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Archives of Disease in Childhood. Fetal and Neonatal Edition|May 1, 1995
Aplasia cutis congenita with chromosome 12q abnormalityJ Y Khan, C Moss, H P RoperScandinavian Journal of Medicine & Science in Sports|November 19, 2005
Muscle connective tissue content of endurance-trained and inactive individualsA L Mackey, A E Donnelly, H P RoperArchives of Disease in Childhood|April 1, 1988
Referrals to a regional neonatal intensive care unitH P Roper, M L Chiswick, D G SimsEuropean Journal of Applied Physiology and Occupational Physiology|January 1, 1994
Indices of free-radical-mediated damage following maximum voluntary eccentric and concentric muscular workJ M Saxton, A E Donnelly, H P RoperNephron|May 13, 1998
Variable presentation of primary hyperoxaluria type 1 in 2 patients homozygous for a novel combined deletion and insertion mutation in exon 8 of the AGXT geneC von Schnakenburg, S A Hulton, D V Milford, et al.The British Journal of Dermatology|August 14, 2002
Mild ichthyosis in a 4-year-old boy with multiple sulphatase deficiencyA Loffeld, R G F Gray, S H Green, et al.Postgraduate Medical Journal|July 27, 2001
Mitochondrial cytopathy presenting with focal segmental glomerulosclerosis, hypoparathyroidism, sensorineural deafness, and progressive neurological diseaseR Hameed, F Raafat, P Ramani, et al.Pediatric Hematology and Oncology|January 1, 1986
Nasopharyngeal carcinoma in childrenH P Roper, A Essex-Cater, H B Marsden, et al.Neurology|July 24, 2002
Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with coresH Jungbluth, C R Müller, B Halliger-Keller, et al.Pageof 2