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

Year Number of Results
2002 3
2003 3
2004 3
2005 6
2006 3
2007 3
2008 5
2009 13
2010 13
2011 24
2012 22
2013 14
2014 20
2015 10
2016 11
2017 5
2019 3
2020 9
2021 7
2022 3
2023 4
2024 2

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162 results

Results by year

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Page 1
Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities.
Chowdhury F, Wang L, Al-Raqad M, Amor DJ, Baxová A, Bendová Š, Biamino E, Brusco A, Caluseriu O, Cox NJ, Froukh T, Gunay-Aygun M, Hančárová M, Haynes D, Heide S, Hoganson G, Kaname T, Keren B, Kosaki K, Kubota K, Lemons JM, Magriña MA, Mark PR, McDonald MT, Montgomery S, Morley GM, Ohnishi H, Okamoto N, Rodriguez-Buritica D, Rump P, Sedláček Z, Schatz K, Streff H, Uehara T, Walia JS, Wheeler PG, Wiesener A, Zweier C, Kawakami K, Wentzensen IM, Lalani SR, Siu VM, Bi W, Balci TB. Chowdhury F, et al. Among authors: kubota k. Genet Med. 2021 Jul;23(7):1234-1245. doi: 10.1038/s41436-021-01129-6. Epub 2021 Apr 6. Genet Med. 2021. PMID: 33824499 Free article.
Amyloid imaging mismatch.
Minamimoto R, Ishii K, Kubota K, Morooka M, Okasaki M, Ito K, Mitsumoto T, Nakajima K, Sato T, Mochizuki M, Okazaki O. Minamimoto R, et al. Among authors: kubota k. Clin Nucl Med. 2012 Aug;37(8):807-9. doi: 10.1097/RLU.0b013e318251e1d3. Clin Nucl Med. 2012. PMID: 22785519
Levetiracetam-Associated Decrease in Pitch Perception.
Kubota K, Shikano H, Fujii H, Nakashima Y, Fukao T. Kubota K, et al. Am J Ther. 2019 Jul/Aug;26(4):e527-e528. doi: 10.1097/MJT.0000000000000754. Am J Ther. 2019. PMID: 31169560 No abstract available.
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: kubota k. 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.
Two novel heterozygous variants in ATP1A3 cause movement disorders.
Furukawa S, Miyamoto S, Fukumura S, Kubota K, Taga T, Nakashima M, Saitsu H. Furukawa S, et al. Among authors: kubota k. Hum Genome Var. 2022 Feb 18;9(1):7. doi: 10.1038/s41439-022-00184-y. Hum Genome Var. 2022. PMID: 35181663 Free PMC article.
162 results