Below are the most recent publications written about "Movement Disorders" by people in Profiles.
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Harvey HB, Watson LC, Subramaniam RM, Burns J, Bykowski J, Chakraborty S, Ledbetter LN, Lee RK, Pannell JS, Pollock JM, Powers WJ, Rosenow JM, Shih RY, Slavin K, Utukuri PS, Corey AS. ACR Appropriateness Criteria? Movement Disorders and Neurodegenerative Diseases. J Am Coll Radiol. 2020 May; 17(5S):S175-S187.
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Valentino WL, Park J, Alnouri G, Gracely EJ, Tami A, Vance D, Palmer J, Sataloff RT. Diagnostic Value of Acoustic and Aerodynamic Measurements in Vocal Fold Movement Disorders and their Correlation with Laryngeal Electromyography and Voice Handicap Index. J Voice. 2021 May; 35(3):497.e1-497.e4.
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Therrien AS, Bastian AJ. The cerebellum as a movement sensor. Neurosci Lett. 2019 01 01; 688:37-40.
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Zou F, McWalter K, Schmidt L, Decker A, Picker JD, Lincoln S, Sweetser DA, Briere LC, Harini C, Marsh E, Medne L, Wang RY, Leydiker K, Mower A, Visser G, Cuppen I, van Gassen KL, van der Smagt J, Yousaf A, Tennison M, Shanmugham A, Butler E, Richard G, McKnight D. Expanding the phenotypic spectrum of GABRG2 variants: a recurrent GABRG2 missense variant associated with a severe phenotype. J Neurogenet. 2017 Mar - Jun; 31(1-2):30-36.
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Thickbroom GW, Cortes M, Rykman A, Volpe BT, Fregni F, Krebs HI, Pascual-Leone A, Edwards DJ. Stroke subtype and motor impairment influence contralesional excitability. Neurology. 2015 Aug 11; 85(6):517-20.
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Therrien AS, Bastian AJ. Cerebellar damage impairs internal predictions for sensory and motor function. Curr Opin Neurobiol. 2015 Aug; 33:127-33.
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Spinelli BA, Wattananon P, Silfies S, Talaty M, Ebaugh D. Using kinematics and a dynamical systems approach to enhance understanding of clinically observed aberrant movement patterns. Man Ther. 2015 Feb; 20(1):221-6.
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Enns GM, Shashi V, Bainbridge M, Gambello MJ, Zahir FR, Bast T, Crimian R, Schoch K, Platt J, Cox R, Bernstein JA, Scavina M, Walter RS, Bibb A, Jones M, Hegde M, Graham BH, Need AC, Oviedo A, Schaaf CP, Boyle S, Butte AJ, Chen R, Chen R, Clark MJ, Haraksingh R, Cowan TM, He P, Langlois S, Zoghbi HY, Snyder M, Gibbs RA, Freeze HH, Goldstein DB. Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathway. Genet Med. 2014 Oct; 16(10):751-8.
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Peeraully T, Hameed S, Cheong PT, Pavanni R, Hussein K, Fook-Chong SM, Tan EK. Complementary therapies in hemifacial spasm and comparison with other movement disorders. Int J Clin Pract. 2013 Aug; 67(8):801-6.
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Milla SS, Coley BD, Karmazyn B, Dempsey-Robertson ME, Dillman JR, Dory CE, Garber M, Hayes LL, Keller MS, Meyer JS, Paidas C, Raske ME, Rigsby CK, Spottswood S, Strouse PJ, Widmann RF, Wootton-Gorges SL. ACR Appropriateness Criteria? limping child--ages 0 to 5 years. J Am Coll Radiol. 2012 Aug; 9(8):545-53.