| Year |
Citation |
Score |
| 2020 |
Verheijen BM, Morimoto S, Sasaki R, Oyanagi K, Kokubo Y, Kuzuhara S, van Leeuwen FW. Expression of Mutant Ubiquitin and Proteostasis Impairment in Kii Amyotrophic Lateral Sclerosis/Parkinsonism-Dementia Complex Brains. Journal of Neuropathology and Experimental Neurology. 79: 902-907. PMID 32647880 DOI: 10.1093/Jnen/Nlaa056 |
0.371 |
|
| 2020 |
Morimoto S, Ishikawa M, Watanabe H, Isoda M, Takao M, Nakamura S, Ozawa F, Hirokawa Y, Kuzuhara S, Okano H, Kokubo Y. Brain Transcriptome Analysis Links Deficiencies of Stress-Responsive Proteins to the Pathomechanism of Kii ALS/PDC. Antioxidants (Basel, Switzerland). 9. PMID 32422904 DOI: 10.3390/Antiox9050423 |
0.349 |
|
| 2018 |
Mimuro M, Yoshida M, Kuzuhara S, Kokubo Y. Amyotrophic lateral sclerosis and parkinsonism-dementia complex of the Hohara focus of the Kii Peninsula: A multiple proteinopathy? Neuropathology. 38: 98-107. PMID 29063640 DOI: 10.1111/Neup.12434 |
0.424 |
|
| 2017 |
Hata Y, Ma N, Yoneda M, Morimoto S, Okano H, Murayama S, Kawanishi S, Kuzuhara S, Kokubo Y. Nitrative Stress and Tau Accumulation in Amyotrophic Lateral Sclerosis/Parkinsonism-Dementia Complex (ALS/PDC) in the Kii Peninsula, Japan. Frontiers in Neuroscience. 11: 751. PMID 29403345 DOI: 10.3389/Fnins.2017.00751 |
0.343 |
|
| 2017 |
Tsunoda K, Yamashita T, Shimada H, Nomura E, Takahashi Y, Shang J, Sato K, Takemoto M, Hishikawa N, Ohta Y, Higuchi M, Suhara T, Kokubo Y, Kuzuhara S, Abe K. A migration case of Kii amyotrophic lateral sclerosis/parkinsonism dementia complex with the shortest stay in the endemic area and the longest incubation to develop the disease. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. PMID 28890043 DOI: 10.1016/J.Jocn.2017.08.057 |
0.404 |
|
| 2017 |
Kokubo Y, Banack SA, Morimoto S, Murayama S, Togashi T, Metcalf JS, Cox PA, Kuzuhara S. β-N-methylamino-L-alanine analysis in the brains of patients with Kii ALS/PDC. Neurology. PMID 28794246 DOI: 10.1212/Wnl.0000000000004310 |
0.331 |
|
| 2017 |
Morimoto S, Hatsuta H, Kokubo Y, Nakano Y, Hasegawa M, Yoneda M, Hirokawa Y, Kuzuhara S, Shiraishi T, Murayama S. Unusual tau pathology of the cerebellum in patients with amyotrophic lateral sclerosis/parkinsonism-dementia complex from the kii peninsula, Japan. Brain Pathology (Zurich, Switzerland). PMID 28236345 DOI: 10.1111/Bpa.12500 |
0.378 |
|
| 2017 |
Kokubo Y, Ishii K, Morimoto S, Mimuro M, Sasaki R, Murayama S, Kuzuhara S. Dopaminergic Positron Emission Tomography Study on Amyotrophic Lateral Sclerosis/Parkinsonism–Dementia Complex in Kii, Japan Journal of Alzheimer’S Disease & Parkinsonism. 7. DOI: 10.4172/2161-0460.1000311 |
0.346 |
|
| 2017 |
Kuzuhara S. My memorable dementia cases and studies on dementiaーALS with frontal dementia, Gerstmann-Sträussler-Scheinkerʼs disease, Lewy body disease, parkinsonism-dementia complex, and other atypical dementias Higher Brain Function Research. 37: 187-194. DOI: 10.2496/Hbfr.37.187 |
0.338 |
|
| 2017 |
Shinotoh H, Shimada H, Kokubo Y, Kitamura S, Niwa F, Tagai K, Hirano S, Morimoto S, Yamashita T, Kuzuhara S, Sahara N, Zhang MR, Suhara T, Higuchi M. Tau imaging in patients with amyotrophic lateral sclerosis/parkinsonism dementia complex in the Kii Peninsula Journal of the Neurological Sciences. 381: 1016. DOI: 10.1016/J.Jns.2017.08.2866 |
0.347 |
|
| 2017 |
Okumiya K, Fujisawa M, Wada T, Saz EGd, Hirata Y, Kuzuhara S, Kokubo Y, Matsubayashi K, Manuaba I, Kareth MF, Mollet JA, Rantetampang AL, Sakamoto R. Longitudinal study for amyotrophic lateral sclerosis and parkinsonism in Papua, Indonesia: 2001–2017 survey results Journal of the Neurological Sciences. 381: 706-707. DOI: 10.1016/J.Jns.2017.08.1990 |
0.325 |
|
| 2017 |
Kokubo Y, Morimoto S, Sasaki R, Kuzuhara S. A new concept and registry system for Amyotrophic Lateral Sclerosis (ALS) and Parkinsonism-dementia complex (PDC) of the Kii peninsula of Japan Journal of the Neurological Sciences. 381: 561-562. DOI: 10.1016/J.Jns.2017.08.1581 |
0.364 |
|
| 2015 |
Funayama M, Ohe K, Amo T, Furuya N, Yamaguchi J, Saiki S, Li Y, Ogaki K, Ando M, Yoshino H, Tomiyama H, Nishioka K, Hasegawa K, Saiki H, Satake W, ... ... Kuzuhara S, et al. CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study. The Lancet. Neurology. 14: 274-82. PMID 25662902 DOI: 10.1016/S1474-4422(14)70266-2 |
0.354 |
|
| 2015 |
Kuzuhara S, Kokubo Y. Clinicopathological study of familial ALS/Parkinsonism-Dementia Complex (ALS/PDC) cases in the Kii Peninsula Journal of the Neurological Sciences. 357: 223-224. DOI: 10.1016/J.Jns.2015.08.773 |
0.357 |
|
| 2015 |
Kokubo Y, Morimoto S, Minuro M, Kuzuhara S. Clinical data base of amyotophic lateral sclerosis/parkinsonism-dementia complex of Kii, Japan Journal of the Neurological Sciences. 357. DOI: 10.1016/J.Jns.2015.08.769 |
0.326 |
|
| 2014 |
Shindo A, Ueda Y, Kuzuhara S, Kokubo Y. Neuropsychological study of amyotrophic lateral sclerosis and parkinsonism-dementia complex in Kii peninsula, Japan. Bmc Neurology. 14: 151. PMID 25041813 DOI: 10.1186/1471-2377-14-151 |
0.384 |
|
| 2014 |
Okumiya K, Wada T, Fujisawa M, Ishine M, Garcia Del Saz E, Hirata Y, Kuzuhara S, Kokubo Y, Seguchi H, Sakamoto R, Manuaba I, Watofa P, Rantetampang AL, Matsubayashi K. Amyotrophic lateral sclerosis and parkinsonism in Papua, Indonesia: 2001-2012 survey results. Bmj Open. 4: e004353. PMID 24740977 DOI: 10.1136/Bmjopen-2013-004353 |
0.368 |
|
| 2014 |
Nishioka K, Funayama M, Vilariño-Güell C, Ogaki K, Li Y, Sasaki R, Kokubo Y, Kuzuhara S, Kachergus JM, Cobb SA, Takahashi H, Mizuno Y, Farrer MJ, Ross OA, Hattori N. EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population. Parkinsonism & Related Disorders. 20: 659-61. PMID 24704100 DOI: 10.1016/J.Parkreldis.2014.03.004 |
0.337 |
|
| 2013 |
Ogaki K, Li Y, Takanashi M, Ishikawa K, Kobayashi T, Nonaka T, Hasegawa M, Kishi M, Yoshino H, Funayama M, Tsukamoto T, Shioya K, Yokochi M, Imai H, Sasaki R, ... ... Kuzuhara S, et al. Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBS. Parkinsonism & Related Disorders. 19: 15-20. PMID 22818528 DOI: 10.1016/J.Parkreldis.2012.06.019 |
0.331 |
|
| 2013 |
Morimoto S, Kokubo Y, Hatsuta H, Kuzuhara S, Murayama S. O2-10-05: Immunohistochemical study of the cerebellum in amyotrophic lateral screlosis (ALS)/ parkinson-dementia complex (PDC) in Kii peninsula (ALS/PDC- Kii, Muro disease) Alzheimer's & Dementia. 9: P336-P336. DOI: 10.1016/J.Jalz.2013.04.193 |
0.359 |
|
| 2012 |
Ando M, Funayama M, Li Y, Kashihara K, Murakami Y, Ishizu N, Toyoda C, Noguchi K, Hashimoto T, Nakano N, Sasaki R, Kokubo Y, Kuzuhara S, Ogaki K, Yamashita C, et al. VPS35 mutation in Japanese patients with typical Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 27: 1413-7. PMID 22991136 DOI: 10.1002/Mds.25145 |
0.315 |
|
| 2012 |
Kokubo Y, Taniguchi A, Hasegawa M, Hayakawa Y, Morimoto S, Yoneda M, Hirokawa Y, Shiraishi T, Saito Y, Murayama S, Kuzuhara S. α-Synuclein pathology in the amyotrophic lateral sclerosis/parkinsonism dementia complex in the Kii Peninsula, Japan. Journal of Neuropathology and Experimental Neurology. 71: 625-30. PMID 22710962 DOI: 10.1097/Nen.0B013E31825B9680 |
0.361 |
|
| 2012 |
Naruse H, Takahashi Y, Kihira T, Yoshida S, Kokubo Y, Kuzuhara S, Ishiura H, Amagasa M, Murayama S, Tsuji S, Goto J. Mutational analysis of familial and sporadic amyotrophic lateral sclerosis with OPTN mutations in Japanese population. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 13: 562-6. PMID 22708870 DOI: 10.3109/17482968.2012.684213 |
0.334 |
|
| 2012 |
Ishiura H, Takahashi Y, Mitsui J, Yoshida S, Kihira T, Kokubo Y, Kuzuhara S, Ranum LP, Tamaoki T, Ichikawa Y, Date H, Goto J, Tsuji S. C9ORF72 repeat expansion in amyotrophic lateral sclerosis in the Kii peninsula of Japan. Archives of Neurology. 69: 1154-8. PMID 22637429 DOI: 10.1001/Archneurol.2012.1219 |
0.361 |
|
| 2012 |
Kaji R, Izumi Y, Adachi Y, Kuzuhara S. ALS-parkinsonism-dementia complex of Kii and other related diseases in Japan. Parkinsonism & Related Disorders. 18: S190-1. PMID 22166431 DOI: 10.1016/S1353-8020(11)70059-1 |
0.418 |
|
| 2012 |
Kokubo Y, Nomura Y, Morimoto S, Kuzuhara S. Cardiac ¹²³I-meta-iodobenzylguanidine scintigraphy in patients with amyotrophic lateral sclerosis and parkinsonism-dementia complex of the Kii peninsula, Japan. Parkinsonism & Related Disorders. 18: 306-8. PMID 21885322 DOI: 10.1016/J.Parkreldis.2011.08.005 |
0.339 |
|
| 2012 |
Murayama S, Morimoto S, Kokubo Y, Saito Y, Hasegawa M, Kihira T, Yoshida S, Takahashi H, Yoshida M, Kuzuhara S. P1-196: Establishment of pathology center for amyotrophic lateral sclerosis/Parkinson's disease complex in Kii Peninsula Alzheimer's & Dementia. 8: P175-P175. DOI: 10.1016/J.Jalz.2012.05.474 |
0.345 |
|
| 2011 |
Kokubo Y, Morimoto S, Shindo A, Hirokawa Y, Shiraishi T, Saito Y, Murayama S, Kuzuhara S. Cardiac ¹²³I-meta-iodobenzylguanidine scintigraphy and lewy body pathology in a patient with amyotrophic lateral sclerosis and parkinsonism-dementia complex of Kii, Japan. Movement Disorders : Official Journal of the Movement Disorder Society. 26: 2300-1. PMID 21780178 DOI: 10.1002/Mds.23850 |
0.344 |
|
| 2011 |
Tomiyama H, Yoshino H, Ogaki K, Li L, Yamashita C, Li Y, Funayama M, Sasaki R, Kokubo Y, Kuzuhara S, Hattori N. PLA2G6 variant in Parkinson's disease. Journal of Human Genetics. 56: 401-3. PMID 21368765 DOI: 10.1038/Jhg.2011.22 |
0.331 |
|
| 2011 |
Kokubo Y, Murayama S, Tomiyama H, Hirokawa Y, Hasegawa M, Okamoto K, Kihira T, Takashima A, Tsuji S, Kuzuhara S. P4-151: Research consortium of amyotrophic lateral sclerosis/parkinsonism-dementia complex of the Kii peninsula of Japan Alzheimer's & Dementia. 7: S756-S757. DOI: 10.1016/J.Jalz.2011.05.2173 |
0.321 |
|
| 2011 |
Yamada M, Sakai K, Nozaki I, Hamaguchi T, Sanjo N, Noguchi-Shinohara M, Sadakane A, Nakamura Y, Sato T, Kitamoto T, Moriwaka F, Shiga Y, Kuroiwa Y, Nishizawa M, Kuzuhara S, et al. Human prion diseases in Japan: analysis of 1,552 patients in a prospective 11-year surveillance Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.1984 |
0.301 |
|
| 2010 |
Nozaki I, Hamaguchi T, Sanjo N, Noguchi-Shinohara M, Sakai K, Nakamura Y, Sato T, Kitamoto T, Mizusawa H, Moriwaka F, Shiga Y, Kuroiwa Y, Nishizawa M, Kuzuhara S, Inuzuka T, et al. Prospective 10-year surveillance of human prion diseases in Japan. Brain : a Journal of Neurology. 133: 3043-57. PMID 20855418 DOI: 10.1093/Brain/Awq216 |
0.345 |
|
| 2010 |
Li L, Funayama M, Tomiyama H, Li Y, Yoshino H, Sasaki R, Kokubo Y, Kuzuhara S, Mizuno Y, Hattori N. No evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patients. Neuroscience Letters. 479: 245-8. PMID 20641165 DOI: 10.1016/J.Neulet.2010.05.071 |
0.307 |
|
| 2010 |
Hara K, Kokubo Y, Ishiura H, Fukuda Y, Miyashita A, Kuwano R, Sasaki R, Goto J, Nishizawa M, Kuzuhara S, Tsuji S. TRPM7 is not associated with amyotrophic lateral sclerosis-parkinsonism dementia complex in the Kii peninsula of Japan. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 310-3. PMID 19405049 DOI: 10.1002/Ajmg.B.30966 |
0.364 |
|
| 2009 |
Kokubo Y, Kuzuhara S, Isoda K, Sato K, Kawada N, Narita Y. Neuro-Sweet disease: report of the first autopsy case. Bmj Case Reports. 2009. PMID 21686758 DOI: 10.1136/Bcr.07.2008.0534 |
0.331 |
|
| 2009 |
Kuzuhara S. [Development of neurology in Japan and its contribution to elucidate and resolve the sociomedical problems]. Rinshå Shinkeigaku = Clinical Neurology. 49: 741-4. PMID 20030198 DOI: 10.5692/Clinicalneurol.49.741 |
0.314 |
|
| 2009 |
Kajikawa H, Kokubo Y, Taniguchi A, Naito Y, Kuzuhara S. Juvenile muscular atrophy of the distal upper extremity (hirayama disease) in two lanky look-alike brothers. The Neurologist. 15: 220-2. PMID 19590383 DOI: 10.1097/Nrl.0B013E3181942880 |
0.345 |
|
| 2009 |
Satoh M, Takeda K, Kuzuhara S. Agraphia in intellectually normal Japanese patients with ALS: omission of kana letters. Journal of Neurology. 256: 1455-60. PMID 19377859 DOI: 10.1007/S00415-009-5136-0 |
0.354 |
|
| 2009 |
Morimoto S, Kuzuhara S, Kokubo Y. Increased oxidative stress in patients with amyotrophic lateral sclerosis/Parkinsonism-dementia complex in the Kii peninsula, Japan. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 123-6. PMID 18972548 DOI: 10.1002/Mds.22362 |
0.362 |
|
| 2009 |
Atsuta N, Watanabe H, Ito M, Tanaka F, Tamakoshi A, Nakano I, Aoki M, Tsuji S, Yuasa T, Takano H, Hayashi H, Kuzuhara S, Sobue G. Age at onset influences on wide-ranged clinical features of sporadic amyotrophic lateral sclerosis. Journal of the Neurological Sciences. 276: 163-9. PMID 18962725 DOI: 10.1016/J.Jns.2008.09.024 |
0.34 |
|
| 2009 |
Kuzuhara S. 5. Recent Topics and Progress in Treatment of Parkinson's Disease Nihon Naika Gakkai Zasshi. 98: 2131-2140. DOI: 10.2169/Naika.98.2131 |
0.303 |
|
| 2008 |
Kuzuhara S. [Treatment of Parkinson's disease at present and in the future]. Rinshå Shinkeigaku = Clinical Neurology. 48: 835-43. PMID 19198095 DOI: 10.5692/Clinicalneurol.48.835 |
0.307 |
|
| 2008 |
Tomiyama H, Kokubo Y, Sasaki R, Li Y, Imamichi Y, Funayama M, Mizuno Y, Hattori N, Kuzuhara S. Mutation analyses in amyotrophic lateral sclerosis/parkinsonism-dementia complex of the Kii peninsula, Japan. Movement Disorders : Official Journal of the Movement Disorder Society. 23: 2344-8. PMID 18759352 DOI: 10.1002/Mds.22262 |
0.353 |
|
| 2008 |
Satoh M, Kuzuhara S. Training in mental singing while walking improves gait disturbance in Parkinson's disease patients. European Neurology. 60: 237-43. PMID 18756088 DOI: 10.1159/000151699 |
0.321 |
|
| 2008 |
Taniguchi A, Narita Y, Naito Y, Kuzuhara S. [Analysis of application form for Parkinson's disease provided by the specific diseases treatment research program of Ministry of Health, Labour and Welfare of Japan]. Rinshå Shinkeigaku = Clinical Neurology. 48: 106-13. PMID 18326303 DOI: 10.5692/Clinicalneurol.48.106 |
0.347 |
|
| 2008 |
Maki T, Kokubo Y, Nishida S, Suzuki H, Kuzuhara S. An autopsy case with non-herpetic acute limbic encephalitis (NHALE). Neuropathology : Official Journal of the Japanese Society of Neuropathology. 28: 521-5. PMID 18282167 DOI: 10.1111/J.1440-1789.2008.00872.X |
0.338 |
|
| 2007 |
Hayashi T, Narita Y, Okugawa N, Hamaguchi E, Shibahara M, Kuzuhara S. Pressure ulcers in ALS patients on admission at a university hospital in Japan. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 8: 310-3. PMID 17852025 DOI: 10.1080/17482960701538825 |
0.324 |
|
| 2007 |
Kokubo Y, Kuzuhara S, Isoda K, Sato K, Kawada N, Narita Y. Neuro-Sweet disease: report of the first autopsy case. Journal of Neurology, Neurosurgery, and Psychiatry. 78: 997-1000. PMID 17702783 DOI: 10.1136/Jnnp.2006.105650 |
0.331 |
|
| 2007 |
Shibata N, Kawaguchi M, Uchida K, Kakita A, Takahashi H, Nakano R, Fujimura H, Sakoda S, Ihara Y, Nobukuni K, Takehisa Y, Kuroda S, Kokubo Y, Kuzuhara S, Honma T, et al. Protein-bound crotonaldehyde accumulates in the spinal cord of superoxide dismutase-1 mutation-associated familial amyotrophic lateral sclerosis and its transgenic mouse model. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 27: 49-61. PMID 17319283 DOI: 10.1111/J.1440-1789.2006.00746.X |
0.308 |
|
| 2007 |
Mimuro M, Kokubo Y, Kuzuhara S. Similar topographical distribution of neurofibrillary tangles in amyotrophic lateral sclerosis and parkinsonism-dementia complex in people living in the Kii peninsula of Japan suggests a single tauopathy. Acta Neuropathologica. 113: 653-8. PMID 17277950 DOI: 10.1007/S00401-007-0197-6 |
0.361 |
|
| 2006 |
Itoh N, Maeda M, Naito Y, Narita Y, Kuzuhara S. An adult case of megalencephalic leukoencephalopathy with subcortical cysts with S93L mutation in MLC1 gene: a case report and diffusion MRI. European Neurology. 56: 243-5. PMID 17077634 DOI: 10.1159/000096672 |
0.329 |
|
| 2006 |
Yokota O, Tsuchiya K, Itoh Y, Ishizu H, Akiyama H, Ikeda M, Kuzuhara S, Otomo E. Frontotemporal lobar degeneration with ubiquitin pathology: an autopsy case presenting with semantic dementia and upper motor neuron signs with a clinical course of 19 years. Acta Neuropathologica. 112: 739-49. PMID 17016698 DOI: 10.1007/S00401-006-0149-6 |
0.352 |
|
| 2006 |
Kokubo Y, Murayama S, Kuzuhara S. P3-320: Immunohistochemical study on the isoform of tau protein in amyotrophic lateral sclerosis/parkinsonism-dementia complex of the Kii peninsula of Japan Alzheimer's & Dementia. 2: S469-S469. DOI: 10.1016/J.Jalz.2006.05.1590 |
0.334 |
|
| 2006 |
Kuzuhara S, Kokubo Y. P3-146: Marked increase of parkinsonism-dementia (P-D) phenotypes in the high incidence amyotrophic lateral sclerosis (ALS) focus in the Kii peninsula of Japan Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.1414 |
0.332 |
|
| 2005 |
Kuzuhara S, Kokubo Y. Atypical parkinsonism of Japan: amyotrophic lateral sclerosis-parkinsonism-dementia complex of the Kii peninsula of Japan (Muro disease): an update. Movement Disorders : Official Journal of the Movement Disorder Society. 20: S108-13. PMID 16092099 DOI: 10.1002/Mds.20548 |
0.43 |
|
| 2004 |
Kokubo Y, Kuzuhara S. Neurofibrillary tangles in ALS and Parkinsonism-dementia complex focus in Kii, Japan. Neurology. 63: 2399-401. PMID 15623711 DOI: 10.1212/01.Wnl.0000147241.52694.6A |
0.372 |
|
| 2004 |
Kuzuhara S, Saito Y, Murayama S. P3-161 Cotton-wool plaques, plaque-like angiopathy, neurofibrillary tangles and leukoencephalopathy in a Japanese man clinically presenting with binswanger's disease Neurobiology of Aging. 25: S401-S402. DOI: 10.1016/S0197-4580(04)81313-7 |
0.312 |
|
| 2003 |
Kokubo Y, Kuzuhara S. Neuroradiological study of patients with amyotrophic lateral sclerosis and parkinsonism-dementia complex on the Kii peninsula of Japan. Archives of Neurology. 60: 1257-61. PMID 12975292 DOI: 10.1001/Archneur.60.9.1257 |
0.336 |
|
| 2003 |
Itoh N, Ishiguro K, Arai H, Kokubo Y, Sasaki R, Narita Y, Kuzuhara S. Biochemical and ultrastructural study of neurofibrillary tangles in amyotrophic lateral sclerosis/parkinsonism-dementia complex in the Kii peninsula of Japan. Journal of Neuropathology and Experimental Neurology. 62: 791-8. PMID 12901704 DOI: 10.1093/Jnen/62.7.791 |
0.34 |
|
| 2003 |
Kokubo Y, Ito K, Kuzuhara S. Ophthalmomyiasis-like pigmentary retinopathy in ALS/PDC in the Kii peninsula of Japan. Neurology. 60: 1725-6. PMID 12771286 DOI: 10.1212/01.Wnl.0000061487.16841.72 |
0.335 |
|
| 2003 |
Machii K, Ugawa Y, Kokubo Y, Sasaki R, Kuzuhara S. Somatosensory evoked potential recovery in kii amyotrophic lateral sclerosis/parkinsonism-dementia complex (kii AlS/PDC). Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology. 114: 564-8. PMID 12705437 DOI: 10.1016/S1388-2457(02)00416-9 |
0.355 |
|
| 2002 |
Saito Y, Geyer A, Sasaki R, Kuzuhara S, Nanba E, Miyasaka T, Suzuki K, Murayama S. Early-onset, rapidly progressive familial tauopathy with R406W mutation. Neurology. 58: 811-3. PMID 11889249 DOI: 10.1212/Wnl.58.5.811 |
0.348 |
|
| 2001 |
Sasaki R, Ito N, Shimamura M, Murakami T, Kuzuhara S, Uchino M, Uyama E. A novel CLCN1 mutation: P480T in a Japanese family with Thomsen's myotonia congenita. Muscle & Nerve. 24: 357-63. PMID 11353420 DOI: 10.1002/1097-4598(200103)24:3<357::Aid-Mus1006>3.0.Co;2-E |
0.323 |
|
| 2001 |
Kuzuhara S, Kokubo Y, Sasaki R, Narita Y, Yabana T, Hasegawa M, Iwatsubo T. Familial amyotrophic lateral sclerosis and parkinsonism-dementia complex of the Kii Peninsula of Japan: clinical and neuropathological study and tau analysis. Annals of Neurology. 49: 501-11. PMID 11310628 DOI: 10.1002/Ana.100 |
0.413 |
|
| 2000 |
Kokubo Y, Kuzuhara S, Narita Y. Geographical distribution of amyotrophic lateral sclerosis with neurofibrillary tangles in the Kii Peninsula of Japan. Journal of Neurology. 247: 850-2. PMID 11151416 DOI: 10.1007/S004150070071 |
0.361 |
|
| 2000 |
Yamamura Y, Hattori N, Matsumine H, Kuzuhara S, Mizuno Y. Autosomal recessive early-onset parkinsonism with diurnal fluctuation: clinicopathologic characteristics and molecular genetic identification. Brain & Development. 22: S87-91. PMID 10984666 DOI: 10.1016/S0387-7604(00)00130-3 |
0.371 |
|
| 2000 |
Saito Y, Kawai M, Inoue K, Sasaki R, Arai H, Nanba E, Kuzuhara S, Ihara Y, Kanazawa I, Murayama S. Widespread expression of alpha-synuclein and tau immunoreactivity in Hallervorden-Spatz syndrome with protracted clinical course. Journal of the Neurological Sciences. 177: 48-59. PMID 10967182 DOI: 10.1016/S0022-510X(00)00337-3 |
0.338 |
|
| 1999 |
Sasaki R, Ichiyasu H, Ito N, Ikeda T, Takano H, Ikeuchi T, Kuzuhara S, Uchino M, Tsuji S, Uyama E. Novel chloride channel gene mutations in two unrelated Japanese families with Becker's autosomal recessive generalized myotonia. Neuromuscular Disorders : Nmd. 9: 587-92. PMID 10619717 DOI: 10.1016/S0960-8966(99)00050-4 |
0.31 |
|
| 1999 |
Kokubo Y, Kuzuhara S, Narita Y, Kikugawa K, Nakano R, Inuzuka T, Tsuji S, Watanabe M, Miyazaki T, Murayama S, Ihara Y. Accumulation of neurofilaments and SOD1-immunoreactive products in a patient with familial amyotrophic lateral sclerosis with I113T SOD1 mutation. Archives of Neurology. 56: 1506-8. PMID 10593307 DOI: 10.1001/Archneur.56.12.1506 |
0.329 |
|
| 1999 |
Shimizu S, Hoshi K, Muramoto T, Homma M, Ironside JW, Kuzuhara S, Sato T, Yamamoto T, Kitamoto T. Creutzfeldt-Jakob disease with florid-type plaques after cadaveric dura mater grafting. Archives of Neurology. 56: 357-62. PMID 10190828 DOI: 10.1001/Archneur.56.3.357 |
0.35 |
|
| 1999 |
Kuzuhara S, Kokubo Y, Sasaki R, Narita Y, Yabana T. A Family Of Amyotrophic Lateral Sclerosis And Parkinsonism-Dementia Complex (Als/Pdc) Of The Kii Peninsula Of Japan Suggesting A Familial Tauopathy. Report Of Three Autopsy Cases Journal of Neuropathology and Experimental Neurology. 58: 548. DOI: 10.1097/00005072-199905000-00166 |
0.356 |
|
| 1998 |
Yamamura Y, Kuzuhara S, Kondo K, Yanagi T, Uchida M, Matsumine H, Mizuno Y. Clinical, pathologic and genetic studies on autosomal recessive early-onset parkinsonism with diurnal fluctuation. Parkinsonism & Related Disorders. 4: 65-72. PMID 18591091 DOI: 10.1016/S1353-8020(98)00015-7 |
0.352 |
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| 1998 |
Sasaki R, Naito Y, Kuzuhara S. A novel de novo point mutation in the GTP cyclohydrolase I gene in a Japanese patient with hereditary progressive and dopa responsive dystonia. Journal of Neurology, Neurosurgery, and Psychiatry. 65: 947. PMID 9854983 DOI: 10.1136/Jnnp.65.6.947 |
0.32 |
|
| 1998 |
Matsumine H, Yamamura Y, Kobayashi T, Nakamura S, Kuzuhara S, Mizuno Y. Early onset parkinsonism with diurnal fluctuation maps to a locus for juvenile parkinsonism. Neurology. 50: 1340-5. PMID 9595984 DOI: 10.1212/Wnl.50.5.1340 |
0.355 |
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| 1997 |
Kikugawa K, Nakano R, Inuzuka T, Kokubo Y, Narita Y, Kuzuhara S, Yoshida S, Tsuji S. A missense mutation in the SOD1 gene in patients with amyotrophic lateral sclerosis from the Kii Peninsula and its vicinity, Japan. Neurogenetics. 1: 113-5. PMID 10732812 DOI: 10.1007/S100480050016 |
0.343 |
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| 1996 |
Kuzuhara S, Kokubo Y, Narita Y. Neuropathology Of A Kii Als Case From A Family Of Als And Parkinsonism-Dementia In Hobara In Kii Peninsula Of Japan Journal of Neuropathology and Experimental Neurology. 55: 633. DOI: 10.1097/00005072-199605000-00123 |
0.355 |
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| 1992 |
Kuzuhara S. [Recent therapeutic advances in geriatric neurology]. Nihon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics. 29: 531-9. PMID 1434048 DOI: 10.3143/Geriatrics.29.531 |
0.334 |
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| 1989 |
Murayama S, Ookawa Y, Mori H, Nakano I, Ihara Y, Kuzuhara S, Tomonaga M. Immunocytochemical and ultrastructural study of Lewy body-like hyaline inclusions in familial amyotrophic lateral sclerosis. Acta Neuropathologica. 78: 143-52. PMID 2473594 DOI: 10.1007/Bf00688202 |
0.327 |
|
| 1987 |
Ugawa Y, Kohara N, Hirasawa H, Kuzuhara S, Iwata M, Mannen T. Myoclonus in Alzheimer's disease. Journal of Neurology. 235: 90-4. PMID 3430197 DOI: 10.1007/Bf00718016 |
0.321 |
|
| 1984 |
Yoshimura M, Mori H, Tomonaga M, Yamanouchi H, Kuzuhara S. [Loss of neurons in the nucleus basalis of Meynert in Parkinson disease with dementia, "diffuse Lewy body disease" and senile dementia of Alzheimer type]. Nihon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics. 21: 580-7. PMID 6533352 DOI: 10.3143/Geriatrics.21.580 |
0.321 |
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