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South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|June 4, 2002
Problems in the optimal management of myasthenia gravis patients--a prospective clinical survey at Kalafong HospitalN A Mafojane, P L A Bill, B P LotzJournal of Neurology, Neurosurgery, and Psychiatry|May 1, 1984
Short-latency somatosensory evoked potentials in dystrophia myotonicaP R Bartel, B P Lotz, C H Van der MeydenSleep|October 1, 1993
Recurrent attacks of unconsciousness with diffuse EEG alpha activityB P Lotz, C M Schutte, P R Bartel, et al.Pediatric Neurology|January 1, 1997
Muscle pathology and clinical features of the sarcolemmopathiesR Fadic, A J Waclawik, P J Lewandoski, et al.Muscle & Nerve|January 1, 1995
Expression of heat-shock/stress proteins in Duchenne muscular dystrophyL Bornman, B S Polla, B P Lotz, et al.South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|September 1, 1993
Sneddon's syndrome with anticardiolipin antibodies--complications and treatmentB P Lotz, C M Schutte, P F Colin, et al.Journal of Child Neurology|April 6, 1999
Infantile botulism: pitfalls in electrodiagnosisR D Sheth, B P Lotz, K E Hecox, et al.Brain : a Journal of Neurology|June 1, 1989
Inclusion body myositis. Observations in 40 patientsB P Lotz, A G Engel, H Nishino, et al.Pediatric Neurology|May 1, 1995
Congenital myopathy with ringlike distribution of myonuclei and mitochondria and accumulation of nemaline rods. A variant of centronuclear myopathy?A J Waclawik, T S Edgar, B P Lotz, et al.Neurology|November 1, 1995
Merosin-negative congenital muscular dystrophy associated with extensive brain abnormalitiesY Sunada, T S Edgar, B P Lotz, et al.Pageof 3