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Page 1
Phenotype of adult Refsum disease due to a defect in peroxin 7.
Horn MA, van den Brink DM, Wanders RJ, Duran M, Poll-The BT, Tallaksen CM, Stokke OH, Moser H, Skjeldal OH. Horn MA, et al. Neurology. 2007 Feb 27;68(9):698-700. doi: 10.1212/01.wnl.0000255960.01644.39. Neurology. 2007. PMID: 17325280
[Refsum disease--a rare cause of polyneuropathy].
Horn MA, Skjeldal OH. Horn MA, et al. Tidsskr Nor Laegeforen. 2007 Aug 9;127(15):1960. Tidsskr Nor Laegeforen. 2007. PMID: 17700744 Free article. Norwegian. No abstract available.
Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophy.
Nicole S, Chaouch A, Torbergsen T, Bauché S, de Bruyckere E, Fontenille MJ, Horn MA, van Ghelue M, Løseth S, Issop Y, Cox D, Müller JS, Evangelista T, Stålberg E, Ioos C, Barois A, Brochier G, Sternberg D, Fournier E, Hantaï D, Abicht A, Dusl M, Laval SH, Griffin H, Eymard B, Lochmüller H. Nicole S, et al. Among authors: horn ma. Brain. 2014 Sep;137(Pt 9):2429-43. doi: 10.1093/brain/awu160. Epub 2014 Jun 20. Brain. 2014. PMID: 24951643
FEMSEC-thematic issue "Rhizosphere-a One Health concept".
Hartmann A, de Bashan L, Wassermann B, Horn MA, Sessitsch A. Hartmann A, et al. Among authors: horn ma. FEMS Microbiol Ecol. 2024 Oct 25;100(11):fiae136. doi: 10.1093/femsec/fiae136. FEMS Microbiol Ecol. 2024. PMID: 39471462 Free PMC article.
Amyotrophic lateral sclerosis caused by the C9orf72 expansion in Norway - prevalence, ancestry, clinical characteristics and sociodemographic status.
Olsen CG, Malmberg VN, Fahlström M, Alstadhaug KB, Bjørnå IK, Braathen GJ, Bråthen G, Demic N, Hallerstig E, Hogenesch I, Horn MA, Kampman MT, Kleveland G, Ljøstad U, Maniaol A, Morsund ÅH, Nakken O, Schlüter K, Schuler S, Seim E, Flemmen HØ, Tysnes OB, Holmøy T, Høyer H. Olsen CG, et al. Among authors: horn ma. Amyotroph Lateral Scler Frontotemporal Degener. 2024 Sep 24:1-9. doi: 10.1080/21678421.2024.2405118. Online ahead of print. Amyotroph Lateral Scler Frontotemporal Degener. 2024. PMID: 39316038
143 results