia mutations in KIF5A kinesin on ...
academic.oup.com
by B Ebbing · · Cited by 156 — Rebecca Schüle,. Rebecca Schüle. 2. Hertie-Institute for Clinical Brain Research. ,. , Tübingen. › hmg › article-abstract
The Impact of Catechol-O-Methyltransferase and Dopamine ...
www.jneurosci.org
by UM Krämer · · Cited by 88 — ... David Cucurell, Wido Nager, Peter Bauer, Rebecca Schüle, Ludger Schöls, Antoni Rodriguez-Fornells and Thomas F. Münte. › content › abstract
an integrated multimodal progression chart in spastic ataxias
www.hsp-info.de
Rebecca Schüle, Matthis Synofzik. Spastic ataxias (SPAX) present an expanding group of >100 rare neurodegenerative diseases with. › Abstract_Schuele
Scientific Publications
Generation of the CRISPR/Cas9-mediated KIF1C knock-out ...
www.sciencedirect.com
by M Nagel · · Cited by 1 — Contact information of distributor, Rebecca Schüle . Type of cell line, Induced pluripotent stem cell (iPSC). › science › article › pii
First de novo KCND3 mutation causes severe Kv4.3 channel ...
bmcmedgenet.biomedcentral.com
by K Smets · · Cited by 52 — Rebecca Schüle obtained funding from the 7th European Community Framework program through a Marie Curie International Outgoing Fellowship (grant ... › articles
Genomik seltener Bewegungsstörungen
www.hih-tuebingen.de
... Rebecca Schüle – Universität Tübingen), Frankreich (Giovanni Stevanin – INSERM Paris) und Italien (Maria Teresa Bassi – IRCCS Bosisio Parini) hat zum ... › geno...
Publications
Create a SciFeed alert for new publications - MDPI
www.mdpi.com
By following authors. Dietmar R. Thal. Stephan Züchner. Stephan Gierer. Claudia Schulte. Ludger Schöls. Rebecca Schüle. Matthis Synofzik ... › scifeed_display
PROSPAX: an integrated multimodal progression Ataxia UK
www.ataxia.org.uk
Rebecca Schüle at the University of Tübingen (Germany). The aim of this project is to establish an integrated trial-ready model of disease progression in ... › uploads › › r...
Publications Authored by Rebecca Schule | PubFacts
www.pubfacts.com
Publications Authored by Rebecca Schule
Video & Audio
Frau PD Dr. Rebecca Schüle: Vortrag auf dem HSP-Info-Tag ...www.youtube.com › watch
www.youtube.com
▶ 1:14:47Frau Dr. Schüle spricht über Neues aus der HSP-Forschung und aus der HSP-Therapie. Des Weiteren ...
Rebecca Schüle - YouTube
www.youtube.com
Teile deine Videos mit Freunden, Verwandten oder der ganzen Welt
Reports & Statements
6th International Meeting on Spastic Paraparesis and Ataxia ...
spatax.wordpress.com
5 Mar — Rebecca Schüle (Germany) IP3 Receptor Degradation – A Mutational Hotspot for Hereditary Ataxia and Motor Neuron Disease ... ›
Rebecca Schüle | SPATAX Network : Clinical and Genetic Analysis of...
spatax.wordpress.com
Posts about Rebecca Schüle written by spatax
Mutations Link Cerebellar Ataxia, Spastic Paraplegia to Lipid Biology...
www.alzforum.org
Co-first author Rebecca Schüle of the Hertie-Institute for Clinical Brain Research and Center for Neurology in Tübingen, Germany, was visiting ...
Miscellaneous
"Solving unsolved rare neurological diseases-a Solve-RD viewpoint ...
mouseion.jax.org
By Rebecca Schüle, Dagmar Timmann, Corrie E Erasmus, et al., Published on › stfb2021
Analysis of CYP7B1 in non-consanguineous cases INFONA
www.infona.pl
by R Schüle · · Cited by 69 — Rebecca Schüle, Elisabeth Brandt, Kathrin N. Karle, Maria Tsaousidou, Stephan Klebe, Sven Klimpe, Michaela Auer-Grumbach, … [ more ]. › resource
Center of Neurology, University of Tübingen - Solve-RD
solve-rd.eu
Clinician, research group leader systems neurodegeneration. Rebecca Schüle-Freyer. Clinician, research group leader genomic of rare movement disorders ... › the-group › consortium › center-of...
Clinical, neuropathological, and genetic characterization of ...
www.gimjournal.org
by T Roux · — Rebecca Schüle. Affiliations. Department of Neurology and Hertie-Institute for Clinical Brain Research University of Tübingen, Tübingen, Germany. › article › fulltext
ERN-RND centres – Hereditary Spastic Paraplegias
www.ern-rnd.eu
Behandlungs und Forschungszentrum für Seltene Erkrankungen ZSE Tübingen Contact: PD Dr Rebecca SCHÜLE, Prof. Ludger SCHÖLS Phone: +49 (0) › disease-knowledge-hub › ataxia
Enrichment of SARM1 alleles encoding variants with eLife
elifesciences.org
Henry Houlden); HSP study (available on request from Dr. Rebecca Schüle); Lothian Birth Cohort (https://www.ed.ac.uk/lothian-birth-cohorts/data-access › articles
Featured Plenary Speakers | Peripheral Nerve Society
www.pnsociety.com
Rebecca Schüle is a neurologist and neuroscientist at the University of Tübingen, Germany. She is the coordinator of the TreatHSP.net consortium, ... › pages
Gene, Mechanism, Therapy: A Network for Precision Medicine ...
www.ekfs.de
Institution: Zentrum für Neurologie, Universität Tübingen Applicants: Prof Dr Matthis Synofzik (Speaker), PD Dr. Rebecca Schüle (deputy speaker), Prof. › currently-funded-projects › gene-...
Hereditary Spastic Paraplegia (HSP): clinical disease course
www.world-wide.org
Rebecca Schüle | University of Tübingen, Germany. @uktuebingen www.ern-rnd.eu/education-tra ... ↗ Hereditary Spastic Paraplegia (HSP): clinical disease ... › seminar
Hereditary spastic paraplegia: Clinicogenetic Read by QxMD
read.qxmd.com
Rebecca Schüle, Sarah Wiethoff, Peter Martus, Kathrin N Karle, Susanne Otto, Stephan Klebe, Sven Klimpe, Constanze Gallenmüller, Delia Kurzwelly, ... › read › hereditary-spastic-parap...
Hertie Institute for Clinical Brain Research, AG Schüle (HIHRS)
hpscreg.eu
Contact for cell line registrations, Rebecca Schüle . Cell lines. HIHRSi001-A (iPSC-GBA-1) · HIHRSi002-A ... › browse › provider
PLA2G6 MUTATIONS ASSOCIATED WITH A CONTINUOUS ...
scholarship.miami.edu
by B Ozes · · Cited by 33 — Burcak Ozes, Nazan Karagoz, Rebecca Schüle, Adriana Rebelo, María-Jesús Sobrido, Florian Harmuth, Matthis Synofzik, Samuel Ignacio Pascual Pascual, ... › outputs › journalArticle
Phenotype and frequency of STUB1 mutations: next ...
cyberleninka.org
Similar topics of scientific paper in Biological sciences , author of scholarly article — Matthis Synofzik, Rebecca Schüle, Martin Schulze, ... › article
Projektbeschreibung von Frau Dr. Schüle -
hsp-hilfe.de
Rebecca Schüle (Bild links). Fast jede fünfte HSP wird durch eine ‚Nonsense-Mutation' verursacht – einen Gendefekt, der durch ein falsches Stoppsignal die ... › projektbeschrei...
Who We Are | N=1 Collaborative
www.n1collaborative.org
Rebecca Schüle, MD. University of Tübingen. Read Full Bio. Victoria Suslovitch, MS, CGC. Boston Children's Hospital. Read Full Bio. Matthis Synofzik, MD. › who-we-are
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