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

Year Number of Results
2002 2
2004 1
2006 1
2007 1
2009 1
2010 3
2011 4
2012 5
2013 1
2014 2
2015 1
2016 1
2017 2
2018 2
2019 4
2020 6
2021 8
2022 9
2023 1
2024 0

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45 results

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Page 1
IGF2 Mutations.
Masunaga Y, Inoue T, Yamoto K, Fujisawa Y, Sato Y, Kawashima-Sonoyama Y, Morisada N, Iijima K, Ohata Y, Namba N, Suzumura H, Kuribayashi R, Yamaguchi Y, Yoshihashi H, Fukami M, Saitsu H, Kagami M, Ogata T. Masunaga Y, et al. Among authors: yoshihashi h. J Clin Endocrinol Metab. 2020 Jan 1;105(1):dgz034. doi: 10.1210/clinem/dgz034. J Clin Endocrinol Metab. 2020. PMID: 31544945 Review.
Vanishing basal ganglia in ATP1A3-related polymicrogyria.
Ogawa E, Sakaguchi Y, Enokizono M, Yoshihashi H, Yamada M, Suzuki H, Kosaki K, Miyama S, Takenouchi T. Ogawa E, et al. Among authors: yoshihashi h. Am J Med Genet A. 2022 Feb;188(2):665-667. doi: 10.1002/ajmg.a.62531. Epub 2021 Oct 11. Am J Med Genet A. 2022. PMID: 34633143 No abstract available.
Long-term clinical course of Heyn-Sproul-Jackson syndrome.
Futagawa H, Ito S, Kosaki K, Yoshihashi H. Futagawa H, et al. Among authors: yoshihashi h. Congenit Anom (Kyoto). 2023 Sep;63(5):174-175. doi: 10.1111/cga.12532. Epub 2023 Jul 30. Congenit Anom (Kyoto). 2023. PMID: 37517811 No abstract available.
Myoclonic Epilepsy with Ragged-red Fibers with Intranuclear Inclusions.
Kawazoe T, Tobisawa S, Sugaya K, Uruha A, Miyamoto K, Komori T, Goto YI, Nishino I, Yoshihashi H, Mizuguchi T, Matsumoto N, Egawa N, Kawata A, Isozaki E. Kawazoe T, et al. Among authors: yoshihashi h. Intern Med. 2022 Feb 15;61(4):547-552. doi: 10.2169/internalmedicine.7767-21. Epub 2021 Aug 24. Intern Med. 2022. PMID: 34433719 Free PMC article.
SATB2-associated syndrome in patients from Japan: Linguistic profiles.
Yamada M, Uehara T, Suzuki H, Takenouchi T, Yoshihashi H, Suzumura H, Mizuno S, Kosaki K. Yamada M, et al. Among authors: yoshihashi h. Am J Med Genet A. 2019 Jun;179(6):896-899. doi: 10.1002/ajmg.a.61114. Epub 2019 Mar 7. Am J Med Genet A. 2019. PMID: 30848049
Genome Analysis in Sick Neonates and Infants: High-yield Phenotypes and Contribution of Small Copy Number Variations.
Suzuki H, Nozaki M, Yoshihashi H, Imagawa K, Kajikawa D, Yamada M, Yamaguchi Y, Morisada N, Eguchi M, Ohashi S, Ninomiya S, Seto T, Tokutomi T, Hida M, Toyoshima K, Kondo M, Inui A, Kurosawa K, Kosaki R, Ito Y, Okamoto N, Kosaki K, Takenouchi T. Suzuki H, et al. Among authors: yoshihashi h. J Pediatr. 2022 May;244:38-48.e1. doi: 10.1016/j.jpeds.2022.01.033. Epub 2022 Feb 4. J Pediatr. 2022. PMID: 35131284 Free article.
45 results