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Page 1
Monogenic variants in dystonia: an exome-wide sequencing study.
Zech M, Jech R, Boesch S, Škorvánek M, Weber S, Wagner M, Zhao C, Jochim A, Necpál J, Dincer Y, Vill K, Distelmaier F, Stoklosa M, Krenn M, Grunwald S, Bock-Bierbaum T, Fečíková A, Havránková P, Roth J, Příhodová I, Adamovičová M, Ulmanová O, Bechyně K, Danhofer P, Veselý B, Haň V, Pavelekova P, Gdovinová Z, Mantel T, Meindl T, Sitzberger A, Schröder S, Blaschek A, Roser T, Bonfert MV, Haberlandt E, Plecko B, Leineweber B, Berweck S, Herberhold T, Langguth B, Švantnerová J, Minár M, Ramos-Rivera GA, Wojcik MH, Pajusalu S, Õunap K, Schatz UA, Pölsler L, Milenkovic I, Laccone F, Pilshofer V, Colombo R, Patzer S, Iuso A, Vera J, Troncoso M, Fang F, Prokisch H, Wilbert F, Eckenweiler M, Graf E, Westphal DS, Riedhammer KM, Brunet T, Alhaddad B, Berutti R, Strom TM, Hecht M, Baumann M, Wolf M, Telegrafi A, Person RE, Zamora FM, Henderson LB, Weise D, Musacchio T, Volkmann J, Szuto A, Becker J, Cremer K, Sycha T, Zimprich F, Kraus V, Makowski C, Gonzalez-Alegre P, Bardakjian TM, Ozelius LJ, Vetro A, Guerrini R, Maier E, Borggraefe I, Kuster A, Wortmann SB, Hackenberg A, Steinfeld R, Assmann B, Staufner C, Opladen T, Růžička E, Cohn RD, Dyment D, Chung WK, Engels H, Ceballos-Bauman… See abstract for full author list ➔ Zech M, et al. Among authors: danhofer p. Lancet Neurol. 2020 Nov;19(11):908-918. doi: 10.1016/S1474-4422(20)30312-4. Lancet Neurol. 2020. PMID: 33098801 Free PMC article.
Next-generation sequencing in children with epilepsy: The importance of precise genotype-phenotype correlation.
Horák O, Burešová M, Kolář S, Španělová K, Jeřábková B, Gaillyová R, Česká K, Réblová K, Šoukalová J, Zídková J, Fajkusová L, Ošlejšková H, Rektor I, Danhofer P. Horák O, et al. Among authors: danhofer p. Epilepsy Behav. 2022 Mar;128:108564. doi: 10.1016/j.yebeh.2022.108564. Epub 2022 Jan 19. Epilepsy Behav. 2022. PMID: 35065395
Cerebrovascular Complications of COVID-19 Disease in Children: A Single-Center Case Series.
Španělová K, Skříšovská T, Mužlayová P, Horák O, Šenkyřík J, Seehofnerová A, Homola L, Klučka J, Blatný J, Ošlejšková H, Danhofer P. Španělová K, et al. Among authors: danhofer p. Pediatr Neurol. 2022 Sep;134:18-24. doi: 10.1016/j.pediatrneurol.2022.06.007. Epub 2022 Jun 16. Pediatr Neurol. 2022. PMID: 35780679 Free PMC article.
Decreased quality of life in Duchenne muscular disease patients related to functional neurological and cardiac impairment.
Juříková L, Masárová L, Panovský R, Pešl M, Revendová KŽ, Volný O, Feitová V, Holeček T, Kincl V, Danhofer P, Voháňka S, Haberlová J, Podolská K. Juříková L, et al. Among authors: danhofer p. Front Neurol. 2024 Feb 8;15:1360385. doi: 10.3389/fneur.2024.1360385. eCollection 2024. Front Neurol. 2024. PMID: 38390598 Free PMC article.
Prognostic factors and seizure outcome in posterior reversible encephalopathy syndrome (PRES) in children with hematological malignancies and bone marrow failure: A retrospective monocentric study.
Danhofer P, Tomečková M, Černá D, Zapletalová D, Horák O, Aulická Š, Juříková L, Domanský J, Kovalčíková P, Pavlík T, Štěrba J, Ošlejšková H. Danhofer P, et al. Seizure. 2019 Nov;72:1-10. doi: 10.1016/j.seizure.2019.08.007. Epub 2019 Aug 15. Seizure. 2019. PMID: 31521834 Free article.
Autosomal dominant temporal lobe epilepsy associated with heterozygous reelin mutation: 3 T brain MRI study with advanced neuroimaging methods.
Česká K, Aulická Š, Horák O, Danhofer P, Říha P, Mareček R, Šenkyřík J, Rektor I, Brázdil M, Ošlejšková H. Česká K, et al. Among authors: danhofer p. Epilepsy Behav Case Rep. 2018 Nov 1;11:39-42. doi: 10.1016/j.ebcr.2018.10.003. eCollection 2019. Epilepsy Behav Case Rep. 2018. PMID: 30619712 Free PMC article.
11 results