Apolipoprotein E-epsilon4 alleles in cerebral amyloid angiopathy and cerebrovascular pathology associated with Alzheimer's disease. DR Premkumar, DL Cohen, P Hedera, RP Friedland, RN Kalaria The American journal of pathology 148 (6), 2083, 1996 | 454 | 1996 |
Identification of vascular structures as a major source of signal contrast in high resolution 2D and 3D functional activation imaging of the motor cortex at l. 5T preliminary … S Lai, AL Hopkins, EM Haacke, D Li, BA Wasserman, P Buckley, ... Magnetic Resonance in Medicine 30 (3), 387-392, 1993 | 449 | 1993 |
Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia X Zhao, D Alvarado, S Rainier, R Lemons, P Hedera, CH Weber, T Tukel, ... Nature genetics 29 (3), 326-331, 2001 | 419 | 2001 |
Treatment of Wilson disease with ammonium tetrathiomolybdate: IV. Comparison of tetrathiomolybdate and trientine in a double-blind study of treatment of the neurologic … GJ Brewer, F Askari, MT Lorincz, M Carlson, M Schilsky, KJ Kluin, ... Archives of neurology 63 (4), 521-527, 2006 | 402 | 2006 |
Treatment of Wilson disease with ammonium tetrathiomolybdate: III. Initial therapy in a total of 55 neurologically affected patients and follow-up with zinc therapy GJ Brewer, P Hedera, KJ Kluin, M Carlson, F Askari, RB Dick, J Sitterly, ... Archives of neurology 60 (3), 379-385, 2003 | 276 | 2003 |
Treatment of Wilson’s disease with zinc. XVII: treatment during pregnancy GJ Brewer, VD Johnson, RD Dick, P Hedera, JK Fink, KJ Kluin Hepatology 31 (2), 364-370, 2000 | 255 | 2000 |
Differential degeneration of the cerebral microvasculature in Alzheimer's disease RN Kalaria, P Hedera Neuroreport 6 (3), 477-480, 1995 | 245 | 1995 |
Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1) C Meredith, R Herrmann, C Parry, K Liyanage, DE Dye, HJ Durling, ... The American Journal of Human Genetics 75 (4), 703-708, 2004 | 237 | 2004 |
Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3 J Senderek, SM Garvey, M Krieger, V Guergueltcheva, A Urtizberea, ... The American Journal of Human Genetics 84 (4), 511-518, 2009 | 212 | 2009 |
Cortical localization of human sustained attention: detection with functional MR using a visual vigilance paradigm JS Lewin, L Friedman, D Wu, DA Miller, LA Thompson, SK Klein, AL Wise, ... Journal of computer assisted tomography 20 (5), 695-701, 1996 | 191 | 1996 |
2D and 3D high resolution gradient echo functional imaging of the brain: venous contributions to signal in motor cortex studies EM Haacke, A Hopkins, S Lai, P Buckley, L Friedman, H Meltzer, ... NMR in Biomedicine 7 (1‐2), 54-62, 1994 | 190 | 1994 |
Hereditary spastic paraplegia overview P Hedera | 175 | 2021 |
Myelopolyneuropathy and pancytopenia due to copper deficiency and high zinc levels of unknown origin II. The denture cream is a primary source of excessive zinc P Hedera, A Peltier, JK Fink, S Wilcock, Z London, GJ Brewer Neurotoxicology 30 (6), 996-999, 2009 | 152 | 2009 |
Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q. JK Fink, S Rainer, J Wilkowski, SM Jones, A Kume, P Hedera, R Albin, ... American journal of human genetics 59 (1), 140, 1996 | 149 | 1996 |
Stroke risk factors and development of collateral flow in carotid occlusive disease P Hedera, J Bujdakova, P Traubner, J Pancak Acta neurologica scandinavica 98 (3), 182-186, 1998 | 146 | 1998 |
Subthalamic nucleus deep brain stimulation in early stage Parkinson's disease D Charles, PE Konrad, JS Neimat, AL Molinari, MG Tramontana, ... Parkinsonism & related disorders 20 (7), 731-737, 2014 | 142 | 2014 |
Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations JJ Johnston, JC Sapp, JT Turner, D Amor, S Aftimos, KA Aleck, M Bocian, ... Human mutation 31 (10), 1142-1154, 2010 | 142 | 2010 |
Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q P Hedera, S Rainier, D Alvarado, X Zhao, J Williamson, B Otterud, ... The American Journal of Human Genetics 64 (2), 563-569, 1999 | 125 | 1999 |
Novel THAP1 sequence variants in primary dystonia J Xiao, Y Zhao, RW Bastian, JS Perlmutter, BA Racette, SD Tabbal, ... Neurology 74 (3), 229-238, 2010 | 121 | 2010 |
Myelopolyneuropathy and pancytopenia due to copper deficiency and high zinc levels of unknown origin: further support for existence of a new zinc overload syndrome P Hedera, JK Fink, PL Bockenstedt, GJ Brewer Archives of Neurology 60 (9), 1303-1306, 2003 | 121 | 2003 |