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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1994 1
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1997 5
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2010 4
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69 results

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Page 1
Hereditary Neuropathies.
Eggermann K, Gess B, Häusler M, Weis J, Hahn A, Kurth I. Eggermann K, et al. Among authors: gess b. Dtsch Arztebl Int. 2018 Feb 9;115(6):91-97. doi: 10.3238/arztebl.2018.0091. Dtsch Arztebl Int. 2018. PMID: 29478438 Free PMC article. Review.
Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies.
Lischka A, Eggermann K, Record CJ, Dohrn MF, Laššuthová P, Kraft F, Begemann M, Dey D, Eggermann T, Beijer D, Šoukalová J, Laura M, Rossor AM, Mazanec R, Van Lent J, Tomaselli PJ, Ungelenk M, Debus KY, Feely SME, Gläser D, Jagadeesh S, Martin M, Govindaraj GM, Singhi P, Baineni R, Biswal N, Ibarra-Ramírez M, Bonduelle M, Gess B, Romero Sánchez J, Suthar R, Udani V, Nalini A, Unnikrishnan G, Marques W Junior, Mercier S, Procaccio V, Bris C, Suresh B, Reddy V, Skorupinska M, Bonello-Palot N, Mochel F, Dahl G, Sasidharan K, Devassikutty FM, Nampoothiri S, Rodovalho Doriqui MJ, Müller-Felber W, Vill K, Haack TB, Dufke A, Abele M, Stucka R, Siddiqi S, Ullah N, Spranger S, Chiabrando D, Bolgül BS, Parman Y, Seeman P, Lampert A, Schulz JB, Wood JN, Cox JJ, Auer-Grumbach M, Timmerman V, de Winter J, Themistocleous AC, Shy M, Bennett DL, Baets J, Hübner CA, Leipold E, Züchner S, Elbracht M, Çakar A, Senderek J, Hornemann T, Woods CG, Reilly MM, Kurth I. Lischka A, et al. Among authors: gess b. Brain. 2023 Dec 1;146(12):4880-4890. doi: 10.1093/brain/awad328. Brain. 2023. PMID: 37769650 Free PMC article.
[Genetics of neuropathies].
Gess B, Schirmacher A, Young P. Gess B, et al. Nervenarzt. 2013 Feb;84(2):157-65. doi: 10.1007/s00115-012-3640-4. Nervenarzt. 2013. PMID: 23325310 Review. German.
NCAM1 and GDF15 are biomarkers of Charcot-Marie-Tooth disease in patients and mice.
Jennings MJ, Kagiava A, Vendredy L, Spaulding EL, Stavrou M, Hathazi D, Grüneboom A, De Winter V, Gess B, Schara U, Pogoryelova O, Lochmüller H, Borchers CH, Roos A, Burgess RW, Timmerman V, Kleopa KA, Horvath R. Jennings MJ, et al. Among authors: gess b. Brain. 2022 Nov 21;145(11):3999-4015. doi: 10.1093/brain/awac055. Brain. 2022. PMID: 35148379 Free PMC article.
Image-to-Image Translation for Simplified MRI Muscle Segmentation.
Gadermayr M, Heckmann L, Li K, Bähr F, Müller M, Truhn D, Merhof D, Gess B. Gadermayr M, et al. Among authors: gess b. Front Radiol. 2021 Jul 6;1:664444. doi: 10.3389/fradi.2021.664444. eCollection 2021. Front Radiol. 2021. PMID: 37492182 Free PMC article.
Ascorbic acid for the treatment of Charcot-Marie-Tooth disease.
Gess B, Baets J, De Jonghe P, Reilly MM, Pareyson D, Young P. Gess B, et al. Cochrane Database Syst Rev. 2015 Dec 11;2015(12):CD011952. doi: 10.1002/14651858.CD011952. Cochrane Database Syst Rev. 2015. PMID: 26662471 Free PMC article. Review.
CMTX Disorder and CamKinase.
Bihel F, Gess B, Fontés M. Bihel F, et al. Among authors: gess b. Front Cell Neurosci. 2016 Mar 1;10:49. doi: 10.3389/fncel.2016.00049. eCollection 2016. Front Cell Neurosci. 2016. PMID: 26973463 Free PMC article. No abstract available.
Behr syndrome with homozygous C19ORF12 mutation.
Kleffner I, Wessling C, Gess B, Korsukewitz C, Allkemper T, Schirmacher A, Young P, Senderek J, Husstedt IW. Kleffner I, et al. Among authors: gess b. J Neurol Sci. 2015 Oct 15;357(1-2):115-8. doi: 10.1016/j.jns.2015.07.009. Epub 2015 Jul 9. J Neurol Sci. 2015. PMID: 26187298
The Babinski-2 sign in hemifacial spasm.
Pawlowski M, Gess B, Evers S. Pawlowski M, et al. Among authors: gess b. Mov Disord. 2013 Aug;28(9):1298-300. doi: 10.1002/mds.25472. Epub 2013 May 1. Mov Disord. 2013. PMID: 23637014
69 results