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Peter Hedera
Peter Hedera
Verified email at louisville.edu
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Cited by
Cited by
Year
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
4501993
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
4481996
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
4172001
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
3852006
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
2692003
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
2462000
Differential degeneration of the cerebral microvasculature in Alzheimer's disease
RN Kalaria, P Hedera
Neuroreport 6 (3), 477-480, 1995
2431995
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
2352004
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
2062009
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
1941996
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
1901994
Hereditary spastic paraplegia overview
P Hedera
GeneReviews®[Internet], 2021
1702021
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
1522009
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
1501996
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
1451998
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
1422010
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
1412014
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
1241999
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
1202010
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
1192003
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