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Anzahl der Publikationen: 3
Zeitschriftenartikel
Mandler, Julia M.; Härtl, Johanna; Cordts, Isabell; Sturm, Marc 
ORCID: https://orcid.org/0000-0002-6552-8362; Hedderich, Dennis M.; Bafligil, Cemsel; Baki, Enayatullah; Becker, Benedikt; Machetanz, Gerrit; Haack, Tobias B. ORCID: https://orcid.org/0000-0001-6033-4836; Berthele, Achim; Hemmer, Bernhard ORCID: https://orcid.org/0000-0001-5985-6784 und Deschauer, Marcus ORCID: https://orcid.org/0000-0001-6116-6790
(2024):
Uncovering genetic mimics in multiple sclerosis. A single-center clinical exome sequencing study.
In: Multiple Sclerosis Journal - Experimental, Translational and Clinical, Bd. 10, Nr. 3
[PDF, 570kB]
ORCID: https://orcid.org/0000-0002-6552-8362; Hedderich, Dennis M.; Bafligil, Cemsel; Baki, Enayatullah; Becker, Benedikt; Machetanz, Gerrit; Haack, Tobias B. ORCID: https://orcid.org/0000-0001-6033-4836; Berthele, Achim; Hemmer, Bernhard ORCID: https://orcid.org/0000-0001-5985-6784 und Deschauer, Marcus ORCID: https://orcid.org/0000-0001-6116-6790
(2024):
Uncovering genetic mimics in multiple sclerosis. A single-center clinical exome sequencing study.
In: Multiple Sclerosis Journal - Experimental, Translational and Clinical, Bd. 10, Nr. 3
[PDF, 570kB]
Haertl, Johanna; Hartberger, Julia; Wunderlich, Silke; Cordts, Isabell; Bafligil, Cemsel; Sturm, Marc; Westphal, Dominik; Haack, Tobias; Hemmer, Bernhard; Ikenberg, Benno David und Deschauer, Marcus
(2023):
Exome-based gene panel analysis in a cohort of acute juvenile ischemic stroke patients:relevance of NOTCH3 and GLA variants.
In: Journal of Neurology, Bd. 270, Nr. 3: S. 1501-1511
[PDF, 779kB]
Gasperi, Christiane; Wiltgen, Tun; Mcginnis, Julian; Cerri, Stefano; Moridi, Thomas; Ouellette, Russell; Pukaj, Albert; Voon, Cuici; Bafligil, Cemsel; Lauerer, Markus; Andlauer, Till F. M.; Held, Friederike; Aly, Lilian; Shchetynsky, Klementy; Stridh, Pernilla; Harroud, Adil; Wiestler, Benedikt; Kirschke, Jan S.; Zimmer, Claus; Baras, Aris; Piehl, Fredrik; Berthele, Achim; Granberg, Tobias; Kockum, Ingrid; Hemmer, Bernhard und Muehlau, Mark
(2023):
A Genetic Risk Variant for Multiple Sclerosis Severity is Associated with Brain Atrophy.
In: Annals of Neurology, Bd. 94, Nr. 6: S. 1080-1085
[PDF, 906kB]