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Page 1
Genetic Determined Iron Starvation Signature in Friedreich's Ataxia.
Grander M, Haschka D, Indelicato E, Kremser C, Amprosi M, Nachbauer W, Henninger B, Stefani A, Högl B, Fischer C, Seifert M, Kiechl S, Weiss G, Boesch S. Grander M, et al. Among authors: hogl b. Mov Disord. 2024 Jul;39(7):1088-1098. doi: 10.1002/mds.29819. Epub 2024 Apr 30. Mov Disord. 2024. PMID: 38686449
HLA dependency and possible clinical relevance of intrathecally synthesized anti-IgLON5 IgG4 in anti-IgLON5 disease.
Koneczny I, Macher S, Hutterer M, Seifert-Held T, Berger-Sieczkowski E, Blaabjerg M, Breu M, Dreyhaupt J, Dutra LA, Erdler M, Fae I, Fischer G, Frommlet F, Heidbreder A, Högl B, Klose V, Klotz S, Liendl H, Nissen MS, Rahimi J, Reinecke R, Ricken G, Stefani A, Süße M, Teive HAG, Weis S, Berger T, Sabater L, Gaig C, Lewerenz J, Höftberger R. Koneczny I, et al. Among authors: hogl b. Front Immunol. 2024 May 16;15:1376456. doi: 10.3389/fimmu.2024.1376456. eCollection 2024. Front Immunol. 2024. PMID: 38827736 Free PMC article.
Neuropathological spectrum of anti-IgLON5 disease and stages of brainstem tau pathology: updated neuropathological research criteria of the disease-related tauopathy.
Gelpi E, Reinecke R, Gaig C, Iranzo A, Sabater L, Molina-Porcel L, Aldecoa I, Endmayr V, Högl B, Schmutzhard E, Poewe W, Pfausler B, Popovic M, Pretnar-Oblak J, Leypoldt F, Matschke J, Glatzel M, Erro EM, Jerico I, Caballero MC, Zelaya MV, Mariotto S, Heidbreder A, Kalev O, Weis S, Macher S, Berger-Sieczkowski E, Ferrari J, Reisinger C, Klupp N, Tienari P, Rautila O, Niemelä M, Yilmazer-Hanke D, Guasp M, Bloem B, Van Gaalen J, Kusters B, Titulaer M, Fransen NL, Santamaria J, Dawson T, Holton JL, Ling H, Revesz T, Myllykangas L, Budka H, Kovacs GG, Lewerenz J, Dalmau J, Graus F, Koneczny I, Höftberger R. Gelpi E, et al. Among authors: hogl b. Acta Neuropathol. 2024 Oct 14;148(1):53. doi: 10.1007/s00401-024-02805-y. Acta Neuropathol. 2024. PMID: 39400557 Free PMC article.
Daytime sleepiness and BMI exhibit gender and age differences in patients with central disorders of hypersomnolence.
Ferrazzini L, Schmidt M, Zhang Z, Khatami R, Dauvilliers Y, Barateau L, Mayer G, Pizza F, Plazzi G, Gool JK, Fronczek R, Lammers GJ, Del Rio-Villegas R, Peraita-Adrados R, Partinen M, Overeem S, Sonka K, Santamaria J, Heinzer R, Canellas F, da Silva AM, Högl B, Veauthier C, Wierzbicka A, Feketeova E, Buskova J, Lecendreux M, Miano S, Kallweit U, Heidbreder A, Bassetti CLA, van der Meer J. Ferrazzini L, et al. Among authors: hogl b. J Sleep Res. 2024 Oct 21:e14365. doi: 10.1111/jsr.14365. Online ahead of print. J Sleep Res. 2024. PMID: 39428908
Rethinking clinical trials in restless legs syndrome: A roadmap.
Garcia-Borreguero D, Black J, Earley CJ, Fulda S, Högl B, Manconi M, Ondo W, Roth T, Trenkwalder C, Winkelman JW; International Restless Legs Syndrome Study Group (IRLSSG). Garcia-Borreguero D, et al. Among authors: hogl b. Sleep Med Rev. 2024 Oct;77:101978. doi: 10.1016/j.smrv.2024.101978. Epub 2024 Jul 18. Sleep Med Rev. 2024. PMID: 39102777 Review.
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction.
Schormair B, Zhao C, Bell S, Didriksen M, Nawaz MS, Schandra N, Stefani A, Högl B, Dauvilliers Y, Bachmann CG, Kemlink D, Sonka K, Paulus W, Trenkwalder C, Oertel WH, Hornyak M, Teder-Laving M, Metspalu A, Hadjigeorgiou GM, Polo O, Fietze I, Ross OA, Wszolek ZK, Ibrahim A, Bergmann M, Kittke V, Harrer P, Dowsett J, Chenini S, Ostrowski SR, Sørensen E, Erikstrup C, Pedersen OB, Topholm Bruun M, Nielsen KR, Butterworth AS, Soranzo N, Ouwehand WH, Roberts DJ, Danesh J, Burchell B, Furlotte NA, Nandakumar P; 23andMe Research Team; D.E.S.I.R. study group; Earley CJ, Ondo WG, Xiong L, Desautels A, Perola M, Vodicka P, Dina C, Stoll M, Franke A, Lieb W, Stewart AFR, Shah SH, Gieger C, Peters A, Rye DB, Rouleau GA, Berger K, Stefansson H, Ullum H, Stefansson K, Hinds DA, Di Angelantonio E, Oexle K, Winkelmann J. Schormair B, et al. Among authors: hogl b. Nat Genet. 2024 Jun;56(6):1090-1099. doi: 10.1038/s41588-024-01763-1. Epub 2024 Jun 5. Nat Genet. 2024. PMID: 38839884 Free PMC article.
347 results