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464 results
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Cramps and small-fiber neuropathy.
Lopate G, Streif E, Harms M, Weihl C, Pestronk A. Lopate G, et al. Among authors: harms m. Muscle Nerve. 2013 Aug;48(2):252-5. doi: 10.1002/mus.23757. Epub 2013 Jun 28. Muscle Nerve. 2013. PMID: 23813593
Multifocal radiculoneuropathy during ipilimumab treatment of melanoma.
Manousakis G, Koch J, Sommerville RB, El-Dokla A, Harms MB, Al-Lozi MT, Schmidt RE, Pestronk A. Manousakis G, et al. Muscle Nerve. 2013 Sep;48(3):440-4. doi: 10.1002/mus.23830. Epub 2013 Jul 27. Muscle Nerve. 2013. PMID: 23447136
Ultrasound of inherited vs. acquired demyelinating polyneuropathies.
Zaidman CM, Harms MB, Pestronk A. Zaidman CM, et al. Among authors: harms mb. J Neurol. 2013 Dec;260(12):3115-21. doi: 10.1007/s00415-013-7123-8. Epub 2013 Oct 8. J Neurol. 2013. PMID: 24101129 Free PMC article.
Pre-morbid type 2 diabetes mellitus is not a prognostic factor in amyotrophic lateral sclerosis.
Paganoni S, Hyman T, Shui A, Allred P, Harms M, Liu J, Maragakis N, Schoenfeld D, Yu H, Atassi N, Cudkowicz M, Miller TM. Paganoni S, et al. Among authors: harms m. Muscle Nerve. 2015 Sep;52(3):339-43. doi: 10.1002/mus.24688. Epub 2015 Jun 1. Muscle Nerve. 2015. PMID: 25900666 Free PMC article.
Neuromuscular Emergencies.
Bucelli R, Harms MB. Bucelli R, et al. Semin Neurol. 2015 Dec;35(6):683-9. doi: 10.1055/s-0035-1564303. Epub 2015 Nov 23. Semin Neurol. 2015. PMID: 26595869 Review.
Dominant spinal muscular atrophy with lower extremity predominance: linkage to 14q32.
Harms MB, Allred P, Gardner R Jr, Fernandes Filho JA, Florence J, Pestronk A, Al-Lozi M, Baloh RH. Harms MB, et al. Neurology. 2010 Aug 10;75(6):539-46. doi: 10.1212/WNL.0b013e3181ec800c. Neurology. 2010. PMID: 20697106 Free PMC article.
Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes.
Cady J, Allred P, Bali T, Pestronk A, Goate A, Miller TM, Mitra RD, Ravits J, Harms MB, Baloh RH. Cady J, et al. Among authors: harms mb. Ann Neurol. 2015 Jan;77(1):100-13. doi: 10.1002/ana.24306. Epub 2014 Nov 27. Ann Neurol. 2015. PMID: 25382069 Free PMC article.
Novel mutations expand the clinical spectrum of DYNC1H1-associated spinal muscular atrophy.
Scoto M, Rossor AM, Harms MB, Cirak S, Calissano M, Robb S, Manzur AY, Martínez Arroyo A, Rodriguez Sanz A, Mansour S, Fallon P, Hadjikoumi I, Klein A, Yang M, De Visser M, Overweg-Plandsoen WC, Baas F, Taylor JP, Benatar M, Connolly AM, Al-Lozi MT, Nixon J, de Goede CG, Foley AR, Mcwilliam C, Pitt M, Sewry C, Phadke R, Hafezparast M, Chong WK, Mercuri E, Baloh RH, Reilly MM, Muntoni F. Scoto M, et al. Among authors: harms mb. Neurology. 2015 Feb 17;84(7):668-79. doi: 10.1212/WNL.0000000000001269. Epub 2015 Jan 21. Neurology. 2015. PMID: 25609763 Free PMC article.
MORC2 mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signs.
Albulym OM, Kennerson ML, Harms MB, Drew AP, Siddell AH, Auer-Grumbach M, Pestronk A, Connolly A, Baloh RH, Zuchner S, Reddel SW, Nicholson GA. Albulym OM, et al. Among authors: harms mb. Ann Neurol. 2016 Mar;79(3):419-27. doi: 10.1002/ana.24575. Epub 2016 Jan 13. Ann Neurol. 2016. PMID: 26659848 Free PMC article.
C9orf72 is required for proper macrophage and microglial function in mice.
O'Rourke JG, Bogdanik L, Yáñez A, Lall D, Wolf AJ, Muhammad AK, Ho R, Carmona S, Vit JP, Zarrow J, Kim KJ, Bell S, Harms MB, Miller TM, Dangler CA, Underhill DM, Goodridge HS, Lutz CM, Baloh RH. O'Rourke JG, et al. Among authors: harms mb. Science. 2016 Mar 18;351(6279):1324-9. doi: 10.1126/science.aaf1064. Science. 2016. PMID: 26989253 Free PMC article.
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