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Page 1
Acute onset spinal muscular atrophy in siblings.
Robb SA, McShane MA, Wilson J, Payan J. Robb SA, et al. Neuropediatrics. 1991 Feb;22(1):45-6. doi: 10.1055/s-2008-1071415. Neuropediatrics. 1991. PMID: 2038428
Prenatal onset spinal muscular atrophy.
MacLeod MJ, Taylor JE, Lunt PW, Mathew CG, Robb SA. MacLeod MJ, et al. Among authors: robb sa. Eur J Paediatr Neurol. 1999;3(2):65-72. doi: 10.1053/ejpn.1999.0184. Eur J Paediatr Neurol. 1999. PMID: 10700541
Rett syndrome: an EEG study in 52 girls.
Robb SA, Harden A, Boyd SG. Robb SA, et al. Neuropediatrics. 1989 Nov;20(4):192-5. doi: 10.1055/s-2008-1071290. Neuropediatrics. 1989. PMID: 2608163
Novel mutations expand the clinical spectrum of DYNC1H1-associated spinal muscular atrophy.
Scoto M, Rossor AM, Harms MB, Cirak S, Calissano M, Robb S, Manzur AY, Martínez Arroyo A, Rodriguez Sanz A, Mansour S, Fallon P, Hadjikoumi I, Klein A, Yang M, De Visser M, Overweg-Plandsoen WC, Baas F, Taylor JP, Benatar M, Connolly AM, Al-Lozi MT, Nixon J, de Goede CG, Foley AR, Mcwilliam C, Pitt M, Sewry C, Phadke R, Hafezparast M, Chong WK, Mercuri E, Baloh RH, Reilly MM, Muntoni F. Scoto M, et al. Neurology. 2015 Feb 17;84(7):668-79. doi: 10.1212/WNL.0000000000001269. Epub 2015 Jan 21. Neurology. 2015. PMID: 25609763 Free PMC article.
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
Interfamilial phenotypic heterogeneity in SMARD1.
Joseph S, Robb SA, Mohammed S, Lillis S, Simonds A, Manzur AY, Walter S, Wraige E. Joseph S, et al. Among authors: robb sa. Neuromuscul Disord. 2009 Mar;19(3):193-5. doi: 10.1016/j.nmd.2008.11.013. Epub 2009 Jan 20. Neuromuscul Disord. 2009. PMID: 19157874
102 results