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Archives of Disease in Childhood|October 23, 2002
Fat oxidation defect presenting with overwhelming ketonuriaE Wraige, M P Champion, C Turner, et al.Journal of Neuroimmunology|August 19, 2008
Congenital myasthenic syndromes in childhood: diagnostic and management challengesM Kinali, D Beeson, M C Pitt, et al.Pediatric Neurology|May 18, 1999
Retrospective study of late febrile seizuresD W Webb, R R Jones, A Y Manzur, et al.Neuromuscular Disorders : NMD|November 26, 1998
A severe clinical and pathological variant of central core disease with possible autosomal recessive inheritanceA Y Manzur, C A Sewry, J Ziprin, et al.Neuropediatrics|January 4, 2005
Bone mineral density in a paediatric spinal muscular atrophy populationM Kinali, L M Banks, E Mercuri, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 1, 1997
Arthrogryposis multiplex congenita and bilateral mid-brain infarction following maternal overdose of co-proxamolE F Maalouf, M Battin, S J Counsell, et al.Pediatric Neurology|October 1, 1995
Hydrocephalus, mineralizing angiopathy, hypercholesterolemia, and hyperlipoprotein (a)A Y Manzur, K J Poskitt, M G Norman, et al.Developmental Medicine and Child Neurology|May 17, 2006
Management of scoliosis in Duchenne muscular dystrophy: a large 10-year retrospective studyM Kinali, S Messina, E Mercuri, et al.Pageof 275