| Year |
Citation |
Score |
| 2023 |
Nakahara Y, Mitsui J, Date H, Porto KJ, Hayashi Y, Yamashita A, Kusakabe Y, Matsukawa T, Ishiura H, Yasuda T, Iwata A, Goto J, Ichikawa Y, Momose Y, Takahashi Y, ... ... Kato T, et al. Genome-wide association study identifies a new susceptibility locus in for Multiple System Atrophy. Medrxiv : the Preprint Server For Health Sciences. PMID 37425910 DOI: 10.1101/2023.05.02.23289328 |
0.381 |
|
| 2019 |
Kato H, Takahashi Y, Iseki C, Igari R, Sato H, Sato H, Koyama S, Tobita M, Kawanami T, Iino M, Ishizawa K, Kato T. Tooth Loss-associated Cognitive Impairment in the Elderly: A Community-based Study in Japan. Internal Medicine (Tokyo, Japan). PMID 30626824 DOI: 10.2169/Internalmedicine.1896-18 |
0.478 |
|
| 2017 |
Koyama S, Sato H, Kobayashi R, Kawakatsu S, Kurimura M, Wada M, Kawanami T, Kato T. Clinical and radiological diversity in genetically confirmed primary familial brain calcification. Scientific Reports. 7: 12046. PMID 28935882 DOI: 10.1038/S41598-017-11595-1 |
0.511 |
|
| 2017 |
Koyama S, Sato H, Wada M, Kawanami T, Emi M, Kato T. Whole-exome sequencing and digital PCR identified a novel compound heterozygous mutation in the NPHP1 gene in a case of Joubert syndrome and related disorders. Bmc Medical Genetics. 18: 37. PMID 28347285 DOI: 10.1186/S12881-017-0399-2 |
0.492 |
|
| 2016 |
Sato H, Takahashi Y, Kimihira L, Iseki C, Kato H, Suzuki Y, Igari R, Sato H, Koyama S, Arawaka S, Kawanami T, Miyajima M, Samejima N, Sato S, Kameda M, ... ... Kato T, et al. A Segmental Copy Number Loss of the SFMBT1 Gene Is a Genetic Risk for Shunt-Responsive, Idiopathic Normal Pressure Hydrocephalus (iNPH): A Case-Control Study. Plos One. 11: e0166615. PMID 27861535 DOI: 10.1371/Journal.Pone.0166615 |
0.495 |
|
| 2016 |
Susa S, Sato-Monma F, Ishii K, Hada Y, Takase K, Tada K, Wada K, Kameda W, Watanabe K, Oizumi T, Suzuki T, Daimon M, Kato T. Transient Worsening of Photosensitivity due to Cholelithiasis in a Variegate Porphyria Patient. Internal Medicine (Tokyo, Japan). 55: 2965-2969. PMID 27746433 DOI: 10.2169/Internalmedicine.55.7108 |
0.321 |
|
| 2016 |
Tanji H, Okada H, Igari R, Yamaguchi Y, Sato H, Takahashi Y, Koyama S, Arawaka S, Wada M, Kawanami T, Wakabayashi K, Kato T. Inflammatory Pseudotumor of the Brain Parenchyma with IgG4 Hypergammaglobulinemia. Internal Medicine (Tokyo, Japan). 55: 1911-6. PMID 27432102 DOI: 10.2169/Internalmedicine.55.5854 |
0.521 |
|
| 2015 |
Mitsui J, Matsukawa T, Sasaki H, Yabe I, Matsushima M, Dürr A, Brice A, Takashima H, Kikuchi A, Aoki M, Ishiura H, Yasuda T, Date H, Ahsan B, Iwata A, ... ... Kato T, et al. Variants associated with Gaucher disease in multiple system atrophy. Annals of Clinical and Translational Neurology. 2: 417-26. PMID 25909086 DOI: 10.1002/Acn3.185 |
0.489 |
|
| 2015 |
Yamaguchi Y, Wada M, Sato H, Nagasawa H, Koyama S, Takahashi Y, Kawanami T, Kato T. Impact of nocturnal heart rate variability on cerebral small-vessel disease progression: a longitudinal study in community-dwelling elderly Japanese. Hypertension Research : Official Journal of the Japanese Society of Hypertension. PMID 25787037 DOI: 10.1038/Hr.2015.38 |
0.488 |
|
| 2014 |
Yoshinaga T, Sekijima Y, Koyama S, Maruyama K, Yoshida T, Kato T, Ikeda S. Clinical and radiological findings of a cerebrotendinous xanthomatosis patient with a novel p.A335V mutation in the CYP27A1 gene. Internal Medicine (Tokyo, Japan). 53: 2725-9. PMID 25447658 DOI: 10.2169/Internalmedicine.53.2996 |
0.313 |
|
| 2014 |
Watanabe K, Ouchi M, Ohara M, Kameda W, Susa S, Oizumi T, Wada M, Suzuki T, Kawanami T, Oba K, Kato T. Change of carotid intima-media thickness is associated with age in elderly Japanese patients without a history of cardiovascular disease. Geriatrics & Gerontology International. PMID 25312290 DOI: 10.1111/Ggi.12402 |
0.498 |
|
| 2014 |
Konno Y, Kanoto M, Hosoya T, Toyoguchi Y, Kawanami T, Kato T. Clinical significance of mammillary body enhancement in Wernicke encephalopathy: report of 2 cases and review of the literature. Magnetic Resonance in Medical Sciences : Mrms : An Official Journal of Japan Society of Magnetic Resonance in Medicine. 13: 123-6. PMID 24769631 DOI: 10.2463/Mrms.2013-0073 |
0.488 |
|
| 2014 |
Iseki C, Takahashi Y, Wada M, Kawanami T, Adachi M, Kato T. Incidence of idiopathic normal pressure hydrocephalus (iNPH): a 10-year follow-up study of a rural community in Japan. Journal of the Neurological Sciences. 339: 108-12. PMID 24656600 DOI: 10.1016/J.Jns.2014.01.033 |
0.493 |
|
| 2014 |
Yamaguchi Y, Wada M, Sato H, Nagasawa H, Koyama S, Takahashi Y, Kawanami T, Kato T. Impact of ambulatory blood pressure variability on cerebral small vessel disease progression and cognitive decline in community-based elderly Japanese. American Journal of Hypertension. 27: 1257-67. PMID 24651635 DOI: 10.1093/Ajh/Hpu045 |
0.485 |
|
| 2014 |
Kayama T, Yamashita H, Fukao A, Kubota I, Kato T, Kitanaka C, Sato S, Ueno Y, Konta T, Shibata Y, Watanabe T, Abe S, Miyamoto T, Inoue S, Miyashita T, et al. Pleiotropic effect of common variants at ABO glycosyltranferase locus in 9q32 on plasma levels of pancreatic lipase and angiotensin converting enzyme Plos One. 9. PMID 24586218 DOI: 10.1371/Journal.Pone.0055903 |
0.493 |
|
| 2014 |
Iseki C, Kawanami T, Tsunoda T, Chinuki Y, Kato T. Chronic headaches and sleepiness caused by facial soap (containing hydrolyzed wheat proteins)-induced wheat allergy. Internal Medicine (Tokyo, Japan). 53: 151-4. PMID 24429457 DOI: 10.2169/Internalmedicine.53.0744 |
0.48 |
|
| 2013 |
Okada H, Wada M, Sato H, Yamaguchi Y, Tanji H, Kurokawa K, Kawanami T, Takahashi T, Kato T. Neuromyelitis optica preceded by hyperCKemia and a possible association with coxsackie virus group A10 infection. Internal Medicine (Tokyo, Japan). 52: 2665-8. PMID 24292760 DOI: 10.2169/Internalmedicine.52.1042 |
0.495 |
|
| 2013 |
Sato H, Takahashi Y, Wada M, Shiono Y, Suzuki I, Kohno K, Kato Y, Kawanami T, Sakurada K, Kayama T, Kato T. Lymphomatosis cerebri with intramedullary spinal cord involvement. Internal Medicine (Tokyo, Japan). 52: 2561-5. PMID 24240797 DOI: 10.2169/Internalmedicine.52.0748 |
0.485 |
|
| 2013 |
Iseki C, Takahashi Y, Wada M, Kawanami T, Kato T. Subclinical declines in the verbal fluency and motor regulation of patients with AVIM (asymptomatic ventriculomegaly with features of idiopathic NPH on MRI): a case-controlled study. Internal Medicine (Tokyo, Japan). 52: 1687-90. PMID 23903500 DOI: 10.2169/Internalmedicine.52.8914 |
0.499 |
|
| 2013 |
Mitsui J, Matsukawa T, Ishiura H, Fukuda Y, Ichikawa Y, Date H, Ahsan B, Nakahara Y, Momose Y, Takahashi Y, Iwata A, Goto J, Yamamoto Y, Komata M, Shirahige K, ... ... Kato T, et al. Mutations in COQ2 in familial and sporadic multiple-system atrophy the multiple-system atrophy research collaboration New England Journal of Medicine. 369: 233-244. PMID 23758206 DOI: 10.1056/Nejmoa1212115 |
0.493 |
|
| 2013 |
Yamaguchi Y, Wada M, Tanji H, Kurokawa K, Kawanami T, Tanji K, Yoneda M, Kato T. Steroid-responsive thalamic lesions accompanying microbleeds in a case of Hashimoto's encephalopathy with autoantibodies against α-enolase. Internal Medicine (Tokyo, Japan). 52: 1249-53. PMID 23728565 DOI: 10.2169/Internalmedicine.52.9373 |
0.501 |
|
| 2013 |
Tanji H, Koyama S, Wada M, Kawanami T, Kurita K, Tamiya G, Saito N, Suzuki K, Kato T, Anderson KE, Gruber-Baldini AL, Fishman PS, Reich SG, Weiner WJ, Shulman LM. Comparison of caregiver strain in Parkinson's disease between Yamagata, Japan, and Maryland, The United States. Parkinsonism & Related Disorders. 19: 628-33. PMID 23514630 DOI: 10.1016/J.Parkreldis.2013.02.014 |
0.46 |
|
| 2013 |
Takahashi M, Obayashi M, Ishiguro T, Sato N, Niimi Y, Ozaki K, Mogushi K, Mahmut Y, Tanaka H, Tsuruta F, Dolmetsch R, Yamada M, Takahashi H, Kato T, Mori O, et al. Cytoplasmic location of α1A voltage-gated calcium channel C-terminal fragment (Cav2.1-CTF) aggregate is sufficient to cause cell death. Plos One. 8: e50121. PMID 23505410 DOI: 10.1371/Journal.Pone.0050121 |
0.464 |
|
| 2013 |
Yamaguchi Y, Wada M, Tanji H, Kurokawa K, Kawanami T, Ohtake H, Kato T. Marked improvement in opsoclonus and cerebellar ataxia after the surgical removal of a squamous cell carcinoma of the thymus: a case report. Journal of the Neurological Sciences. 325: 156-9. PMID 23235139 DOI: 10.1016/J.Jns.2012.11.011 |
0.501 |
|
| 2012 |
Mizuta K, Kuroda M, Kurimura M, Yahata Y, Sekizuka T, Aoki Y, Ikeda T, Abiko C, Noda M, Kimura H, Mizutani T, Kato T, Kawanami T, Ahiko T. Epidemic myalgia in adults associated with human parechovirus type 3 infection, Yamagata, Japan, 2008. Emerging Infectious Diseases. 18: 1787-93. PMID 23095469 DOI: 10.3201/Eid1811.111570 |
0.479 |
|
| 2012 |
Kato T, Tamiya G, Koyama S, Nakamura T, Makino S, Arawaka S, Kawanami T, Tooyama I. UBR5 Gene Mutation Is Associated with Familial Adult Myoclonic Epilepsy in a Japanese Family. Isrn Neurology. 2012: 508308. PMID 23029623 DOI: 10.5402/2012/508308 |
0.491 |
|
| 2012 |
Takahashi Y, Koyama S, Tanaka H, Arawaka S, Wada M, Kawanami T, Haga H, Watanabe H, Toyota K, Numakura C, Hayasaka K, Kato T. An elderly Japanese patient with adult-onset type II citrullinemia with a novel D493G mutation in the SLC25A13 gene. Internal Medicine (Tokyo, Japan). 51: 2131-4. PMID 22892490 DOI: 10.2169/Internalmedicine.51.7644 |
0.5 |
|
| 2012 |
Hiraka T, Koyama S, Kurokawa K, Tanji H, Iseki C, Wada M, Kawanami T, Oda A, Hosoya T, Kato T. Reversible distension of the subarachnoid space around the optic nerves in a case of idiopathic hypertrophic pachymeningitis. Magnetic Resonance in Medical Sciences : Mrms : An Official Journal of Japan Society of Magnetic Resonance in Medicine. 11: 141-4. PMID 22790301 DOI: 10.2463/Mrms.11.141 |
0.47 |
|
| 2012 |
Iseki C, Takahashi Y, Wada M, Arawaka S, Kawanami T, Kato T. Changes in the subarachnoid space precede ventriculomegaly in idiopathic normal pressure hydrocephalus (iNPH). Internal Medicine (Tokyo, Japan). 51: 1751-3. PMID 22790139 DOI: 10.2169/Internalmedicine.51.7254 |
0.477 |
|
| 2012 |
Takahashi M, Ishikawa K, Sato N, Obayashi M, Niimi Y, Ishiguro T, Yamada M, Toyoshima Y, Takahashi H, Kato T, Takao M, Murayama S, Mori O, Eishi Y, Mizusawa H. Reduced brain-derived neurotrophic factor (BDNF) mRNA expression and presence of BDNF-immunoreactive granules in the spinocerebellar ataxia type 6 (SCA6) cerebellum. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 32: 595-603. PMID 22393909 DOI: 10.1111/J.1440-1789.2012.01302.X |
0.462 |
|
| 2012 |
Koyama S, Kawanami T, Arawaka S, Wada M, Kato T. A Japanese adult case of megalencephalic leukoencephalopathy with subcortical cysts with a good long-term prognosis. Internal Medicine (Tokyo, Japan). 51: 503-6. PMID 22382567 DOI: 10.2169/Internalmedicine.51.6462 |
0.518 |
|
| 2012 |
Koyama S, Kawanami T, Tanji H, Arawaka S, Wada M, Saito N, Kato T. A case of cerebrotendinous xanthomatosis presenting with epilepsy as an initial symptom with a novel V413D mutation in the CYP27A1 gene. Clinical Neurology and Neurosurgery. 114: 1021-3. PMID 22336472 DOI: 10.1016/J.Clineuro.2012.01.032 |
0.481 |
|
| 2012 |
Koike H, Tanaka F, Hashimoto R, Tomita M, Kawagashira Y, Iijima M, Fujitake J, Kawanami T, Kato T, Yamamoto M, Sobue G. Natural history of transthyretin Val30Met familial amyloid polyneuropathy: analysis of late-onset cases from non-endemic areas. Journal of Neurology, Neurosurgery, and Psychiatry. 83: 152-8. PMID 22228785 DOI: 10.1136/Jnnp-2011-301299 |
0.511 |
|
| 2012 |
Koyama S, Kawanami T, Kurokawa K, Tanji H, Iseki C, Arawaka S, Wada M, Kato T. Carpal tunnel syndrome as an initial manifestation in a case of transthyretin-related familial amyloid polyneuropathy with a novel A120T mutation. Clinical Neurology and Neurosurgery. 114: 707-9. PMID 22209138 DOI: 10.1016/J.Clineuro.2011.11.030 |
0.502 |
|
| 2011 |
Kimura H, Kurimura M, Kurokawa K, Nagaoka U, Arawaka S, Wada M, Kawanami T, Kurita K, Kato T. A comprehensive study of repetitive transcranial magnetic stimulation in Parkinson's disease. Isrn Neurology. 2011: 845453. PMID 22389830 DOI: 10.5402/2011/845453 |
0.472 |
|
| 2011 |
Takahashi Y, Iseki C, Wada M, Momma T, Ueki M, Kawanami T, Daimon M, Suzuki K, Tamiya G, Kato T. Impaired glucose metabolism slows executive function independent of cerebral ischemic lesions in Japanese elderly: the Takahata study. Internal Medicine (Tokyo, Japan). 50: 1671-8. PMID 21841324 DOI: 10.2169/Internalmedicine.50.4871 |
0.49 |
|
| 2011 |
Takahashi Y, Kawanami T, Nagasawa H, Iseki C, Hanyu H, Kato T. Familial normal pressure hydrocephalus (NPH) with an autosomal-dominant inheritance: a novel subgroup of NPH. Journal of the Neurological Sciences. 308: 149-51. PMID 21704338 DOI: 10.1016/J.Jns.2011.06.018 |
0.506 |
|
| 2011 |
Wada M, Takahashi Y, Iseki C, Kawanami T, Daimon M, Kato T. Plasma fibrinogen, global cognitive function, and cerebral small vessel disease: results of a cross-sectional study in community-dwelling Japanese elderly. Internal Medicine (Tokyo, Japan). 50: 999-1007. PMID 21532222 DOI: 10.2169/Internalmedicine.50.4752 |
0.51 |
|
| 2011 |
Kato T, Sato H, Emi M, Seino T, Arawaka S, Iseki C, Takahashi Y, Wada M, Kawanami T. Segmental copy number loss of SFMBT1 gene in elderly individuals with ventriculomegaly: a community-based study. Internal Medicine (Tokyo, Japan). 50: 297-303. PMID 21325761 DOI: 10.2169/Internalmedicine.50.4505 |
0.505 |
|
| 2010 |
Kato T, Iseki C, Takahashi Y, Wada M, Kawanami T, Sato H, Emi M. [iNPH (Idiopathic normal pressure hydrocephalus) and AVIM (asymptomatic ventriculomegaly with features of iNPH on MRI)]. Rinshå Shinkeigaku = Clinical Neurology. 50: 963-5. PMID 21921528 DOI: JST.JSTAGE/clinicalneurol/50.963 |
0.453 |
|
| 2010 |
Tanji H, Koyama S, Kawanami T, Kato T. Late-onset familial amyloid polyneuropathy unrelated to known endemics. Internal Medicine (Tokyo, Japan). 49: 2367. PMID 21048379 DOI: 10.2169/Internalmedicine.49.4052 |
0.464 |
|
| 2010 |
Kato T, Emi M, Sato H, Arawaka S, Wada M, Kawanami T, Katagiri T, Tsuburaya K, Toyoshima I, Tanaka F, Sobue G, Matsubara K. Segmental copy-number gain within the region of isopentenyl diphosphate isomerase genes in sporadic amyotrophic lateral sclerosis. Biochemical and Biophysical Research Communications. 402: 438-42. PMID 20955688 DOI: 10.1016/J.Bbrc.2010.10.056 |
0.494 |
|
| 2010 |
Maruyama H, Morino H, Ito H, Izumi Y, Kato H, Watanabe Y, Kinoshita Y, Kamada M, Nodera H, Suzuki H, Komure O, Matsuura S, Kobatake K, Morimoto N, Abe K, ... ... Kato T, et al. Mutations of optineurin in amyotrophic lateral sclerosis. Nature. 465: 223-6. PMID 20428114 DOI: 10.1038/Nature08971 |
0.707 |
|
| 2010 |
Ishiguro T, Ishikawa K, Takahashi M, Obayashi M, Amino T, Sato N, Sakamoto M, Fujigasaki H, Tsuruta F, Dolmetsch R, Arai T, Sasaki H, Nagashima K, Kato T, Yamada M, et al. The carboxy-terminal fragment of alpha(1A) calcium channel preferentially aggregates in the cytoplasm of human spinocerebellar ataxia type 6 Purkinje cells. Acta Neuropathologica. 119: 447-64. PMID 20043227 DOI: 10.1007/S00401-009-0630-0 |
0.566 |
|
| 2010 |
Wada M, Nagasawa H, Kawanami T, Kurita K, Daimon M, Kubota I, Kayama T, Kato T. Cystatin C as an index of cerebral small vessel disease: results of a cross-sectional study in community-based Japanese elderly. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 17: 383-90. PMID 19832902 DOI: 10.1111/J.1468-1331.2009.02809.X |
0.498 |
|
| 2010 |
Kato T, Iseki C, Takahashi Y, Wada M, Kawanami T, Sato H, Emi M. iNPH (Idiopathic normal pressure hydrocephalus) and AVIM (asymptomatic ventriculomegaly with features of iNPH on MRI) Rinsho Shinkeigaku. 50: 963-965. DOI: 10.5692/Clinicalneurol.50.963 |
0.463 |
|
| 2009 |
Iseki C, Takahashi Y, Wada M, Kawanami T, Kurita K, Kato T. [A case of neurofibromatosis type 2 (NF2) presenting with late-onset axonal polyneuropathy]. Rinshå Shinkeigaku = Clinical Neurology. 49: 419-23. PMID 19715170 DOI: 10.5692/clinicalneurol.49.419 |
0.45 |
|
| 2009 |
Sakamoto M, Arawaka S, Hara S, Sato H, Cui C, Machiya Y, Koyama S, Wada M, Kawanami T, Kurita K, Kato T. Contribution of endogenous G-protein-coupled receptor kinases to Ser129 phosphorylation of alpha-synuclein in HEK293 cells. Biochemical and Biophysical Research Communications. 384: 378-82. PMID 19410557 DOI: 10.1016/J.Bbrc.2009.04.130 |
0.46 |
|
| 2009 |
Iseki C, Kawanami T, Nagasawa H, Wada M, Koyama S, Kikuchi K, Arawaka S, Kurita K, Daimon M, Mori E, Kato T. Asymptomatic ventriculomegaly with features of idiopathic normal pressure hydrocephalus on MRI (AVIM) in the elderly: a prospective study in a Japanese population. Journal of the Neurological Sciences. 277: 54-7. PMID 18990411 DOI: 10.1016/J.Jns.2008.10.004 |
0.49 |
|
| 2008 |
Karube H, Sakamoto M, Arawaka S, Hara S, Sato H, Ren CH, Goto S, Koyama S, Wada M, Kawanami T, Kurita K, Kato T. N-terminal region of alpha-synuclein is essential for the fatty acid-induced oligomerization of the molecules. Febs Letters. 582: 3693-700. PMID 18848547 DOI: 10.1016/J.Febslet.2008.10.001 |
0.452 |
|
| 2008 |
Wada M, Daimon M, Emi M, Iijima H, Sato H, Koyano S, Tajima K, Kawanami T, Kurita K, Hunt SC, Hopkins PN, Kubota I, Kawata S, Kato T. Genetic association between aldehyde dehydrogenase 2 (ALDH2) variation and high-density lipoprotein cholesterol (HDL-C) among non-drinkers in two large population samples in Japan. Journal of Atherosclerosis and Thrombosis. 15: 179-84. PMID 18776700 DOI: 10.5551/Jat.E542 |
0.473 |
|
| 2008 |
Wada M, Nagasawa H, Iseki C, Takahashi Y, Sato H, Arawaka S, Kawanami T, Kurita K, Daimon M, Kato T. Cerebral small vessel disease and chronic kidney disease (CKD): results of a cross-sectional study in community-based Japanese elderly. Journal of the Neurological Sciences. 272: 36-42. PMID 18541269 DOI: 10.1016/J.Jns.2008.04.029 |
0.512 |
|
| 2008 |
Wada M, Nagasawa H, Kurita K, Koyama S, Arawaka S, Kawanami T, Tajima K, Daimon M, Kato T. Cerebral small vessel disease and C-reactive protein: results of a cross-sectional study in community-based Japanese elderly. Journal of the Neurological Sciences. 264: 43-9. PMID 17673235 DOI: 10.1016/J.Jns.2007.06.053 |
0.517 |
|
| 2007 |
Nomoto T, Seta T, Nomura K, Shikama Y, Katagiri T, Katsura K, Kato T, Katayama Y. A case of reversible encephalopathy accompanied by demyelination occurring after ingestion of Sugihiratake mushrooms. Journal of Nippon Medical School = Nippon Ika Daigaku Zasshi. 74: 261-4. PMID 17625378 DOI: 10.1272/Jnms.74.261 |
0.318 |
|
| 2007 |
Nagasawa H, Wada M, Arawaka S, Kawanami T, Kurita K, Daimon M, Adachi M, Hosoya T, Emi M, Muramatsu M, Kato T. A polymorphism of the aldehyde dehydrogenase 2 gene is a risk factor for multiple lacunar infarcts in Japanese men: the Takahata Study. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 14: 428-34. PMID 17388993 DOI: 10.1111/J.1468-1331.2007.01700.X |
0.509 |
|
| 2007 |
Wada M, Nagasawa H, Kurita K, Koyama S, Arawaka S, Kawanami T, Tajima K, Daimon M, Kato T. Microalbuminuria is a risk factor for cerebral small vessel disease in community-based elderly subjects. Journal of the Neurological Sciences. 255: 27-34. PMID 17320908 DOI: 10.1016/J.Jns.2007.01.066 |
0.517 |
|
| 2006 |
Adachi M, Kawanami T, Ohshima F, Kato T. Upper midbrain profile sign and cingulate sulcus sign: MRI findings on sagittal images in idiopathic normal-pressure hydrocephalus, Alzheimer's disease, and progressive supranuclear palsy. Radiation Medicine. 24: 568-72. PMID 17041793 DOI: 10.1007/S11604-006-0074-6 |
0.495 |
|
| 2006 |
Arawaka S, Wada M, Goto S, Karube H, Sakamoto M, Ren CH, Koyama S, Nagasawa H, Kimura H, Kawanami T, Kurita K, Tajima K, Daimon M, Baba M, Kido T, ... ... Kato T, et al. The role of G-protein-coupled receptor kinase 5 in pathogenesis of sporadic Parkinson's disease. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 9227-38. PMID 16957079 DOI: 10.1523/Jneurosci.0341-06.2006 |
0.49 |
|
| 2006 |
Koyama S, Arawaka S, Chang-Hong R, Wada M, Kawanami T, Kurita K, Kato M, Nagai M, Aoki M, Itoyama Y, Sobue G, Chan PH, Kato T. Alteration of familial ALS-linked mutant SOD1 solubility with disease progression: its modulation by the proteasome and Hsp70. Biochemical and Biophysical Research Communications. 343: 719-30. PMID 16563356 DOI: 10.1016/J.Bbrc.2006.02.170 |
0.494 |
|
| 2005 |
Nagasawa H, Wada M, Koyama S, Kawanami T, Kurita K, Kato T. [A case of methanol intoxication with optic neuropathy visualized on STIR sequence of MR images]. Rinshå Shinkeigaku = Clinical Neurology. 45: 527-30. PMID 16119839 |
0.416 |
|
| 2005 |
Nagasawa H, Kurita K, Wada M, Kawanami T, Kato T. Blood transfusion-induced irreversible brain damage. Journal of Neurology. 252: 1541-2. PMID 15940385 DOI: 10.1007/S00415-005-0878-9 |
0.463 |
|
| 2005 |
Chang-Hong R, Wada M, Koyama S, Kimura H, Arawaka S, Kawanami T, Kurita K, Kadoya T, Aoki M, Itoyama Y, Kato T. Neuroprotective effect of oxidized galectin-1 in a transgenic mouse model of amyotrophic lateral sclerosis. Experimental Neurology. 194: 203-11. PMID 15899257 DOI: 10.1016/J.Expneurol.2005.02.011 |
0.488 |
|
| 2005 |
Kurokawa K, Sato H, Nakajima K, Kawanami T, Kato T. [Clinical, neuroimaging and electroencephalographic findings of encephalopathy occuring after the ingestion of "sugihiratake" (Pleurocybella porrigens), an autumn mashroom: a report of two cases]. Rinshå Shinkeigaku = Clinical Neurology. 45: 111-6. PMID 15782609 |
0.462 |
|
| 2004 |
Kato T, Kawanami T, Shimizu H, Kurokawa K, Sato H, Nakajima K, Nomoto T, Seta T, Kamei T, Yoshino H, Sasagawa I, Ito M, Karasawa S, Kimura H, Suzuki Y, et al. [An outbreak of encephalopathy after eating autumn mushroom (Sugihiratake; Pleurocybella porrigens) in patients with renal failure: a clinical analysis of ten cases in Yamagata, Japan]. Nå to Shinkei = Brain and Nerve. 56: 999-1007. PMID 15729876 |
0.446 |
|
| 2004 |
Yamaguchi H, Igarashi M, Hirata A, Tsuchiya H, Sugiyama K, Morita Y, Jimbu Y, Ohnuma H, Daimon M, Tominaga M, Kato T. Progression of diabetic nephropathy enhances the plasma osteopontin level in type 2 diabetic patients. Endocrine Journal. 51: 499-504. PMID 15516785 DOI: 10.1507/Endocrj.51.499 |
0.603 |
|
| 2004 |
Karasawa S, Kawanami T, Kimura H, Kurita K, Kato T. An unusual case of hypertensive encephalopathy involving the brain stem. Internal Medicine (Tokyo, Japan). 43: 448-9. PMID 15206565 DOI: 10.2169/Internalmedicine.43.448 |
0.476 |
|
| 2004 |
Wada M, Ren CH, Koyama S, Arawaka S, Kawakatsu S, Kimura H, Nagasawa H, Kawanami T, Kurita K, Daimon M, Hirano A, Kato T. A human granin-like neuroendocrine peptide precursor (proSAAS) immunoreactivity in tau inclusions of Alzheimer's disease and parkinsonism-dementia complex on Guam. Neuroscience Letters. 356: 49-52. PMID 14746899 DOI: 10.1016/J.Neulet.2003.11.028 |
0.611 |
|
| 2003 |
Wada M, Kimura M, Daimon M, Kurita K, Kato T, Johmura Y, Johkura K, Kuroiwa Y, Sobue G. An unusual phenotype of McLeod syndrome with late onset axonal neuropathy Journal of Neurology, Neurosurgery, and Psychiatry. 74: 1697-1698. PMID 14638894 DOI: 10.1136/Jnnp.74.12.1697 |
0.303 |
|
| 2003 |
Kikuchi K, Arawaka S, Koyama S, Kimura H, Ren CH, Wada M, Kawanami T, Kurita K, Daimon M, Kawakatsu S, Kadoya T, Goto K, Kato T. An N-terminal fragment of ProSAAS (a granin-like neuroendocrine peptide precursor) is associated with tau inclusions in Pick's disease. Biochemical and Biophysical Research Communications. 308: 646-54. PMID 12914799 DOI: 10.1016/S0006-291X(03)01391-3 |
0.502 |
|
| 2003 |
Daimon M, Sugiyama K, Kameda W, Saitoh T, Oizumi T, Hirata A, Yamaguchi H, Ohnuma H, Igarashi M, Kato T. Increased urinary levels of pentosidine, pyrraline and acrolein adduct in type 2 diabetes. Endocrine Journal. 50: 61-7. PMID 12733710 DOI: 10.1507/Endocrj.50.61 |
0.517 |
|
| 2003 |
Wada M, Ono S, Kadoya T, Kawanami T, Kurita K, Kato T. Decreased galectin-1 immunoreactivity of the skin in amyotrophic lateral sclerosis. Journal of the Neurological Sciences. 208: 67-70. PMID 12639727 DOI: 10.1016/S0022-510X(02)00424-0 |
0.491 |
|
| 2003 |
Wada M, Kurita K, Tajima K, Kawanami T, Kato T. A case of inflammatory demyelinating polyradiculoneuropathy associated with T-cell lymphoma. Acta Neurologica Scandinavica. 107: 62-6. PMID 12542515 DOI: 10.1034/J.1600-0404.2003.02094.X |
0.487 |
|
| 2002 |
Kawanami T, Kurita K, Yamakawa M, Omoto E, Kato T. Cerebrovascular disease in acute leukemia: a clinicopathological study of 14 patients. Internal Medicine (Tokyo, Japan). 41: 1130-4. PMID 12521201 DOI: 10.2169/Internalmedicine.41.1130 |
0.52 |
|
| 2002 |
Saitoh T, Daimon M, Eguchi H, Hosoya T, Kawanami T, Kurita K, Tominaga M, Kato T. Type 2 diabetes is not a risk factor for asymptomatic ischemic brain lesion--the Funagata study. Internal Medicine (Tokyo, Japan). 41: 351-6. PMID 12058882 DOI: 10.2169/Internalmedicine.41.351 |
0.504 |
|
| 2001 |
Moriai S, Daimon M, Susa S, Kurimura M, Kawanami T, Kurita K, Kato T. Hypoceruloplasminemia in neurological diseases. Internal Medicine (Tokyo, Japan). 40: 548-9. PMID 11446685 DOI: 10.2169/Internalmedicine.40.548 |
0.48 |
|
| 2001 |
Kato T, Kurita K, Seino T, Kadoya T, Horie H, Wada M, Kawanami T, Daimon M, Hirano A. Galectin-1 is a component of neurofilamentous lesions in sporadic and familial amyotrophic lateral sclerosis. Biochemical and Biophysical Research Communications. 282: 166-72. PMID 11263987 DOI: 10.1006/Bbrc.2001.4556 |
0.616 |
|
| 2000 |
Adachi M, Hosoya T, Yamaguchi K, Kawanami T, Kato T. Diffusion- and T2-weighted MRI of the transverse pontine fibres in spinocerebellar degeneration. Neuroradiology. 42: 803-9. PMID 11151684 DOI: 10.1007/S002340000336 |
0.493 |
|
| 2000 |
Daimon M, Susa S, Ohizumi T, Moriai S, Kawanami T, Hirata A, Yamaguchi H, Ohnuma H, Igarashi M, Kato T. A novel mutation of the ceruloplasmin gene in a patient with heteroallelic ceruloplasmin gene mutation (HypoCPGM). The Tohoku Journal of Experimental Medicine. 191: 119-25. PMID 10997552 DOI: 10.1620/Tjem.191.119 |
0.495 |
|
| 1999 |
Kurita K, Kawanami T, Katagiri T, Fuyama S, Kato T. T-cell lymphoma showing a non-enhancing diffuse white matter lesion with marked brain atrophy. Internal Medicine (Tokyo, Japan). 38: 507-11. PMID 10411359 DOI: 10.2169/Internalmedicine.38.507 |
0.485 |
|
| 1999 |
Nagaoka U, Suzuki Y, Kawanami T, Kurita K, Shikama Y, Honda K, Abe K, Nakajima T, Kato T. Regional differences in genetic subgroup frequency in hereditary cerebellar ataxia, and a morphometrical study of brain MR images in SCA1, MJD and SCA6. Journal of the Neurological Sciences. 164: 187-94. PMID 10402032 DOI: 10.1016/S0022-510X(99)00076-3 |
0.496 |
|
| 1999 |
Nakamura R, Kurita K, Kawanami T, Kato T. An immunohistochemical study of Purkinje cells in a case of hereditary cerebellar cortical atrophy. Acta Neuropathologica. 97: 196-200. PMID 9928832 DOI: 10.1007/S004010050974 |
0.427 |
|
| 1998 |
Kawanami T, Kato T, Kurita K, Sasaki H. The pallidoreticular pattern of brain damage on MRI in a patient with carbon monoxide poisoning. Journal of Neurology, Neurosurgery, and Psychiatry. 64: 282. PMID 9489555 DOI: 10.1136/Jnnp.64.2.282 |
0.489 |
|
| 1998 |
Yamaguchi K, Takahashi S, Kawanami T, Kato T, Sasaki H. Retinal degeneration in hereditary ceruloplasmin deficiency. Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fã¼R Augenheilkunde. 212: 11-4. PMID 9438577 DOI: 10.1159/000027251 |
0.473 |
|
| 1997 |
Kato T, Daimon M, Kawanami T, Ikezawa Y, Sasaki H, Maeda K. Islet changes in hereditary ceruloplasmin deficiency. Human Pathology. 28: 499-502. PMID 9104952 DOI: 10.1016/S0046-8177(97)90041-1 |
0.484 |
|
| 1997 |
Kato T, Suzuki J, Hayakawa H, Wada M, Kawanami T, Kurita K, Ikezawa Y, Ishikawa K, Sasaki H. Binding of IDPN (β,β′‐iminodipropionitrile) to rat spinal cord: Possible implication in the mechanism of spheroid formation in amyotrophic lateral sclerosis Neuropathology. 17: 76-79. DOI: 10.1111/J.1440-1789.1997.Tb00017.X |
0.483 |
|
| 1997 |
Kato T, Kawanami T, Daimon M, Sasaki H. Hereditary ceruloplasmin deficiency: A cerebro-retino-diabetic disease Neuropathology. 17: 71-75. DOI: 10.1111/J.1440-1789.1997.Tb00016.X |
0.531 |
|
| 1997 |
Kurita K, Kato T, Wada M, Kawanami T, Sasaki H. Ultrastructural localization of heparan sulfate-like immunoreactivity in spinal spheroids of motor neuron disease Neuropathology. 17: 15-20. DOI: 10.1111/J.1440-1789.1997.Tb00005.X |
0.506 |
|
| 1996 |
Kawanami T, Kato T, Daimon M, Tominaga M, Sasaki H, Maeda K, Arai S, Shikama Y, Katagiri T. Hereditary caeruloplasmin deficiency: clinicopathological study of a patient. Journal of Neurology, Neurosurgery, and Psychiatry. 61: 506-9. PMID 8937346 DOI: 10.1136/Jnnp.61.5.506 |
0.521 |
|
| 1996 |
Sasaki H, Yamatani K, Kato T, Kawanami T. Hereditary ceruloplasmin deficiency--a new type of diabetes mellitus. Internal Medicine (Tokyo, Japan). 35: 596-7. PMID 8894730 DOI: 10.2169/Internalmedicine.35.596 |
0.458 |
|
| 1996 |
Shibata N, Hirano A, Kobayashi M, Siddique T, Deng HX, Hung WY, Kato T, Asayama K. Intense superoxide dismutase-1 immunoreactivity in intracytoplasmic hyaline inclusions of familial amyotrophic lateral sclerosis with posterior column involvement. Journal of Neuropathology and Experimental Neurology. 55: 481-90. PMID 8786408 DOI: 10.1097/00005072-199604000-00011 |
0.615 |
|
| 1995 |
Daimon M, Kato T, Kawanami T, Tominaga M, Igarashi M, Yamatani K, Sasaki H. A nonsense mutation of the ceruloplasmin gene in hereditary ceruloplasmin deficiency with diabetes mellitus. Biochemical and Biophysical Research Communications. 217: 89-95. PMID 8526944 DOI: 10.1006/Bbrc.1995.2749 |
0.499 |
|
| 1995 |
Daimon M, Morita Y, Yamatani K, Igarashi M, Fukase N, Kawanami T, Kato T, Tominaga M, Sasaki H. Dinucleotide repeat polymorphism in the human ceruloplasmin gene. Human Genetics. 96: 736. PMID 8522337 DOI: 10.1007/Bf00210309 |
0.464 |
|
| 1995 |
Daimon M, Yamatani K, Igarashi M, Fukase N, Kawanami T, Kato T, Tominaga M, Sasaki H. Fine structure of the human ceruloplasmin gene. Biochemical and Biophysical Research Communications. 208: 1028-35. PMID 7702601 DOI: 10.1006/Bbrc.1995.1437 |
0.464 |
|
| 1994 |
Kawanami T, Kato T, Llena JF, Hirano A, Sasaki H. Altered synaptophysin-immunoreactive pattern in human olivary hypertrophy. Neuroscience Letters. 176: 178-80. PMID 7830941 DOI: 10.1016/0304-3940(94)90076-0 |
0.609 |
|
| 1994 |
Kato T, Kurita K, Kawanami T, Sasaki H. Detection of a 23 kDa human brain protein that shares epitope(s) with the 17 kDa core protein of human immunodeficiency virus (HIV). Neuroscience Letters. 181: 134-6. PMID 7534890 DOI: 10.1016/0304-3940(94)90577-0 |
0.47 |
|
| 1993 |
Kato T, Katagiri T, Shikama Y, Kurita K, Toyoshima I, Hirano A, Wada M, Sasaki H. Heparin sulfate-like immunoreactivity in the spinal cord in motor neuron disease. Acta Neuropathologica. 85: 663-5. PMID 8337944 DOI: 10.1007/Bf00334678 |
0.515 |
|
| 1992 |
Manaka H, Kato T, Kurita K, Katagiri T, Shikama Y, Kujirai K, Kawanami T, Suzuki Y, Nihei K, Sasaki H. Marked increase in cerebrospinal fluid ubiquitin in Creutzfeldt-Jakob disease. Neuroscience Letters. 139: 47-9. PMID 1328965 DOI: 10.1016/0304-3940(92)90854-Z |
0.49 |
|
| 1991 |
Kato T, Katagiri T, Hirano A, Kawanami T, Shikama Y, Kurita K, Sasaki H, Arai S. Calcitonin gene-related peptide immunoreactivity in spinal spheroids in motor neuron disease. Acta Neuropathologica. 82: 302-5. PMID 1759561 DOI: 10.1007/Bf00308816 |
0.623 |
|
| 1991 |
Kato T, Hirano A, Manaka H, Sasaki H, Katagiri T, Kawanami T, Shikama Y, Seino T, Sasaki H. Calcitonin gene-related peptide immunoreactivity in familial amyotrophic lateral sclerosis. Neuroscience Letters. 133: 163-7. PMID 1667811 DOI: 10.1016/0304-3940(91)90560-G |
0.617 |
|
| 1989 |
Kato T, Katagiri T, Hirano A, Kawanami T, Sasaki H. Lewy body-like hyaline inclusions in sporadic motor neuron disease are ubiquitinated. Acta Neuropathologica. 77: 391-6. PMID 2469287 DOI: 10.1007/Bf00687373 |
0.622 |
|
| 1988 |
Kato T, Katagiri T, Hirano A, Sasaki H, Arai S. Sporadic lower motor neuron disease with Lewy body-like inclusions: a new subgroup? Acta Neuropathologica. 76: 208-11. PMID 3407398 DOI: 10.1007/Bf00688105 |
0.508 |
|
| 1987 |
Kato T, Dembitzer HM, Hirano A, Llena JF. HTLV-III-like particles within a cell process surrounded by a myelin sheath in an AIDS brain. Acta Neuropathologica. 73: 306-8. PMID 3650020 DOI: 10.1007/Bf00686627 |
0.408 |
|
| 1987 |
Kato T, Hirano A, Llena JF, Dembitzer HM. Neuropathology of acquired immune deficiency syndrome (AIDS) in 53 autopsy cases with particular emphasis on microglial nodules and multinucleated giant cells. Acta Neuropathologica. 73: 287-94. PMID 3618121 DOI: 10.1007/Bf00686624 |
0.441 |
|
| 1987 |
Kato T, Hirano A, Donnenfeld H. A Golgi study of the large anterior horn cells of the lumbar cords in normal spinal cords and in amyotrophic lateral sclerosis. Acta Neuropathologica. 75: 34-40. PMID 3434213 DOI: 10.1007/Bf00686790 |
0.433 |
|
| 1987 |
Kato T, Hirano A, Dembitzer HM, Llena JF. HTLV-III-LIXE PARTICLES WITHIN A CELL PROCESS SURROUNDED BY MYELIN IN AN AIDS BRAIN. Journal of Neuropathology and Experimental Neurology. 46: 348. DOI: 10.1097/00005072-198705000-00056 |
0.4 |
|
| 1986 |
Kato T, Hirano A, Weinberg MN, Jacobs AK. Spinal cord lesions in progressive supranuclear palsy: some new observations. Acta Neuropathologica. 71: 11-4. PMID 3776465 DOI: 10.1007/Bf00687955 |
0.427 |
|
| 1986 |
Kato T, Hirano A, Jacobs AK, Weinberg MN. SPINAL CORD LESIONS IN PROGRESSIVE SUPRANUCLEAR PALSY Journal of Neuropathology and Experimental Neurology. 45: 377. DOI: 10.1097/00005072-198605000-00189 |
0.473 |
|
| 1985 |
Kato T, Hirano A, Llena JF. A Golgi study of the human Purkinje cell soma and dendrites. Acta Neuropathologica. 68: 145-8. PMID 4072621 DOI: 10.1007/Bf00688636 |
0.404 |
|
| 1985 |
Kato T, Hirano A. A Golgi study of the proximal portion of the human Purkinje cell axon. Acta Neuropathologica. 68: 191-5. PMID 3909727 DOI: 10.1007/Bf00690193 |
0.388 |
|
| 1985 |
Kato T, Hirano A. TRANSIENT RETINO-INFERIOR COLLICULAR FIBERS IN NEONATAL RATS Journal of Neuropathology and Experimental Neurology. 44: 342. DOI: 10.1097/00005072-198505000-00115 |
0.438 |
|
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