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Plos One|September 13, 2018
Adding insult to injury: Ship groundings are associated with coral disease in a pristine reefL J Raymundo, W Y Licuanan, A M KerrJournal of Medical Genetics|November 1, 1988
Palmoplantar keratoderma, nail dystrophy, and hereditary motor and sensory neuropathy: an autosomal dominant traitJ L Tolmie, D E Wilcox, R McWilliam, et al.American Journal of Medical Genetics|July 1, 1987
Microcephaly: genetic counselling and antenatal diagnosis after the birth of an affected childJ L Tolmie, M McNay, J B Stephenson, et al.Journal of Medical Genetics|January 1, 1989
Genetic aspects of tuberous sclerosis in the west of ScotlandJ R Sampson, S J Scahill, J B Stephenson, et al.Australian Paediatric Journal|February 1, 1986
Biotin-reversible neurodegenerative disease in infancyL C Low, J B Stephenson, K Bartlett, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 13, 2000
Abnormalities in urinary pterin levels in Rett syndromeS Messahel, A E Pheasant, H Pall, et al.Neuromuscular Disorders : NMD|July 10, 1999
Muscle ultrasound in the assessment of suspected neuromuscular disease in childhoodS M Zuberi, N Matta, S Nawaz, et al.Developmental Medicine and Child Neurology|April 1, 1996
X-linked hydrocephalus masquerading as spina bifida and destructive porencephaly in successive generations in one familyC M Brewer, B J Fredericks, J M Pont, et al.Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1996
Familial hemiplegic migraine in the west of Scotland: a clinical and genetic study of seven familiesM A Ahmed, E Reid, A Cooke, et al.Archives of Disease in Childhood|January 6, 1999
Hyperammonaemic encephalopathy after a subureteric injection for vesicoureteric refluxS M Zuberi, J B Stephenson, A F Azmy, et al.Pageof 9