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Peikert, Kevin 
ORCID: https://orcid.org/0000-0002-0845-2453 und Danek, Adrian ORCID: https://orcid.org/0000-0001-8857-5383
(2023):
VPS13 Forum Proceedings: XK, XK-Related and VPS13 Proteins in Membrane Lipid Dynamics.
In: Contact, Bd. 6
[PDF, 1MB]
ORCID: https://orcid.org/0000-0002-0845-2453 und Danek, Adrian ORCID: https://orcid.org/0000-0001-8857-5383
(2023):
VPS13 Forum Proceedings: XK, XK-Related and VPS13 Proteins in Membrane Lipid Dynamics.
In: Contact, Bd. 6
[PDF, 1MB]
Peikert, Kevin; Hermann, Andreas und Danek, Adrian
(2022):
XK-Associated McLeod Syndrome: Nonhematological Manifestations and Relation to VPS13A Disease.
In: Transfusion Medicine and Hemotherapy, Bd. 49, Nr. 1: S. 4-12
Federti, Enrica; Matte, Alessandro; Riccardi, Veronica; Peikert, Kevin; Alper, Seth L.; Danek, Adrian; Walker, Ruth H.; Siciliano, Angela; Iatcenko, Iana; Hermann, Andreas und De Franceschi, Lucia
(2022):
Adaptative Up-Regulation of PRX2 and PRX5 Expression Characterizes Brain from a Mouse Model of Chorea-Acanthocytosis.
In: Antioxidants, Bd. 11, Nr. 1, 76
Recktenwald, Steffen M.; Lopes, Marcelle G. M.; Peter, Stephana; Hof, Sebastian; Simionato, Greta; Peikert, Kevin; Hermann, Andreas; Danek, Adrian; Bentum, Kai van; Eichler, Hermann; Wagner, Christian; Quint, Stephan und Kaestner, Lars
(2022):
Erysense, a Lab-on-a-Chip-Based Point-of-Care Device to Evaluate Red Blood Cell Flow Properties With Multiple Clinical Applications.
In: Frontiers in Physiology, Bd. 13, 884690
Peikert, Kevin; Federti, Enrica; Matte, Alessandro; Constantin, Gabriela; Pietronigro, Enrica Caterina; Fabene, Paolo Francesco; Defilippi, Paola; Turco, Emilia; Del Gallo, Federico; Pucci, Pietro; Amoresano, Angela; Illiano, Anna; Cozzolino, Flora; Monti, Maria; Garello, Francesca; Terreno, Enzo; Alper, Seth Leo; Glass, Hannes; Pelzl, Lisann; Akguen, Katja; Ziemssen, Tjalf; Ordemann, Rainer; Lang, Florian; Brunati, Anna Maria; Tibaldi, Elena; Andolfo, Immacolata; Iolascon, Achille; Bertini, Giuseppe; Buffelli, Mario; Zancanaro, Carlo; Lorenzetto, Erika; Siciliano, Angela; Bonifacio, Massimiliano; Danek, Adrian; Walker, Ruth Helen; Hermann, Andreas und De Franceschi, Lucia
(2021):
Therapeutic targeting of Lyn kinase to treat chorea-acanthocytosis.
In: Acta Neuropathologica Communications, Bd. 9, Nr. 1, 81
Quick, Silvio; Heidrich, Felix Matthias; Winkler, Max-Valentin; Winkler, Anna Helene; Ibrahim, Karim; Linke, Axel; Speiser, Uwe; Grabmaier, Ulrich; Buhmann, Carsten; Marxreiter, Franz; Saft, Carsten; Danek, Adrian; Hermann, Andreas und Peikert, Kevin
(2021):
Cardiac manifestation is evident in chorea-acanthocytosis but different from McLeod syndrome.
In: Parkinsonism & Related Disorders, Bd. 88: S. 90-95
Rabe, Antonia; Kihm, Alexander; Darras, Alexis; Peikert, Kevin; Simionato, Greta; Dasanna, Anil Kumar; Glass, Hannes; Geisel, Jürgen; Quint, Stephan; Danek, Adrian; Wagner, Christian; Fedosov, Dmitry A.; Hermann, Andreas und Kaestner, Lars
(2021):
The Erythrocyte Sedimentation Rate and Its Relation to Cell Shape and Rigidity of Red Blood Cells from Chorea-Acanthocytosis Patients in an Off-Label Treatment with Dasatinib.
In: Biomolecules, Bd. 11, Nr. 5, 727
Peikert, Kevin; Akgun, Katja; Beste, Christian; Ziemssen, Tjalf; Buhmann, Carsten; Danek, Adrian und Hermann, Andreas
(2020):
Neurofilament light chain in serum is significantly increased in chorea-acanthocytosis.
In: Parkinsonism & Related Disorders, Bd. 80: S. 28-31
Naumann, Marcel; Peikert, Kevin; Guenther, Rene; van der Kooi, Anneke J.; Aronica, Eleonora; Huebers, Annemarie; Danel, Veronique; Corcia, Philippe; Pan-Montojo, Francisco; Cirak, Sebahattin; Haliloglu, Goeknur; Ludolph, Albert C.; Goswami, Anand; Andersen, Peter M.; Prudlo, Johannes; Wegner, Florian; Van Damme, Philip; Weishaupt, Jochen H. und Hermann, Andreas
(2019):
Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis.
In: Annals of Clinical and Translational Neurology
[PDF, 626kB]
Peikert, Kevin; Danek, Adrian und Hermann, Andreas
(2018):
Current state of knowledge in Chorea-Acanthocytosis as core Neuroacanthocytosis syndrome.
In: European Journal of Medical Genetics, Bd. 61, Nr. 11: S. 699-705