Search Results - Denecke, Jonas

Long-term neuropsychologic outcome of pre-emptive mTOR inhibitor treatment in children with tuberous sclerosis complex (TSC) under 4 months of age (PROTECT), a two-arm, randomized,... by Driedger, Jan Henje (Author) , Schröter, Julian (Author) , Hertzberg, Christoph (Author) , Weschke, Bernhard (Author) , Kaindl, Angela M. (Author) , Lücke, Thomas (Author) , Thiels, Charlotte (Author) , Klotz, Kerstin A. (Author) , Fazeli, Walid (Author) , Rostásy, Kevin (Author) , Wiethoff-Ubrig, Lucia (Author) , Kaiser, Olaf (Author) , Trollmann, Regina (Author) , Mammadova, Dilbar (Author) , Schubert-Bast, Susanne (Author) , Bach, Alexia (Author) , Eckenweiler, Matthias (Author) , Schönberger, Jan (Author) , Martakis, Kyriakos (Author) , Hahn, Andreas (Author) , Brockmann, Knut (Author) , Dreha-Kulaczewski, Steffi (Author) , Weiss, Deike (Author) , Denecke, Jonas (Author) , Muhle, Hiltrud (Author) , Arélin, Maria (Author) , Merkenschlager, Andreas (Author) , Borggräfe, Ingo (Author) , Roser, Timo (Author) , Ebrahimi-Fakhari, Daniel (Author) , Fiedler, Barbara (Author) , Schlump, Jan-Ulrich (Author) , Köster, Ilka (Author) , Korenke, Christoph (Author) , Alber, Michael (Author) , Ruf, Susanne (Author) , Feucht, Martha (Author) , Scholl, Theresa (Author) , Syrbe, Steffen (Author) , Saffari, Afshin (Author) ,

• Verlag, lizenzpflichtig, Volltext

Prolonged apnea in a boy with epilepsy and a novel gain-of-function missense CACNA1A variant indicating SUDEP risk by Pelizzari, Simone (Author) , Campiglio, Marta (Author) , El Ghaleb, Yousra (Author) , Bierhals, Tatjana (Author) , Hempel, Maja (Author) , Denecke, Jonas (Author) , Flucher, Bernhard E. (Author) , Johannsen, Jessika (Author) ,

• Verlag, kostenfrei, Volltext
• Verlag, kostenfrei, Volltext

Etiological involvement of KCND1 variants in an X-linked neurodevelopmental disorder with variable expressivity by Kalm, Tassja (Author) , Schob, Claudia (Author) , Völler, Hanna (Author) , Gardeitchik, Thatjana (Author) , Gilissen, Christian (Author) , Pfundt, Rolph (Author) , Klöckner, Chiara (Author) , Platzer, Konrad (Author) , Klabunde-Cherwon, Annick (Author) , Ries, Markus (Author) , Syrbe, Steffen (Author) , Beccaria, Francesca (Author) , Madia, Francesca (Author) , Scala, Marcello (Author) , Zara, Federico (Author) , Hofstede, Floris (Author) , Simon, Marleen E. H. (Author) , Jaarsveld, Richard H. van (Author) , Oegema, Renske (Author) , Gassen, Koen L. I. van (Author) , Holwerda, Sjoerd J. B. (Author) , Barakat, Tahsin Stefan (Author) , Bouman, Arjan (Author) , Slegtenhorst, Marjon van (Author) , Álvarez, Sara (Author) , Fernández-Jaén, Alberto (Author) , Porta, Javier (Author) , Accogli, Andrea (Author) , Mancardi, Margherita Maria (Author) , Striano, Pasquale (Author) , Iacomino, Michele (Author) , Chae, Jong-Hee (Author) , Jang, SeSong (Author) , Kim, Soo Y. (Author) , Chitayat, David (Author) , Mercimek-Andrews, Saadet (Author) , Depienne, Christel (Author) , Kampmeier, Antje (Author) , Kuechler, Alma (Author) , Surowy, Harald (Author) , Bertini, Enrico Silvio (Author) , Radio, Francesca Clementina (Author) , Mancini, Cecilia (Author) , Pizzi, Simone (Author) , Tartaglia, Marco (Author) , Gauthier, Lucas (Author) , Genevieve, David (Author) , Tharreau, Mylène (Author) , Azoulay, Noy (Author) , Zaks-Hoffer, Gal (Author) , Gilad, Nesia K. (Author) , Orenstein, Naama (Author) , Bernard, Geneviève (Author) , Thiffault, Isabelle (Author) , Denecke, Jonas (Author) , Herget, Theresia (Author) , Kortüm, Fanny (Author) , Kubisch, Christian (Author) , Bähring, Robert (Author) , Kindler, Stefan (Author) ,

• Verlag, kostenfrei, Volltext
• Verlag, kostenfrei, Volltext

Cognitive function in SMA patients with 2 or 3 SMN2 copies treated with SMN-modifying or gene addition therapy during the first year of life by Steffens, Paula (Author) , Weiss, Deike (Author) , Perez, Anna (Author) , Appel, Manuel (Author) , Weber, Philipp (Author) , Weiss, Claudia (Author) , Stoltenburg, Corinna (Author) , Ehinger, Ute (Author) , von der Hagen, Maja (Author) , Schallner, Jens (Author) , Claussen, Birte (Author) , Lode, Ilka (Author) , Hahn, Andreas (Author) , Schuler, Rahel (Author) , Ruß, Lena (Author) , Ziegler, Andreas (Author) , Denecke, Jonas (Author) , Johannsen, Jessika (Author) ,

• Verlag, kostenfrei, Volltext
• Verlag, kostenfrei, Volltext

Natural history and developmental trajectories of individuals with disease-causing variants in STXBP1 by Thalwitzer, Kim M. (Author) , Driedger, Jan Henje (Author) , Xian, Julie (Author) , Saffari, Afshin (Author) , Zacher, Pia (Author) , Bölsterli, Bigna K. (Author) , McKeown Ruggiero, Sarah (Author) , Sullivan, Katie Rose (Author) , Datta, Alexandre N. (Author) , Kellinghaus, Christoph (Author) , Althaus, Jürgen (Author) , Wiemer-Kruel, Adelheid (Author) , van Baalen, Andreas (Author) , Pampel, Armin (Author) , Alber, Michael (Author) , Braakman, Hilde M. H. (Author) , Debus, Otfried Martin (Author) , Denecke, Jonas (Author) , Hobbiebrunken, Elke (Author) , Breitweg, Ina (Author) , Diehl, Danielle (Author) , Eitel, Hans Christian (Author) , Gburek-Augustat, Janina (Author) , Preisel, Martin (Author) , Schlump, Jan-Ulrich (Author) , Laufs, Mirjam (Author) , Mammadova, Dilbar (Author) , Wurst, Carsten (Author) , Prager, Christine (Author) , Löhr-Nilles, Christa (Author) , Martin, Peter (Author) , Garbade, Sven (Author) , Platzer, Konrad (Author) , Benkel-Herrenbrueck, Ira (Author) , Egler, Kerstin (Author) , Fazeli, Walid (Author) , Lemke, Johannes R. (Author) , Runkel, Eva (Author) , Klein, Barbara (Author) , Linden, Tobias (Author) , Schröter, Julian (Author) , Steffeck, Heike (Author) , Thies, Bastian (Author) , Deimling, Florian von (Author) , Illsinger, Sabine (Author) , Borggräfe, Ingo (Author) , Classen, Georg (Author) , Wieczorek, Dagmar (Author) , Ramantani, Georgia (Author) , Kölker, Stefan (Author) , Hoffmann, Georg F. (Author) , Ries, Markus (Author) , Helbig, Ingo (Author) , Syrbe, Steffen (Author) ,

• Resolving-System, lizenzpflichtig

Gene replacement therapy with onasemnogene abeparvovec in children with spinal muscular atrophy aged 24 months or younger and bodyweight up to 15 kg: an observational cohort study by Weiß, Claudia (Author) , Ziegler, Andreas (Author) , Becker, Lena-Luise (Author) , Johannsen, Jessika (Author) , Brennenstuhl, Heiko (Author) , Schreiber, Gudrun (Author) , Flotats-Bastardas, Marina (Author) , Stoltenburg, Corinna (Author) , Hartmann, Hans (Author) , Illsinger, Sabine (Author) , Denecke, Jonas (Author) , Pechmann, Astrid (Author) , Müller-Felber, Wolfgang (Author) , Vill, Katharina (Author) , Blaschek, Astrid (Author) , Smitka, Martin (Author) , van der Stam, Lieske (Author) , Weiss, Katja (Author) , Winter, Benedikt (Author) , Goldhahn, Klaus (Author) , Plecko, Barbara (Author) , Horber, Veronka (Author) , Bernert, Günther (Author) , Husain, Ralf A (Author) , Rauscher, Christian (Author) , Trollmann, Regina (Author) , Garbade, Sven (Author) , Hahn, Andreas (Author) , von der Hagen, Maja (Author) , Kaindl, Angela M (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Germline AGO2 mutations impair RNA interference and human neurological development by Lessel, Davor (Author) , Zeitler, Daniela M. (Author) , Reijnders, Margot R. F. (Author) , Kazantsev, Andriy (Author) , Hassani Nia, Fatemeh (Author) , Bartholomäus, Alexander (Author) , Martens, Victoria (Author) , Bruckmann, Astrid (Author) , Graus, Veronika (Author) , McConkie-Rosell, Allyn (Author) , McDonald, Marie (Author) , Lozic, Bernarda (Author) , Tan, Ee-Shien (Author) , Gerkes, Erica (Author) , Johannsen, Jessika (Author) , Denecke, Jonas (Author) , Telegrafi, Aida (Author) , Zonneveld-Huijssoon, Evelien (Author) , Lemmink, Henny H. (Author) , Cham, Breana W. M. (Author) , Kovacevic, Tanja (Author) , Ramsdell, Linda (Author) , Foss, Kimberly (Author) , Le Duc, Diana (Author) , Mitter, Diana (Author) , Syrbe, Steffen (Author) , Merkenschlager, Andreas (Author) , Sinnema, Margje (Author) , Panis, Bianca (Author) , Lazier, Joanna (Author) , Osmond, Matthew (Author) , Hartley, Taila (Author) , Mortreux, Jeremie (Author) , Busa, Tiffany (Author) , Missirian, Chantal (Author) , Prasun, Pankaj (Author) , Lüttgen, Sabine (Author) , Mannucci, Ilaria (Author) , Lessel, Ivana (Author) , Schob, Claudia (Author) , Kindler, Stefan (Author) , Pappas, John (Author) , Rabin, Rachel (Author) , Willemsen, Marjolein (Author) , Gardeitchik, Thatjana (Author) , Löhner, Katharina (Author) , Rump, Patrick (Author) , Dias, Kerith-Rae (Author) , Evans, Carey-Anne (Author) , Andrews, Peter Ian (Author) , Roscioli, Tony (Author) , Brunner, Han G. (Author) , Chijiwa, Chieko (Author) , Lewis, M. E. Suzanne (Author) , Abou Jamra, Rami (Author) , Dyment, David A. (Author) , Boycott, Kym M. (Author) , Stegmann, Alexander P. A. (Author) , Kubisch, Christian (Author) , Tan, Ene-Choo (Author) , Mirzaa, Ghayda M. (Author) , McWalter, Kirsty (Author) , Kleefstra, Tjitske (Author) , Pfundt, Rolph (Author) , Ignatova, Zoya (Author) , Meister, Gunter (Author) , Kreienkamp, Hans-Jürgen (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Phenotypic and molecular insights into CASK-related disorders in males by Moog, Ute (Author) , Bierhals, Tatjana (Author) , Brand, Kristina (Author) ,

Other Authors: “…Denecke, Jonas…”

• Verlag, Abstract, Volltext

Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridization by Weber, Stefanie (Author) , Landwehr, Christina (Author) , Renkert-Baudis, Miriam (Author) , Hoischen, Alexander (Author) , Wühl, Elke (Author) , Denecke, Jonas (Author) , Radlwimmer, Bernhard (Author) , Haffner, Dieter (Author) , Schaefer, Franz (Author) , Weber, Ruthild (Author) ,

• Verlag, lizenzpflichtig, Volltext

Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridization

Other Authors: “…Denecke, Jonas…”