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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1966 1
1967 3
1968 1
1969 2
1975 1
1978 2
1979 2
1980 1
1981 1
1982 1
1983 2
1984 3
1985 5
1986 2
1988 3
1989 5
1990 5
1991 2
1994 1
1997 4
1998 3
1999 2
2000 1
2002 3
2003 2
2004 1
2005 1
2006 2
2007 3
2008 4
2009 2
2010 2
2011 2
2012 4
2013 4
2014 9
2015 6
2016 4
2017 6
2018 9
2019 6
2020 8
2021 9
2022 11
2023 4
2024 0

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Search Results

137 results

Results by year

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Page 1
Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophy.
Sakamoto M, Iwama K, Sasaki M, Ishiyama A, Komaki H, Saito T, Takeshita E, Shimizu-Motohashi Y, Haginoya K, Kobayashi T, Goto T, Tsuyusaki Y, Iai M, Kurosawa K, Osaka H, Tohyama J, Kobayashi Y, Okamoto N, Suzuki Y, Kumada S, Inoue K, Mashimo H, Arisaka A, Kuki I, Saijo H, Yokochi K, Kato M, Inaba Y, Gomi Y, Saitoh S, Shirai K, Morimoto M, Izumi Y, Watanabe Y, Nagamitsu SI, Sakai Y, Fukumura S, Muramatsu K, Ogata T, Yamada K, Ishigaki K, Hirasawa K, Shimoda K, Akasaka M, Kohashi K, Sakakibara T, Ikuno M, Sugino N, Yonekawa T, Gürsoy S, Cinleti T, Kim CA, Teik KW, Yan CM, Haniffa M, Ohba C, Ito S, Saitsu H, Saida K, Tsuchida N, Uchiyama Y, Koshimizu E, Fujita A, Hamanaka K, Misawa K, Miyatake S, Mizuguchi T, Miyake N, Matsumoto N. Sakamoto M, et al. Among authors: akasaka m. Genet Med. 2022 Dec;24(12):2453-2463. doi: 10.1016/j.gim.2022.08.007. Epub 2022 Oct 28. Genet Med. 2022. PMID: 36305856 Free article.
Acute encephalopathy in children with tuberous sclerosis complex.
Numoto S, Kurahashi H, Sato A, Kubota M, Shiihara T, Okanishi T, Tanaka R, Kuki I, Fukuyama T, Kashiwagi M, Ikeno M, Kubota K, Akasaka M, Mimaki M, Okumura A. Numoto S, et al. Among authors: akasaka m. Orphanet J Rare Dis. 2021 Jan 6;16(1):5. doi: 10.1186/s13023-020-01646-8. Orphanet J Rare Dis. 2021. PMID: 33407677 Free PMC article.
Tapping into non-English-language science for the conservation of global biodiversity.
Amano T, Berdejo-Espinola V, Christie AP, Willott K, Akasaka M, Báldi A, Berthinussen A, Bertolino S, Bladon AJ, Chen M, Choi CY, Bou Dagher Kharrat M, de Oliveira LG, Farhat P, Golivets M, Hidalgo Aranzamendi N, Jantke K, Kajzer-Bonk J, Kemahlı Aytekin MÇ, Khorozyan I, Kito K, Konno K, Lin DL, Littlewood N, Liu Y, Liu Y, Loretto MC, Marconi V, Martin PA, Morgan WH, Narváez-Gómez JP, Negret PJ, Nourani E, Ochoa Quintero JM, Ockendon N, Oh RRY, Petrovan SO, Piovezan-Borges AC, Pollet IL, Ramos DL, Reboredo Segovia AL, Rivera-Villanueva AN, Rocha R, Rouyer MM, Sainsbury KA, Schuster R, Schwab D, Şekercioğlu ÇH, Seo HM, Shackelford G, Shinoda Y, Smith RK, Tao SD, Tsai MS, Tyler EHM, Vajna F, Valdebenito JO, Vozykova S, Waryszak P, Zamora-Gutierrez V, Zenni RD, Zhou W, Sutherland WJ. Amano T, et al. Among authors: akasaka m. PLoS Biol. 2021 Oct 7;19(10):e3001296. doi: 10.1371/journal.pbio.3001296. eCollection 2021 Oct. PLoS Biol. 2021. PMID: 34618803 Free PMC article.
GNAO1 mutation-related severe involuntary movements treated with gabapentin.
Akasaka M, Kamei A, Tanifuji S, Asami M, Ito J, Mizuma K, Oyama K, Tokutomi T, Yamamoto K, Fukushima A, Takenouchi T, Uehara T, Suzuki H, Kosaki K. Akasaka M, et al. Brain Dev. 2021 Apr;43(4):576-579. doi: 10.1016/j.braindev.2020.12.002. Epub 2020 Dec 23. Brain Dev. 2021. PMID: 33358199
Lactulose: A treatment for hyperammonemia in a lysinuric protein-intolerant patient with dynamic blood amino acid concentrations.
Kakisaka K, Sato T, Wada Y, Ito A, Eto H, Abe H, Kanazawa J, Yusa K, Kooka Y, Endo K, Yoshida Y, Oikawa T, Kuroda H, Miyasaka A, Akasaka M, Matsumoto T. Kakisaka K, et al. Among authors: akasaka m. Mol Genet Metab Rep. 2022 Jul 15;32:100898. doi: 10.1016/j.ymgmr.2022.100898. eCollection 2022 Sep. Mol Genet Metab Rep. 2022. PMID: 35865266 Free PMC article. No abstract available.
137 results