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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 4
2021
Lotz-Havla, Amelie S.; Weiß, Katharina J.; Schiergens, Katharina A.; Brunet, Theresa; Kohlhase, Jürgen; Regenauer-Vandewiele, Stephanie und Maier, Esther M.
(2021):
Subcutaneous vitamin B12 administration using a portable infusion pump in cobalamin-related remethylation disorders: a gentle and easy to use alternative to intramuscular injections.
In: Orphanet journal of rare diseases, Bd. 16, Nr. 1, 215
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Lotz-Havla, Amelie S.; Weiß, Katharina J.; Schiergens, Katharina A.; Brunet, Theresa; Kohlhase, Jürgen; Regenauer-Vandewiele, Stephanie und Maier, Esther M.
(2021):
Subcutaneous vitamin B12 administration using a portable infusion pump in cobalamin-related remethylation disorders: a gentle and easy to use alternative to intramuscular injections.
In: Orphanet Journal of Rare Diseases, Bd. 16, Nr. 1, 215
2017
Minnerop, Martina; Kurzwelly, Delia; Wagner, Holger; Söhn, Anne S.; Reichbauer, Jennifer; Tao, Feifei; Rattay, Tim W.; Peitz, Michael; Rehbach, Kristina; Giorgetti, Alejandro; Pyle, Angela; Thiele, Holger; Altmüller, Janine; Timmann, Dagmar; Karaca, Ilker; Lennarz, Martina; Bäts, Jonathan; Hengel, Holger; Synofzik, Matthis; Atasu, Burcu; Feely, Shawna; Kennerson, Marina; Stendel, Claudia; Lindig, Tobias; Gonzalez, Michael A.; Stirnberg, Rüdiger; Sturm, Marc; Röske, Sandra; Jung, Johanna; Bauer, Peter; Lohmann, Ebba; Herms, Stefan; Heilmann-Heimbach, Stefanie; Nicholson, Garth; Mahanjah, Muhammad; Sharkia, Rajech; Carloni, Paolo; Brüstle, Oliver; Klopstock, Thomas; Mathews, Katherine D.; Shy, Michael E.; Jonghe, Peter de; Chinnery, Patrick F.; Horvath, Rita; Kohlhase, Jürgen; Schmitt, Ina; Wolf, Michael; Greschus, Susanne; Amunts, Katrin; Maier, Wolfgang; Schöls, Ludger; Nürnberg, Peter; Zuchner, Stephan; Klockgether, Thomas; Ramirez, Alfredo und Schüle, Rebecca
(2017):
Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia.
In: Brain, Bd. 140: S. 1561-1578
2016
Mehraein, Yasmin; Schmid, Irene; Eggert, Marlene; Kohlhase, Jürgen und Steinlein, Ortrud K.
(2016):
DICER1 syndrome can mimic different genetic tumor predispositions.
In: Cancer Letters, Bd. 370, Nr. 2: S. 275-278