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Article : Hertie-Institut für klinische Hirnforschungwww.hih-tuebingen.de › press › article

www.hih-tuebingen.de

In Tübingen wurden Dr. Stefanie Nicole Hayer (Hertie-Institut für klinische Hirnforschung und Universität Tübingen), Dr. Dr. Randolph Helfrich ...

HEIDI: Hayer, Stefanie Nicole: Neuronal activity-dependent...

katalog.ub.uni-heidelberg.de

Titel: Neuronal activity-dependent transcriptional regulation of the synaptic cell adhesion molecules Lrrtm1 and Lrrtm2. Verf.angabe: Stefanie Nicole Hayer.

heiBIB: Hayer, Stefanie Nicole

katalog.ub.uni-heidelberg.de

the synaptic cell adhesion molecules Lrrtm1 and Lrrtm2 / Stefanie Nicole Hayer, ...

Generation of an induced pluripotent stem cell line from a patient...

pubmed.ncbi.nlm.nih.gov

Authors. Stefanie Nicole Hayer , Yvonne Schelling , Philip Hoeflinger , Stefan Hauser , Ludger Schöls. Affiliations. 1 Department of Neurodegenerative Diseases, ...

STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a...

ojrd.biomedcentral.com

Stefanie Nicole Hayer,; Tine Deconinck,; Benjamin Bender,; Katrien Smets,; Stephan Züchner,; Selina Reich,; Ludger Schöls,; Rebecca Schüle, ...

NfL and pNfH are increased in Friedreich's ataxia | SpringerLinklink.springer.com › article

link.springer.com

Stefanie Nicole Hayer ,; Inga Liepelt , ...

Generation of an induced pluripotent stem cell line from a patient...

en.x-mol.com

(SCA3): HIHCNi002-A，Stefanie Nicole Hayer, Yvonne Schelling, Jeannette Huebener-Schmid, Jonasz Jeremiasz Weber, Stefan Hauser, ...

FDI Lab - SciCrunch Infrastructure | Searching in Literaturescicrunch.org › scicrunch

scicrunch.org

Hertie Network of Excellence in Clinical Neuroscience ...www.ghst.de › hertie-network

www.ghst.de

Tübingen. Dr. Stefanie Nicole Hayer, Hertie-Institut für klinische Hirnforschung (HIH). Ich beschäftige mich mit der Erforschung der seltenen ...

Jahrgang Nr Saison PDF Kostenfreier ...docplayer.org › Jahrgang...

docplayer.org

... Steffens, Laura Meeth, Sina Rohlinger, Lisa Diede, Lene Scharfbillig, Hanna Ruppert, Nicole Hayer, Stefanie Summe Einsätze Tore gesamt Feldtore 8 9 m 8.

Publication highlights

rd-neuromics.eu

Stefanie Nicole Hayer, Tine Deconinck, Benjamin Bender, Katrien Smets, Stephan Züchner, Selina Reich, Ludger Schöls, Rebecca Schüle, Peter De Jonghe, ...

KIT-Bibliothek - KVK - Karlsruher Virtueller Katalogkvk.bibliothek.kit.edu › nph-kvk2

kvk.bibliothek.kit.edu

NfL and pNfH are increased in Friedreich's ataxia / Stefanie Nicole Hayer, Inga Liepelt, Christian Barro, Carlo Wilke, Jens Kuhle, Peter Martus, Ludger Schöls, ...

Phenotype and frequency of STUB1 mutations: next-generation...

cyberleninka.org

Stefanie Nicole Hayer, Tine Deconinck, Benjamin Bender, Katrien Smets, Stephan Züchner, et al. STUB1 mutations in autosomal recessive ataxias ...

STUB1/CHIP mutations cause Gordon Holmes syndrome as ...cyberleninka.org › article

cyberleninka.org

Similar topics of scientific paper in Clinical medicine , author of scholarly article — Stefanie Nicole Hayer, Tine Deconinck, Benjamin Bender, Katrien Smets, ...

STUB1/CHIP mutations cause Gordon Holmes syndrome as ...miami.pure.elsevier.com › publications

miami.pure.elsevier.com

Stefanie Nicole Hayer, Tine Deconinck, Benjamin Bender, Katrien Smets, Stephan Züchner, Selina Reich, Ludger Schöls, Rebecca Schüle, ...

搜索页_+Hypogonadism - cglhub.comwww.cglhub.com › auto › search

www.cglhub.com

作者： Stefanie Nicole Hayer ; Tine Deconinck ; Benjamin Bender… 关键词：Neurodegeneration ; Neurodegenerative disease ; CHIP ; Gordon Holmes ...

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