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| Office
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Mailing
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6140 MRB III
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465 21st Avenue, South, 6140 MRB III 6140 MRB III 37232-8552
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| Research
Keywords |
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Movement Disorders, Hereditary Spastic Paraplegia, Epilepsy |
| Research
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Hereditary Spastic Paraplegia/Epilepsy |
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Blair, MA, Ma, S, Abou-Khalil, B, Hedera, P. Genetic variants in the IMPA2 gene do not confer increased risk of febrile
seizures in Caucasian patients. Eur J Neurol, 14(4), 424-7, 2007 Hedera, P, Blair, MA, Andermann, E, Andermann, F, D''Agostino, D, Taylor, KA, Chahine, L, Pandolfo, M, Bradford, Y, Haines, JL, Abou-Khalil, B. Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3. Neurology, , , 2007 Abou-Khalil, B, Krei, L, Lazenby, B, Harris, PA, Haines, JL, Hedera, P. Familial genetic predisposition, epilepsy localization and antecedent febrile
seizures. Epilepsy Res, , , 2006 Blair, MA, Ma, S, Hedera, P. Mutation in KIF5A can also cause adult-onset hereditary spastic paraplegia. Neurogenetics, 7(1), 47-50, 2006 Hedera, P, Ma, S, Blair, MA, Taylor, KA, Hamati, A, Bradford, Y, Abou-Khalil, B, Haines, JL. Identification of a novel locus for febrile seizures and epilepsy on chromosome
21q22. Epilepsia, 47(10), 1622-8, 2006 Ma, S, Abou-Khalil, B, Blair, MA, Sutcliffe, JS, Haines, JL, Hedera, P. Mutations in GABRA1, GABRA5, GABRG2 and GABRD receptor genes are not a major
factor in the pathogenesis of familial focal epilepsy preceded by febrile seizures. Neurosci Lett, 394(1), 74-8, 2006 Ma, S, Blair, MA, Abou-Khalil, B, Lagrange, AH, Gurnett, CA, Hedera, P. Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic
epilepsy. Epilepsy Res, 71(2-3), 129-34, 2006 Ma, S, Davis, TL, Blair, MA, Fang, JY, Bradford, Y, Haines, JL, Hedera, P. Familial essential tremor with apparent autosomal dominant inheritance: should
we also consider other inheritance modes. Mov Disord, 21(9), 1368-74, 2006 Ma, S, Abou-Khalil, B, Sutcliffe, JS, Haines, JL, Hedera, P. The GABBR1 locus and the G1465A variant is not associated with temporal lobe
epilepsy preceded by febrile seizures. BMC Med Genet, 6, 13, 2005 PMCID:1079842 Hedera, P, Abou-Khalil, B, Crunk, AE, Taylor, KA, Haines, JL, Sutcliffe, JS. Autosomal dominant lateral temporal epilepsy: two families with novel mutations
in the LGI1 gene. Epilepsia, 45(3), 218-22, 2004 Hedera, P, Fenichel, GM, Blair, M, Haines, JL. Novel mutation in the SPG3A gene in an African American family with an early
onset of hereditary spastic paraplegia. Arch Neurol, 61(10), 1600-3, 2004 Brewer, George J, Hedera, Peter, Kluin, Karen J, Carlson, Martha, Askari, Fred, Dick, Robert B, Sitterly, Julia, Fink, John K. Treatment of Wilson disease with ammonium tetrathiomolybdate: III. Initial therapy in a total of 55 neurologically affected patients and follow-up with zinc therapy. Arch Neurol, 60(3), 379-85, 2003 Hedera, Peter, Fink, John K, Bockenstedt, Paula L, Brewer, George J. Myelopolyneuropathy and pancytopenia due to copper deficiency and high zinc levels of unknown origin: further support for existence of a new zinc overload syndrome. Arch Neurol, 60(9), 1303-6, 2003 Hedera, Peter, Gorski, Jerome L. Oculo-facio-cardio-dental syndrome: skewed X chromosome inactivation in mother and daughter suggest X-linked dominant Inheritance. Am J Med Genet, 123A(3), 261-6, 2003 Hedera, Peter, Innis, Jeffrey W. Juberg-Hayward syndrome: report of a new patient with severe phenotype and novel clinical features. Am J Med Genet, 122A(3), 257-60, 2003 Hedera, Peter, Petty, Elizabeth M, Bui, Melanie R, Blaivas, Mila, Fink, John K. The second kindred with autosomal dominant distal myopathy linked to chromosome 14q: genetic and clinical analysis. Arch Neurol, 60(9), 1321-5, 2003 Hedera, P. Ethical principles and pitfalls of genetic testing for dementia. J Geriatr Psychiatry Neurol, 14(4), 213-21, 2002 Hedera, P, Rainier, S, Zhao, X P, Schalling, M, Lindblad, K, Yuan, Q-P, Ikeuchi, T, Trobe, J, Wald, J J, Eldevik, O P, Kluin, K, Fink, J K. Spastic paraplegia, ataxia, mental retardation (SPAR): a novel genetic disorder. Neurology, 58(3), 411-6, 2002 Hedera, P, Toriello, H V, Petty, E M. Novel autosomal dominant mandibulofacial dysostosis with ptosis: clinical description and exclusion of TCOF1. J Med Genet, 39(7), 484-8, 2002 PMCID:1735177 Hedera, Peter, Alvarado, David, Beydoun, Ahmad, Fink, John K. Novel mental retardation-epilepsy syndrome linked to Xp21.1-p11.4. Ann Neurol, 51(1), 45-50, 2002 Hedera, Peter, Brewer, George J, Fink, John K. White matter changes in Wilson disease. Arch Neurol, 59(5), 866-7, 2002 Hedera, Peter, Innis, Jeffrey W. Possible third case of Lin-Gettig syndrome. Am J Med Genet, 110(4), 380-3, 2002 Hedera, Peter, Turner, R Scott. Inherited dementias. Neurol Clin, 20(3), 779-808, vii, 2002 Hedera, P, Gorski, J L. Retinitis pigmentosa, growth hormone deficiency, and acromelic skeletal dysplasia in two brothers: possible familial RHYNS syndrome. Am J Med Genet, 101(2), 142-5, 2001 Hedera, P, Williamson, J A, Rainier, S, Alvarado, D, Tukel, T, Apak, M, Fink, J K. Prenatal diagnosis of hereditary spastic paraplegia. Prenat Diagn, 21(3), 202-6, 2001 Rainier, S, Hedera, P, Alvarado, D, Zhao, X, Kleopa, K A, Heiman-Patterson, T, Fink, J K. Hereditary spastic paraplegia linked to chromosome 14q11-q21: reduction of the SPG3 locus interval from 5.3 to 2.7 cM. J Med Genet, 38(11), E39, 2001 PMCID:1734767 Zhao, X, Alvarado, D, Rainier, S, Lemons, R, Hedera, P, Weber, C H, Tukel, T, Apak, M, Heiman-Patterson, T, Ming, L, Bui, M, Fink, J K. Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia. Nat Genet, 29(3), 326-31, 2001 Brewer, G J, Johnson, V D, Dick, R D, Hedera, P, Fink, J K, Kluin, K J. Treatment of Wilson's disease with zinc. XVII: treatment during pregnancy. Hepatology, 31(2), 364-70, 2000 Hedera, P, DiMauro, S, Bonilla, E, Wald, J J, Fink, J K. Mitochondrial analysis in autosomal dominant hereditary spastic paraplegia. Neurology, 55(10), 1591-2, 2000 Brewer, G J, Fink, J K, Hedera, P. Diagnosis and treatment of Wilson's disease. Semin Neurol, 19(3), 261-70, 1999 Fink, J K, Hedera, P. Hereditary spastic paraplegia: genetic heterogeneity and genotype-phenotype correlation. Semin Neurol, 19(3), 301-9, 1999 Hedera, P, DiMauro, S, Bonilla, E, Wald, J, Eldevik, O P, Fink, J K. Phenotypic analysis of autosomal dominant hereditary spastic paraplegia linked to chromosome 8q. Neurology, 53(1), 44-50, 1999 Hedera, P, Rainier, S, Alvarado, D, Zhao, X, Williamson, J, Otterud, B, Leppert, M, Fink, J K. Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q. Am J Hum Genet, 64(2), 563-9, 1999 PMCID:1377766 Hedera, P, Stanton, M, Flöer, B, Wald, J J. Prolonged coma after continuous sedation with propofol. Eur Neurol, 41(2), 116-7, 1999 Hedera, P, Bujdáková, J, Traubner, P, Pancák, J. Stroke risk factors and development of collateral flow in carotid occlusive disease. Acta Neurol Scand, 98(3), 182-6, 1998 Hedera, P, Wu, D, Collins, S, Lewin, J S, Miller, D, Lerner, A J, Klein, S, Friedland, R P. Sex and electroencephalographic synchronization after photic stimulation predict signal changes in the visual cortex on functional MR images. AJNR Am J Neuroradiol, 19(5), 853-7, 1998 Cohen, D L, Hedera, P, Premkumar, D R, Friedland, R P, Kalaria, R N. Amyloid-beta protein angiopathies masquerading as Alzheimer's disease. Ann N Y Acad Sci, 826, 390-5, 1997 Fink, J K, Hedera, P, Mathay, J G, Albin, R L. Paroxysmal dystonic choreoathetosis linked to chromosome 2q: clinical analysis and proposed pathophysiology. Neurology, 49(1), 177-83, 1997 Friedland, R P, Kalaria, R, Berridge, M, Miraldi, F, Hedera, P, Reno, J, Lyle, L, Marotta, C A. Neuroimaging of vessel amyloid in Alzheimer's disease. Ann N Y Acad Sci, 826, 242-7, 1997 Hedera, P, Friedland, R P. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: study of two American families with predominant dementia. J Neurol Sci, 146(1), 27-33, 1997 Lerner, A J, Hedera, P, Koss, E, Stuckey, J, Friedland, R P. Delirium in Alzheimer disease. Alzheimer Dis Assoc Disord, 11(1), 16-20, 1997 Fink, J K, Rainer, S, Wilkowski, J, Jones, S M, Kume, A, Hedera, P, Albin, R, Mathay, J, Girbach, L, Varvil, T, Otterud, B, Leppert, M. Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q. Am J Hum Genet, 59(1), 140-5, 1996 PMCID:1915128 Hedera, P, Lai, S, Lewin, J S, Haacke, E M, Wu, D, Lerner, A J, Friedland, R P. Assessment of cerebral blood flow reserve using functional magnetic resonance imaging. J Magn Reson Imaging, 6(5), 718-25, 1996 Kalaria, R N, Hedera, P. beta-Amyloid vasoactivity in Alzheimer's disease. Lancet, 347(9013), 1492-3, 1996 Lewin, J S, Friedman, L, Wu, D, Miller, D A, Thompson, L A, Klein, S K, Wise, A L, Hedera, P, Buckley, P, Meltzer, H, Friedland, R P, Duerk, J L. Cortical localization of human sustained attention: detection with functional MR using a visual vigilance paradigm. J Comput Assist Tomogr, 20(5), 695-701, 1996 Premkumar, D R, Cohen, D L, Hedera, P, Friedland, R P, Kalaria, R N. Apolipoprotein E-epsilon4 alleles in cerebral amyloid angiopathy and cerebrovascular pathology associated with Alzheimer's disease. Am J Pathol, 148(6), 2083-95, 1996 PMCID:1861657 Hedera, P. Influence of extreme head rotations on brainstem auditory evoked potentials (BAEP). Clin Neurol Neurosurg, 97(4), 290-5, 1995 Hedera, P, Bujdáková, J, Traubner, P. Effect of collateral flow patterns on outcome of carotid occlusion. Eur Neurol, 35(4), 212-6, 1995 Hedera, P, Lerner, A J, Castellani, R, Friedland, R P. Concurrence of Alzheimer's disease, Parkinson's disease, diffuse Lewy body disease, and amyotrophic lateral sclerosis. J Neurol Sci, 128(2), 219-24, 1995 Hedera, P, Wu, D, Lewin, J S, Miller, D, Lerner, A J, Friedland, R P. Temporal patterns of uncoupling between oxidative metabolism and regional cerebral blood flow demonstrated by functional magnetic resonance imaging. Invest Radiol, 30(11), 625-33, 1995 Kalaria, R N, Hedera, P. Differential degeneration of the cerebral microvasculature in Alzheimer's disease. Neuroreport, 6(3), 477-80, 1995 Haacke, E M, Hopkins, A, Lai, S, Buckley, P, Friedman, L, Meltzer, H, Hedera, P, Friedland, R, Klein, S, Thompson, L. 2D and 3D high resolution gradient echo functional imaging of the brain: venous contributions to signal in motor cortex studies. NMR Biomed, 7(1-2), 54-62, 1994 Hedera, P, Bujdáková, J, Traubner, P. Compressions of carotid and vertebral arteries in assessment of intracranial collateral flow: correlation between angiography and transcranial Doppler ultrasonography. Angiology, 45(12), 1039-45, 1994 Hedera, P, Lai, S, Haacke, E M, Lerner, A J, Hopkins, A L, Lewin, J S, Friedland, R P. Abnormal connectivity of the visual pathways in human albinos demonstrated by susceptibility-sensitized MRI. Neurology, 44(10), 1921-6, 1994 Lerner, A J, Koss, E, Patterson, M B, Ownby, R L, Hedera, P, Friedland, R P, Whitehouse, P J. Concomitants of visual hallucinations in Alzheimer's disease. Neurology, 44(3 Pt 1), 523-7, 1994 Friedland, R P, Koss, E, Lerner, A, Hedera, P, Ellis, W, Dronkers, N, Ober, B A, Jagust, W J. Functional imaging, the frontal lobes, and dementia. Dementia, 4(3-4), 192-203, 1993 Friedland, R P, Lerner, A J, Hedera, P, Brass, E P. Encephalopathy associated with bismuth subgallate therapy. Clin Neuropharmacol, 16(2), 173-6, 1993 Hedera, P, Bujdáková, J, Traubner, P. Blood flow velocities in basilar artery during rotation of the head. Acta Neurol Scand, 88(3), 229-33, 1993 Hedera, P, Friedland, R P. Duane's syndrome with giant aneurysm of the vertebral basilar arterial junction. J Clin Neuroophthalmol, 13(4), 271-4, 1993 Lai, S, Hopkins, A L, Haacke, E M, Li, D, Wasserman, B A, Buckley, P, Friedman, L, Meltzer, H, Hedera, P, Friedland, R. 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 1.5T: preliminary results. Magn Reson Med, 30(3), 387-92, 1993 Hedera, P, Traubner, P, Bujdáková, J. Short-term prognosis of stroke due to occlusion of internal carotid artery based on transcranial Doppler ultrasonography. Stroke, 23(8), 1069-72, 1992 |
| Postdoctoral
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N/A |
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