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Brain : a Journal of Neurology|June 1, 1995
The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic studyS R Hammans, M G Sweeney, M G Hanna, et al.Journal of the Neurological Sciences|November 1, 1996
Mitochondrial encephalopathy with multiple mitochondrial DNA deletions: a report of two families and two sporadic cases with unusual clinical and neuropathological featuresR M Chalmers, M Brockington, R S Howard, et al.Neuropediatrics|May 1, 1999
Merosin-positive congenital muscular dystrophy: a large inbred familyI Mahjneh, K Bushby, L Anderson, et al.Neurology|March 26, 2003
FKRP gene mutations cause congenital muscular dystrophy, mental retardation, and cerebellar cystsH Topaloglu, M Brockington, Y Yuva, et al.Experimental Cell Research|August 2, 2005
Mutated fukutin-related protein (FKRP) localises as wild type in differentiated muscle cellsN F Dolatshad, M Brockington, S Torelli, et al.Veterinary Oncology (London, England)|February 17, 2025
Comparative oncology in action: vignettes on immunotherapy developmentAmy LeBlanc, Christina N Mazcko, Nicola J Mason, et al.Human Genetics|May 12, 2005
Localisation of merosin-positive congenital muscular dystrophy to chromosome 4p16.3G S Sellick, C Longman, M Brockington, et al.Neurology|May 16, 2002
Collagen VI involvement in Ullrich syndrome: a clinical, genetic, and immunohistochemical studyE Mercuri, Y Yuva, S C Brown, et al.Neuropediatrics|November 9, 2000
Congenital muscular dystrophy with secondary merosin deficiency and normal brain MRI: a novel entity?E Mercuri, C A Sewry, S C Brown, et al.Diabetologia|April 1, 1994
Mitochondrial gene defects in patients with NIDDMJ C Alcolado, A Majid, M Brockington, et al.Pageof 4