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Archives of Neurology|July 1, 1981
Loss of strength and functional decline in Duchenne's dystrophyK G Allsop, F A ZiterPhysical Therapy|November 1, 1979
The value of orthoses for patients with Duchenne muscular dystrophyF A Ziter, K G AllsopDevelopmental Medicine and Child Neurology|December 1, 1979
Epidemiology of myelomeningocele in UtahD E Nesbit, F A ZiterArchives of Neurology|July 1, 1977
Three-generation pedigree of a Möbius syndrome variant with chromosome translocationF A Ziter, W C Wiser, A RobinsonThe Journal of Pediatrics|April 1, 1984
Emery-Dreifuss muscular dystrophyR P Dickey, F A Ziter, R A SmithArchives of Neurology|February 1, 1977
Rigid spine syndrome. A type I fiber myopathyA R Seay, F A Ziter, J H PetajanJournal of the Neurological Sciences|December 1, 1979
Abnormal leukocyte electrophoretic mobility in myotonic dystrophyA R Seay, F A Ziter, H R HillThe Journal of Pediatrics|November 1, 1982
The Robin sequence as a consequence of malformation, dysplasia, and neuromuscular syndromesJ C Carey, R M Fineman, F A ZiterElectroencephalography and Clinical Neurophysiology|October 1, 1985
Identification of minimal expression of myotonic dystrophy using electroretinographyD J Creel, A S Crandall, F A ZiterPageof 20