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Specific MRI Abnormalities Reveal Severe Perrault Syndrome due to CLPP Defects.
Theunissen TE, Szklarczyk R, Gerards M, Hellebrekers DM, Mulder-Den Hartog EN, Vanoevelen J, Kamps R, de Koning B, Rutledge SL, Schmitt-Mechelke T, van Berkel CG, van der Knaap MS, de Coo IF, Smeets HJ. Theunissen TE, et al. Among authors: rutledge sl. Front Neurol. 2016 Nov 16;7:203. doi: 10.3389/fneur.2016.00203. eCollection 2016. Front Neurol. 2016. PMID: 27899912 Free PMC article.
SPECT abnormalities in generalized dystonia.
LeDoux MS, Rutledge SL, Mountz JM, Darji JT. LeDoux MS, et al. Among authors: rutledge sl. Pediatr Neurol. 1995 Jul;13(1):5-10. doi: 10.1016/0887-8994(95)00109-s. Pediatr Neurol. 1995. PMID: 7575848
Chiari I malformation and neurofibromatosis type 1.
Tubbs RS, Rutledge SL, Kosentka A, Bartolucci AA, Oakes WJ. Tubbs RS, et al. Among authors: rutledge sl. Pediatr Neurol. 2004 Apr;30(4):278-80. doi: 10.1016/j.pediatrneurol.2003.09.013. Pediatr Neurol. 2004. PMID: 15087107
Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome.
Bainbridge MN, Mazumder A, Ogasawara D, Abou Jamra R, Bernard G, Bertini E, Burglen L, Cope H, Crawford A, Derksen A, Dure L, Gantz E, Koch-Hogrebe M, Hurst ACE, Mahida S, Marshall P, Micalizzi A, Novelli A, Peng H; Rady Children's Institute for Genomic Medicine; Rodriguez D, Robbins SL, Rutledge SL, Scalise R, Schließke S, Shashi V, Srivastava S, Thiffault I, Topol S; Undiagnosed Disease Network; Qebibo L, Wieczorek D, Cravatt B, Haricharan S, Torkamani A, Friedman J. Bainbridge MN, et al. Among authors: rutledge sl. Brain. 2022 Oct 21;145(10):3383-3390. doi: 10.1093/brain/awac223. Brain. 2022. PMID: 35737950 Free PMC article.
37 results