Auflistung 4 Medizinische Fakultät nach Titel

DSpace Repositorium (Manakin basiert)

Auflistung 4 Medizinische Fakultät nach Titel

Sortiert nach: Sortierung: Ergebnisse:

  • Genomic surveillance of SARS-CoV-2 in the Republic of Congo
    Ntoumi, Francine; Mapanguy, Claujens Chastel Mfoutou; Tomazatos, Alexandru; Pallerla, Srinivas Reddy; Le Thi Kieu Linh; Casadei, Nicolas; Angelov, Angel; Sonnabend, Michael; Peter, Silke; Kremsner, Peter G.; Velavan, Thirumalaisamy P. (2021)
  • Genomics of ADME gene expression: mapping expression quantitative trait loci relevant for absorption, distribution, metabolism and excretion of drugs in human liver
    Schroeder, A.; Klein, K.; Winter, S.; Schwab, M.; Bonin, M.; Zell, A.; Zanger, U. M. (2013)
  • Genomics, epigenomics and pharmacogenomics of familial hypercholesterolemia (FHBGEP): A study protocol
    Borges, Jessica Bassani; de Oliveira, Victor Fernandes; Ferreira, Glaucio Monteiro; Los, Bruna; Almendros Afonso Barbosa, Thais Kristini; Rodrigues Marcal, Elisangela da Silva; Dagli-Hernandez, Carolina; Costa de Freitas, Renata Caroline; Bortolin, Raul Hernandes; Mori, Augusto Akira; Crespo Hirata, Thiago Dominguez; Imoto Nakaya, Helder Takashi; Bastos, Gisele Medeiros; Thurow, Helena Strelow; Goncalves, Rodrigo Marques; de Araujo, Daniel Branco; Zatz, Henry Paulo; Bertolami, Adriana; Faludi, Andre Arpad; Bertolami, Marcelo Chiara; de Moraes Rego Sousa, Amanda Guerra; Franca, Joao Italo Dias; Jannes, Cinthia Elim; Pereira, Alexandre da Costa; Nakazone, Marcelo Arruda; Silva Souza, Doroteia Rossi; Carmo, Tayanne Silva; Sampaio, Marcelo Ferraz; Gorjao, Renata; Pithon-Curi, Tania Cristina; Moriel, Patricia; Silbiger, Vivian Nogueira; Luchessi, Andre Ducati; Goes de Araujo, Jessica Nayara; Naslavsky, Michel Satya; Wang, Jaqueline Yu Ting; Kronenberger, Thales; Cerda, Alvaro; Lin-Wang, Hui Tzu; Garofalo, Adriana Regina; Fajardo, Cristina Moreno; Crespo Hirata, Rosario Dominguez; Hirata, Mario Hiroyuki (2021)
  • Genotyp-Phänotyp-Korrelation bei Schwerhörigkeit: Genetische Varianten im peripheren Hörsystem und die Hörleistung mit Cochlea-Implantat
    Dofek, Saskia Jasmin (2019)
  • Genotyp-Phänotyp-Korrelationen bei Kindern und Jugendlichen mit nichtklassischem adrenogenitalen Syndrom mit 21-Hydroxylase-Defekt
    Doerr, H. G.; Schulze, N.; Bettendorf, M.; Binder, G.; Bonfig, W.; Denzer, C.; Dunstheimer, D.; Salzgeber, K.; Schmidt, H.; Schwab, K. O.; Voss, E.; Wabitsch, M.; Woelfle, J. (2020)
  • Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation
    Kouz, Karim; Lissewski, Christina; Spranger, Stephanie; Mitter, Diana; Riess, Angelika; Lopez-Gonzalez, Vanesa; Luettgen, Sabine; Aydin, Hatip; von Deimling, Florian; Evers, Christina; Hahn, Andreas; Hempel, Maja; Issa, Ulrike; Kahlert, Anne-Karin; Lieb, Adrian; Villavicencio-Lorini, Pablo; Juliana Ballesta-Martinez, Maria; Nampoothiri, Sheela; Ovens-Raeder, Angela; Puchmajerova, Alena; Satanovskij, Robin; Seidel, Heide; Unkelbach, Stephan; Zabel, Bernhard; Kutsche, Kerstin; Zenker, Martin (2016)
  • Genotype correlates with the natural history of severe bile salt export pump deficiency
    van Wessel, Daan B. E.; Thompson, Richard J.; Gonzales, Emmanuel; Jankowska, Irena; Sokal, Etienne; Grammatikopoulos, Tassos; Kadaristiana, Agustina; Jacquemin, Emmanuel; Spraul, Anne; Lipinski, Patryk; Czubkowski, Piotr; Rock, Nathalie; Shagrani, Mohammad; Broering, Dieter; Algoufi, Talal; Mazhar, Nejat; Nicastro, Emanuele; Kelly, Deirdre A.; Nebbia, Gabriella; Arnell, Henrik; Fischler, Bjoern; Hulscher, Jan B. F.; Serranti, Daniele; Arikan, Cigdem; Polat, Esra; Debray, Dominique; Lacaille, Florence; Goncalves, Cristina; Hierro, Loreto; Bartolo, Gema Munoz; Mozer-Glassberg, Yael; Azaz, Amer; Brecelj, Jernej; Dezsofi, Antal; Calvo, Pier Luigi; Grabhorn, Enke; Sturm, Ekkehard; van der Woerd, Wendy J.; Kamath, Binita M.; Wang, Jian-She; Li, Liting; Durmaz, Oezlem; Onal, Zerrin; Bunt, Ton M. G.; Hansen, Bettina E.; Verkade, Henkjan J. (2020)
  • Genotype-Phenotype Association and Impact on Outcomes following Guided De-Escalation of Anti-Platelet Treatment in Acute Coronary Syndrome Patients : The TROPICAL-ACS Genotyping Substudy
    Gross, Lisa; Trenk, Dietmar; Jacobshagen, Claudius; Krieg, Anne; Gawaz, Meinrad; Massberg, Steffen; Baylacher, Monika; Aradi, Daniel; Stimpfle, Fabian; Hromek, Julia; Vogelgesang, Anja; Hadamitzky, Martin; Sibbing, Dirk; Geisler, Tobias (2018)
  • Genotype-phenotype correlations in RHOBTB2- associated neurodevelopmental disorders
    Langhammer, Franziska; Maroofian, Reza; Badar, Rueda; Gregor, Anne; Rochman, Michelle; Ratliff, Jeffrey B.; Koopmans, Marije; Herget, Theresia; Hempel, Maja; Kortuem, Fanny; Heron, Delphine; Mignot, Cyril; Keren, Boris; Brooks, Susan; Botti, Christina; Ben-Zeev, Bruria; Argilli, Emanuela; Sherr, Elliot H.; Gowda, Vykuntaraju K.; Srinivasan, Varunvenkat M.; Bakhtiari, Somayeh; Kruer, Michael C.; Salih, Mustafa A.; Kuechler, Alma; Muller, Eric A.; Blocker, Karli; Kuismin, Outi; Park, Kristen L.; Kochhar, Aaina; Brown, Kathleen; Ramanathan, Subhadra; Clark, Robin D.; Elgizouli, Magdeldin; Melikishvili, Gia; Tabatadze, Nazhi; Stark, Zornitza; Mirzaa, Ghayda M.; Ong, Jinfon; Grasshoff, Ute; Bevot, Andrea; von Wintzingerode, Lydia; Jamra, Rami A.; Hennig, Yvonne; Goldenberg, Paula; Al Alam, Chadi; Charif, Majida; Boulouiz, Redouane; Bellaoui, Mohammed; Amrani, Rim; Al Mutairi, Fuad; Tamim, Abdullah M.; Abdulwahab, Firdous; Alkuraya, Fowzan S.; Khouj, Ebtissal M.; Alvi, Javeria R.; Sultan, Tipu; Hashemi, Narges; Karimiani, Ehsan G.; Ashrafzadeh, Farah; Imannezhad, Shima; Efthymiou, Stephanie; Houlden, Henry; Sticht, Heinrich; Zweier, Christiane (2023)
  • Genotype-phenotype correlations in syndromic forms of hereditary retinal diseases
    Nasser, Fadi (2021)
  • Genotype-Phenotype correlations of SCARB2 associated clinical presentation: a case report and in-depth literature review
    Atasu, Burcu; Acarli, Ayse Nur Ozdag; Bilgic, Basar; Baykan, Betul; Demir, Erol; Ozluk, Yasemin; Turkmen, Aydin; Hauser, Ann-Kathrin; Guven, Gamze; Hanagasi, Hasmet; Gurvit, Hakan; Emre, Murat; Gasser, Thomas; Lohmann, Ebba (2022)
  • Genotype-Phenotype Correlations, Dystonia and Disease Progression in Spinocerebellar Ataxia Type 14
    Chelban, Viorica; Wiethoff, Sarah; Fabian-Jessing, Bjorn K.; Haridy, Nourelhoda A.; Khan, Alaa; Efthymiou, Stephanie; Becker, Esther B. E.; O'Connor, Emer; Hersheson, Joshua; Newland, Katrina; Hojland, Allan Thomas; Gregersen, Pernille A.; Lindquist, Suzanne G.; Petersen, Michael B.; Nielsen, Jorgen E.; Nielsen, Michael; Wood, Nicholas W.; Giunti, Paola; Houlden, Henry (2018)
  • Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6
    Reetz, Kathrin; Costa, Ana S.; Mirzazade, Shahram; Lehmann, Anna; Juzek, Agnes; Rakowicz, Maria; Boguslawska, Romana; Schoels, Ludger; Linnemann, Christoph; Mariotti, Caterina; Grisoli, Marina; Duerr, Alexandra; van de Warrenburg, Bart P.; Timmann, Dagmar; Pandolfo, Massimo; Bauer, Peter; Jacobi, Heike; Hauser, Till-Karsten; Klockgether, Thomas; Schulz, Joerg B. (2013)
  • Genotypic and Phenotypic Spectrum of Foveal Hypoplasia A Multicenter Study
    Kuht, Helen J.; Maconachie, Gail D. E.; Han, Jinu; Kessel, Line; van Genderen, Maria M.; McLean, Rebecca J.; Hisaund, Michael; Tu, Zhanhan; Hertle, Richard W.; Gronskov, Karen; Bai, Dayong; Wei, Aihua; Li, Wei; Jiao, Yonghong; Smirnov, Vasily; Choi, Jae-Hwan; Tobin, Martin D.; Sheth, Viral; Purohit, Ravi; Dawar, Basu; Girach, Ayesha; Strul, Sasha; May, Laura; Chen, Fred K.; Jeffery, Rachael C. Heath; Aamir, Abdullah; Sano, Ronaldo; Jin, Jing; Brooks, Brian P.; Kohl, Susanne; Arveiler, Benoit; Montoliu, Lluis; Engle, Elizabeth C.; Proudlock, Frank A.; Nishad, Garima; Pani, Prateek; Varma, Girish; Gottlob, Irene; Thomas, Mervyn G. (2022)
  • Genotypic diversity and phenotypic spectrum of infantile liver failure syndrome type 1 due to variants inLARS1
    Lenz, Dominic; Smith, Desiree E. C.; Crushell, Ellen; Husain, Ralf A.; Salomons, Gajja S.; Alhaddad, Bader; Bernstein, Jonathan A.; Bianzano, Alyssa; Biskup, Saskia; Brennenstuhl, Heiko; Caldari, Dominique; Dikow, Nicola; Haack, Tobias B.; Hanson-Kahn, Andrea; Harting, Inga; Horn, Denise; Hughes, Joanne; Huijberts, Maya; Isidor, Bertrand; Kathemann, Simone; Kopajtich, Robert; Kotzaeridou, Urania; Kuery, Sebastien; Lainka, Elke; Laugwitz, Lucia; Lupski, James R.; Posey, Jennifer E.; Reynolds, Claire; Rosenfeld, Jill A.; Schroeter, Julian; Vansenne, Fleur; Wagner, Matias; Weiss, Claudia; Wolffenbuttel, Bruce H. R.; Wortmann, Saskia B.; Koelker, Stefan; Hoffmann, Georg F.; Prokisch, Holger; Mendes, Marisa, I; Staufner, Christian (2020)
  • Genotyping circulating tumor DNA of pediatric Hodgkin lymphoma
    Desch, Ann-Kathrin; Hartung, Kristin; Botzen, Ante; Brobeil, Alexander; Rummel, Mathias; Kurch, Lars; Georgi, Thomas; Jox, Theresa; Bielack, Stefan; Burdach, Stefan; Classen, Carl Friedrich; Claviez, Alexander; Debatin, Klaus-Michael; Ebinger, Martin; Eggert, Angelika; Faber, Joerg; Flotho, Christian; Fruehwald, Michael; Graf, Norbert; Jorch, Norbert; Kontny, Udo; Kramm, Christof; Kulozik, Andreas; Kuehr, Joachim; Sykora, Karl-Walter; Metzler, Markus; Mueller, Hermann L.; Nathrath, Michaela; Nuesslein, Thomas; Paulussen, Michael; Pekrun, Arnulf; Reinhardt, Dirk; Reinhard, Harald; Roessig, Claudia; Sauerbrey, Axel; Schlegel, Paul-Gerhardt; Schneider, Dominik T.; Scheurlen, Wolfram; Schweigerer, Lothar; Simon, Thorsten; Suttorp, Meinolf; Vorwerk, Peter; Schmitz, Roland; Kluge, Regine; Mauz-Koerholz, Christine; Koerholz, Dieter; Gattenloehner, Stefan; Braeuninger, Andreas (2020)
  • Genotyping single nucleotide polymorphisms for allele-selective therapy in Huntington disease
    Claassen, Daniel O.; Corey-Bloom, Jody; Dorsey, E. Ray; Edmondson, Mary; Kostyk, Sandra K.; LeDoux, Mark S.; Reilmann, Ralf; Rosas, H. Diana; Walker, Francis; Wheelock, Vicki; Svrzikapa, Nenad; Longo, Kenneth A.; Goyal, Jaya; Hung, Serena; Panzara, Michael A. (2020)
  • Gentamicin Concentration Gradients in Scala Tympani Perilymph following Systemic Applications
    Hahn, Hartmut; Salt, Alec N.; Schumacher, Ulrike; Plontke, Stefan K. (2013)
  • Gentherapie als Behandlungskonzept für erbliche Netzhauterkrankungen
    Bellingrath, J. -S.; Fischer, M. D. (2015)
  • Gentherapie zur Behandlung von Netzhauterkrankungen
    Ochakovski, G. Alex; Bartz-Schmidt, Karl Ulrich; Fischer, M. Dominik (2017)