CSF1R-related leukoencephalopathy: A major player in primary microgliopathies

gan Konno, Takuya, Kasanuki, Koji, Ikeuchi, Takeshi, Dickson, Dennis W., Wszolek, Zbigniew K.
Cyhoeddwyd yn Neurology (2018)

Autosomal dominant Parkinson’s disease caused by SNCA duplications

gan Konno, Takuya, Ross, Owen A., Puschmann, Andreas, Dickson, Dennis W., Wszolek, Zbigniew K.
Cyhoeddwyd yn Parkinsonism Relat Disord (2015)

Hypertrophic olivary degeneration: A clinico-radiologic study

gan Konno, Takuya, Broderick, Daniel F., Tacik, Pawel, Caviness, John N., Wszolek, Zbigniew K.
Cyhoeddwyd yn Parkinsonism Relat Disord (2016)

Deep brain stimulation for levodopa-refractory benign tremulous parkinsonism

gan Konno, Takuya, Ross, Owen A., Wharen, Robert E., Uitti, Ryan J., Wszolek, Zbigniew K.
Cyhoeddwyd yn Neurol Neurochir Pol (2016)

Cerebral Peduncle Angle: Unreliable in Differentiating Progressive Supranuclear Palsy From Other Neurodegenerative Diseases

gan Tipton, Philip W., Konno, Takuya, Broderick, Daniel F., Dickson, Dennis W., Wszolek, Zbigniew K.
Cyhoeddwyd yn Parkinsonism Relat Disord (2016)

Robustness and Vulnerability of the Autoregulatory System That Maintains Nuclear TDP-43 Levels: A Trade-off Hypothesis for ALS Pathology Based on in Silico Data

gan Sugai, Akihiro, Kato, Taisuke, Koyama, Akihide, Koike, Yuka, Kasahara, Sou, Konno, Takuya, Ishihara, Tomohiko, Onodera, Osamu
Cyhoeddwyd yn Front Neurosci (2018)

DCTN1-related neurodegeneration: Perry syndrome and beyond

gan Konno, Takuya, Ross, Owen A., Teive, Hélio A.G., Sławek, Jarosław, Dickson, Dennis W., Wszolek, Zbigniew K.
Cyhoeddwyd yn Parkinsonism Relat Disord (2017)

A patient clinically diagnosed as multiple system atrophy harboring LRRK2 p.G2019S

gan Ando, Shoichiro, Konno, Takuya, Ishihara, Tomohiko, Hayashi, Hideki, Saito, Natsumi, Nishioka, Kenya, Hattori, Nobutaka, Wszolek, Zbigniew K., Onodera, Osamu
Cyhoeddwyd yn Clin Park Relat Disord (2019)

Efficacy of teriparatide in the treatment of nontraumatic osteonecrosis of the femoral head: a retrospective comparative study with alendronate

gan Arai, Ryuta, Takahashi, Daisuke, Inoue, Masahiro, Irie, Tohru, Asano, Tsuyoshi, Konno, Takuya, Terkawi, Mohamad Alaa, Onodera, Tomohiro, Kondo, Eiji, Iwasaki, Norimasa
Cyhoeddwyd yn BMC Musculoskelet Disord (2017)

Diagnostic Criteria for Adult-onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia Due to CSF1R mutation

gan Konno, Takuya, Yoshida, Kunihiro, Mizuta, Ikuko, Mizuno, Toshiki, Kawarai, Toshitaka, Tada, Masayoshi, Nozaki, Hiroaki, Ikeda, Shu-ichi, Onodera, Osamu, Wszolek, Zbigniew K., Ikeuchi, Takeshi
Cyhoeddwyd yn Eur J Neurol (2017)

Partial Loss of Function of CSF1R in a Patient with White Matter Abnormalities

gan Konno, Takuya, Miura, Takeshi, Harriott, Andrea M., Mezaki, Naomi, Edwards, Emily S., Rademakers, Rosa, Ross, Owen A., Meschia, James F., Ikeuchi, Takeshi, Wszolek, Zbigniew K.
Cyhoeddwyd yn Eur J Neurol (2018)

Coexistence of Progressive Supranuclear Palsy With Pontocerebellar Atrophy and Myotonic Dystrophy Type 1

gan Koga, Shunsuke, Eric Ahlskog, J, DeTure, Michael A, Baker, Matt, Roemer, Shanu F, Konno, Takuya, Rademakers, Rosa, Ross, Owen A, Dickson, Dennis W
Cyhoeddwyd yn J Neuropathol Exp Neurol (2019)

Increased cytoplasmic TARDBP mRNA in affected spinal motor neurons in ALS caused by abnormal autoregulation of TDP-43

gan Koyama, Akihide, Sugai, Akihiro, Kato, Taisuke, Ishihara, Tomohiko, Shiga, Atsushi, Toyoshima, Yasuko, Koyama, Misaki, Konno, Takuya, Hirokawa, Sachiko, Yokoseki, Akio, Nishizawa, Masatoyo, Kakita, Akiyoshi, Takahashi, Hitoshi, Onodera, Osamu
Cyhoeddwyd yn Nucleic Acids Res (2016)

Distinct spatiotemporal accumulation of N-truncated and full-length amyloid-β(42) in Alzheimer’s disease

gan Shinohara, Mitsuru, Koga, Shunsuke, Konno, Takuya, Nix, Jeremy, Shinohara, Motoko, Aoki, Naoya, Das, Pritam, Parisi, Joseph E, Petersen, Ronald C, Rosenberry, Terrone L, Dickson, Dennis W, Bu, Guojun
Cyhoeddwyd yn Brain (2017)

Association of MAPT subhaplotypes with clinical and demographic features in Parkinson’s disease

gan Deutschlander, Angela B., Konno, Takuya, Soto‐Beasley, Alexandra I., Walton, Ronald L., van Gerpen, Jay A., Uitti, Ryan J., Heckman, Michael G., Wszolek, Zbigniew K., Ross, Owen A.
Cyhoeddwyd yn Ann Clin Transl Neurol (2020)

Heterogeneity of cerebral TDP-43 pathology in sporadic amyotrophic lateral sclerosis: Evidence for clinico-pathologic subtypes

gan Takeuchi, Ryoko, Tada, Mari, Shiga, Atsushi, Toyoshima, Yasuko, Konno, Takuya, Sato, Tomoe, Nozaki, Hiroaki, Kato, Taisuke, Horie, Masao, Shimizu, Hiroshi, Takebayashi, Hirohide, Onodera, Osamu, Nishizawa, Masatoyo, Kakita, Akiyoshi, Takahashi, Hitoshi
Cyhoeddwyd yn Acta Neuropathol Commun (2016)

Diffuse Lewy body disease manifesting as corticobasal syndrome: A rare form of Lewy body disease

gan Kasanuki, Koji, Josephs, Keith A., Ferman, Tanis J., Murray, Melissa E., Koga, Shunsuke, Konno, Takuya, Sakae, Nobutaka, Parks, Adam, Uitti, Ryan J., Van Gerpen, Jay A., Graff-Radford, Neill R., Wszolek, Zbigniew K., Dickson, Dennis W.
Cyhoeddwyd yn Neurology (2018)

Duplication and deletion upstream of LMNB1 in autosomal dominant adult-onset leukodystrophy

gan Mezaki, Naomi, Miura, Takeshi, Ogaki, Kotaro, Eriguchi, Makoto, Mizuno, Yuri, Komatsu, Kenichi, Yamazaki, Hiroki, Suetsugi, Natsuki, Kawajiri, Sumihiro, Yamasaki, Ryo, Ishiguro, Takanobu, Konno, Takuya, Nozaki, Hiroaki, Kasuga, Kensaku, Okuma, Yasuyuki, Kira, Jun-Ichi, Hara, Hideo, Onodera, Osamu, Ikeuchi, Takeshi
Cyhoeddwyd yn Neurol Genet (2018)

Haploinsufficiency of CSF-1R and clinicopathologic characterization in patients with HDLS

gan Konno, Takuya, Tada, Masayoshi, Tada, Mari, Koyama, Akihide, Nozaki, Hiroaki, Harigaya, Yasuo, Nishimiya, Jin, Matsunaga, Akiko, Yoshikura, Nobuaki, Ishihara, Kenji, Arakawa, Musashi, Isami, Aiko, Okazaki, Kenichi, Yokoo, Hideaki, Itoh, Kyoko, Yoneda, Makoto, Kawamura, Mitsuru, Inuzuka, Takashi, Takahashi, Hitoshi, Nishizawa, Masatoyo, Onodera, Osamu, Kakita, Akiyoshi, Ikeuchi, Takeshi
Cyhoeddwyd 2014

Identification and functional characterization of novel mutations including frameshift mutation in exon 4 of CSF1R in patients with adult-onset leukoencephalopathy with axonal sphe...

gan Miura, Takeshi, Mezaki, Naomi, Konno, Takuya, Iwasaki, Akio, Hara, Naoyuki, Miura, Masatomo, Funayama, Michitaka, Unai, Yuki, Tashiro, Yuichi, Okita, Kenji, Kihara, Takeshi, Ito, Nobuo, Kanatsuka, Yoichi, Jones, David T., Hara, Norikazu, Ishiguro, Takanobu, Tokutake, Takayoshi, Kasuga, Kensaku, Nozaki, Hiroaki, Dickson, Dennis W., Onodera, Osamu, Wszolek, Zbigniew K., Ikeuchi, Takeshi
Cyhoeddwyd yn J Neurol (2018)