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289 results

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Page 1
Cardiorespiratory Progression Over 5 Years and Role of Corticosteroids in Duchenne Muscular Dystrophy: A Single-Site Retrospective Longitudinal Study.
Trucco F, Domingos JP, Tay CG, Ridout D, Maresh K, Munot P, Sarkozy A, Robb S, Quinlivan R, Riley M, Burch M, Fenton M, Wallis C, Chan E, Abel F, Manzur AY, Muntoni F. Trucco F, et al. Among authors: robb s. Chest. 2020 Oct;158(4):1606-1616. doi: 10.1016/j.chest.2020.04.043. Epub 2020 May 7. Chest. 2020. PMID: 32387519
Infantile axonal neuropathy in two siblings.
Quinlivan RM, Robb SA, Hall SM, Honavar M, Hughes RA, Dubowitz V. Quinlivan RM, et al. Among authors: robb sa. Neuromuscul Disord. 1994 May;4(3):227-32. doi: 10.1016/0960-8966(94)90023-x. Neuromuscul Disord. 1994. PMID: 7919970
Bladder dysfunction in Duchenne muscular dystrophy.
MacLeod M, Kelly R, Robb SA, Borzyskowski M. MacLeod M, et al. Among authors: robb sa. Arch Dis Child. 2003 Apr;88(4):347-9. doi: 10.1136/adc.88.4.347. Arch Dis Child. 2003. PMID: 12651768 Free PMC article.
Analysis of an adult Duchenne muscular dystrophy population.
Parker AE, Robb SA, Chambers J, Davidson AC, Evans K, O'Dowd J, Williams AJ, Howard RS. Parker AE, et al. Among authors: robb sa. QJM. 2005 Oct;98(10):729-36. doi: 10.1093/qjmed/hci113. Epub 2005 Aug 31. QJM. 2005. PMID: 16135534
Backache in a Duchenne boy.
Kinali M, Robinson R, Manzur AY, Burren CP, Robb SA. Kinali M, et al. Among authors: robb sa. Neuromuscul Disord. 2007 Apr;17(4):346-8. doi: 10.1016/j.nmd.2007.01.008. Epub 2007 Mar 6. Neuromuscul Disord. 2007. PMID: 17339110 No abstract available.
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies.
Zhou H, Jungbluth H, Sewry CA, Feng L, Bertini E, Bushby K, Straub V, Roper H, Rose MR, Brockington M, Kinali M, Manzur A, Robb S, Appleton R, Messina S, D'Amico A, Quinlivan R, Swash M, Müller CR, Brown S, Treves S, Muntoni F. Zhou H, et al. Among authors: robb s. Brain. 2007 Aug;130(Pt 8):2024-36. doi: 10.1093/brain/awm096. Epub 2007 May 4. Brain. 2007. PMID: 17483490 Free article.
Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan.
Godfrey C, Clement E, Mein R, Brockington M, Smith J, Talim B, Straub V, Robb S, Quinlivan R, Feng L, Jimenez-Mallebrera C, Mercuri E, Manzur AY, Kinali M, Torelli S, Brown SC, Sewry CA, Bushby K, Topaloglu H, North K, Abbs S, Muntoni F. Godfrey C, et al. Among authors: robb s. Brain. 2007 Oct;130(Pt 10):2725-35. doi: 10.1093/brain/awm212. Epub 2007 Sep 18. Brain. 2007. PMID: 17878207
289 results