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For: Iwasaki Y, Hashizume Y, Yoshida M, Kitamoto T, Sobue G. Neuropathologic characteristics of brainstem lesions in sporadic Creutzfeldt-Jakob disease. Acta Neuropathol 2005;109:557-66. [PMID: 15933870 DOI: 10.1007/s00401-005-0981-0] [Cited by in Crossref: 41] [Cited by in F6Publishing: 39] [Article Influence: 2.4] [Reference Citation Analysis]
Number Citing Articles
1 Na S, Lee SA, Lee JD, Lee ES, Lee TK. Creutzfeldt-Jakob disease presenting with bilateral hearing loss: A case report. World J Clin Cases 2022; 10(18): 6333-6337 [DOI: 10.12998/wjcc.v10.i18.6333] [Cited by in CrossRef: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Matsuo K, Goto D, Hasegawa M, Ogita K, Koyama T, Akagi A, Kitamoto T, Yoshida M, Iwasaki Y. An autopsy case of MV2K-type sporadic Creutzfeldt-Jakob disease presenting with characteristic clinical, radiological, and neuropathological findings. Neuropathology 2022. [PMID: 35441383 DOI: 10.1111/neup.12804] [Reference Citation Analysis]
3 Iwasaki Y, Mori K, Ito M, Kawai Y, Akagi A, Riku Y, Miyahara H, Kobayashi A, Kitamoto T, Yoshida M. System degeneration in an MM1-type sporadic Creutzfeldt-Jakob disease case with an unusually prolonged akinetic mutism state. Prion 2021;15:12-20. [PMID: 33472525 DOI: 10.1080/19336896.2020.1868931] [Reference Citation Analysis]
4 Andereggen L, Remonda L. Pontine Neoplasm or Myelinolysis Despite Normal Sodium Levels. World Neurosurg. 2020;140:63-64. [PMID: 32416240 DOI: 10.1016/j.wneu.2020.05.061] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
5 Iwasaki Y. The Braak hypothesis in prion disease with a focus on Creutzfeldt-Jakob disease. Neuropathology 2020;40:436-49. [PMID: 32363728 DOI: 10.1111/neup.12654] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
6 Katsikaki G, Dagklis IE, Angelopoulos P, Ntantos D, Prevezianou A, Bostantjopoulou S. Atypical and early symptoms of sporadic Creutzfeldt – Jakob disease: case series and review of the literature. International Journal of Neuroscience 2021;131:927-38. [DOI: 10.1080/00207454.2020.1759594] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
7 Ikeda T, Iwasaki Y, Sakurai K, Akagi A, Riku Y, Mimuro M, Miyahara H, Kitamoto T, Matsukawa N, Yoshida M. Correlating diffusion-weighted MRI intensity with type 2 pathology in mixed MM-type sporadic Creutzfeldt-Jakob disease. J Neurol Sci 2020;408:116515. [PMID: 31675505 DOI: 10.1016/j.jns.2019.116515] [Reference Citation Analysis]
8 Iwasaki Y, Hiraga K, Ito S, Ando T, Akagi A, Riku Y, Mimuro M, Miyahara H, Kobayashi A, Kitamoto T, Yoshida M. Autopsy case of MV2K‐type sporadic Creutzfeldt‐Jakob disease with spongiform changes of the cerebral cortex. Neuropathology 2019;39:452-60. [DOI: 10.1111/neup.12595] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
9 Kresl P, Rahimi J, Gelpi E, Aldecoa I, Ricken G, Danics K, Keller E, Kovacs GG. Accumulation of prion protein in the vagus nerve in creutzfeldt-jakob disease. Ann Neurol 2019;85:782-7. [PMID: 30801763 DOI: 10.1002/ana.25451] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
10 Iwasaki Y, Hashimoto R, Saito Y, Aiba I, Inukai A, Akagi A, Mimuro M, Miyahara H, Kitamoto T, Yoshida M. An autopsied case of MM1-type sporadic Creutzfeldt-Jakob disease with pathology of Wernicke encephalopathy. Prion 2019;13:13-20. [PMID: 30409087 DOI: 10.1080/19336896.2018.1545525] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
11 Akagi A, Iwasaki Y, Mimuro M, Kitamoto T, Yamada M, Yoshida M. Pathological progression of genetic Creutzfeldt-Jakob disease with a PrP V180I mutation. Prion 2018;12:54-62. [PMID: 29264994 DOI: 10.1080/19336896.2017.1414130] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 1.8] [Reference Citation Analysis]
12 Hayashi Y, Iwasaki Y, Yoshikura N, Asano T, Mimuro M, Kimura A, Satoh K, Kitamoto T, Yoshida M, Inuzuka T. An autopsy-verified case of steroid-responsive encephalopathy with convulsion and a false-positive result from the real-time quaking-induced conversion assay. Prion 2017;11:284-92. [PMID: 28749249 DOI: 10.1080/19336896.2017.1345416] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 1.8] [Reference Citation Analysis]
13 Iwasaki Y, Kato H, Ando T, Mimuro M, Kitamoto T, Yoshida M. MM1-type sporadic Creutzfeldt-Jakob disease with 1-month total disease duration and early pathologic indicators. Neuropathology 2017;37:420-5. [PMID: 28402042 DOI: 10.1111/neup.12379] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.2] [Reference Citation Analysis]
14 Iwasaki Y. Creutzfeldt-Jakob disease. Neuropathology 2017;37:174-88. [PMID: 28028861 DOI: 10.1111/neup.12355] [Cited by in Crossref: 57] [Cited by in F6Publishing: 46] [Article Influence: 9.5] [Reference Citation Analysis]
15 Hayashi Y, Iwasaki Y, Takekoshi A, Yoshikura N, Asano T, Mimuro M, Kimura A, Satoh K, Kitamoto T, Yoshida M, Inuzuka T. An autopsy-verified case of FTLD-TDP type A with upper motor neuron-predominant motor neuron disease mimicking MM2-thalamic-type sporadic Creutzfeldt-Jakob disease. Prion 2016;10:492-501. [PMID: 27929803 DOI: 10.1080/19336896.2016.1243192] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 1.7] [Reference Citation Analysis]
16 Iwasaki Y, Saito Y, Aiba I, Kobayashi A, Mimuro M, Kitamoto T, Yoshida M. An autopsied case of MV2K + C-type sporadic Creutzfeldt-Jakob disease presenting with widespread cerebral cortical involvement and Kuru plaques: MV2K + C-type sporadic CJD. Neuropathology 2017;37:241-8. [DOI: 10.1111/neup.12350] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
17 Hayashi Y, Iwasaki Y, Yoshikura N, Asano T, Hatano T, Tatsumi S, Satoh K, Kimura A, Kitamoto T, Yoshida M, Inuzuka T. Decreased regional cerebral blood flow in the bilateral thalami and medulla oblongata determined by an easy Z-score (eZIS) analysis of 99mTc-ECD-SPECT images in a case of MM2-thalamic-type sporadic Creutzfeldt–Jakob disease. Journal of the Neurological Sciences 2015;358:447-52. [DOI: 10.1016/j.jns.2015.09.356] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 1.7] [Reference Citation Analysis]
18 Iacono D, Ferrari S, Gelati M, Zanusso G, Mariotto S, Monaco S. Sporadic Creutzfeldt-Jakob Disease: Prion Pathology in Medulla Oblongata-Possible Routes of Infection and Host Susceptibility. Biomed Res Int 2015;2015:396791. [PMID: 26457299 DOI: 10.1155/2015/396791] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
19 Reis R, Hennessy E, Murray C, Griffin ÉW, Cunningham C. At the centre of neuronal, synaptic and axonal pathology in murine prion disease: degeneration of neuroanatomically linked thalamic and brainstem nuclei. Neuropathol Appl Neurobiol 2015;41:780-97. [PMID: 25727649 DOI: 10.1111/nan.12232] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.6] [Reference Citation Analysis]
20 Mirabile I, Jat PS, Brandner S, Collinge J. Identification of clinical target areas in the brainstem of prion-infected mice. Neuropathol Appl Neurobiol 2015;41:613-30. [PMID: 25311251 DOI: 10.1111/nan.12189] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 0.9] [Reference Citation Analysis]
21 Salazar R, Cerghet M, Ramachandran V. Bilateral hearing loss heralding sporadic Creutzfeldt-Jakob disease: a case report and literature review. Otol Neurotol 2014;35:1327-9. [PMID: 25122149 DOI: 10.1097/MAO.0000000000000485] [Cited by in Crossref: 8] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
22 Iwasaki Y, Tatsumi S, Mimuro M, Kitamoto T, Yoshida M. Comparison of the clinical course of Japanese MM1-type sporadic Creutzfeldt-Jakob disease between subacute spongiform encephalopathy and panencephalopathic-type. Clin Neurol Neurosurg 2014;121:59-63. [PMID: 24793477 DOI: 10.1016/j.clineuro.2014.03.024] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
23 Iwasaki Y, Tatsumi S, Mimuro M, Kitamoto T, Hashizume Y, Yoshida M. Relation between clinical findings and progression of cerebral cortical pathology in MM1-type sporadic Creutzfeldt-Jakob disease: proposed staging of cerebral cortical pathology. J Neurol Sci 2014;341:97-104. [PMID: 24787503 DOI: 10.1016/j.jns.2014.04.011] [Cited by in Crossref: 19] [Cited by in F6Publishing: 19] [Article Influence: 2.4] [Reference Citation Analysis]
24 Fujita K, Matsui N, Takahashi Y, Iwasaki Y, Yoshida M, Yuasa T, Izumi Y, Kaji R. Increased interleukin-17 in the cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease: a case-control study of rapidly progressive dementia. J Neuroinflammation 2013;10:135. [PMID: 24219883 DOI: 10.1186/1742-2094-10-135] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 0.8] [Reference Citation Analysis]
25 Iwasaki Y, Yokoi F, Tatsumi S, Mimuro M, Iwai K, Kitamoto T, Yoshida M. An autopsied case of Creutzfeldt-Jakob disease with mutation in the prion protein gene codon 232 and type 1+2 prion protein. Neuropathology 2013;33:568-75. [PMID: 23320809 DOI: 10.1111/neup.12013] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
26 Iwasaki Y, Mori K, Ito M, Nagaoka M, Ieda T, Kitamoto T, Yoshida M, Hashizume Y. An autopsied case of V180I Creutzfeldt-Jakob disease presenting with panencephalopathic-type pathology and a characteristic prion protein type: Panencephalopathic-type V180I CJD. Neuropathology 2011;31:540-8. [DOI: 10.1111/j.1440-1789.2010.01192.x] [Cited by in Crossref: 22] [Cited by in F6Publishing: 23] [Article Influence: 2.0] [Reference Citation Analysis]
27 Saito Y, Iwasaki Y, Aiba I, Kitamoto T, Yoshida M, Hashizume Y. An autopsy case of MM2-cortical + thalamic-type sporadic Creutzfeldt-Jakob disease: MM2-cortical + thalamic-type CJD. Neuropathology 2011;31:523-30. [DOI: 10.1111/j.1440-1789.2010.01181.x] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 1.0] [Reference Citation Analysis]
28 Iwasaki Y, Mimuro M, Yoshida M, Kitamoto T, Hashizume Y. Survival to akinetic mutism state in Japanese cases of MM1-type sporadic Creutzfeldt-Jakob disease is similar to Caucasians. Eur J Neurol 2011;18:999-1002. [PMID: 20722706 DOI: 10.1111/j.1468-1331.2010.03185.x] [Cited by in Crossref: 13] [Cited by in F6Publishing: 9] [Article Influence: 1.1] [Reference Citation Analysis]
29 Hama T, Iwasaki Y, Niwa H, Yoshida M, Hashizume Y, Kitamoto T, Murakami N, Sobue G. An autopsied case of panencephalopathic-type Creutzfeldt-Jakob disease with mutation in the prion protein gene at codon 232 and type 1 prion protein. Neuropathology 2009;29:727-34. [PMID: 19422533 DOI: 10.1111/j.1440-1789.2009.01016.x] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 0.8] [Reference Citation Analysis]
30 Iwasaki Y, Mimuro M, Yoshida M, Hashizume Y, Kitamoto T, Sobue G. Clinicopathologic characteristics of five autopsied cases of dura mater-associated Creutzfeldt-Jakob disease. Neuropathology 2008;28:51-61. [PMID: 18181835 DOI: 10.1111/j.1440-1789.2007.00847.x] [Cited by in Crossref: 18] [Cited by in F6Publishing: 14] [Article Influence: 1.3] [Reference Citation Analysis]
31 Niimi Y, Iwasaki Y, Umemura T, Tanaka F, Yoshida M, Hashizume Y, Kitamoto T, Hirayama M, Sobue G. MM2-cortical-type sporadic Creutzfeldt-Jakob disease with early stage cerebral cortical pathology presenting with a rapidly progressive clinical course. Neuropathology 2008;28:645-51. [PMID: 18410280 DOI: 10.1111/j.1440-1789.2008.00904.x] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
32 Hoshino A, Iwasaki Y, Izumi M, Kimura S, Ibi T, Kitamoto T, Yoshida M, Hashizume Y, Sahashi K. MM1-type sporadic Creutzfeldt-Jakob disease with unusually prolonged disease duration presenting with panencephalopathic-type pathology. Neuropathology 2008;28:326-32. [PMID: 18248577 DOI: 10.1111/j.1440-1789.2007.00854.x] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.2] [Reference Citation Analysis]
33 Iwasaki Y, Yoshida M, Hashizume Y, Kitamoto T, Sobue G. Pyramidal tract degeneration in sporadic Creutzfeldt-Jakob disease: Pyramidal tract degeneration in CJD. Neuropathology 2007;27:434-41. [DOI: 10.1111/j.1440-1789.2007.00812.x] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.3] [Reference Citation Analysis]
34 Iwasaki Y, Mimuro M, Yoshida M, Hashizume Y, Ito M, Kitamoto T, Wakayama Y, Sobue G. Enhanced Aquaporin-4 immunoreactivity in sporadic Creutzfeldt-Jakob disease. Neuropathology 2007;27:314-23. [DOI: 10.1111/j.1440-1789.2007.00781.x] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 0.7] [Reference Citation Analysis]
35 Iwasaki Y, Iijima M, Kimura S, Yoshida M, Hashizume Y, Yamada M, Kitamoto T, Sobue G. Autopsy case of sporadic Creutzfeldt-Jakob disease presenting with signs suggestive of brainstem and spinal cord involvement. Neuropathology 2006;26:550-6. [PMID: 17203592 DOI: 10.1111/j.1440-1789.2006.00723.x] [Cited by in Crossref: 11] [Cited by in F6Publishing: 8] [Article Influence: 0.7] [Reference Citation Analysis]
36 Jung KY, Seo DW, Na DL, Chung CS, Lee IK, Oh K, Im CH, Jung HK. Source localization of periodic sharp wave complexes using independent component analysis in sporadic Creutzfeldt-Jakob disease. Brain Res 2007;1143:228-37. [PMID: 17331477 DOI: 10.1016/j.brainres.2007.01.127] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 1.1] [Reference Citation Analysis]
37 Reñé R, Campdelacreu J, Ferrer I, Escrig A, Povedano M, Gascón-Bayarri J, Moral E. Familial Creutzfeldt-Jakob disease with E200K mutation presenting with neurosensorial hypoacusis. J Neurol Neurosurg Psychiatry 2007;78:103-4. [PMID: 17172576 DOI: 10.1136/jnnp.2006.095588] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 0.3] [Reference Citation Analysis]
38 Iwasaki Y, Yoshida M, Hashizume Y, Kitamoto T, Sobue G. Clinicopathologic characteristics of sporadic Japanese Creutzfeldt-Jakob disease classified according to prion protein gene polymorphism and prion protein type. Acta Neuropathol 2006;112:561-71. [PMID: 16847689 DOI: 10.1007/s00401-006-0111-7] [Cited by in Crossref: 46] [Cited by in F6Publishing: 45] [Article Influence: 2.9] [Reference Citation Analysis]
39 Hirose K, Iwasaki Y, Izumi M, Yoshida M, Hashizume Y, Kitamoto T, Sahashi K. MM2-thalamic-type sporadic Creutzfeldt-Jakob disease with widespread neocortical pathology. Acta Neuropathol 2006;112:503-11. [PMID: 16957926 DOI: 10.1007/s00401-006-0131-3] [Cited by in Crossref: 23] [Cited by in F6Publishing: 21] [Article Influence: 1.4] [Reference Citation Analysis]
40 Iwasaki Y, Yoshida M, Hashizume Y, Kitamoto T, Sobue G. Neuropathologic characteristics of spinal cord lesions in sporadic Creutzfeldt-Jakob disease. Acta Neuropathol 2005;110:490-500. [PMID: 16175355 DOI: 10.1007/s00401-005-1076-7] [Cited by in Crossref: 18] [Cited by in F6Publishing: 20] [Article Influence: 1.1] [Reference Citation Analysis]