Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Yaz Y, Kisanuki"'
Publikováno v:
Neurology. 100:S195-S197
A 39-year-old previously healthy man presented with insidiously progressive paresthesia in his lower extremities and worsening of gait and balance. MRI demonstrated T2-hyperintense signal abnormalities involving the thalami, midbrain, dentate nuclei,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ce638f5682339c303c65cecea9a0ebe
https://doi.org/10.1212/wnl.0000000000207008
https://doi.org/10.1212/wnl.0000000000207008
Publikováno v:
The Clinical Neuropsychologist. 36:1787-1798
Objective: The alpha-synuclein gene (SNCA) is implicated in both Parkinson's disease (PD) and dementia with Lewy bodies (DLB). The purpose of this case study was to describe the neuropsychological profile, clinical trajectory, and treatment course of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65c0d8b99a75914b115032b9dcaa0986
https://doi.org/10.1080/13854046.2021.1914735
https://doi.org/10.1080/13854046.2021.1914735
Autor:
Sabrina, Paganoni, Fabiola, De Marchi, James, Chan, Sara K, Thrower, Nathan P, Staff, Neil, Datta, Yaz Y, Kisanuki, Vivian, Drory, Christina, Fournier, Erik P, Pioro, Stephen A, Goutman, Nazem, Atassi, Maryangel, Jeon, Sarah, Caldwell, Timothy, Mcdonough, Caroline, Gentile, Jianing, Liu, Michelle, Turner, Carol, Denny, Kevin, Felice, Misty, Green, Stephanie, Scarberry, Saad, Abu-Saleh, Beatrice, Nefussy, Debbie, Hastings, Sangri, Kim, Blake, Swihart, Ximena, Arcila-Londono, Daniel S, Newman, Michael, Silverman, Angela, Genge, Kristiana, Salmon, Lauren, Elman, Leo, Mccluskey, Kelly, Almasy, Marc, Gotkine, Kimberly, Goslin, Arlena, Cummings, Eli K, Edwards, Michael, Rivner, Kristy, Bouchard, Brandy, Quarles, Justin, Kwan, Matthew, Jaffa, Robert, Baloh, Peggy, Allred, David, Walk, Samuel, Maiser, Georgios, Manousakis, Valerie, Ferment, J Americo M, Fernandes, Pariwat, Thaisetthawatkul, Deborah, Heimes, Melissa, Phillips, Laura, Sams, Melissa, Kahler, Alecia, Corcoran, Daniel G, Larriviere, Sadie, Chotto, Gracy, Juba
Publikováno v:
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 21:74-81
Primary lateral sclerosis (PLS) is a neurodegenerative disease characterized by progressive upper motor neuron dysfunction. Because PLS patients represent only 1 to 4% of patients with adult motor neuron diseases, there is limited information about t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb97f3bb52c2556e6bc12b50b853c0c5
https://doi.org/10.1080/21678421.2020.1804591
https://doi.org/10.1080/21678421.2020.1804591
Autor:
Hiroshi, Mitsumoto, Grace, Jang, Ikjae, Lee, Zachary, Simmons, Alexander V, Sherman, Daragh, Heitzman, Eric, Sorenson, Ken, Cheung, Jinsy, Andrews, Matthew, Harms, Neil A, Shneider, Regina, Santella, Sabrina, Paganoni, Senda, Ajroud-Driss, J Americo M, Fernandes, Katherine M, Burke, Kelly, Gwathmey, Ali A, Habib, Nicholas J, Maragakis, David, Walk, Christina, Fournier, Terry, Heiman-Patterson, James, Wymer, Frank, Diaz, Stephen N, Scelsa, Lauren, Elman, Angela, Genge, Stephen A, Goutman, Ghazala, Hayat, Omar, Jawdat, Wendy S, Johnston, Nanette C, Joyce, Edward J, Kasarskis, Yaz Y, Kisanuki, Catherine, Lomen-Hoerth, Michael T, Pulley, Jaimin S, Shah, Christen, Shoesmith, Lorne, Zinman
Introduction/Aims. Primary lateral sclerosis (PLS) is exceedingly rare and has been an enigmatic disease. Recent progress has drastically changed this perception, with early biomarkers being investigated and potential medications for PLS emerging at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::199e0ab7e9df901d229ea3fce3df5843
Publikováno v:
The Clinical neuropsychologist. 36(7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e5bcf0436dbf54a5cf2a156e4135b386
https://pubmed.ncbi.nlm.nih.gov/33983072
https://pubmed.ncbi.nlm.nih.gov/33983072
Publikováno v:
Molecular Genetics and Metabolism. 135:S52
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14d0a5f261324fb6a3b34ae73d59af1a
https://doi.org/10.1016/j.ymgme.2021.11.127
https://doi.org/10.1016/j.ymgme.2021.11.127
Autor:
Mike Kalogiannis, Emily Hsu, Jon T Willie, Richard M Chemelli, Yaz Y Kisanuki, Masashi Yanagisawa, Christopher S Leonard
Publikováno v:
PLoS ONE, Vol 6, Iss 4, p e18697 (2011)
To investigate how cholinergic systems regulate aspects of the sleep disorder narcolepsy, we video-monitored mice lacking both orexin (hypocretin) receptors (double knockout; DKO mice) while pharmacologically altering cholinergic transmission. Sponta
Externí odkaz:
https://doaj.org/article/d71b6efbd3824739b64c34d8ee10a411
Autor:
Shoichi Ozaki, Kazuo Yudoh, Mari Ikeda, Yaz Y. Kisanuki, Kimito Kawahata, Takahiro Okazaki, Shoshi Shinagawa, Masashi Yanagisawa
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Scientific Reports
Scientific Reports
Endothelin 1 (ET-1), mainly produced from vascular endothelial cells, induces vasoconstriction in physiological conditions. The endothelin receptor antagonist is among the most effective agents for pulmonary hypertension. However, little is known abo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f335529da310b54f4b1077d3a60e797
http://link.springer.com/article/10.1038/s41598-017-14202-5
http://link.springer.com/article/10.1038/s41598-017-14202-5
Publikováno v:
The neuroradiology journal. 32(2)
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is a rare white matter degenerative disease characterized by both axonal and glial injury due to a defect in the CSF1R gene. In this report, we describe ALSP in a previou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe799e015baaae676d7909f72ff9ae25
https://pubmed.ncbi.nlm.nih.gov/30614382
https://pubmed.ncbi.nlm.nih.gov/30614382
Autor:
Ahmed Hashmi, Amita Sneh, Fumihiro Watanabe, Harmeet Moti, Anthony Hernandez, Robert E. Hammer, Yaz Y. Kisanuki, Mackenzie Schumer, Odelia Ghodsizadeh, William D. Arnold, Zarife Sahenk
Publikováno v:
Journal of Neuropathology and Experimental Neurology
Supplemental Digital Content is available in the text.
Hereditary spastic paraplegias (HSPs) are characterized by progressive spasticity and weakness in the lower extremities that result from length-dependent central to peripheral axonal degener
Hereditary spastic paraplegias (HSPs) are characterized by progressive spasticity and weakness in the lower extremities that result from length-dependent central to peripheral axonal degener
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbe7dd58ca453e9529e82bf72570dd92
https://doi.org/10.1097/nen.0000000000000000
https://doi.org/10.1097/nen.0000000000000000