1
0
0
News
Netzwerk-Profile
LinkedIn: Sebahattin Cirak | LinkedIn
Sebahattin Ciraks berufliches Profil anzeigen LinkedIn ist das weltweit größte berufliche Netzwerk, das Fach- und Führungskräften wie Sebahattin Cirak dabei ...
LinkedIn: Sebahattin Cirak | Berufsprofil - LinkedIn
Sehen Sie sich das Profil von Sebahattin Cirak auf LinkedIn an, dem weltweit größten beruflichen Netzwerk. Sebahattin Cirak hat 2 Jobs im Profil angegeben. Sehen Sie sich auf LinkedIn das vollständige Profil an und erfahren Sie mehr über die Kontakte von Sebahattin Cirak und über Jobs bei ähnlichen Unternehmen.
LinkedIn: Beitrag von Sebahattin Ciraklinkedin.com
› posts › sebahattin-cirak-b115b6...
Interessen
Table of contents | Journal of Neurology, Neurosurgery & Psychiatry
jnnp.bmj.com
... Volker Straub,; Mariacristina Scoto,; Sebahattin Cirak,; Véronique Humbertclaude,; Mireille Claustres,; Chiara Scotton,; Chiara Passarelli,; Hanns Lochmüller, ...
Business-Profile
Xing: Sebahattin Cirak - Senior Research Associate - Washington Childrens...
Berufserfahrung, Kontaktdaten, Portfolio und weitere Infos: Erfahren Sie mehr – oder kontaktieren Sie Sebahattin Cirak direkt bei XING.
Private Homepages
216th ENMC international workshop - Neurology
ikm.ku.dk
author = "Isabelle Richard and Jean-Pierre Laurent and Sebahattin Cirak and John Vissing and {ENMC FKRP Study Group}",. year = "2016",. month = "10",.
Ausbildung
Mutations in GDP-mannose pyrophosphorylase B cause congenital and...
kclpure.kcl.ac.uk
author = "Carss, {Keren J} and Elizabeth Stevens and Foley, {A Reghan} and Sebahattin Cirak and Moniek Riemersma and Silvia Torelli and Alexander ...
Bücher
Sebahattin Cirak | XanEdu Customization Platform
www.academicpub.com
Author: Sebahattin Cirak. Results. Co-existence of chronic renal failure, renal clear cell carcinoma, and Blau syndrome Springer Science+Business ...
Search Results
molecularcasestudies.cshlp.org
An open-access, peer-reviewed, international journal in the field of precision medicine. Articles in the journal present genomic and molecular analyses of...
Differenzialdiagnose Pädiatrie - Google Books
books.google.hr
Schnell und sicher zur richtigen Diagnose – das ist das Ziel eines jeden Pädiaters und dabei unterstützt Sie Differenzialdiagnose Pädiatrie! Über
Isolierung und Charakterisierung des Schabenallergens Per a
books.google.de
Sebahattin Cirak pages. 0 Reviewshttp://books.google.com/books/ about/Isolierung_und_Charakterisierung_des_Sch.html?id=SQi5tgAACAAJ ...
Dokumente zum Namen
Sebahattin Cirak - Academia.edu
independent.academia.edu
Academia.edu is a place to share and follow research.
Abstracts of the 52nd Workshop for Pediatric Research : Frankfurt,...
www.ikmb.uni-kiel.de
ikmb - Institut für Klinische ... Holly H Zimmerman, Joachim Weis, Emma L Baple, Andrew H Crosby, Sebahattin Cirak, C Hellmuth, O Uhl, M Standl, J ...
Late diagnosis of a truncating WISP3 mutation entails a severe...
www.scienceopen.com
Authors: Salem Alawbathani,, Amit Kawalia, Mert Karakaya,, Janine Altmüller, Peter Nürnberg, Sebahattin Cirak,. Publication date ( Print ): February
Publications from the ProNova Centre
www.biotech.kth.se
Niks, Francesca Gualandi, Fredrik Pontén, Kate. Bushby, Annemieke Aartsma-Rus, Elena. Schwartz, Yannick Le Priol, Volker. Straub, Mathias Uhlén, Sebahattin Cirak, Peter A. C 't Hoen, Francesco Muntoni, Alessandra. Ferlini, Jochen M Schwenk, Peter. Nilsson, Cristina Al-Khalili. Szigyarto (2014) Affinity proteomics within.
Wissenschaftliche Veröffentlichungen
DFG GEPRIS - Privatdozent Dr. Sebahattin Cirak
gepris.dfg.de
Privatdozent Dr. Sebahattin Cirak, Zentrum für Molekulare Medizin Köln (ZMMK)Köln
A novel SPEG mutation causes non-compaction cardiomyopathy and...
actaneurocomms.biomedcentral.com
Funding. This work was supported by the Deutsche Forschungsgemeinschaft, Germany grant (CI –1) to Dr. Sebahattin Cirak.
Cirak, Sebahattin: Molekulare Charkterisierung einer distalen...
bibliographie.ub.uni-due.de
Medizinische Fakultät » Universitätsklinikum Essen » Zentrum für Kinder- und Jugendmedizin » Klinik für Kinderheilkunde I/Perinatalzentrum
DFG - GEPRIS - Aufklärung der molekularen Pathophysiologie ...
gepris.dfg.de
Antragsteller Dr. Sebahattin Cirak Uniklinik Köln Klinik und Poliklinik für Kinder- und Jugendmedizin. Fachliche Zuordnung Humangenetik Kinder- und Jugendmedizin Förderung Förderung seit Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer Projektbeschreibung ...
Veröffentlichungen allgemein
Importance of Skin Changes in the Differential Diagnosis of...
www.hindawi.com
Didem Ardicli, Rahsan Gocmen, Beril Talim, Rosanne Sprute, Goknur Haliloglu, Sebahattin Cirak, and Haluk Topaloglu, “Congenital mirror ...
ISPD gene mutations are a common cause of BioMedSearch
www.biomedsearch.com
congenital and limb-girdle muscular dystrophies. Sebahattin Cirak,1 Aileen Reghan Foley,1 Ralf Herrmann,2 Tobias Willer,3,4,5,6 Shu Yau,7. Elizabeth Stevens,1 Silvia Torelli,1 Lina Brodd,7 Alisa Kamynina,1 Petr Vondracek,8 Helen Roper,9. Cheryl Longman,10 Rudolf Korinthenberg,11 Gianni Marrosu ...
Exercise as it relates to Disease/Exercising with muscular dystrophy...
en.wikibooks.org
Jump up ↑ Local restoration of dystrophin expression with the morpholino oligomer AVI in Duchenne muscular dystrophy: a single-blind, placebo-controlled, dose-escalation, proof-of-concept study. Maria Kinali*, Virginia Arechavala-Gomeza*, Lucy Feng, Sebahattin Cirak, David Hunt, Carl Adkin, Michela Guglieri, ...
A novel SPEG mutation causes non-compaction cardiomyopathy and...
link.springer.com
... Daimagüler; Thushiha Logeswaran; Hannah Schlierbach; Jutta Petzinger; Harald Ehrhardt; Andreas Hahn; Sebahattin Cirak Email author.
Artikel & Meinungen
Molecular medicine for Duchenne muscular dystrophy (DMD) and parent...
www.thescienceforum.com
Here are a few parent-advocacy articles on Duchenne muscular dystrophy and eteplirsen, a Morpholino antisense drug in clinical trials. Eteplirsen
An organelle-specific protein landscape identifies novel diseases and...
www.nature.com
Cellular organelles provide opportunities to relate biological mechanisms to disease. Here we use affinity proteomics, genetics and cell biology to interrogate...
Homozygous mutation in Atlastin GTPase 1 causes recessive hereditary...
www.nature.com
Short Communication
Sonstiges
Sebahattin Cirak | LinkedIn
www.linkedin.com
View Sebahattin Cirak's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Sebahattin Cirak discover ...
SELECTBIO - Next-Gen Sequencing Speaker Biography
selectbiosciences.com
Sebahattin CirakInstitute of Child Health. Sorry, There is currently no biography for this presenter. Sebahattin Cirak Image. Add to Calendar ▽ :00: :00:00 Europe/London Next-Gen Sequencing SELECTBIO . iCalendar · Google Calendar · Outlook ...
Supplemental Data. Biallelic Loss of Proprioception-Related PIEZO2....
docplayer.net
1 The American Journal of Human Genetics, Volume 99 Supplemental Data Biallelic Loss of Proprioception-Related PIEZO2 Causes Muscular Atrophy with Perinatal Respiratory Distress, Arthrogryposis, and Scoliosis Andrea Delle Vedove, Markus Storbeck, Raoul Heller, Irmgard Hölker, Malavika Hebbar, Anju Shukla, Olafur Magnusson, Sebahattin Cirak, Katta M. Girisha, Mary …
Neuromuskuläre Zentren in Nordrhein-Westfalen | Deutsche Gesellschaft...
www.dgm.org
Dr. Sebahattin Cirak in Zusammenarbeit mit OA Dr. P. -Herkenrath, PD Dr. J.-C. von Kleist-Retzow, Universitätskinderklinik Köln...
Burcu Ayoglu - Publications List
publicationslist.org
... Fredrik Pontén, Kate Bushby, Annemieke Aartsma-Rus, Elena Schwartz, Yannick Le Priol, Volker Straub, Mathias Uhlén, Sebahattin Cirak, Peter A C 't Hoen, ...
CCDC115 Deficiency Causes a Disorder of Golgi Homeostasis with...
www.infona.pl
Jos C. Jansen, Sebahattin Cirak, Monique van Scherpenzeel, Sharita Timal, Janine Reunert, Stephan Rust, Belén Pérez, Dorothée Vicogne, Peter Krawitz, ...
Chavarria-Soley, Mol Vis 2006; 12:
www.molvis.org
Primary congenital glaucoma and Rieger's anomaly: extended haplotypes reveal founder effects for eight distinct CYP1B1 mutations. Gabriela Chavarria-Soley,1 Karin Michels-Rautenstrauss,1 Francesca Pasutto,1 David Flikier,2 Paul Flikier,3Sebahattin Cirak,4 Bassem Bejjani,5 Daniel L. Winters,5 ...
Characterisation and validation of insertions and deletions in
discovery.ucl.ac.uk
UCL Discovery is UCL's open access repository, showcasing and providing access to UCL research outputs from all UCL disciplines.
Funding Portfolio | curecmd
www.curecmd.org
Cure CMD is a nonprofit organization dedicated to curing Congenital Muscular Dystrophy by advancing research and empowering families.
EPMA-World Congress 2015: Bonn, Germany September 2015
dash.harvard.edu
... Agnieszka Migasiewicz, Maria-Luiza Podbielska, Markus Pelleter, Agnieszka Giemza, Halina Podbielska A17 Personalized molecular treatment for muscular dystrophies Sebahattin Cirak A18 Secondary mutations in circulating tumour DNA for acquired drug resistance in patients with advanced ALK + NSCLC Marzia Del ...
A translational approach to dystroglycanopathies: a frequent type of...
molcellped.springeropen.com
Sebahattin Cirak,; Haicui Wang,; Raul Heredia,; Francesco Muntoni,; Yetrib Hathout,; Peter Herkenrath,; Jörg Dötsch and; Peter Nürnberg.
Abstracts of the 52nd Workshop for Pediatric Research
www.infona.pl
... Holly Hardy, Osama Refai, Katy E. S. Barwick, Holly H. Zimmerman, Joachim Weis, Emma L. Baple, Andrew H. Crosby, Sebahattin Cirak, C. Hellmuth, O. Uhl, ...
Biallelic Loss of Proprioception-Related PIEZO2 Causes Muscular...
manipal.pure.elsevier.com
Andrea Delle Vedove, Markus Storbeck, Raoul Heller, Irmgard Hölker, Malavika Hebbar, Anju Shukla, Olafur Magnusson, Sebahattin Cirak, ...
Dystromirs as Serum Biomarkers for Monitoring the Disease Severity in...
figshare.com
Dystromirs as Serum Biomarkers for Monitoring the Disease Severity in Duchenne Muscular Dystrophy
CCDC115 Deficiency Causes a Disorder of Golgi Homeostasis with...
cris.maastrichtuniversity.nl
author = "Jansen, {Jos C.} and Sebahattin Cirak and {van Scherpenzeel}, Monique and Sharita Timal and Janine Reunert and Stephan Rust and Belen Perez ...
Cirak - Patent applications
www.patentsencyclopedia.com
Sebahattin Cirak, Washington, DC US. Patent application number, Description, Published , IN VITRO GENETIC DIAGNOSTIC OF INHERITED ...
Dystromirs as Serum Biomarkers for Monitoring the Disease Severity in...
journals.plos.org
Sebahattin Cirak,. Affiliations: The Dubowitz Neuromuscular Centre, Institute of Child Health, University College London, London, United ...
ISPD gene mutations are a common cause of congenital and limb-girdle...
www.muni.cz
Original title: ISPD gene mutations are a common cause of congenital and limb -girdle muscular dystrophies. Authors: Sebahattin Cirak, Aileen Reghan Foley, ...
Verwandte Suchanfragen zu Sebahattin Cirak
| Irmgard Hölker Raoul Heller Markus Storbeck | Andrea Delle Vedove Carl Adkin Janine Reunert | Thomas Voit Lucy Feng Joachim Weis |
Personen Vorname "Sebahattin" (215) Name "Cirak" (81) |
sortiert nach Relevanz / Datum