| Year |
Citation |
Score |
| 2019 |
Downs AM, Roman KM, Campbell SA, Pisani A, Hess EJ, Bonsi P. The neurobiological basis for novel experimental therapeutics in dystonia. Neurobiology of Disease. 104526. PMID 31279827 DOI: 10.1016/J.Nbd.2019.104526 |
0.346 |
|
| 2019 |
Downs AM, Fan X, Donsante C, Jinnah HA, Hess EJ. Trihexyphenidyl rescues the deficit in dopamine neurotransmission in a mouse model of DYT1 dystonia. Neurobiology of Disease. PMID 30707939 DOI: 10.1016/J.Nbd.2019.01.012 |
0.391 |
|
| 2018 |
Tara E, Vitenzon A, Hess E, Khodakhah K. Aberrant cerebellar Purkinje cell activity as the cause of motor attacks in a mouse model of episodic ataxia type 2. Disease Models & Mechanisms. 11. PMID 30279196 DOI: 10.1242/Dmm.034181 |
0.372 |
|
| 2018 |
Yalcin-Cakmakli G, Rose SJ, Villalba RM, Williams L, Jinnah HA, Hess EJ, Smith Y. Striatal Cholinergic Interneurons in a Knock-in Mouse Model of L-DOPA-Responsive Dystonia. Frontiers in Systems Neuroscience. 12: 28. PMID 29997483 DOI: 10.3389/Fnsys.2018.00028 |
0.421 |
|
| 2018 |
Fan X, Donsante Y, Jinnah HA, Hess EJ. Dopamine receptor agonist treatment for idiopathic dystonia: A reappraisal in humans and mice. The Journal of Pharmacology and Experimental Therapeutics. PMID 29348266 DOI: 10.1124/Jpet.117.246348 |
0.329 |
|
| 2017 |
Rose SJ, Harrast P, Donsante C, Fan X, Joers V, Tansey MG, Jinnah HA, Hess EJ. Parkinsonism without dopamine neuron degeneration in aged l-dopa-responsive dystonia knockin mice. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 28949038 DOI: 10.1002/Mds.27169 |
0.307 |
|
| 2016 |
Shakkottai VG, Batla A, Bhatia K, Dauer WT, Dresel C, Niethammer M, Eidelberg D, Raike RS, Smith Y, Jinnah HA, Hess EJ, Meunier S, Hallett M, Fremont R, Khodakhah K, et al. Current Opinions and Areas of Consensus on the Role of the Cerebellum in Dystonia. Cerebellum (London, England). PMID 27734238 DOI: 10.1007/S12311-016-0825-6 |
0.345 |
|
| 2015 |
Rose SJ, Yu XY, Heinzer AK, Harrast P, Fan X, Raike RS, Thompson VB, Pare JF, Weinshenker D, Smith Y, Jinnah HA, Hess EJ. A new knock-in mouse model of l-DOPA-responsive dystonia. Brain : a Journal of Neurology. 138: 2987-3002. PMID 26220941 DOI: 10.1093/Brain/Awv212 |
0.392 |
|
| 2015 |
Raike RS, Hess EJ, Jinnah HA. Dystonia and cerebellar degeneration in the leaner mouse mutant. Brain Research. 1611: 56-64. PMID 25791619 DOI: 10.1016/J.Brainres.2015.03.011 |
0.366 |
|
| 2014 |
Rose SJ, Kriener LH, Heinzer AK, Fan X, Raike RS, van den Maagdenberg AM, Hess EJ. The first knockin mouse model of episodic ataxia type 2. Experimental Neurology. 261: 553-62. PMID 25109669 DOI: 10.1016/J.Expneurol.2014.08.001 |
0.409 |
|
| 2014 |
Lohr KM, Bernstein AI, Stout KA, Dunn AR, Lazo CR, Alter SP, Wang M, Li Y, Fan X, Hess EJ, Yi H, Vecchio LM, Goldstein DS, Guillot TS, Salahpour A, et al. Increased vesicular monoamine transporter enhances dopamine release and opposes Parkinson disease-related neurodegeneration in vivo. Proceedings of the National Academy of Sciences of the United States of America. 111: 9977-82. PMID 24979780 DOI: 10.1073/Pnas.1402134111 |
0.35 |
|
| 2014 |
Prudente CN, Hess EJ, Jinnah HA. Dystonia as a network disorder: what is the role of the cerebellum? Neuroscience. 260: 23-35. PMID 24333801 DOI: 10.1016/J.Neuroscience.2013.11.062 |
0.335 |
|
| 2014 |
Song CH, Bernhard D, Hess EJ, Jinnah HA. Subtle microstructural changes of the cerebellum in a knock-in mouse model of DYT1 dystonia. Neurobiology of Disease. 62: 372-80. PMID 24121114 DOI: 10.1016/J.Nbd.2013.10.003 |
0.422 |
|
| 2013 |
Wilson BK, Hess EJ. Animal models for dystonia. Movement Disorders : Official Journal of the Movement Disorder Society. 28: 982-9. PMID 23893454 DOI: 10.1002/Mds.25526 |
0.383 |
|
| 2013 |
Song CH, Bernhard D, Bolarinwa C, Hess EJ, Smith Y, Jinnah HA. Subtle microstructural changes of the striatum in a DYT1 knock-in mouse model of dystonia. Neurobiology of Disease. 54: 362-71. PMID 23336980 DOI: 10.1016/J.Nbd.2013.01.008 |
0.388 |
|
| 2013 |
Raike RS, Weisz C, Hoebeek FE, Terzi MC, De Zeeuw CI, van den Maagdenberg AM, Jinnah HA, Hess EJ. Stress, caffeine and ethanol trigger transient neurological dysfunction through shared mechanisms in a mouse calcium channelopathy. Neurobiology of Disease. 50: 151-9. PMID 23009754 DOI: 10.1016/J.Nbd.2012.09.005 |
0.343 |
|
| 2013 |
Raike RS, Pizoli CE, Weisz C, van den Maagdenberg AM, Jinnah HA, Hess EJ. Limited regional cerebellar dysfunction induces focal dystonia in mice. Neurobiology of Disease. 49: 200-10. PMID 22850483 DOI: 10.1016/J.Nbd.2012.07.019 |
0.727 |
|
| 2012 |
Song CH, Fan X, Exeter CJ, Hess EJ, Jinnah HA. Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia. Neurobiology of Disease. 48: 66-78. PMID 22659308 DOI: 10.1016/J.Nbd.2012.05.009 |
0.404 |
|
| 2012 |
Lee HY, Nakayama J, Xu Y, Fan X, Karouani M, Shen Y, Pothos EN, Hess EJ, Fu YH, Edwards RH, Ptácek LJ. Dopamine dysregulation in a mouse model of paroxysmal nonkinesigenic dyskinesia. The Journal of Clinical Investigation. 122: 507-18. PMID 22214848 DOI: 10.1172/Jci58470 |
0.389 |
|
| 2012 |
Fan X, Hughes KE, Jinnah HA, Hess EJ. Selective and sustained α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor activation in cerebellum induces dystonia in mice. The Journal of Pharmacology and Experimental Therapeutics. 340: 733-41. PMID 22171094 DOI: 10.1124/Jpet.111.190082 |
0.349 |
|
| 2012 |
Todorov B, Kros L, Shyti R, Plak P, Haasdijk ED, Raike RS, Frants RR, Hess EJ, Hoebeek FE, De Zeeuw CI, van den Maagdenberg AM. Purkinje cell-specific ablation of Cav2.1 channels is sufficient to cause cerebellar ataxia in mice. Cerebellum (London, England). 11: 246-58. PMID 21870131 DOI: 10.1007/S12311-011-0302-1 |
0.326 |
|
| 2012 |
Fan X, Bruno KJ, Hess EJ. Rodent models of ADHD. Current Topics in Behavioral Neurosciences. 9: 273-300. PMID 21516392 DOI: 10.1007/7854_2011_121 |
0.711 |
|
| 2012 |
Lee H, Pothos E, Hess EJ, Fu Y, Edwards R, Ptacek L. Dopamine Dysregulation in a Mouse Model of Paroxysmal Non-Kinesigenic Dyskinesia (IN6-1.003) Neurology. 78: IN6-1.003-IN6-1.003. DOI: 10.1212/Wnl.78.1_Meetingabstracts.In6-1.003 |
0.341 |
|
| 2011 |
Thompson VB, Jinnah HA, Hess EJ. Convergent mechanisms in etiologically-diverse dystonias. Expert Opinion On Therapeutic Targets. 15: 1387-403. PMID 22136648 DOI: 10.1517/14728222.2011.641533 |
0.316 |
|
| 2011 |
Neychev VK, Gross RE, Lehéricy S, Hess EJ, Jinnah HA. The functional neuroanatomy of dystonia. Neurobiology of Disease. 42: 185-201. PMID 21303695 DOI: 10.1016/J.Nbd.2011.01.026 |
0.317 |
|
| 2010 |
Scholle HC, Jinnah HA, Arnold D, Biedermann FH, Faenger B, Grassme R, Hess EJ, Schumann NP. Kinematic and electromyographic tools for characterizing movement disorders in mice. Movement Disorders : Official Journal of the Movement Disorder Society. 25: 265-74. PMID 20077474 DOI: 10.1002/Mds.22933 |
0.43 |
|
| 2010 |
Fan X, Xu M, Hess EJ. D2 dopamine receptor subtype-mediated hyperactivity and amphetamine responses in a model of ADHD Neurobiology of Disease. 37: 228-236. PMID 19840852 DOI: 10.1016/J.Nbd.2009.10.009 |
0.374 |
|
| 2009 |
Chen G, Popa LS, Wang X, Gao W, Barnes J, Hendrix CM, Hess EJ, Ebner TJ. Low-frequency oscillations in the cerebellar cortex of the tottering mouse. Journal of Neurophysiology. 101: 234-45. PMID 18987121 DOI: 10.1152/Jn.90829.2008 |
0.332 |
|
| 2008 |
Neychev VK, Fan X, Mitev VI, Hess EJ, Jinnah HA. The basal ganglia and cerebellum interact in the expression of dystonic movement. Brain : a Journal of Neurology. 131: 2499-509. PMID 18669484 DOI: 10.1093/brain/awn168 |
0.307 |
|
| 2008 |
Shirley TL, Rao LM, Hess EJ, Jinnah HA. Paroxysmal dyskinesias in mice. Movement Disorders : Official Journal of the Movement Disorder Society. 23: 259-64. PMID 17999434 DOI: 10.1002/Mds.21829 |
0.4 |
|
| 2007 |
Devanagondi R, Egami K, LeDoux MS, Hess EJ, Jinnah HA. Neuroanatomical substrates for paroxysmal dyskinesia in lethargic mice. Neurobiology of Disease. 27: 249-57. PMID 17561408 DOI: 10.1016/J.Nbd.2007.05.001 |
0.434 |
|
| 2007 |
Fan X, Hess EJ. D2-like dopamine receptors mediate the response to amphetamine in a mouse model of ADHD. Neurobiology of Disease. 26: 201-11. PMID 17291774 DOI: 10.1016/J.Nbd.2006.12.011 |
0.432 |
|
| 2007 |
Bruno KJ, Freet CS, Twining RC, Egami K, Grigson PS, Hess EJ. Abnormal latent inhibition and impulsivity in coloboma mice, a model of ADHD. Neurobiology of Disease. 25: 206-16. PMID 17064920 DOI: 10.1016/J.Nbd.2006.09.009 |
0.725 |
|
| 2006 |
Kasim S, Blake BL, Fan X, Chartoff E, Egami K, Breese GR, Hess EJ, Jinnah HA. The role of dopamine receptors in the neurobehavioral syndrome provoked by activation of L-type calcium channels in rodents. Developmental Neuroscience. 28: 505-17. PMID 17028428 DOI: 10.1159/000095113 |
0.366 |
|
| 2006 |
Bruno KJ, Hess EJ. The alpha(2C)-adrenergic receptor mediates hyperactivity of coloboma mice, a model of attention deficit hyperactivity disorder. Neurobiology of Disease. 23: 679-88. PMID 16839770 DOI: 10.1016/J.Nbd.2006.05.007 |
0.726 |
|
| 2006 |
von Coelln R, Thomas B, Andrabi SA, Lim KL, Savitt JM, Saffary R, Stirling W, Bruno K, Hess EJ, Lee MK, Dawson VL, Dawson TM. Inclusion body formation and neurodegeneration are parkin independent in a mouse model of alpha-synucleinopathy. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 3685-96. PMID 16597723 DOI: 10.1523/Jneurosci.0414-06.2006 |
0.702 |
|
| 2005 |
Raike RS, Jinnah HA, Hess EJ. Animal models of generalized dystonia. Neurorx : the Journal of the American Society For Experimental Neurotherapeutics. 2: 504-12. PMID 16389314 DOI: 10.1602/Neurorx.2.3.504 |
0.409 |
|
| 2005 |
Fureman BE, Hess EJ. Noradrenergic blockade prevents attacks in a model of episodic dysfunction caused by a channelopathy. Neurobiology of Disease. 20: 227-32. PMID 16242631 DOI: 10.1016/J.Nbd.2005.03.004 |
0.383 |
|
| 2005 |
Pan B, Fromholt SE, Hess EJ, Crawford TO, Griffin JW, Sheikh KA, Schnaar RL. Myelin-associated glycoprotein and complementary axonal ligands, gangliosides, mediate axon stability in the CNS and PNS: neuropathology and behavioral deficits in single- and double-null mice. Experimental Neurology. 195: 208-17. PMID 15953602 DOI: 10.1016/J.Expneurol.2005.04.017 |
0.335 |
|
| 2005 |
Weisz CJ, Raike RS, Soria-Jasso LE, Hess EJ. Potassium channel blockers inhibit the triggers of attacks in the calcium channel mouse mutant tottering. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 4141-5. PMID 15843617 DOI: 10.1523/Jneurosci.0098-05.2005 |
0.322 |
|
| 2005 |
Jinnah HA, Hess EJ, Ledoux MS, Sharma N, Baxter MG, Delong MR. Rodent models for dystonia research: characteristics, evaluation, and utility. Movement Disorders : Official Journal of the Movement Disorder Society. 20: 283-92. PMID 15641011 DOI: 10.1002/Mds.20364 |
0.335 |
|
| 2004 |
Von Coelln R, Thomas B, Savitt JM, Lim KL, Sasaki M, Hess EJ, Dawson VL, Dawson TM. Loss of locus coeruleus neurons and reduced startle in parkin null mice. Proceedings of the National Academy of Sciences of the United States of America. 101: 10744-9. PMID 15249681 DOI: 10.1073/Pnas.0401297101 |
0.373 |
|
| 2004 |
von Coelln R, Thomas B, Lim K, Hess E, Lee M, Dawson V, Dawson T. Alpha-Synuclein-induzierte Proteinaggregation und Neurodegeneration in vivo sind Parkin-unabhängig Aktuelle Neurologie. 31. DOI: 10.1055/S-2004-833018 |
0.335 |
|
| 2003 |
Fureman BE, Campbell DB, Hess EJ. Regulation of tyrosine hydroxylase expression in tottering mouse Purkinje cells. Neurotoxicity Research. 5: 521-8. PMID 14715436 DOI: 10.1007/Bf03033162 |
0.318 |
|
| 2003 |
Jones MD, Hess EJ. Norepinephrine regulates locomotor hyperactivity in the mouse mutant coloboma. Pharmacology, Biochemistry, and Behavior. 75: 209-16. PMID 12759129 DOI: 10.1016/S0091-3057(03)00073-X |
0.482 |
|
| 2002 |
Pizoli CE, Jinnah HA, Billingsley ML, Hess EJ. Abnormal cerebellar signaling induces dystonia in mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 22: 7825-33. PMID 12196606 DOI: 10.1523/Jneurosci.22-17-07825.2002 |
0.734 |
|
| 2002 |
Fureman BE, Jinnah HA, Hess EJ. Triggers of paroxysmal dyskinesia in the calcium channel mouse mutant tottering. Pharmacology, Biochemistry, and Behavior. 73: 631-7. PMID 12151038 DOI: 10.1016/S0091-3057(02)00854-7 |
0.363 |
|
| 2001 |
Jones MD, Williams ME, Hess EJ. Expression of catecholaminergic mRNAs in the hyperactive mouse mutant coloboma. Brain Research. Molecular Brain Research. 96: 114-21. PMID 11731016 DOI: 10.1016/S0169-328X(01)00281-9 |
0.455 |
|
| 2001 |
Jones MD, Williams ME, Hess EJ. Abnormal presynaptic catecholamine regulation in a hyperactive SNAP-25-deficient mouse mutant. Pharmacology, Biochemistry, and Behavior. 68: 669-76. PMID 11526963 DOI: 10.1016/S0091-3057(01)00481-6 |
0.461 |
|
| 2000 |
Jinnah HA, Sepkuty JP, Ho T, Yitta S, Drew T, Rothstein JD, Hess EJ. Calcium channel agonists and dystonia in the mouse. Movement Disorders : Official Journal of the Movement Disorder Society. 15: 542-51. PMID 10830422 DOI: 10.1002/1531-8257(200005)15:3<542::Aid-Mds1019>3.0.Co;2-2 |
0.332 |
|
| 1996 |
Hess EJ, Collins KA, Wilson MC. Mouse model of hyperkinesis implicates SNAP-25 in behavioral regulation. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 16: 3104-11. PMID 8622140 |
0.368 |
|
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