Auflistung Universitätsbibliographie nach Autor "Bauer, Peter"

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Auflistung Universitätsbibliographie nach Autor "Bauer, Peter"

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  • Personalized peptide vaccine-induced immune response associated with long-term survival of a metastatic cholangiocarcinoma patient
    Loeffler, Markus W.; Chandran, P. Anoop; Laske, Karoline; Schroeder, Christopher; Bonzheim, Irina; Walzer, Mathias; Hilke, Franz J.; Trautwein, Nico; Kowalewski, Daniel J.; Schuster, Heiko; Guender, Marc; Yanez, Viviana A. Carcamo; Mohr, Christopher; Sturm, Marc; Huu-Phuc Nguyen; Riess, Olaf; Bauer, Peter; Nahnsen, Sven; Nadalin, Silvio; Zieker, Derek; Glatzle, Joerg; Thiel, Karolin; Schneiderhan-Marra, Nicole; Clasen, Stephan; Boesmueller, Hans; Fend, Falko; Kohlbacher, Oliver; Gouttefangeas, Cecile; Stevanovic, Stefan; Koenigsrainer, Alfred; Rammensee, Hans-Georg (2016)
  • Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts
    Synofzik, Matthis; Schuele, Rebecca; Schulze, Martin; Gburek-Augustat, Janina; Schweizer, Roland; Schirmacher, Anja; Kraegeloh-Mann, Ingeborg; Gonzalez, Michael; Young, Peter; Zuechner, Stephan; Schoels, Ludger; Bauer, Peter (2014)
  • PIK3R1 mutations in SHORT syndrome
    Schroeder, C.; Riess, A.; Bonin, M.; Bauer, P.; Riess, O.; Doebler-Neumann, M.; Wieser, S.; Moog, U.; Tzschach, A. (2014)
  • Prediction of Survival With Long-Term Disease Progression in Most Common Spinocerebellar Ataxia
    Diallo, Alhassane; Jacobi, Heike; Cook, Arron; Giunti, Paola; Parkinson, Michael H.; Labrum, Robyn; Durr, Alexandra; Brice, Alexis; Charles, Perrine; Marelli, Cecilia; Mariotti, Caterina; Nanetti, Lorenzo; Panzeri, Marta; Castaldo, Anna; Rakowicz, Maria; Rola, Rafal; Sulek, Anna; Schmitz-Huebsch, Tanja; Schoels, Ludger; Hengel, Holger; Baliko, Laszlo; Melegh, Bela; Filla, Alessandro; Antenora, Antonella; Infante, Jon; Berciano, Jose; van de Warrenburg, Bart P.; Timmann, Dagmar; Boesch, Sylvia; Nachbauer, Wolfgang; Pandolfo, Massimo; Schulz, Joerg B.; Bauer, Peter; Jun-Suk, Kang; Klockgether, Thomas; du Montcel, Sophie Tezenas (2019)
  • Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6
    du Montcel, Sophie Tezenas; Durr, Alexandra; Rakowicz, Maria; Nanetti, Lorenzo; Charles, Perrine; Sulek, Anna; Mariotti, Caterina; Rola, Rafal; Schols, Ludger; Bauer, Peter; Dufaure-Gare, Isabelle; Jacobi, Heike; Forlani, Sylvie; Schmitz-Huebsch, Tanja; Filla, Alessandro; Timmann, Dagmar; van de Warrenburg, Bart P.; Marelli, Cecila; Kang, Jun-Suk; Giunti, Paola; Cook, Arron; Baliko, Laszlo; Bela, Melegh; Boesch, Sylvia; Szymanski, Sandra; Berciano, Jose; Infante, Jon; Buerk, Katrin; Masciullo, Marcella; Di Fabio, Roberto; Depondt, Chantal; Ratka, Susanne; Stevanin, Giovanni; Klockgether, Thomas; Brice, Alexis; Golmard, Jean-Louis (2014)
  • PRRT2 Mutations Are the Major Cause of Benign Familial Infantile Seizures
    Schubert, Julian; Paravidino, Roberta; Becker, Felicitas; Berger, Andrea; Bebek, Nerses; Bianchi, Amedeo; Brockmann, Knut; Capovilla, Giuseppe; Bernardina, Bernardo Dalla; Fukuyama, Yukio; Hoffmann, Georg F.; Jurkat-Rott, Karin; Anttonen, Anna-Kaisa; Kurlemann, Gerhard; Lehesjoki, Anna-Elina; Lehmann-Horn, Frank; Mastrangelo, Massimo; Mause, Ulrike; Mueller, Stephan; Neubauer, Bernd; Puest, Burkhard; Rating, Dietz; Robbiano, Angela; Ruf, Susanne; Schroeder, Christopher; Seidel, Andreas; Specchio, Nicola; Stephani, Ulrich; Striano, Pasquale; Teichler, Jens; Turkdogan, Dilsad; Vigevano, Federico; Viri, Maurizio; Bauer, Peter; Zara, Federico; Lerche, Holger; Weber, Yvonne G. (2012)
  • Recommendations for patient screening in ultra-rare inherited metabolic diseases : what have we learned from Niemann-Pick disease type C?
    Sobrido, Maria-Jesus; Bauer, Peter; de Koning, Tom; Klopstock, Thomas; Nadjar, Yann; Patterson, Marc C.; Synofzik, Matthis; Hendriksz, Chris J. (2019)
  • Screening of Mutations in GNAL in Sporadic Dystonia Patients
    Dufke, Claudia; Sturm, Marc; Schroeder, Christopher; Moll, Susanne; Ott, Thomas; Riess, Olaf; Bauer, Peter; Grundmann, Kathrin (2014)
  • SeqPurge: highly-sensitive adapter trimming for paired-end NGS data
    Sturm, Marc; Schroeder, Christopher; Bauer, Peter (2016)
  • SIL1 mutations and clinical spectrum in patients with Marinesco-Sjogren syndrome
    Krieger, Michael; Roos, Andreas; Stendel, Claudia; Claeys, Kristl G.; Sonmez, Fatma Mujgan; Baudis, Michael; Bauer, Peter; Bornemann, Antje; de Goede, Christian; Dufke, Andreas; Finkel, Richard S.; Goebel, Hans H.; Haeussler, Martin; Kingston, Helen; Kirschner, Janbernd; Medne, Livija; Muschke, Petra; Rivier, Francois; Rudnik-Schoeneborn, Sabine; Spengler, Sabrina; Inzana, Francesca; Stanzial, Franco; Benedicenti, Francesco; Synofzik, Matthis; Lia Taratuto, Ana; Pirra, Laura; Tay, Stacey Kiat-Hong; Topaloglu, Haluk; Uyanik, Goekhan; Wand, Dorothea; Williams, Denise; Zerres, Klaus; Weis, Joachim; Senderek, Jan (2013)
  • Spinocerebellar ataxia type 14: refining clinicogenetic diagnosis in a rare adult-onset disorder
    Schmitz-Huebsch, Tanja; Lux, Silke; Bauer, Peter; Brandt, Alexander U.; Schlapakow, Elena; Greschus, Susanne; Scheel, Michael; Gaertner, Hanna; Kirlangic, Mehmet E.; Gras, Vincent; Timmann, Dagmar; Synofzik, Matthis; Giorgetti, Alejandro; Carloni, Paolo; Shah, Jon N.; Schoels, Ludger; Kopp, Ute; Bussenius, Lisa; Oberwahrenbrock, Timm; Zimmermann, Hanna; Pfueller, Caspar; Kadas, Ella-Maria; Roennefarth, Maria; Grosch, Anne-Sophie; Endres, Matthias; Amunts, Katrin; Paul, Friedemann; Doss, Sarah; Minnerop, Martina (2021)
  • Spinocerebellar Ataxia Types 1, 2, 3 and 6: the Clinical Spectrum of Ataxia and Morphometric Brainstem and Cerebellar Findings
    Jacobi, Heike; Hauser, Till-Karsten; Giunti, Paola; Globas, Christoph; Bauer, Peter; Schmitz-Huebsch, Tanja; Baliko, Laszlo; Filla, Alessandro; Mariotti, Caterina; Rakowicz, Maria; Charles, Perine; Ribai, Pascale; Szymanski, Sandra; Infante, Jon; van de Warrenburg, Bart P. C.; Duerr, Alexandra; Timmann, Dagmar; Boesch, Sylvia; Fancellu, Roberto; Rola, Rafal; Depondt, Chantal; Schoels, Ludger; Zdzienicka, Elzbieta; Kang, Jun-Suk; Ratzka, Susanne; Kremer, Berry; Stephenson, Dennis A.; Melegh, Bela; Pandolfo, Massimo; du Montcel, Sophie Tezenas; Borkert, Johannes; Schulz, Joerg B.; Klockgether, Thomas (2012)
  • Survival in patients with spinocerebellar ataxia types 1, 2, 3, and 6 (EUROSCA): a longitudinal cohort study
    Diallo, Alhassane; Jacobi, Heike; Cook, Arron; Labrum, Robyn; Durr, Alexandra; Brice, Alexis; Charles, Perrine; Marelli, Cecilia; Mariotti, Caterina; Nanetti, Lorenzo; Panzeri, Marta; Rakowicz, Maria; Sobanska, Anna; Sulek, Anna; Schmitz-Huebsch, Tanja; Hengel, Holger; Melegh, Bela; Filla, Alessandro; Antenora, Antonella; Infante, Jon; Berciano, Jose; van de Warrenburg, Bart P.; Timmann, Dagmar; Boesch, Sylvia; Pandolfo, Massimo; Schulz, Jorg B.; Bauer, Peter; Giunti, Paola; Kang, Jun-Suk; Klockgether, Thomas; du Montcel, Sophie Tezenas; Schöls, Ludger (2018)
  • SYNE1 ataxia is a common recessive ataxia with major non-cerebellar features: a large multi-centre study
    Synofzik, Matthis; Smets, Katrien; Mallaret, Martial; Di Bella, Daniela; Gallenmueller, Constanze; Baets, Jonathan; Schulze, Martin; Magri, Stefania; Sarto, Elisa; Mustafa, Mona; Deconinck, Tine; Haack, Tobias; Zuechner, Stephan; Gonzalez, Michael; Timmann, Dagmar; Stendel, Claudia; Klopstock, Thomas; Durr, Alexandra; Tranchant, Christine; Sturm, Marc; Hamza, Wahiba; Nanetti, Lorenzo; Mariotti, Caterina; Koenig, Michel; Schoels, Ludger; Schuele, Rebecca; de Jonghe, Peter; Anheim, Mathieu; Taroni, Franco; Bauer, Peter (2016)
  • Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathies
    Waldmueller, Stephan; Schroeder, Christopher; Sturm, Marc; Scheffold, Thomas; Imbrich, Kerstin; Junker, Sandra; Frische, Christian; Hofbeck, Michael; Bauer, Peter; Bonin, Michael; Gawaz, Meinrad; Gramlich, Michael (2015)
  • The hidden Niemann-Pick type C patient: clinical niches for a rare inherited metabolic disease
    Hendriksz, Christian J.; Anheim, Mathieu; Bauer, Peter; Bonnot, Olivier; Chakrapani, Anupam; Corvol, Jean-Christophe; de Koning, Tom J.; Degtyareva, Anna; Dionisi-Vici, Carlo; Doss, Sarah; Duning, Thomas; Giunti, Paola; Iodice, Rosa; Johnston, Tracy; Kelly, Dierdre; Kluenemann, Hans-Hermann; Lorenzl, Stefan; Padovani, Alessandro; Pocovi, Miguel; Synofzik, Matthis; Terblanche, Alta; Bergh, Florian Then; Topcu, Meral; Tranchant, Christine; Walterfang, Mark; Velten, Christian; Kolb, Stefan A. (2017)
  • The modulation of Amyotrophic Lateral Sclerosis risk by Ataxin-2 intermediate polyglutamine expansions is a specific effect
    Gispert, Suzana; Kurz, Alexander; Waibel, Stefan; Bauer, Peter; Liepelt, Inga; Geisen, Christof; Gitler, Aaron D.; Becker, Tim; Weber, Markus; Berg, Daniela; Andersen, Peter M.; Krueger, Rejko; Riess, Olaf; Ludolph, Albert C.; Auburger, Georg (2012)
  • The Reciprocal Cerebellar Circuitry in Human Hereditary Ataxia
    Koeppen, Arnulf H.; Ramirez, R. Liane; Bjork, Sarah T.; Bauer, Peter; Feustel, Paul J. (2013)
  • The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation
    Mallaret, Martial; Synofzik, Matthis; Lee, Jaeho; Sagum, Cari A.; Mahajnah, Muhammad; Sharkia, Rajech; Drouot, Nathalie; Renaud, Mathilde; Klein, Fabrice A. C.; Anheim, Mathieu; Tranchant, Christine; Mignot, Cyril; Mandel, Jean-Louis; Bedford, Mark; Bauer, Peter; Salih, Mustafa A.; Schuele, Rebecca; Schoels, Ludger; Aldaz, C. Marcelo; Koenig, Michel (2014)
  • Understanding the role of genetic variability in LRRK2 in Indian population
    Kishore, Asha; Sreelatha, Ashwin Ashok Kumar; Sturm, Marc; von-Zweydorf, Felix; Pihlstrom, Lasse; Raimondi, Francesco; Russell, Rob; Lichtner, Peter; Banerjee, Moinak; Krishnan, Syam; Rajan, Roopa; Puthenveedu, Divya Kalikavil; Chung, Sun Ju; Bauer, Peter; Riess, Olaf; Gloeckner, Christian Johannes; Kruger, Rejko; Gasser, Thomas; Sharma, Manu (2019)