| Year |
Citation |
Score |
| 2022 |
Graves TD, Griggs RC, Bundy BN, Jen JC, Baloh RW, Hanna MG. Correction to: Episodic Ataxia Type 1: Natural History and Effect on Quality of Life. Cerebellum (London, England). PMID 35904745 DOI: 10.1007/s12311-022-01450-z |
0.578 |
|
| 2022 |
Graves TD, Griggs RC, Bundy BN, Jen JC, Baloh RW, Hanna MG. Episodic Ataxia Type 1: Natural History and Effect on Quality of Life. Cerebellum (London, England). PMID 35655106 DOI: 10.1007/s12311-021-01360-6 |
0.623 |
|
| 2020 |
Cha YH, Baloh RW, Cho C, Magnusson M, Song JJ, Strupp M, Wuyts F, Staab JP. Mal de débarquement syndrome: Diagnostic criteria consensus document of the classification committee of the bárány society. Journal of Vestibular Research : Equilibrium & Orientation. PMID 32986636 DOI: 10.3233/VES-200714 |
0.632 |
|
| 2018 |
Cha YH, Cui YY, Baloh RW. Comprehensive Clinical Profile of Mal De Debarquement Syndrome. Frontiers in Neurology. 9: 261. PMID 29867709 DOI: 10.3389/fneur.2018.00261 |
0.628 |
|
| 2016 |
Stam AH, Kothari PH, Shaikh A, Gschwendter A, Jen JC, Hodgkinson S, Hardy TA, Hayes M, Kempster PA, Kotschet KE, Bajema IM, van Duinen SG, Maat-Schieman ML, de Jong PT, de Smet MD, ... ... Baloh RW, et al. Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations. Brain : a Journal of Neurology. PMID 27604306 DOI: 10.1093/Brain/Aww217 |
0.646 |
|
| 2014 |
Graves TD, Cha YH, Hahn AF, Barohn R, Salajegheh MK, Griggs RC, Bundy BN, Jen JC, Baloh RW, Hanna MG. Episodic ataxia type 1: clinical characterization, quality of life and genotype-phenotype correlation. Brain : a Journal of Neurology. 137: 1009-18. PMID 24578548 DOI: 10.1093/brain/awu012 |
0.769 |
|
| 2013 |
Cha YH, Cui Y, Baloh RW. Repetitive transcranial magnetic stimulation for mal de debarquement syndrome Otology and Neurotology. 34: 175-179. PMID 23202153 DOI: 10.1097/MAO.0b013e318278bf7c |
0.618 |
|
| 2012 |
Cha YH, Chakrapani S, Craig A, Baloh RW. Metabolic and functional connectivity changes in mal de debarquement syndrome. Plos One. 7: e49560. PMID 23209584 DOI: 10.1371/journal.pone.0049560 |
0.623 |
|
| 2012 |
Kerber KA, Burke JF, Skolarus LE, Callaghan BC, Fife TD, Baloh RW, Fendrick AM. A prescription for the Epley maneuver: www.youtube.com? Neurology. 79: 376-80. PMID 22826542 DOI: 10.1212/WNL.0b013e3182604533 |
0.481 |
|
| 2012 |
Jen JC, Lopez I, Baloh RW. Opsoclonus: clinical and immunological features. Journal of the Neurological Sciences. 320: 61-5. PMID 22818114 DOI: 10.1016/j.jns.2012.06.017 |
0.576 |
|
| 2011 |
Kerber KA, Baloh RW. The evaluation of a patient with dizziness. Neurology. Clinical Practice. 1: 24-33. PMID 23634356 DOI: 10.1212/CPJ.0b013e31823d07b6 |
0.491 |
|
| 2011 |
Wan J, Mamsa H, Johnston JL, Spriggs EL, Singer HS, Zee DS, Al-Bayati AR, Baloh RW, Jen JC. Large Genomic Deletions in CACNA1A Cause Episodic Ataxia Type 2. Frontiers in Neurology. 2: 51. PMID 21927611 DOI: 10.3389/fneur.2011.00051 |
0.668 |
|
| 2010 |
Kim HA, Lee H, Sohn SI, Kim JS, Baloh RW. Perverted head shaking nystagmus in focal pontine infarction. Journal of the Neurological Sciences. 301: 93-5. PMID 21146834 DOI: 10.1016/j.jns.2010.11.009 |
0.374 |
|
| 2009 |
Jen JC, Baloh RW. Familial episodic ataxia: a model for migrainous vertigo. Annals of the New York Academy of Sciences. 1164: 252-6. PMID 19645908 DOI: 10.1111/j.1749-6632.2008.03723.x |
0.673 |
|
| 2009 |
de Vries B, Mamsa H, Stam AH, Wan J, Bakker SL, Vanmolkot KR, Haan J, Terwindt GM, Boon EM, Howard BD, Frants RR, Baloh RW, Ferrari MD, Jen JC, van den Maagdenberg AM. Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake. Archives of Neurology. 66: 97-101. PMID 19139306 DOI: 10.1001/Archneurol.2008.535 |
0.663 |
|
| 2008 |
Cha YH, Brodsky J, Ishiyama G, Sabatti C, Baloh RW. Clinical features and associated syndromes of mal de debarquement. Journal of Neurology. 255: 1038-44. PMID 18500497 DOI: 10.1007/S00415-008-0837-3 |
0.64 |
|
| 2008 |
Marti S, Baloh RW, Jen JC, Straumann D, Jung HH. Progressive cerebellar ataxia with variable episodic symptoms--phenotypic diversity of R1668W CACNA1A mutation. European Neurology. 60: 16-20. PMID 18437043 DOI: 10.1159/000127974 |
0.677 |
|
| 2008 |
Lee H, Jen JC, Cha YH, Nelson SF, Baloh RW. Phenotypic and genetic analysis of a large family with migraine-associated vertigo Headache. 48: 1460-1467. PMID 18081823 DOI: 10.1111/j.1526-4610.2007.01002.x |
0.762 |
|
| 2008 |
Cha YH, Kane MJ, Baloh RW. Familial clustering of migraine, episodic vertigo, and Ménière's disease. Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 29: 93-6. PMID 18046258 DOI: 10.1097/mao.0b013e31815c2abb |
0.637 |
|
| 2008 |
Shook SJ, Mamsa H, Jen JC, Baloh RW, Zhou L. Novel mutation in KCNA1 causes episodic ataxia with paroxysmal dyspnea Muscle and Nerve. 37: 399-402. PMID 17912752 DOI: 10.1002/mus.20904 |
0.677 |
|
| 2008 |
Wiest G, Baloh RW. The personal and scientific feud between Ernst Brücke and Josef Hyrtl. Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 27: 570-5. PMID 16791051 DOI: 10.1097/01.mao.0000217348.02173.6b |
0.675 |
|
| 2007 |
Cha YH, Baloh RW. Migraine associated vertigo. Journal of Clinical Neurology (Seoul, Korea). 3: 121-6. PMID 19513278 DOI: 10.3988/jcn.2007.3.3.121 |
0.672 |
|
| 2007 |
Richards A, van den Maagdenberg AM, Jen JC, Kavanagh D, Bertram P, Spitzer D, Liszewski MK, Barilla-Labarca ML, Terwindt GM, Kasai Y, McLellan M, Grand MG, Vanmolkot KR, de Vries B, Wan J, ... ... Baloh RW, et al. C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy. Nature Genetics. 39: 1068-70. PMID 17660820 DOI: 10.1038/Ng2082 |
0.619 |
|
| 2007 |
Lee H, Sininger L, Jen JC, Cha YH, Baloh RW, Nelson SF. Association of progesterone receptor with migraine-associated vertigo Neurogenetics. 8: 195-200. PMID 17609999 DOI: 10.1007/s10048-007-0091-3 |
0.738 |
|
| 2007 |
Kerber KA, Jen JC, Lee H, Nelson SF, Baloh RW. A new episodic ataxia syndrome with linkage to chromosome 19q13. Archives of Neurology. 64: 749-52. PMID 17502476 DOI: 10.1001/archneur.64.5.749 |
0.705 |
|
| 2006 |
Ishiyama G, Ishiyama A, Kerber K, Baloh RW. Gentamicin ototoxicity: Clinical features and the effect on the human vestibulo-ocular reflex Acta Oto-Laryngologica. 126: 1057-1061. PMID 16923710 DOI: 10.1080/00016480600606673 |
0.528 |
|
| 2006 |
Kerber KA, Whitman GT, Brown DL, Baloh RW. Increased risk of death in community-dwelling older people with white matter hyperintensities on MRI. Journal of the Neurological Sciences. 250: 33-8. PMID 16889799 DOI: 10.1016/j.jns.2006.06.022 |
0.496 |
|
| 2006 |
Lee H, Jen JC, Wang H, Chen Z, Mamsa H, Sabatti C, Baloh RW, Nelson SF. A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity. Human Molecular Genetics. 15: 251-8. PMID 16330481 DOI: 10.1093/Hmg/Ddi441 |
0.653 |
|
| 2006 |
Kerber KA, Ishiyama GP, Baloh RW. A longitudinal study of oculomotor function in normal older people Neurobiology of Aging. 27: 1346-1353. PMID 16122840 DOI: 10.1016/j.neurobiolaging.2005.07.009 |
0.493 |
|
| 2006 |
Bhidayasiri R, Jen JC, Baloh RW. Three brothers with a very-late-onset writer's cramp. Movement Disorders : Official Journal of the Movement Disorder Society. 20: 1375-7. PMID 15954129 DOI: 10.1002/mds.20568 |
0.622 |
|
| 2005 |
Kerber KA, Rasmussen PA, Masaryk TJ, Baloh RW. Recurrent vertigo attacks cured by stenting a basilar artery stenosis Neurology. 65: 962. PMID 16186549 DOI: 10.1212/01.wnl.0000175975.67488.e9 |
0.473 |
|
| 2005 |
Kerber KA, Jen JC, Perlman S, Baloh RW. Late-onset pure cerebellar ataxia: Differentiating those with and without identifiable mutations Journal of the Neurological Sciences. 238: 41-45. PMID 16109427 DOI: 10.1016/j.jns.2005.06.006 |
0.728 |
|
| 2005 |
Jen J, Baloh RH, Ishiyama A, Baloh RW. Dejerine-Sottas syndrome and vestibular loss due to a point mutation in the PMP22 gene. Journal of the Neurological Sciences. 237: 21-4. PMID 15992829 DOI: 10.1016/j.jns.2005.05.003 |
0.644 |
|
| 2005 |
Rucker JC, Jen J, Stahl JS, Natesan N, Baloh RW, Leigh RJ. Internuclear ophthalmoparesis in episodic ataxia type 2. Annals of the New York Academy of Sciences. 1039: 571-4. PMID 15827025 DOI: 10.1196/annals.1325.070 |
0.646 |
|
| 2005 |
Wan J, Carr JR, Baloh RW, Jen JC. Nonconsensus intronic mutations cause episodic ataxia. Annals of Neurology. 57: 131-5. PMID 15622542 DOI: 10.1002/Ana.20343 |
0.652 |
|
| 2004 |
Lee H, Wang H, Jen JC, Sabatti C, Baloh RW, Nelson SF. A novel mutation in KCNA1 causes episodic ataxia without myokymia. Human Mutation. 24: 536. PMID 15532032 DOI: 10.1002/Humu.9295 |
0.68 |
|
| 2004 |
Baloh RW. Genes and migraine. Drugs of Today (Barcelona, Spain : 1998). 40: 577-88. PMID 15510232 DOI: 10.1358/dot.2004.40.7.850476 |
0.3 |
|
| 2004 |
Jen JC, Kim GW, Dudding KA, Baloh RW. No mutations in CACNA1A and ATP1A2 in probands with common types of migraine. Archives of Neurology. 61: 926-8. PMID 15210532 DOI: 10.1001/archneur.61.6.926 |
0.641 |
|
| 2004 |
Baloh RH, Jen JC, Kim G, Baloh RW. Chronic cough due to Thr124Met mutation in the peripheral myelin protein zero (MPZ gene). Neurology. 62: 1905-6. PMID 15159512 |
0.616 |
|
| 2004 |
Jen JC, Chan WM, Bosley TM, Wan J, Carr JR, Rüb U, Shattuck D, Salamon G, Kudo LC, Ou J, Lin DD, Salih MA, Kansu T, Al Dhalaan H, Al Zayed Z, ... ... Baloh RW, et al. Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis. Science (New York, N.Y.). 304: 1509-13. PMID 15105459 DOI: 10.1126/Science.1096437 |
0.587 |
|
| 2003 |
Sasaki O, Jen JC, Baloh RW, Kim GW, Isawa M, Usami S. Neurotological findings in a family with episodic ataxia. Journal of Neurology. 250: 373-5. PMID 12749331 DOI: 10.1007/s00415-003-0994-3 |
0.624 |
|
| 2002 |
Wiest G, Baloh RW. The pioneering work of Josef Breuer on the vestibular system. Archives of Neurology. 59: 1647-53. PMID 12374505 DOI: 10.1001/archneur.59.10.1647 |
0.665 |
|
| 2002 |
Jen JC, Baloh RW. Genetics of episodic ataxia. Advances in Neurology. 89: 459-61. PMID 11968470 |
0.595 |
|
| 2002 |
Baloh RW, Jen JC. Genetics of familial episodic vertigo and ataxia. Annals of the New York Academy of Sciences. 956: 338-45. PMID 11960817 DOI: 10.1111/j.1749-6632.2002.tb02832.x |
0.682 |
|
| 2002 |
Wiest G, Baloh RW. Sigmund Freud and the VIIIth Cranial Nerve. Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 23: 228-32. PMID 11875355 DOI: 10.1097/00129492-200203000-00021 |
0.661 |
|
| 2002 |
Baloh RW. Episodic vertigo: central nervous system causes. Current Opinion in Neurology. 15: 17-21. PMID 11796946 DOI: 10.1097/00019052-200202000-00004 |
0.315 |
|
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