| Year |
Citation |
Score |
| 2021 |
Vandael D, Okamoto Y, Jonas P. Transsynaptic modulation of presynaptic short-term plasticity in hippocampal mossy fiber synapses. Nature Communications. 12: 2912. PMID 34006874 DOI: 10.1038/s41467-021-23153-5 |
0.74 |
|
| 2019 |
Okamoto Y. Presynaptic mechanisms underlying post-tetanic potentiation at hippocampal mossy fiber synapses Intrinsic Activity. 7: A3.36. DOI: 10.25006/IA.7.S1-A3.36 |
0.647 |
|
| 2016 |
Okamoto Y, Lipstein N, Hua Y, Lin KH, Brose N, Sakaba T, Midorikawa M. Distinct modes of endocytotic presynaptic membrane and protein uptake at the calyx of Held terminal of rats and mice. Elife. 5. PMID 27154627 DOI: 10.7554/eLife.14643 |
0.373 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2019 |
Li J, Suda K, Ueoka I, Tanaka R, Yoshida H, Okada Y, Okamoto Y, Hiramatsu Y, Takashima H, Yamaguchi M. Neuron-specific knockdown of Drosophila HADHB induces a shortened lifespan, deficient locomotive ability, abnormal motor neuron terminal morphology and learning disability. Experimental Cell Research. PMID 30953623 DOI: 10.1016/j.yexcr.2019.03.040 |
0.272 |
|
| 2014 |
Midorikawa M, Okamoto Y, Sakaba T. Developmental changes in Ca2+ channel subtypes regulating endocytosis at the calyx of Held. The Journal of Physiology. 592: 3495-510. PMID 24907302 DOI: 10.1113/jphysiol.2014.273243 |
0.253 |
|
| 2016 |
Okamoto Y, Lipstein N, Hua Y, Lin K, Brose N, Sakaba T, Midorikawa M. Author response: Distinct modes of endocytotic presynaptic membrane and protein uptake at the calyx of Held terminal of rats and mice Elife. DOI: 10.7554/Elife.14643.018 |
0.211 |
|
| 2021 |
Vandael D, Okamoto Y, Borges-Merjane C, Vargas-Barroso V, Suter BA, Jonas P. Subcellular patch-clamp techniques for single-bouton stimulation and simultaneous pre- and postsynaptic recording at cortical synapses. Nature Protocols. 16: 2947-2967. PMID 33990799 DOI: 10.1038/s41596-021-00526-0 |
0.201 |
|
| 2018 |
Higuchi Y, Okunushi R, Hara T, Hashiguchi A, Yuan J, Yoshimura A, Murayama K, Ohtake A, Ando M, Hiramatsu Y, Ishihara S, Tanabe H, Okamoto Y, Matsuura E, Ueda T, et al. Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy. Brain : a Journal of Neurology. PMID 29718187 DOI: 10.1093/brain/awy104 |
0.163 |
|
| 2017 |
Yuan JH, Hashiguchi A, Yoshimura A, Yaguchi H, Tsuzaki K, Ikeda A, Wada-Isoe K, Ando M, Nakamura T, Higuchi Y, Hiramatsu Y, Okamoto Y, Takashima H. Clinical diversity caused by novel IGHMBP2 variants. Journal of Human Genetics. PMID 28202949 DOI: 10.1038/jhg.2017.15 |
0.124 |
|
| 2024 |
Kojima F, Okamoto Y, Ando M, Higuchi Y, Hobara T, Yuan J, Yoshimura A, Hashiguchi A, Matsuura E, Takashima H. A novel homozygous HPDL variant in Japanese siblings with autosomal recessive hereditary spastic paraplegia: case report and literature review. Neurogenetics. PMID 38286980 DOI: 10.1007/s10048-024-00746-y |
0.12 |
|
| 2011 |
Sakiyama Y, Okamoto Y, Higuchi I, Inamori Y, Sangatsuda Y, Michizono K, Watanabe O, Hatakeyama H, Goto Y, Arimura K, Takashima H. A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy. Acta Neuropathologica. 121: 775-83. PMID 21424749 DOI: 10.1007/s00401-011-0818-y |
0.114 |
|
| 2019 |
Sawada J, Katayama T, Tokashiki T, Kikuchi S, Kano K, Takahashi K, Saito T, Adachi Y, Okamoto Y, Yoshimura A, Takashima H, Hasebe N. The First Case of Spinocerebellar Ataxia Type 8 in Monozygotic Twins. Internal Medicine (Tokyo, Japan). PMID 31554751 DOI: 10.2169/internalmedicine.2905-19 |
0.108 |
|
| 2007 |
Yoshida T, Tomozawa Y, Arisato T, Okamoto Y, Hirano H, Nakagawa M. The functional alteration of mutant GFAP depends on the location of the domain: morphological and functional studies using astrocytoma-derived cells. Journal of Human Genetics. 52: 362-9. PMID 17318298 DOI: 10.1007/s10038-007-0124-7 |
0.107 |
|
| 2022 |
Ando M, Higuchi Y, Yuan JH, Yoshimura A, Higashi S, Takeuchi M, Hobara T, Kojima F, Noguchi Y, Takei J, Hiramatsu Y, Nozuma S, Sakiyama Y, Hashiguchi A, Matsuura E, ... Okamoto Y, et al. Genetic and clinical features of cerebellar ataxia with biallelic repeat expansions in Japan. Frontiers in Neurology. 13: 952493. PMID 36034314 DOI: 10.3389/fneur.2022.952493 |
0.105 |
|
| 2014 |
Hashiguchi A, Higuchi Y, Nomura M, Nakamura T, Arata H, Yuan J, Yoshimura A, Okamoto Y, Matsuura E, Takashima H. Neurofilament light mutation causes hereditary motor and sensory neuropathy with pyramidal signs. Journal of the Peripheral Nervous System : Jpns. 19: 311-6. PMID 25583183 DOI: 10.1111/jns.12102 |
0.105 |
|
| 2013 |
Okamoto Y, Pehlivan D, Wiszniewski W, Beck CR, Snipes GJ, Lupski JR, Khajavi M. Curcumin facilitates a transitory cellular stress response in Trembler-J mice. Human Molecular Genetics. 22: 4698-705. PMID 23847051 DOI: 10.1093/hmg/ddt318 |
0.097 |
|
| 2015 |
Pehlivan D, Beck CR, Okamoto Y, Harel T, Akdemir ZH, Jhangiani SN, Withers MA, Goksungur MT, Carvalho CM, Czesnik D, Gonzaga-Jauregui C, Wiszniewski W, Muzny DM, Gibbs RA, Rautenstrauss B, et al. The role of combined SNV and CNV burden in patients with distal symmetric polyneuropathy. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 26378787 DOI: 10.1038/Gim.2015.124 |
0.092 |
|
| 2022 |
Ando M, Higuchi Y, Yuan J, Yoshimura A, Taniguchi T, Kojima F, Noguchi Y, Hobara T, Takeuchi M, Takei J, Hiramatsu Y, Sakiyama Y, Hashiguchi A, Okamoto Y, Mitsui J, et al. Comprehensive Genetic Analyses of Inherited Peripheral Neuropathies in Japan: Making Early Diagnosis Possible. Biomedicines. 10. PMID 35884855 DOI: 10.3390/biomedicines10071546 |
0.091 |
|
| 2021 |
Higuchi Y, Ando M, Yoshimura A, Hakotani S, Koba Y, Sakiyama Y, Hiramatsu Y, Tashiro Y, Maki Y, Hashiguchi A, Yuan J, Okamoto Y, Matsuura E, Takashima H. Prevalence of Fragile X-Associated Tremor/Ataxia Syndrome in Patients with Cerebellar Ataxia in Japan. Cerebellum (London, England). PMID 34498198 DOI: 10.1007/s12311-021-01323-x |
0.087 |
|
| 2023 |
Higuchi Y, Ando M, Kojima F, Yuan J, Hashiguchi A, Yoshimura A, Hiramatsu Y, Nozuma S, Fukumura S, Yahikozawa H, Abe E, Toyoshima I, Sugawara M, Okamoto Y, Matsuura E, et al. Dystonia and Parkinsonism in COA7-related disorders: expanding the phenotypic spectrum. Journal of Neurology. PMID 37750949 DOI: 10.1007/s00415-023-11998-3 |
0.086 |
|
| 2015 |
Gonzaga-Jauregui C, Harel T, Gambin T, Kousi M, Griffin LB, Francescatto L, Ozes B, Karaca E, Jhangiani SN, Bainbridge MN, Lawson KS, Pehlivan D, Okamoto Y, Withers M, Mancias P, et al. Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy. Cell Reports. 12: 1169-83. PMID 26257172 DOI: 10.1016/J.Celrep.2015.07.023 |
0.086 |
|
| 2009 |
Hirano R, Takashima H, Okubo R, Okamoto Y, Maki Y, Ishida S, Suehara M, Hokezu Y, Arimura K. Clinical and genetic characterization of 16q-linked autosomal dominant spinocerebellar ataxia in South Kyushu, Japan. Journal of Human Genetics. 54: 377-81. PMID 19444286 DOI: 10.1038/jhg.2009.44 |
0.081 |
|
| 2023 |
Ando M, Higuchi Y, Yuan J, Yoshimura A, Kojima F, Yamanishi Y, Aso Y, Izumi K, Imada M, Maki Y, Nakagawa H, Hobara T, Noguchi Y, Takei J, Hiramatsu Y, ... ... Okamoto Y, et al. Clinical variability associated with intronic FGF14 GAA repeat expansion in Japan. Annals of Clinical and Translational Neurology. PMID 37916889 DOI: 10.1002/acn3.51936 |
0.081 |
|
| 2019 |
Ie Y, Okamoto Y, Inoue T, Tone S, Seo T, Honda Y, Tanaka S, Lee SK, Ohto T, Yamada R, Tada H, Aso Y. Highly Planar and Completely Insulated Oligothiophenes: Effects of π-Conjugation on Hopping Charge Transport. The Journal of Physical Chemistry Letters. PMID 31132274 DOI: 10.1021/acs.jpclett.9b00747 |
0.076 |
|
| 2002 |
Kitamura S, Kohno Y, Okamoto Y, Takeshita M, Ohta S. Reductive metabolism of an alpha,beta-ketoalkyne, 4-phenyl-3-butyn-2-one, by rat liver preparations. Drug Metabolism and Disposition: the Biological Fate of Chemicals. 30: 414-20. PMID 11901095 DOI: 10.1124/dmd.30.4.414 |
0.076 |
|
| 2017 |
Hirayanagi K, Okamoto Y, Takai E, Ishizawa K, Makioka K, Fujita Y, Kaneko Y, Tanaka M, Takashima H, Ikeda Y. Bilateral striatal necrosis caused by a founder mitochondrial 14459G>A mutation in two independent Japanese families. Journal of the Neurological Sciences. 378: 177-181. PMID 28566160 DOI: 10.1016/j.jns.2017.05.015 |
0.075 |
|
| 2023 |
Okamoto Y, Takashima H. The Current State of Charcot-Marie-Tooth Disease Treatment. Genes. 14. PMID 37510296 DOI: 10.3390/genes14071391 |
0.073 |
|
| 2023 |
Ando M, Higuchi Y, Yuan JH, Yoshimura A, Dozono M, Hobara T, Kojima F, Noguchi Y, Takeuchi M, Takei J, Hiramatsu Y, Nozuma S, Nakamura T, Sakiyama Y, Hashiguchi A, ... ... Okamoto Y, et al. Clinical phenotypic diversity of -related disease in the largest case series of inherited peripheral neuropathy in Japan. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 36948577 DOI: 10.1136/jnnp-2022-330769 |
0.071 |
|
| 2022 |
Tokuhisa A, Akinaga Y, Terayama K, Okamoto Y, Okuno Y. Single-Image Super-Resolution Improvement of X-ray Single-Particle Diffraction Images Using a Convolutional Neural Network. Journal of Chemical Information and Modeling. 62: 3352-3364. PMID 35820663 DOI: 10.1021/acs.jcim.2c00660 |
0.071 |
|
| 2017 |
Ando M, Hashiguchi A, Okamoto Y, Yoshimura A, Hiramatsu Y, Yuan J, Higuchi Y, Mitsui J, Ishiura H, Umemura A, Maruyama K, Matsushige T, Morishita S, Nakagawa M, Tsuji S, et al. Clinical and genetic diversities of Charcot-Marie-Tooth disease with MFN2 mutations in a large case study. Journal of the Peripheral Nervous System : Jpns. PMID 28660751 DOI: 10.1111/jns.12228 |
0.069 |
|
| 2007 |
Okamoto Y, Higashiyama H, Inoue H, Kanematsu M, Kinoshita M, Asano S. Quantitative image analysis in adipose tissue using an automated image analysis system: differential effects of peroxisome proliferator-activated receptor-alpha and -gamma agonist on white and brown adipose tissue morphology in AKR obese and db/db diabetic mice. Pathology International. 57: 369-77. PMID 17539968 DOI: 10.1111/j.1440-1827.2007.02109.x |
0.067 |
|
| 2011 |
Yoshida T, Sasaki M, Yoshida M, Namekawa M, Okamoto Y, Tsujino S, Sasayama H, Mizuta I, Nakagawa M. Nationwide survey of Alexander disease in Japan and proposed new guidelines for diagnosis. Journal of Neurology. 258: 1998-2008. PMID 21533827 DOI: 10.1007/s00415-011-6056-3 |
0.067 |
|
| 2004 |
Hirano R, Takashima H, Okubo R, Tajima K, Okamoto Y, Ishida S, Tsuruta K, Arisato T, Arata H, Nakagawa M, Osame M, Arimura K. Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families. Neurogenetics. 5: 215-21. PMID 15455264 DOI: 10.1007/s10048-004-0194-z |
0.067 |
|
| 2017 |
Kawashima K, Okamoto Y, Annayev O, Toyokura N, Takahashi R, Lippmaa M, Itaka K, Suzuki Y, Matsuki N, Koinuma H. Combinatorial screening of halide perovskite thin films and solar cells by mask-defined IR laser molecular beam epitaxy. Science and Technology of Advanced Materials. 18: 307-315. PMID 28567176 DOI: 10.1080/14686996.2017.1314172 |
0.066 |
|
| 2015 |
Ie Y, Okamoto Y, Tone S, Aso Y. Synthesis, Properties, and π-Dimer Formation of Oligothiophenes Partially Bearing Orthogonally Fused Fluorene Units. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 16688-95. PMID 26407071 DOI: 10.1002/chem.201502606 |
0.065 |
|
| 2007 |
Miyazaki Y, Tang J, Maeda Y, Nakano M, Wang L, Nolte RT, Sato H, Sugai M, Okamoto Y, Truesdale AT, Hassler DF, Nartey EN, Patrick DR, Ho ML, Ozawa K. Orally active 4-amino-5-diarylurea-furo[2,3-d]pyrimidine derivatives as anti-angiogenic agent inhibiting VEGFR2 and Tie-2. Bioorganic & Medicinal Chemistry Letters. 17: 1773-8. PMID 17276055 DOI: 10.1016/j.bmcl.2006.12.077 |
0.064 |
|
| 2018 |
Yoshimura A, Yuan JH, Hashiguchi A, Ando M, Higuchi Y, Nakamura T, Okamoto Y, Nakagawa M, Takashima H. Genetic profile and onset features of 1005 patients with Charcot-Marie-Tooth disease in Japan. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 30257968 DOI: 10.1136/jnnp-2018-318839 |
0.064 |
|
| 2011 |
Hayashi T, Nakamura M, Ichiba M, Matsuda M, Kato M, Shiokawa N, Shimo H, Tomiyasu A, Mori S, Tomiyasu Y, Ishizuka T, Inamori Y, Okamoto Y, Umehara F, Arimura K, et al. Adult-type metachromatic leukodystrophy with compound heterozygous ARSA mutations: a case report and phenotypic comparison with a previously reported case. Psychiatry and Clinical Neurosciences. 65: 105-8. PMID 21265945 DOI: 10.1111/j.1440-1819.2010.02169.x |
0.064 |
|
| 2002 |
Okamoto Y, Mitsuyama H, Jonosono M, Hirata K, Arimura K, Osame M, Nakagawa M. Autosomal dominant palatal myoclonus and spinal cord atrophy. Journal of the Neurological Sciences. 195: 71-6. PMID 11867077 DOI: 10.1016/S0022-510X(01)00687-6 |
0.063 |
|
| 2022 |
Hiramatsu Y, Okamoto Y, Yoshimura A, Yuan JH, Ando M, Higuchi Y, Hashiguchi A, Matsuura E, Nozaki F, Kumada T, Murayama K, Suzuki M, Yamamoto Y, Matsui N, Miyazaki Y, et al. Complex hereditary peripheral neuropathies caused by novel variants in mitochondrial-related nuclear genes. Journal of Neurology. PMID 35235001 DOI: 10.1007/s00415-022-11026-w |
0.062 |
|
| 2022 |
Ando M, Higuchi Y, Okamoto Y, Yuan J, Yoshimura A, Takei J, Taniguchi T, Hiramatsu Y, Sakiyama Y, Hashiguchi A, Matsuura E, Nakagawa H, Sonoda K, Yamashita T, Tamura A, et al. An NEFH founder mutation causes broad phenotypic spectrum in multiple Japanese families. Journal of Human Genetics. PMID 35091664 DOI: 10.1038/s10038-022-01019-y |
0.062 |
|
| 2020 |
Ie Y, Okamoto Y, Inoue T, Seo T, Ohto T, Yamada R, Tada H, Aso Y. Improving Intramolecular Hopping Charge Transport via Periodical Segmentation of π-Conjugation in a Molecule. Journal of the American Chemical Society. PMID 33350820 DOI: 10.1021/jacs.0c10560 |
0.06 |
|
| 2003 |
Kinoshita T, Imaizumi T, Miura Y, Fujimoto H, Ayabe M, Shoji H, Okamoto Y, Takashima H, Osame M, Nakagawa M. A case of adult-onset Alexander disease with Arg416Trp human glial fibrillary acidic protein gene mutation. Neuroscience Letters. 350: 169-72. PMID 14550921 DOI: 10.1016/S0304-3940(03)00900-5 |
0.057 |
|
| 2020 |
Okamoto Y, Sumiya M, Nakamura Y, Suzuki Y. Effective silicon production from SiCl source using hydrogen radicals generated and transported at atmospheric pressure. Science and Technology of Advanced Materials. 21: 482-491. PMID 32939173 DOI: 10.1080/14686996.2020.1789438 |
0.057 |
|
| 2018 |
Yuan JH, Hashiguchi A, Okamoto Y, Yoshimura A, Ando M, Shiomi K, Saito K, Takahashi M, Ichinose K, Ohmichi T, Ichikawa K, Tadashi A, Takigawa H, Shibayama H, Takashima H. Clinical and mutational spectrum of Japanese patients with recessive variants in SH3TC2. Journal of Human Genetics. PMID 29321516 DOI: 10.1038/s10038-017-0388-5 |
0.056 |
|
| 2007 |
Higashiyama H, Billin AN, Okamoto Y, Kinoshita M, Asano S. Expression profiling of peroxisome proliferator-activated receptor-delta (PPAR-delta) in mouse tissues using tissue microarray. Histochemistry and Cell Biology. 127: 485-94. PMID 17333240 DOI: 10.1007/s00418-007-0279-5 |
0.055 |
|
| 2014 |
Okamoto Y, Goksungur MT, Pehlivan D, Beck CR, Gonzaga-Jauregui C, Muzny DM, Atik MM, Carvalho CM, Matur Z, Bayraktar S, Boone PM, Akyuz K, Gibbs RA, Battaloglu E, Parman Y, et al. Exonic duplication CNV of NDRG1 associated with autosomal-recessive HMSN-Lom/CMT4D. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 386-94. PMID 24136616 DOI: 10.1038/Gim.2013.155 |
0.055 |
|
| 2012 |
Tokunaga S, Hashiguchi A, Yoshimura A, Maeda K, Suzuki T, Haruki H, Nakamura T, Okamoto Y, Takashima H. Late-onset Charcot-Marie-Tooth disease 4F caused by periaxin gene mutation. Neurogenetics. 13: 359-65. PMID 22847150 DOI: 10.1007/s10048-012-0338-5 |
0.055 |
|
| 2021 |
Douzono M, Nobuhara Y, Maruta K, Okamoto Y, Sonoda Y, Takashima H. [Inherited Creutzfeldt-Jakob disease with four-octapeptide repeat insertional mutation in the prion gene]. Rinsho Shinkeigaku = Clinical Neurology. PMID 33867415 DOI: 10.5692/clinicalneurol.cn-001558 |
0.054 |
|
| 2007 |
Okamoto Y, Higashiyama H, Rong JX, McVey MJ, Kinoshita M, Asano S, Hansen MK. Comparison of mitochondrial and macrophage content between subcutaneous and visceral fat in db/db mice. Experimental and Molecular Pathology. 83: 73-83. PMID 17434481 DOI: 10.1016/j.yexmp.2007.02.007 |
0.051 |
|
| 2022 |
Okamoto Y, Hirano M, Morino K, Kajita MK, Nakaoka S, Tsuda M, Sugimoto KJ, Tamaki S, Hisatake J, Yokoyama H, Igarashi T, Shinagawa A, Sugawara T, Hara S, Fujikawa K, et al. Early dynamics of chronic myeloid leukemia on nilotinib predicts deep molecular response. Npj Systems Biology and Applications. 8: 39. PMID 36229495 DOI: 10.1038/s41540-022-00248-3 |
0.05 |
|
| 2018 |
Tanabe H, Higuchi Y, Yuan JH, Hashiguchi A, Yoshimura A, Ishihara S, Nozuma S, Okamoto Y, Matsuura E, Ishiura H, Mitsui J, Takashima R, Kokubun N, Maeda K, Asano Y, et al. Clinical and genetic features of Charcot-Marie-Tooth disease 2F and hereditary motor neuropathy 2B in Japan. Journal of the Peripheral Nervous System : Jpns. PMID 29381233 DOI: 10.1111/jns.12252 |
0.05 |
|
| 2007 |
Rong JX, Qiu Y, Hansen MK, Zhu L, Zhang V, Xie M, Okamoto Y, Mattie MD, Higashiyama H, Asano S, Strum JC, Ryan TE. Adipose mitochondrial biogenesis is suppressed in db/db and high-fat diet-fed mice and improved by rosiglitazone. Diabetes. 56: 1751-60. PMID 17456854 DOI: 10.2337/db06-1135 |
0.049 |
|
| 2006 |
Okamoto Y, Takashima H, Higuchi I, Matsuyama W, Suehara M, Nishihira Y, Hashiguchi A, Hirano R, Ng AR, Nakagawa M, Izumo S, Osame M, Arimura K. Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene. Neurogenetics. 7: 175-83. PMID 16779558 DOI: 10.1007/s10048-006-0046-0 |
0.048 |
|
| 2022 |
Matsuda A, Imada K, Obara N, Iida H, Yamazaki H, Tomiyama Y, Miyamura K, Sasaki O, Maeda T, Ohta K, Usuki K, Tokumine Y, Imajo K, Okamoto Y, Murakami M, et al. Dysmegakaryopoiesis and Transient Mild Increase in Bone Marrow Blasts in Patients With Aplastic Anemia Treated With Eltrombopag May Be Signs of Hematologic Improvement and Not Portend Clonal Evolution. American Journal of Clinical Pathology. PMID 36018052 DOI: 10.1093/ajcp/aqac094 |
0.044 |
|
| 2020 |
Taniguchi T, Ando M, Okamoto Y, Yoshimura A, Higuchi Y, Hashiguchi A, Shiga K, Hayashida A, Hatano T, Ishiura H, Mitsui J, Hattori N, Mizuno T, Nakagawa M, Tsuji S, et al. Genetic spectrum of Charcot-Marie-Tooth disease associated with myelin protein zero gene variants in Japan. Clinical Genetics. PMID 33179255 DOI: 10.1111/cge.13881 |
0.042 |
|
| 2018 |
Ohkura A, Negoto T, Aoki T, Noguchi K, Okamoto Y, Komatani H, Kawano T, Mukasa A, Morioka M. Stenotic changes of the posterior cerebral artery are a major contributing factor for cerebral infarction in moyamoya disease. Surgical Neurology International. 9: 105. PMID 29930871 DOI: 10.4103/sni.sni_18_18 |
0.04 |
|
| 2014 |
Komeyama K, Okamoto Y, Takaki K. Cobalt-catalyzed formal [4+2] cycloaddition of α,α'-dichloro-ortho-xylenes with alkynes. Angewandte Chemie (International Ed. in English). 53: 11325-8. PMID 25160750 DOI: 10.1002/anie.201406807 |
0.037 |
|
| 2007 |
Higashiyama H, Yoshimoto D, Okamoto Y, Kikkawa H, Asano S, Kinoshita M. Receptor-activated Smad localisation in bleomycin-induced pulmonary fibrosis. Journal of Clinical Pathology. 60: 283-9. PMID 16751304 DOI: 10.1136/jcp.2006.037606 |
0.037 |
|
| 2022 |
Ando M, Higuchi Y, Yuan JH, Yoshimura A, Kitao R, Morimoto T, Taniguchi T, Takeuchi M, Takei J, Hiramatsu Y, Sakiyama Y, Hashiguchi A, Okamoto Y, Mitsui J, Ishiura H, et al. Novel de novo POLR3B mutations responsible for demyelinating Charcot-Marie-Tooth disease in Japan. Annals of Clinical and Translational Neurology. PMID 35482004 DOI: 10.1002/acn3.51555 |
0.035 |
|
| 2015 |
Nozuma S, Okamoto Y, Higuchi I, Yuan J, Hashiguchi A, Sakiyama Y, Yoshimura A, Higuchi Y, Takashima H. Clinical and Electron Microscopic Findings in Two Patients with Mitochondrial Myopathy Associated with Episodic Hyper-creatine Kinase-emia. Internal Medicine (Tokyo, Japan). 54: 3209-14. PMID 26666615 DOI: 10.2169/internalmedicine.54.5444 |
0.032 |
|
| 2013 |
Zhao Z, Hu J, Sakiyama Y, Okamoto Y, Higuchi I, Li N, Shen H, Takashima H. DYSF mutation analysis in a group of Chinese patients with dysferlinopathy Clinical Neurology and Neurosurgery. 115: 1234-1237. PMID 23254335 DOI: 10.1016/j.clineuro.2012.11.010 |
0.032 |
|
| 2009 |
Fukushima S, Hirohata M, Okamoto Y, Yamashita S, Ishida S, Shigemori M. Anterior inferior cerebellar artery dissecting aneurysm in a juvenile: case report. Neurologia Medico-Chirurgica. 49: 81-4. PMID 19246870 DOI: 10.2176/nmc.49.81 |
0.029 |
|
| 2022 |
Ando M, Higuchi Y, Yuan J, Yoshimura A, Taniguchi T, Takei J, Takeuchi M, Hiramatsu Y, Shimizu F, Kubota M, Takeshima A, Ueda T, Koh K, Nagaoka U, Tokashiki T, ... ... Okamoto Y, et al. Novel heterozygous variants of SLC12A6 in Japanese families with Charcot-Marie-Tooth disease. Annals of Clinical and Translational Neurology. PMID 35733399 DOI: 10.1002/acn3.51603 |
0.027 |
|
| 2020 |
Ishihara S, Okamoto Y, Tanabe H, Yoshimura A, Higuchi Y, Yuan JH, Hashiguchi A, Ishiura H, Mitsui J, Suwazono S, Oya Y, Sasaki M, Nakagawa M, Tsuji S, Ohya Y, et al. Clinical features of inherited neuropathy with BSCL2 mutations in Japan. Journal of the Peripheral Nervous System : Jpns. PMID 32108980 DOI: 10.1111/jns.12369 |
0.026 |
|
| 2017 |
Komatani H, Okamoto Y, Aoki T, Noguchi K, Morioka M. Long-term Prognosis after Extracranial-intracranial Bypass Surgery for Symptomatic Cerebrovascular Occlusive Disease. The Kurume Medical Journal. PMID 28603158 DOI: 10.2739/kurumemedj.MS6400016 |
0.024 |
|
| 2016 |
Higuchi Y, Hashiguchi A, Yuan J, Yoshimura A, Mitsui J, Ishiura H, Tanaka M, Ishihara S, Tanabe H, Nozuma S, Okamoto Y, Matsuura E, Ohkubo R, Inamizu S, Shiraishi W, et al. Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2. Annals of Neurology. PMID 26991897 DOI: 10.1002/ana.24612 |
0.019 |
|
| 2015 |
Hiramatsu Y, Yoshimura M, Saigo R, Arata H, Okamoto Y, Matsuura E, Maruyama H, Takashima H. Toxocara canis myelitis involving the lumbosacral region: a case report. The Journal of Spinal Cord Medicine. 1-15. PMID 26832660 DOI: 10.1080/10790268.2015.1114230 |
0.016 |
|
| 2011 |
Okamoto Y, Higuchi I, Sakiyama Y, Tokunaga S, Watanabe O, Arimura K, Nakagawa M, Takashima H. A new mitochondria-related disease showing myopathy with episodic hyper-creatine kinase-emia. Annals of Neurology. 70: 486-92. PMID 21905081 DOI: 10.1002/ana.22498 |
0.013 |
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| 2022 |
Lee J, Iwasaki T, Kaida T, Chuman H, Yoshimura A, Okamoto Y, Takashima H, Miyata K. A case of adult-onset Wolfram syndrome with compound heterozygous mutations of the WFS1 gene. American Journal of Ophthalmology Case Reports. 25: 101315. PMID 35112031 DOI: 10.1016/j.ajoc.2022.101315 |
0.01 |
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| 2022 |
Taniguchi T, Ando M, Okamoto Y, Yoshimura A, Higuchi Y, Hashiguchi A, Matsuda N, Yamamoto M, Dohi E, Takahashi M, Yoshino M, Nomura T, Matsushima M, Yabe I, Sanpei Y, et al. Elderly patients with suspected Charcot-Marie-Tooth disease should be tested for the TTR gene for effective treatments. Journal of Human Genetics. PMID 35027655 DOI: 10.1038/s10038-021-01005-w |
0.01 |
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| 2015 |
Sakiyama Y, Kanda N, Higuchi Y, Yoshimura M, Wakaguri H, Takata Y, Watanabe O, Yuan J, Tashiro Y, Saigo R, Nozuma S, Yoshimura A, Arishima S, Ikeda K, Shinohara K, ... ... Okamoto Y, et al. New type of encephalomyelitis responsive to trimethoprim/sulfamethoxazole treatment in Japan. Neurology® Neuroimmunology & Neuroinflammation. 2: e143. PMID 26309903 DOI: 10.1212/NXI.0000000000000143 |
0.01 |
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| 2012 |
Miyake H, Kajimoto Y, Murai H, Nomura S, Ono S, Okamoto Y, Sumi Y. Assessment of a quick reference table algorithm for determining initial postoperative pressure settings of programmable pressure valves in patients with idiopathic normal pressure hydrocephalus: SINPHONI subanalysis. Neurosurgery. 71: 722-8; discussion 72. PMID 22653392 DOI: 10.1227/NEU.0b013e318260fef7 |
0.01 |
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