Risultati della ricerca - Sandra Nagl
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1
Underwater vs Conventional Endoscopic Mucosal Resection of Large Sessile or Flat Colorectal Polyps: A Prospective Randomized Controlled Trial di Sandra Nagl, Alanna Ebigbo, Stefan Goelder, Christoph Roemmele, Lukas Neuhaus, Tobias Weber, Georg Braun, Andreas Probst, Elisabeth Schnoy, Agnieszka Kafel, Anna Muzalyova, Helmut Messmann
Pubblicazione 2021Artigo -
2
A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes di Marwan Shinawi, Christian P. Schaaf, Samarth Bhatt, Zhilian Xia, Ankita Patel, Sau Wai Cheung, Brendan C. Lanpher, Sandra Nagl, Heinrich Stephan Herding, Claudia Nevinny-Stickel, LaDonna Immken, Gayle Patel, Jennifer R. German, Arthur L. Beaudet, Paweł Stankiewicz
Pubblicazione 2009Artigo -
3
Influence of artificial intelligence on the diagnostic performance of endoscopists in the assessment of Barrett’s esophagus: a tandem randomized and video trial di M. Meinikheim, Robert Mendel, Christoph Palm, Andreas Probst, Anna Muzalyova, M. W. Scheppach, Sandra Nagl, Elisabeth Schnoy, Christoph Römmele, Dominik Schulz, J. Schlottmann, Friederike Prinz, David Rauber, T. Rückert, Tomoaki Matsumura, Glòria Fernández–Esparrach, Nasim Parsa, Michael F. Byrne, Helmut Messmann, Alanna Ebigbo
Pubblicazione 2024Artigo -
4
Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1 di Anne Gregor, Beate Albrecht, Ingrid Bader, Emilia K. Bijlsma, Arif B. Ekici, Hartmut Engels, Karl Hackmann, Denise Horn, Juliane Hoyer, Jakub Klapecki, Jürgen Kohlhase, Isabelle Maystadt, Sandra Nagl, Eva Christina Prott, Sigrid Tinschert, Reinhard Ullmann, Eva Wohlleber, Geoffrey Woods, André Reis, Anita Rauch, Christiane Zweier
Pubblicazione 2011Artigo -
5
Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read... di Christine Neuhaus, Tobias Eisenberger, Christian Decker, Sandra Nagl, Cornelia Blank, Markus Pfister, Ingo Kennerknecht, Cornelie Müller-Hofstede, Peter Charbel Issa, Raoul Heller, Bodo B. Beck, Klaus Rüther, Diana Mitter, Klaus Rohrschneider, Ute Steinhauer, Heike Korbmacher, Dagmar Huhle, Solaf M. Elsayed, Hesham M. Taha, Shahid Mahmood Baig, Heidi Stöhr, Markus N. Preising, Susanne Markus, Fabian Moeller, Birgit Lorenz, Kerstin Nagel‐Wolfrum, Arif O. Khan, Hanno J. Bolz
Pubblicazione 2017Artigo
Strumenti per la ricerca:
Soggetti correlati
Biology
Copy-number variation
Gene
Genetics
Genome
Medicine
Intellectual disability
Internal medicine
Mutation
Phenotype
Randomized controlled trial
Surgery
Adenocarcinoma
Adverse effect
Allele
Barrett's esophagus
Bioinformatics
Biopsy
Cancer
Chromosome
Compound heterozygosity
Confidence interval
Diagnostic accuracy
Endoscopic mucosal resection
Endoscopy
Epilepsy
Esophageal disease
Esophagus
Exon
Frameshift mutation