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Showing articles 0 to 13 of 13 Filter Applied: genetic linkage (Click to remove) Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations Neurol 47:1269-1277, Baser,M.E., 1996 Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease NEJM 360:1729-1739, Hara,K.,et al, 2009 Alexander Disease, Ventricular Garlands and Abnormalities of the Medulla and Spinal Cord Neurol 66:494-498,468, van der Knaap,M.S.,et al, 2006 Linkiage of Locus for Cerebral Cavernous Hemagiomas to Chromosome 7q in 4 Families of Mexican-American Descent Neurol 48:752-757, Polymeropoulos,M.H.,et al, 1997 Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients Lancet 350:1511-1515, 14901997., Joutel,A.,et al, 1997 Hereditary Spastic Paraplegia:Advances in Genetic Research Neurol 46:1507-1514, Fink,J.K.,et al, 1996 Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family Neurol 45:325-331, Fink,J.K.,et al, 1995 Late-Onset Friedreich's Ataxia, Molecular Genetics, Clinical Neurophysiology, and Magnetic Resonance Imaging Arch Neurol 50:803-806, Klockgether,T.,et al, 1993 DNA Diagnosis of Neurofibromatosis 2:Altered Coding Sequence of the Merlin Tumor Suppressor in an Extended Pedigree JAMA 270:2316-2320, MacCollin,M.,et al, 1993 Central Nervous System Lesions in von Hippel-Lindau Syndrome JNNP 55:898-901, Neumann,H.P.H.,et al, 1992 Genetic Susceptibility to Multiple Sclerosis Linked to Myelin Basic Protein Gene Lancet 340:987-991, Tienari,P.J.,et al, 1992 Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis Medicine 70:99-117, Gatti,R.A.,et al, 1991 Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update Ann Int Med 113:39-52, Mulvihill,J.J.,et al, 1990 Showing articles 0 to 13 of 13