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Page 1
Genetic Risk Factors in Isolated Dystonia Escape Genome-Wide Association Studies.
Laabs BH, Lohmann K, Vollstedt EJ, Reinberger T, Nuxoll LM, Kilic-Berkmen G, Perlmutter JS, Loens S, Cruchaga C, Franke A, Dobricic V, Hinrichs F, Grözinger A, Altenmüller E, Bellows S, Boesch S, Bressman SB, Duque KR, Espay AJ, Ferbert A, Feuerstein JS, Frank S, Gasser T, Haslinger B, Jech R, Kaiser F, Kamm C, Kollewe K, Kühn AA, LeDoux MS, Lohmann E, Mahajan A, Münchau A, Multhaupt-Buell T, Pantelyat A, Pirio Richardson SE, Raymond D, Reich SG, Saunders Pullman R, Schormair B, Sharma N, Sichani AH, Simonyan K, Volkmann J, Wagle Shukla A, Winkelmann J, Wright LJ, Zech M, Zeuner KE, Zittel S, Kasten M, Sun YV, Bäumer T, Brüggemann N, Ozelius LJ, Jinnah HA, Klein C, König IR. Laabs BH, et al. Among authors: hinrichs f. Mov Disord. 2024 Nov;39(11):2110-2116. doi: 10.1002/mds.29968. Epub 2024 Sep 17. Mov Disord. 2024. PMID: 39287592
RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar Ataxia.
Milovanović A, Dragaševic-Mišković N, Thomsen M, Borsche M, Hinrichs F, Westenberger A, Klein C, Brüggemann N, Branković M, Marjanović A, Svetel M, Kostić VS, Lohmann K. Milovanović A, et al. Among authors: hinrichs f. Mov Disord Clin Pract. 2024 Jun;11(6):626-633. doi: 10.1002/mdc3.14020. Epub 2024 Mar 15. Mov Disord Clin Pract. 2024. PMID: 38487929 Free PMC article.
Large-Scale Screening: Phenotypic and Mutational Spectrum in Isolated and Combined Dystonia Genes.
Thomsen M, Marth K, Loens S, Everding J, Junker J, Borngräber F, Ott F, Jesús S, Gelderblom M, Odorfer T, Kuhlenbäumer G, Kim HJ, Schaeffer E, Becktepe J, Kasten M, Brüggemann N, Pfister R, Kollewe K, Krauss JK, Lohmann E, Hinrichs F, Berg D, Jeon B, Busch H, Altenmüller E, Mir P, Kamm C, Volkmann J, Zittel S, Ferbert A, Zeuner KE, Rolfs A, Bauer P, Kühn AA, Bäumer T, Klein C, Lohmann K. Thomsen M, et al. Among authors: hinrichs f. Mov Disord. 2024 Mar;39(3):526-538. doi: 10.1002/mds.29693. Epub 2024 Jan 12. Mov Disord. 2024. PMID: 38214203
Compound Heterozygous DARS2 Mutations as a Mimic of Hereditary Spastic Paraplegia.
Pauly MG, Hellenbroich Y, Grundmann-Hauser K, Hinrichs F, Lohmann K, Brüggemann N. Pauly MG, et al. Among authors: hinrichs f. Mov Disord Clin Pract. 2021 Jun 14;8(6):972-976. doi: 10.1002/mdc3.13258. eCollection 2021 Aug. Mov Disord Clin Pract. 2021. PMID: 34405109 Free PMC article. No abstract available.
Discordant Monozygotic Parkinson Disease Twins: Role of Mitochondrial Integrity.
Dulovic-Mahlow M, König IR, Trinh J, Diaw SH, Urban PP, Knappe E, Kuhnke N, Ingwersen LC, Hinrichs F, Weber J, Kupnicka P, Balck A, Delcambre S, Vollbrandt T, Grünewald A, Klein C, Seibler P, Lohmann K. Dulovic-Mahlow M, et al. Among authors: hinrichs f. Ann Neurol. 2021 Jan;89(1):158-164. doi: 10.1002/ana.25942. Epub 2020 Nov 4. Ann Neurol. 2021. PMID: 33094862
Risk factors for preoperative seizures in intracranial meningiomas.
Hinrichs FL, Brokinkel C, Adeli A, Sporns PB, Hess K, Paulus W, Stummer W, Grauer O, Spille DC, Brokinkel B. Hinrichs FL, et al. J Neurosurg Sci. 2023 Feb;67(1):66-72. doi: 10.23736/S0390-5616.20.05068-7. Epub 2020 Oct 15. J Neurosurg Sci. 2023. PMID: 33056948
38 results