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Showing articles 0 to 8 of 8 Filter Applied: chromosome 17 (Click to remove) Hydrocephalus in Patients with Neurofibromatosis Type 1: MR Imaging Findings and the Outcome of Endoscopic Third Ventriculostomy AJNR 32:643-46, Dincer, A.,et al, 2011 Von Recklinghausen's Neurofibromatosis: Neurofibromatosis Type 1 Lancet 361:1552-1554, Reynolds,R.M., et al, 2003 Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients Neurol 52:1345-1352,1307, Van Domburg,P.H.M.F.,et al, 1999 Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families Ann Neurol 41:150-159, Heutnik,P.,et al, 1997 Mapping of Hereditary Neuralgic Amyotrophy (Familial Brachial Plexus Neuropathy) to Distal Chromosome 17q Neurol 46:1128-1132, Pellegrino,J.E.,et al, 1996 Phenotypic Heterogen in Hered Neurop with Liability to Press Palsies Assoc with Chromosome 17p11. 2-12 Delet Neurol 46:1133-1137, Pareyson,D.,et al, 1996 Hered Neuralgic Amyotrophy & Hered Neuropathy with Liability to Pressure Palsies:Distinct Clin, Electrophy & Genetic Entities Neurol 44:2250-2252, Gouider,R.,et al, 1994 Hereditary Neuralgic Amyotrophy & Hereditary Neuropathy with Liability to Pressure Palsies:Distinct Genetic Dis Neurol 44:2253-2257, Chance,P.F.,et al, 1994 Showing articles 0 to 8 of 8