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Showing articles 0 to 10 of 10 Filter Applied: chromosome 3 (Click to remove) Review of the Neurological Implications of von Hippel-Lindau Disease JAMA Neurol 75:620-627, Dornbos, D.,et al, 2018 Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up AJNR 30:1971-1976, Uggetti,C.,et al, 2009 Neurologic Manifestations of von Hippel-Lindau Disease JAMA 300:1334-1342, Butman,J.A.,et al, 2008 Clinicopath Conf, Von Hippel Lindau Disease, Adrenal Pheochromocytoma, Brain-Stem and Spinal Cord Hemangioblastoma NEJM 355:394-402, Case 23-2006, 2006 A Variant in the HS1-BP3 Gene is Associated with Familial Essential Tremor Neurol 64:417-421, Higgins, J.J., et al, 2005 Variable Presentation of Brugada Syndrome: Lessons from Three Generations with Syncope BMJ 326:1078-1079, Plunkett,A.,et al, 2003 von Hippel-Lindau Disease Lancet 361:2059-2067, Lonser,R.R.,et al, 2003 New Nomenclature and DNA Testing Guidelines for Myotonic Dystrophy Type 1 (DM1) Neurol 54:1218-1221, The International Myotonic Dystrophy Consortium (I, 2000 Getting a Grip on the Myotonic Dystrophies Neurol 52:12-13, Thornton,C.A.&Ashizawa,T., 1999 Linkage of Proximal Myotonic Myopathy to Chromosome 3q Neurol 52:170-171,12, Ricker,K.,et al, 1999 Showing articles 0 to 10 of 10