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Page 1
Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis.
Matthews E, Labrum R, Sweeney MG, Sud R, Haworth A, Chinnery PF, Meola G, Schorge S, Kullmann DM, Davis MB, Hanna MG. Matthews E, et al. Among authors: meola g. Neurology. 2009 May 5;72(18):1544-7. doi: 10.1212/01.wnl.0000342387.65477.46. Epub 2008 Dec 31. Neurology. 2009. PMID: 19118277 Free PMC article.
Diagnosis and new treatment in muscle channelopathies.
Meola G, Hanna MG, Fontaine B. Meola G, et al. J Neurol Neurosurg Psychiatry. 2009 Apr;80(4):360-5. doi: 10.1136/jnnp.2008.164046. J Neurol Neurosurg Psychiatry. 2009. PMID: 19289476 Review.
Randomized, placebo-controlled trials of dichlorphenamide in periodic paralysis.
Sansone VA, Burge J, McDermott MP, Smith PC, Herr B, Tawil R, Pandya S, Kissel J, Ciafaloni E, Shieh P, Ralph JW, Amato A, Cannon SC, Trivedi J, Barohn R, Crum B, Mitsumoto H, Pestronk A, Meola G, Conwit R, Hanna MG, Griggs RC; Muscle Study Group. Sansone VA, et al. Among authors: meola g. Neurology. 2016 Apr 12;86(15):1408-1416. doi: 10.1212/WNL.0000000000002416. Epub 2016 Feb 10. Neurology. 2016. PMID: 26865514 Free PMC article. Clinical Trial.
The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C-terminal peptide of the ClC-1 channel.
Altamura C, Lucchiari S, Sahbani D, Ulzi G, Comi GP, D'Ambrosio P, Petillo R, Politano L, Vercelli L, Mongini T, Dotti MT, Cardani R, Meola G, Lo Monaco M, Matthews E, Hanna MG, Carratù MR, Conte D, Imbrici P, Desaphy JF. Altamura C, et al. Among authors: meola g. Hum Mutat. 2018 Sep;39(9):1273-1283. doi: 10.1002/humu.23581. Epub 2018 Jul 4. Hum Mutat. 2018. PMID: 29935101 Free article.
Guidelines on clinical presentation and management of nondystrophic myotonias.
Stunnenberg BC, LoRusso S, Arnold WD, Barohn RJ, Cannon SC, Fontaine B, Griggs RC, Hanna MG, Matthews E, Meola G, Sansone VA, Trivedi JR, van Engelen BGM, Vicart S, Statland JM. Stunnenberg BC, et al. Among authors: meola g. Muscle Nerve. 2020 Oct;62(4):430-444. doi: 10.1002/mus.26887. Epub 2020 May 27. Muscle Nerve. 2020. PMID: 32270509 Free PMC article. Review.
Mexiletine for symptoms and signs of myotonia in nondystrophic myotonia: a randomized controlled trial.
Statland JM, Bundy BN, Wang Y, Rayan DR, Trivedi JR, Sansone VA, Salajegheh MK, Venance SL, Ciafaloni E, Matthews E, Meola G, Herbelin L, Griggs RC, Barohn RJ, Hanna MG; Consortium for Clinical Investigation of Neurologic Channelopathies. Statland JM, et al. Among authors: meola g. JAMA. 2012 Oct 3;308(13):1357-65. doi: 10.1001/jama.2012.12607. JAMA. 2012. PMID: 23032552 Free PMC article. Clinical Trial.
Andersen's syndrome: a distinct periodic paralysis.
Sansone V, Griggs RC, Meola G, Ptácek LJ, Barohn R, Iannaccone S, Bryan W, Baker N, Janas SJ, Scott W, Ririe D, Tawil R. Sansone V, et al. Among authors: meola g. Ann Neurol. 1997 Sep;42(3):305-12. doi: 10.1002/ana.410420306. Ann Neurol. 1997. PMID: 9307251 Free article.
Treatment for periodic paralysis.
Sansone V, Meola G, Links TP, Panzeri M, Rose MR. Sansone V, et al. Among authors: meola g. Cochrane Database Syst Rev. 2008 Jan 23;(1):CD005045. doi: 10.1002/14651858.CD005045.pub2. Cochrane Database Syst Rev. 2008. PMID: 18254068 Free article. Review.
Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4.
Pagliarani S, Lucchiari S, Scarlato M, Redaelli E, Modoni A, Magri F, Fossati B, Previtali SC, Sansone VA, Lecchi M, Lo Monaco M, Meola G, Comi GP. Pagliarani S, et al. Among authors: meola g. Front Neurol. 2020 Apr 29;11:255. doi: 10.3389/fneur.2020.00255. eCollection 2020. Front Neurol. 2020. PMID: 32411069 Free PMC article.
298 results