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Publications Archives - Face2Gene
www.face2gene.com
Alexej Knaus, Jean Tori Pantel, Manuela Pendziwiat, Nurulhuda Hajjir, Max Zhao, Tzung-Chien Hsieh, Max Schubach, Yaron Gurovich, Nicole Fleischer, Marten ...
Wie eine Genmutation die Zellkraftwerke beeinträchtigt — Institut...
www.biochemie.uni-freiburg.de
Nora Vögtle*, Björn Brändl, Austin Larson, Manuela Pendziwiat, Marisa Friederich, Susan White, Alice Basinger, Cansu Kücükköse, Hiltrud ...
Firmen-Mitarbeiter
Manuela Pendziwiat (Dipl. Biochem.) — Forschungsplattform der...
www.neurologie.uni-kiel.de
Manuela Pendziwiat (Dipl. Biochem.) wiss. Mitarbeiter. Telefon: + · . Arbeitsgruppen der ...
Private Homepages
Defining the phenotypic spectrum of SLC6A1 mutations - Neurology
ikm.ku.dk
... and Chae, {Jong Hee} and Desiree Czapansky-Beilman and Reichert, {Sara Chadwick} and Manuela Pendziwiat and Verhoeven, {Judith S.} and Schelhaas, ...
Ausbildung
De novo variants in neurodevelopmental disorders with epilepsy -...
kclpure.kcl.ac.uk
Manuela Pendziwiat, Pasquale Striano, Sha Tang & 31 others ...
Bücher
Manuela Pendziwiat author profile – Rxivist
rxivist.org
Research profile for Manuela Pendziwiat (University Medical Center, Schleswig Holstein), provided by Rxivist, the site that helps you find the most discussed ...
Dokumente zum Namen
Manuela Pendziwiat - Academia.edu
independent.academia.edu
Academia.edu is a place to share and follow research.
Heterozygous variants in KMT2E cause a spectrum of neurodevelopmental...
www.scienceopen.com
... Esther U Melchinger , Saadet Mercimek-Andrews , Caroline Nava , Manuela Pendziwiat , Richard Person , Gian Paolo Paolo Ramelli , Luiza LP Ramos , Anita ...
Wissenschaftliche Veröffentlichungen
The American Journal of Human Genetics | Vol 102, Issue 4, Pages...
www.sciencedirect.com
F.-Nora Vögtle, Björn Brändl, Austin Larson, Manuela Pendziwiat, ... Ingo Helbig. Pages : Download PDF. Article preview. select article ...
Characterization of glycosylphosphatidylinositol biosynthesis defects...
genomemedicine.biomedcentral.com
Alexej Knaus,; Jean Tori Pantel,; Manuela Pendziwiat,; Nurulhuda Hajjir,; Max Zhao,; Tzung-Chien Hsieh,; Max Schubach,; Yaron Gurovich, ...
Understanding essential tremor: Essential tremor sufferers needed for...
www.sciencedaily.com
Essential tremor affects nearly one per cent of the world’s population, increasing to four per cent of those over 40. The involuntary shaking of hands is the...
PIGT-CDG, a disorder of the glycosylphosphatidylinositol anchor:...
www.igsb.uni-bonn.de
... Line HG Larsen, Karine Lascelles, Ewa Obersztyn, Alistair Pagnamenta, Deb K Pal, Manuela Pendziwiat, Mina Ryten, Jenny Taylor, Julie Vogt, Yvonne Weber ...
Sonstiges
MANUELA PENDZIWIAT - epilepsiegenetiks Webseite!
www.epilepsiegenetik.de
MANUELA PENDZIWIAT. Position. Wissenschaftliche Mitarbeiterin. Stationen. Kiel. Interessen. Genetische Untersuchungen mittels Next Generation ...
Suchmaschine BASE (Bielefeld Academic Search Engine): Trefferliste
www.base-search.net
Ergebnis Ihrer Suche im BASE.
Altmetric – De Novo Mutations in Synaptic Transmission Genes...
www.altmetric.com
... Rikke S. Møller, Hiltrud Muhle, Deb Pal, Aarno Palotie, Manuela Pendziwiat, Angela Robbiano, Filip Roelens, Felix Rosenow, Kaja Selmer, Jose M. Serratosa, ...
Additional file 1: of Characterization of...
figshare.com
Additional file 1: of Characterization of glycosylphosphatidylinositol biosynthesis defects by clinical features, flow cytometry, and automated image analysis
Essentieller Tremor mit starkem Zittern erblich bedingt
medmix.at
Etwa jeder Hundertste leidet an andauerndem, stärker ausgeprägtem Zittern, das bestimmt das genetisch bedingte Krankheitsbild Essentieller Tremor.
Das Zittern liegt in den Genen - Medizin Aspekte
medizin-aspekte.de
... Wolfgang Lieb, Zbigniew K. Wszolek, Manuela Pendziwiat, Oswaldo Lorenzo-Betancor, Werner Poewe, Sara Ortega-Cubero, Klaus Seppi, Alex Rajput, Anna ...
DNM1 encephalopathy | Neurology
n.neurology.org
Sarah von Spiczak, Katherine L. Helbig, Deepali N. Shinde, Robert Huether, Manuela Pendziwiat, Charles Lourenço, Mark E. Nunes, Dean P.
Loss of function of the retinoid-related nuclear receptor (RORB) gene...
www.scholars.northwestern.edu
Salmi, Iben Bache, Nadine Bruneau, Manuela Pendziwiat, Joel ...
Altmetric – Defining the phenotypic spectrum ofSLC6A1mutations
www.altmetric.com
... Desiree Czapansky-Beilman, Sara Chadwick Reichert, Manuela Pendziwiat, Judith S. Verhoeven, Helenius J. Schelhaas, Orrin Devinsky, Jakob Christensen, ...
De novo mutations in synaptic transmission genes including DNM1 cause...
experts.umn.edu
... and Hiltrud Muhle and Deb Pal and Aarno Palotie and Manuela Pendziwiat and Angela Robbiano and Filip Roelens and Felix Rosenow and ...
Defining the phenotypic spectrum of SLC6A1 mutations - Research -...
pure.au.dk
... Yongjin Yoo and Murim Choi and Jong-Hee Chae and Desiree Czapansky-Beilman and Reichert, {Sara Chadwick} and Manuela Pendziwiat and Verhoeven, ...
Differential aggregation properties of alpha-synuclein isoforms - PDF...
coek.info
Pathologic aggregation of α-synuclein is a central process in the pathogenesis of Parkinson's disease. The α-synucl...
Erratum: De Novo Mutations in Synaptic Transmission Genes Including...
research.monash.edu
... Rikke S. Møller, Hiltrud Muhle, Deb Pal, Aarno Palotie, Manuela Pendziwiat, Angela Robbiano, Filip Roelens, Felix Rosenow, Kaja Selmer, ...
EPILEPSIA - New Articles (February 13, 2016)
hosted.verticalresponse.com
Felix Benninger, Zaid Afawi, Amos D. Korczyn, Karen L. Oliver, Manuela Pendziwiat, Masayuki Nakamura, Akira Sano, Ingo Helbig, Samuel F.
Esansiyel Tremora (İyi Huylu Titreme) Neden Olan Gen Bulundu | Yücel...
yucelbinici.com
... Wolfgang Lieb, Zbigniew K. Wszolek, Manuela Pendziwiat, Oswaldo Lorenzo-Betancor, Werner Poewe, Sara Ortega-Cubero, Klaus Seppi, ...
Genome-wide association study in essential tremor identifies three...
mayoclinic.pure.elsevier.com
... Schneider, Colin A. Hodgkinson, Wolfgang Lieb, Zbigniew K Wszolek, Manuela Pendziwiat, Oswaldo Lorenzo-Betancor, Werner Poewe, Sara Ortega-Cubero, ...
Genetik der Epilepsien des Kindes- und Jugendalters - PDF Free...
docplayer.org
Manuela Pendziwiat Arbeitsgruppe Pädiatrische Epilepsiegenetik, Klinik für Neuropädiatrie, UK-SH, Campus Kiel. Wenn Sie in einer anderen Klinik behandelt ...
Most recent papers with the keyword Van baalen, andreas | Read by QxMD
read.qxmd.com
F-Nora Vögtle, Björn Brändl, Austin Larson, Manuela Pendziwiat, Marisa W Friederich, Susan M White, Alice Basinger, Cansu Kücükköse, Hiltrud Muhle, ...
Mutations in PMPCB Encoding the Catalytic Subunit of the...
medworm.com
Mitochondrial disorders causing neurodegeneration in childhood are genetically heterogeneous, and the underlying genetic etiology remains unknown in many...
Wie eine Genmutation die Zellkraftwerke beeinträchtigt • DGP
www.deutschesgesundheitsportal.de
Team um Freiburger Molekularmedizinerin entdeckt neuen Krankheitsmechanismus in den Mitochondrien Dr. Nora Vögtle, Leiterin einer Emmy-Noether-Nachwuchsgruppe...
Verwandte Suchanfragen zu Manuela Pendziwiat
| Jean Tori Pantel Tori Pantel Werner Poewe | Felix Rosenow Ingo Helbig Björn Brändl | Sara Chadwick Alexej Knaus Wolfgang Lieb |
Personen Vorname "Manuela" (35206) Name "Pendziwiat" (1) |
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