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Brain structure in juvenile-onset Huntington disease.
Tereshchenko A, Magnotta V, Epping E, Mathews K, Espe-Pfeifer P, Martin E, Dawson J, Duan W, Nopoulos P. Tereshchenko A, et al. Among authors: mathews k. Neurology. 2019 Apr 23;92(17):e1939-e1947. doi: 10.1212/WNL.0000000000007355. Epub 2019 Apr 10. Neurology. 2019. PMID: 30971481 Free PMC article.
Autosomal recessive cerebellar hypoplasia.
Mathews KD, Afifi AK, Hanson JW. Mathews KD, et al. J Child Neurol. 1989 Jul;4(3):189-94. doi: 10.1177/088307388900400307. J Child Neurol. 1989. PMID: 2768782
Hypertensive encephalopathy in childhood.
Wright RR, Mathews KD. Wright RR, et al. Among authors: mathews kd. J Child Neurol. 1996 May;11(3):193-6. doi: 10.1177/088307389601100305. J Child Neurol. 1996. PMID: 8734020
Urologic and gastrointestinal symptoms in the dystroglycanopathies.
Crockett CD, Bertrand LA, Cooper CS, Rahhal RM, Liu K, Zimmerman MB, Moore SA, Mathews KD. Crockett CD, et al. Among authors: mathews kd. Neurology. 2015 Feb 3;84(5):532-9. doi: 10.1212/WNL.0000000000001213. Epub 2015 Jan 7. Neurology. 2015. PMID: 25568299 Free PMC article. Clinical Trial.
Illness-associated muscle weakness in dystroglycanopathies.
Carlson CR, McGaughey SD, Eskuri JM, Stephan CM, Zimmerman MB, Mathews KD. Carlson CR, et al. Neurology. 2017 Dec 5;89(23):2374-2380. doi: 10.1212/WNL.0000000000004720. Epub 2017 Nov 3. Neurology. 2017. PMID: 29101272 Free PMC article.
Cobblestone Malformation in LAMA2 Congenital Muscular Dystrophy (MDC1A).
Jayakody H, Zarei S, Nguyen H, Dalton J, Chen K, Hudgins L, Day J, Withrow K, Pandya A, Teasley J, Dobyns WB, Mathews KD, Moore SA. Jayakody H, et al. Among authors: mathews kd. J Neuropathol Exp Neurol. 2020 Sep 1;79(9):998-1010. doi: 10.1093/jnen/nlaa062. J Neuropathol Exp Neurol. 2020. PMID: 32827036 Free PMC article.
624 results