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

Year Number of Results
1969 1
1995 1
2001 2
2002 1
2003 4
2004 1
2005 2
2006 4
2007 10
2008 5
2009 3
2010 1
2011 1
2012 4
2013 1
2014 3
2015 3
2016 2
2017 2
2018 3
2019 3
2020 1
2021 3
2022 3
2023 4
2024 1

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61 results

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Page 1
Association between cerebrospinal fluid parameters and developmental and neurological status in glucose transporter 1 deficiency syndrome.
Nabatame S, Tanigawa J, Tominaga K, Kagitani-Shimono K, Yanagihara K, Imai K, Ando T, Tsuyusaki Y, Araya N, Matsufuji M, Natsume J, Yuge K, Bratkovic D, Arai H, Okinaga T, Matsushige T, Azuma Y, Ishihara N, Miyatake S, Kato M, Matsumoto N, Okamoto N, Takahashi S, Hattori S, Ozono K. Nabatame S, et al. Among authors: tanigawa j. J Neurol Sci. 2023 Apr 15;447:120597. doi: 10.1016/j.jns.2023.120597. Epub 2023 Mar 2. J Neurol Sci. 2023. PMID: 36965413 Free article.
Macro-CK and CK-BB Contributing to Sham CK-MB Elevation.
Wada Y, Tanigawa J, Ishizaka N. Wada Y, et al. Among authors: tanigawa j. Intern Med. 2017;56(11):1449-1450. doi: 10.2169/internalmedicine.56.8329. Epub 2017 Jun 1. Intern Med. 2017. PMID: 28566616 Free PMC article. No abstract available.
Thrombectomy and distal protection devices.
Rajagopal R, Musto C, La Manna A, Tanigawa J, Goktekin O, Di Mario C. Rajagopal R, et al. Among authors: tanigawa j. Minerva Cardioangiol. 2005 Oct;53(5):415-30. Minerva Cardioangiol. 2005. PMID: 16179884 Review.
Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy.
Fatima A, Hoeber J, Schuster J, Koshimizu E, Maya-Gonzalez C, Keren B, Mignot C, Akram T, Ali Z, Miyatake S, Tanigawa J, Koike T, Kato M, Murakami Y, Abdullah U, Ali MA, Fadoul R, Laan L, Castillejo-López C, Liik M, Jin Z, Birnir B, Matsumoto N, Baig SM, Klar J, Dahl N. Fatima A, et al. Among authors: tanigawa j. Am J Hum Genet. 2022 Mar 3;109(3):542-546. doi: 10.1016/j.ajhg.2022.02.007. Am J Hum Genet. 2022. PMID: 35245475 Free PMC article. No abstract available.
Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy.
Fatima A, Hoeber J, Schuster J, Koshimizu E, Maya-Gonzalez C, Keren B, Mignot C, Akram T, Ali Z, Miyatake S, Tanigawa J, Koike T, Kato M, Murakami Y, Abdullah U, Ali MA, Fadoul R, Laan L, Castillejo-López C, Liik M, Jin Z, Birnir B, Matsumoto N, Baig SM, Klar J, Dahl N. Fatima A, et al. Among authors: tanigawa j. Am J Hum Genet. 2021 Apr 1;108(4):739-748. doi: 10.1016/j.ajhg.2021.02.015. Epub 2021 Mar 11. Am J Hum Genet. 2021. PMID: 33711248 Free PMC article.
61 results