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Year Number of Results
2011 1
2012 1
2013 4
2014 2
2016 1
2018 1
2020 1
2024 0

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11 results

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Page 1
Atypical periodic paralysis and myalgia: A novel RYR1 phenotype.
Matthews E, Neuwirth C, Jaffer F, Scalco RS, Fialho D, Parton M, Raja Rayan D, Suetterlin K, Sud R, Spiegel R, Mein R, Houlden H, Schaefer A, Healy E, Palace J, Quinlivan R, Treves S, Holton JL, Jungbluth H, Hanna MG. Matthews E, et al. Neurology. 2018 Jan 30;90(5):e412-e418. doi: 10.1212/WNL.0000000000004894. Epub 2018 Jan 3. Neurology. 2018. PMID: 29298851 Free PMC article.
Double trouble in a patient with myotonia.
Hehir MK, Logigian E, Raja Rayan DL, Ciafaloni E. Hehir MK, et al. BMJ Case Rep. 2013 Feb 14;2013:bcr2012008167. doi: 10.1136/bcr-2012-008167. BMJ Case Rep. 2013. PMID: 23417379 Free PMC article.
Non-dystrophic myotonia: prospective study of objective and patient reported outcomes.
Trivedi JR, Bundy B, Statland J, Salajegheh M, Rayan DR, Venance SL, Wang Y, Fialho D, Matthews E, Cleland J, Gorham N, Herbelin L, Cannon S, Amato A, Griggs RC, Hanna MG, Barohn RJ; CINCH Consortium. Trivedi JR, et al. Brain. 2013 Jul;136(Pt 7):2189-200. doi: 10.1093/brain/awt133. Epub 2013 Jun 13. Brain. 2013. PMID: 23771340 Free PMC article.
Call for participation in the neurogenetics consortium within the Human Variome Project.
Haworth A, Bertram L, Carrera P, Elson JL, Braastad CD, Cox DW, Cruts M, den Dunnen JT, Farrer MJ, Fink JK, Hamed SA, Houlden H, Johnson DR, Nuytemans K, Palau F, Rayan DL, Robinson PN, Salas A, Schüle B, Sweeney MG, Woods MO, Amigo J, Cotton RG, Sobrido MJ. Haworth A, et al. Neurogenetics. 2011 Aug;12(3):169-73. doi: 10.1007/s10048-011-0287-4. Epub 2011 Jun 1. Neurogenetics. 2011. PMID: 21630033
11 results