Auflistung 4 Medizinische Fakultät nach Titel

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Auflistung 4 Medizinische Fakultät nach Titel

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  • Rapidly Progressive Hypertrophic Cardiomyopathy in an Infant with Noonan Syndrome with Multiple Lentigines: Palliative Treatment with a Rapamycin Analog
    Hahn, Andreas; Lauriol, Jessica; Thul, Josef; Behnke-Hall, Kachina; Logeswaran, Tushiha; Schaenzer, Anne; Boeguercue, Nuray; Garvalov, Boyan K.; Zenker, Martin; Gelb, Bruce D.; von Gerlach, Susanne; Kandolf, Reinhard; Kontaridis, Maria I.; Schranz, Dietmar (2015)
  • Raptinal bypasses BAX, BAK, and BOK for mitochondrial outer membrane permeabilization and intrinsic apoptosis
    Heimer, Sina; Knoll, Gertrud; Schulze-Osthoff, Klaus; Ehrenschwender, Martin (2019)
  • Rare actinomycetes Nocardia caishijiensis and Pseudonocardia carboxydivorans as endophytes, their bioactivity and metabolites evaluation
    Tanvir, Rabia; Sajid, Imran; Hasnain, Shahida; Kulik, Andreas; Grond, Stephanie (2016)
  • Rare and changeable as a chameleon: paraneoplastic syndromes in renal cell carcinoma
    Hegemann, M.; Kroeger, N.; Stenzl, A.; Bedke, J. (2018)
  • Rare and potentially fatal- Cytogenetically cryptic TNIP1::PDGFRB and PCM1::FGFR1 fusion leading to myeloid/lymphoid neoplasms with eosinophilia in children
    Berking, Ann-Cathrine; Flaadt, Tim; Behrens, Yvonne Lisa; Yoshimi, Ayami; Leipold, Alfred; Holzer, Ursula; Lang, Peter; Quintanilla-Martinez, Leticia; Schlegelberger, Brigitte; Reiter, Andreas; Niemeyer, Charlotte; Strahm, Brigitte; Goehring, Gudrun (2023)
  • Rare BRAF mutations in melanoma patients: implications for molecular testing in clinical practice
    Heinzerling, L.; Kuehnapfel, S.; Meckbach, D.; Baiter, M.; Kaempgen, E.; Keikavoussi, P.; Schuler, G.; Agaimy, A.; Bauer, J.; Hartmann, A.; Kiesewetter, F.; Schneider-Stock, R. (2013)
  • Rare cause of severely impaired left and right ventricular function – Case 7/2014
    Duckheim, Martin; Bigalke, Boris; Artunç, Ferruh Hâdi; Gawaz, Meinrad; Schreieck, Jürgen (2014)
  • Rare causes of early-onset dystonia-parkinsonism with cognitive impairment: a de novo PSEN-1 mutation
    Carecchio, Miryam; Picillo, Marina; Valletta, Lorella; Elia, Antonio E.; Haack, Tobias B.; Cozzolino, Autilia; Vitale, Annalisa; Garavaglia, Barbara; Iuso, Arcangela; Bagella, Caterina F.; Pappata, Sabina; Barone, Paolo; Prokisch, Holger; Romito, Luigi; Tiranti, Valeria (2017)
  • Rare coding variants in genes encoding GABA(A) receptors in genetic generalised epilepsies : an exome-based case-control study
    May, Patrick; Girard, Simon; Harrer, Merle; Bobbili, Dheeraj R.; Schubert, Julian; Wolking, Stefan; Becker, Felicitas; Lachance-Touchette, Pamela; Meloche, Caroline; Gravel, Micheline; Niturad, Cristina E.; Knaus, Julia; De Kovel, Carolien; Toliat, Mohamad; Polvi, Anne; Iacomino, Michele; Guerrero-Lopez, Rosa; Baulac, Stephanie; Marini, Carla; Thiele, Holger; Altmueller, Janine; Jabbari, Kamel; Ruppert, Ann-Kathrin; Jurkowski, Wiktor; Lal, Dennis; Rusconi, Raffaella; Cestele, Sandrine; Terragni, Benedetta; Coombs, Ian D.; Reid, Christopher A.; Striano, Pasquale; Caglayan, Hande; Siren, Auli; Everett, Kate; Moller, Rikke S.; Hjalgrim, Helle; Muhle, Hiltrud; Helbig, Ingo; Kunz, Wolfram S.; Weber, Yvonne G.; Weckhuysen, Sarah; De Jonghe, Peter; Sisodiya, Sanjay M.; Nabbout, Rima; Franceschetti, Silvana; Coppola, Antonietta; Vari, Maria S.; Trenite, Dorothee Kasteleijn-Nolst; Baykan, Betul; Ozbek, Ugur; Bebek, Nerses; Klein, Karl M.; Rosenow, Felix; Nguyen, Dang K.; Dubeau, Francois; Carmant, Lionel; Lortie, Anne; Desbiens, Richard; Clement, Jean-Francois; Cieuta-Walti, Cecile; Sills, Graeme J.; Auce, Pauls; Francis, Ben; Johnson, Michael R.; Marson, Anthony G.; Berghuis, Bianca; Sander, Josemir W.; Avbersek, Andreja; McCormack, Mark; Cavalleri, Gianpiero L.; Delanty, Norman; Depondt, Chantal; Krenn, Martin; Zimprich, Fritz; Peter, Sarah; Nikanorova, Marina; Kraaij, Robert; van Rooij, Jeroen; Balling, Rudi; Ikram, M. Arfan; Uitterlinden, Andre G.; Avanzini, Giuliano; Schorge, Stephanie; Petrou, Steven; Mantegazza, Massimo; Sander, Thomas; LeGuern, Eric; Serratosa, Jose M.; Koeleman, Bobby P. C.; Palotie, Aarno; Lehesjoki, Anna-Elina; Nothnagel, Michael; Nuernberg, Peter; Maljevic, Snezana; Zara, Federico; Cossette, Patrick; Krause, Roland; Lerche, Holger (2018)
  • Rare disease education in Europe and beyond: time to act
    Tumiene, Birute; Peters, Harm; Melegh, Bela; Peterlin, Borut; Utkus, Algirdas; Fatkulina, Natalja; Pfliegler, Gyoergy; Graessner, Holm; Hermanns, Sanja; Scarpa, Maurizio; Blay, Jean-Yves; Ashton, Sharon; McKay, Lucy; Baynam, Gareth (2022)
  • Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy
    Paul, Maimuna S.; Duncan, Anna R.; Genetti, Casie A.; Pan, Hongling; Jackson, Adam; Grant, Patricia E.; Shi, Jiahai; Pinelli, Michele; Brunetti-Pierri, Nicola; Garza-Flores, Alexandra; Shahani, Dave; Saneto, Russell P.; Zampino, Giuseppe; Leoni, Chiara; Agolini, Emanuele; Novelli, Antonio; Bluemlein, Ulrike; Haack, Tobias B.; Heinritz, Wolfram; Matzker, Eva; Alhaddad, Bader; Abou Jamra, Rami; Bartolomaeus, Tobias; AlHamdan, Saber; Carapito, Raphael; Isidor, Bertrand; Bahram, Seiamak; Ritter, Alyssa; Izumi, Kosuke; Shakked, Ben Pode; Barel, Ortal; Ben Zeev, Bruria; Begtrup, Amber; Carere, Deanna Alexis; Mullegama, Sureni, V; Palculict, Timothy Blake; Calame, Daniel G.; Schwan, Katharina; Aycinena, Alicia R. P.; Traberg, Rasa; Douzgou, Sofia; Pirt, Harrison; Ismayilova, Naila; Banka, Siddharth; Chao, Hsiao-Tuan; Agrawal, Pankaj B. (2023)
  • Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy
    Lal, Dennis; Trucks, Holger; Moller, Rikke S.; Hjalgrim, Helle; Koeleman, Bobby P. C.; de Kovel, Carolien G. F.; Visscher, Frank; Weber, Yvonne G.; Lerche, Holger; Becker, Felicitas; Schankin, Christoph J.; Neubauer, Bernd A.; Surges, Rainer; Kunz, Wolfram S.; Zimprich, Fritz; Franke, Andre; Illig, Thomas; Ried, Janina S.; Leu, Costin; Nuernberg, Peter; Sander, Thomas (2013)
  • Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features
    Niturad, Cristina Elena; Lev, Dorit; Kalscheuer, Vera M.; Charzewska, Agnieszka; Schubert, Julian; Lerman-Sagie, Tally; Kroes, Hester Y.; Oegema, Renske; Traverso, Monica; Specchio, Nicola; Lassota, Maria; Chelly, Jamel; Bennett-Back, Odeya; Carmi, Nirit; Koffler-Brill, Tal; Iacomino, Michele; Trivisano, Marina; Capovilla, Giuseppe; Striano, Pasquale; Nawara, Magdalena; Rzonca, Sylwia; Fischer, Ute; Bienek, Melanie; Jensen, Corinna; Hu, Hao; Thiele, Holger; Altmuller, Janine; Krause, Roland; May, Patrick; Becker, Felicitas; Balling, Rudi; Biskup, Saskia; Haas, Stefan A.; Nuernberg, Peter; van Gassen, Koen L. I.; Lerche, Holger; Zara, Federico; Maljevic, Snezana; Leshinsky-Silver, Esther (2017)
  • Rare gene deletions in genetic generalized and Rolandic epilepsies
    Jabbari, Kamel; Bobbili, Dheeraj R.; Lal, Dennis; Reinthaler, Eva M.; Schubert, Julian; Wolking, Stefan; Sinha, Vishal; Motameny, Susanne; Thiele, Holger; Kawalia, Amit; Altmueller, Janine; Toliat, Mohammad Reza; Kraaij, Robert; van Rooij, Jeroen; Uitterlinden, Andre G.; Ikram, M. Arfan; Zara, Federico; Lehesjoki, Anna-Elina; Krause, Roland; Zimprich, Fritz; Sander, Thomas; Neubauer, Bernd A.; May, Patrick; Lerche, Holger; Nuernberg, Peter (2018)
  • Rare genetic variant burden in DPYD predicts severe fluoropyrimidine-related toxicity risk
    De Mattia, Elena; Silvestri, Marco; Polesel, Jerry; Ecca, Fabrizio; Mezzalira, Silvia; Scarabel, Lucia; Zhou, Yitian; Roncato, Rossana; Lauschke, Volker M.; Calza, Stefano; Spina, Michele; Puglisi, Fabio; Toffoli, Giuseppe; Cecchin, Erika (2022)
  • Rare genital malformations in women's health research: sociodemographic, regional, and disease-related characteristics of patients with Mayer-Rokitansky-Kuster-Hauser syndrome
    Brucker, Sara Yvonne; Poesch, Leonie-Sophia; Graf, Joachim; Sokolov, Alexander N.; Schaeffeler, Norbert; Kronenthaler, Andrea; Hiltner, Hanna; Wagner, Anke; Ueding, Esther; Rieger, Monika A.; Schoeller, Dorit; Stefanescu, Diana; Rall, Kristin Katharina; Wallwiener, Diethelm; Simoes, Elisabeth (2020)
  • Rare germline copy number variants (CNVs) and breast cancer risk
    Dennis, Joe; Tyrer, Jonathan P.; Walker, Logan C.; Michailidou, Kyriaki; Dorling, Leila; Bolla, Manjeet K.; Wang, Qin; Ahearn, Thomas U.; Andrulis, Irene L.; Anton-Culver, Hoda; Antonenkova, Natalia N.; Arndt, Volker; Aronson, Kristan J.; Freeman, Laura E. Beane; Beckmann, Matthias W.; Behrens, Sabine; Benitez, Javier; Bermisheva, Marina; Bogdanova, Natalia, V; Bojesen, Stig E.; Brenner, Hermann; Castelao, Jose E.; Chang-Claude, Jenny; Chenevix-Trench, Georgia; Clarke, Christine L.; Collee, J. Margriet; Couch, Fergus J.; Cox, Angela; Cross, Simon S.; Czene, Kamila; Devilee, Peter; Dork, Thilo; Dossus, Laure; Eliassen, A. Heather; Eriksson, Mikael; Evans, D. Gareth; Fasching, Peter A.; Figueroa, Jonine; Fletcher, Olivia; Flyger, Henrik; Fritschi, Lin; Gabrielson, Marike; Gago-Dominguez, Manuela; Garcia-Closas, Montserrat; Giles, Graham G.; Gonzalez-Neira, Anna; Guenel, Pascal; Hahnen, Eric; Haiman, Christopher A.; Hall, Per; Hollestelle, Antoinette; Hoppe, Reiner; Hopper, John L.; Howell, Anthony; Jager, Agnes; Jakubowska, Anna; John, Esther M.; Johnson, Nichola; Jones, Michael E.; Jung, Audrey; Kaaks, Rudolf; Keeman, Renske; Khusnutdinova, Elza; Kitahara, Cari M.; Ko, Yon-Dschun; Kosma, Veli-Matti; Koutros, Stella; Kraft, Peter; Kristensen, Vessela N.; Kubelka-Sabit, Katerina; Kurian, Allison W.; Lacey, James, V; Lambrechts, Diether; Larson, Nicole L.; Linet, Martha; Ogrodniczak, Alicja; Mannermaa, Arto; Manoukian, Siranoush; Margolin, Sara; Mavroudis, Dimitrios; Milne, Roger L.; Muranen, Taru A.; Murphy, Rachel A.; Nevanlinna, Heli; Olson, Janet E.; Olsson, Hakan; Park-Simon, Tjoung-Won; Perou, Charles M.; Peterlongo, Paolo; Plaseska-Karanfilska, Dijana; Pylkas, Katri; Rennert, Gad; Saloustros, Emmanouil; Sandler, Dale P.; Sawyer, Elinor J.; Schmidt, Marjanka K.; Schmutzler, Rita K.; Shibli, Rana; Smeets, Ann; Soucy, Penny; Southey, Melissa C. (2022)
  • Rare hereditary diseases with defects in DNA-repair
    Knoch, Jennifer; Kamenisch, York; Kubisch, Christian; Berneburg, Mark (2012)
  • Rare mature B-cell lymphomas in children and adolescents
    Woessmann, Wilhelm; Quintanilla-Martinez, Leticia (2019)
  • Rare pediatric tumors in Germany - not as rare as expected: a study based on data from the Bavarian Cancer Registry and the German Childhood Cancer Registry
    Achajew, Aisana; Brecht, Ines B.; Radespiel-Troeger, Martin; Meyer, Martin; Metzler, Markus; Bremensdorfer, Claudia; Spix, Claudia; Erdmann, Friederike; Schneider, Dominik T.; Abele, Michael (2022)