Anzahl der Einträge: 8.
2022
Gerling, Stephan ,
Hörl, Maria,
Geis, Tobias,
Zant, Robert,
Dechant, Markus Johann,
Melter, Michael und
Michel, Holger
(2022)
Coronary Artery Z-scores in Febrile Children with Suspected Kawasaki Disease.
The Thoracic and Cardiovascular Surgeon 70(S 03).
Zugang zum Volltext eingeschränkt.
Bölsterli, Bigna K. ,
Boltshauser, Eugen ,
Palmieri, Luigi ,
Spenger, Johannes ,
Brunner-Krainz, Michaela,
Distelmaier, Felix,
Freisinger, Peter ,
Geis, Tobias ,
Gropman, Andrea L. ,
Häberle, Johannes ,
Hentschel, Julia,
Jeandidier, Bruno,
Karall, Daniela ,
Keren, Boris,
Klabunde-Cherwon, Annick,
Konstantopoulou, Vassiliki,
Kottke, Raimund ,
Lasorsa, Francesco M.,
Makowski, Christine,
Mignot, Cyril,
O’Gorman Tuura, Ruth,
Porcelli, Vito,
Santer, René,
Sen, Kuntal,
Steinbrücker, Katja,
Syrbe, Steffen ,
Wagner, Matias,
Ziegler, Andreas,
Zöggeler, Thomas,
Mayr, Johannes A. ,
Prokisch, Holger und
Wortmann, Saskia B.
(2022)
Ketogenic Diet Treatment of Defects in the Mitochondrial Malate Aspartate Shuttle and Pyruvate Carrier.
Nutrients 14 (17), S. 3605.
Volltext nicht vorhanden.
Pfeiffer, Christina K,
Smith, Karen,
Bernard, Stephen,
Dalziel, Stuart R,
Hearps, Stephen ,
Geis, Tobias,
Kabesch, Michael und
Babl, Franz E
(2022)
Prehospital benzodiazepine use and need for respiratory support in paediatric seizures.
Emergency Medicine Journal 39 (8), S. 608-615.
Volltext nicht vorhanden.
2021
Geis, Tobias,
Brandstetter, Susanne,
Toncheva, Antoaneta A. ,
Laub, Otto,
Leipold, Georg,
Wagner, Ralf,
Kabesch, Michael,
Kasser, Severin,
Kuhle, Jens und
Wellmann, Sven
(2021)
Serum neurofilament light chain (sNfL) values in a large cross-sectional population of children with asymptomatic to moderate COVID-19.
Journal of Neurology 268, S. 3969-3974.
2020
Oegema, Renske ,
Barakat, Tahsin Stefan ,
Wilke, Martina,
Stouffs, Katrien ,
Amrom, Dina,
Aronica, Eleonora,
Bahi-Buisson, Nadia,
Conti, Valerio ,
Fry, Andrew E. ,
Geis, Tobias,
Andres, David Gomez,
Parrini, Elena,
Pogledic, Ivana ,
Said, Edith,
Soler, Doriette,
Valor, Luis M.,
Zaki, Maha S. ,
Mirzaa, Ghayda,
Dobyns, William B.,
Reiner, Orly,
Guerrini, Renzo ,
Pilz, Daniela T.,
Hehr, Ute,
Leventer, Richard J.,
Jansen, Anna C. ,
Mancini, Grazia M. S. und
Di Donato, Nataliya
(2020)
International consensus recommendations on the diagnostic work-up for malformations of cortical development.
Nature Reviews Neurology 16 (11), S. 618-635.
Volltext nicht vorhanden.
2019
Geis, Tobias,
Rödl, Tanja,
Topaloğlu, Haluk,
Balci-Hayta, Burcu,
Hinreiner, Sophie,
Müller-Felber, Wolfgang,
Schoser, Benedikt,
Mehraein, Yasmin,
Hübner, Angela,
Zirn, Birgit,
Hoopmann, Markus,
Reutter, Heiko,
Mowat, David,
Schuierer, Gerhard,
Schara, Ulrike,
Hehr, Ute und
Kölbel, Heike
(2019)
Clinical long-time course, novel mutations and genotype-phenotype correlation in a cohort of 27 families with POMT1-related disorders.
Orphanet Journal of Rare Diseases 14 (1).
Volltext nicht vorhanden.
2018
2016
Herbst, Saskia M.,
Proepper, Christiane R.,
Geis, Tobias,
Borggraefe, Ingo,
Hahn, Andreas,
Debus, Otfried,
Haeussler, Martin,
von Gersdorff, Gero,
Kurlemann, Gerhard,
Ensslen, Matthias,
Beaud, Nathalie,
Budde, Joerg,
Gilbert, Michael,
Heiming, Ralf,
Morgner, Rita,
Philippi, Heike,
Ross, Sophia,
Strobl-Wildemann, Gertrud,
Muelleder, Kerstin,
Vosschulte, Paul,
Morris-Rosendahl, Deborah J. ,
Schuierer, Gerhard und
Hehr, Ute
(2016)
LIS1-associated classic lissencephaly: A retrospective, multicenter survey of the epileptogenic phenotype and response to antiepileptic drugs.
Brain and Development 38 (4), S. 399-406.
Volltext nicht vorhanden.
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