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Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan.
Longman C, Brockington M, Torelli S, Jimenez-Mallebrera C, Kennedy C, Khalil N, Feng L, Saran RK, Voit T, Merlini L, Sewry CA, Brown SC, Muntoni F. Longman C, et al. Among authors: kennedy c. Hum Mol Genet. 2003 Nov 1;12(21):2853-61. doi: 10.1093/hmg/ddg307. Epub 2003 Sep 9. Hum Mol Genet. 2003. PMID: 12966029
Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing.
Labrum RW, Rajakulendran S, Graves TD, Eunson LH, Bevan R, Sweeney MG, Hammans SR, Tubridy N, Britton T, Carr LJ, Ostergaard JR, Kennedy CR, Al-Memar A, Kullmann DM, Schorge S, Temple K, Davis MB, Hanna MG. Labrum RW, et al. Among authors: kennedy cr. J Med Genet. 2009 Nov;46(11):786-91. doi: 10.1136/jmg.2009.067967. Epub 2009 Jul 7. J Med Genet. 2009. PMID: 19586927
An inherited dystrophin deletion without muscle weakness.
Collins AL, Leyland KG, Kennedy CR, Robinson D, Spratt HC. Collins AL, et al. Among authors: kennedy cr. J Med Genet. 1994 Jun;31(6):505. doi: 10.1136/jmg.31.6.505. J Med Genet. 1994. PMID: 8071981 Free PMC article. No abstract available.
Short and Long-Term Outcomes of Lung Transplantation from Brain Death vs. Circulatory Death Donors: A Meta-analysis of Comparative Studies.
Spadaccio C, Salsano A, Altarabsheh S, Castro-Varela A, Gallego Navarro C, Juarez Casso F, Abdelrehim A, Andi K, Ribeiro R, Choi K, Knop G, Kennedy CC, Pennington KM, Spencer PJ, Daly R, Villavicencio M, Cypel M, Saddoughi SA. Spadaccio C, et al. Among authors: kennedy cc. J Heart Lung Transplant. 2025 Jan 9:S1053-2498(24)02024-2. doi: 10.1016/j.healun.2024.12.010. Online ahead of print. J Heart Lung Transplant. 2025. PMID: 39798936
3,014 results