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Showing articles 0 to 6 of 6 Filter Applied: neuroaxonal dystrophy,infantile (Click to remove) Neuroaxonal Dystrophy Due to Lysosomal a-N-Acetylgalactosaminidase Deficiency NEJM 320:1735-1740, Schindler,D.,et al, 1989 Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria Neurol 52:1472-1478, Nardocci,N.,et al, 1999 Diagnosis of Infatile Neuroaxonal Dystrophy by Skin Biopsy Ann Neurol 7:377-379, Wisniewski,K.,et al, 1980 Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features Ann Neurol 3:419, Dorfman,L.J.,et al, 1978 Examination of Dental Pulp to Diagnose Infantile Neuroaxonal Dystrophy Arch Neurol 39:422-423, Carlo,J.,et al, 1982 T2* and FSE MRI Distinguishes Four Subtypes of Neurodegeneration With Brain Iron Accumulation Neurol 70:1614-1619, McNeill,A.,et al, 2008 Showing articles 0 to 6 of 6