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Results by year

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

Year Number of Results
1980 2
1984 1
1991 1
1992 1
1993 3
1998 4
1999 2
2000 2
2002 3
2003 2
2004 1
2005 1
2009 2
2010 1
2012 1
2013 1
2014 2
2016 1
2017 1
2018 1
2019 1
2020 1
2021 5
2022 1
2024 0

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37 results

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Page 1
Reply to a Letter to the Editor.
Kimizuka M, Yamakage M. Kimizuka M, et al. J Anesth. 2021 Jun;35(3):465. doi: 10.1007/s00540-021-02918-8. Epub 2021 Mar 17. J Anesth. 2021. PMID: 33728522 No abstract available.
Monomelic muscle atrophy.
Takemitsu M, Murayama K, Saga T, Michihiro N, Shiihara H, Kimizuka M, Nonaka I. Takemitsu M, et al. Among authors: kimizuka m. Neuromuscul Disord. 1993 Jul;3(4):311-7. doi: 10.1016/0960-8966(93)90024-e. Neuromuscul Disord. 1993. PMID: 8268728
Retinal detachment in spondyloepiphyseal dysplasia congenita.
Ikegawa S, Iwaya T, Taniguchi K, Kimizuka M. Ikegawa S, et al. Among authors: kimizuka m. J Pediatr Orthop. 1993 Nov-Dec;13(6):791-2. doi: 10.1097/01241398-199311000-00021. J Pediatr Orthop. 1993. PMID: 8245210
Novel and recurrent EBP mutations in X-linked dominant chondrodysplasia punctata.
Ikegawa S, Ohashi H, Ogata T, Honda A, Tsukahara M, Kubo T, Kimizuka M, Shimode M, Hasegawa T, Nishimura G, Nakamura Y. Ikegawa S, et al. Among authors: kimizuka m. Am J Med Genet. 2000 Oct 2;94(4):300-5. doi: 10.1002/1096-8628(20001002)94:4<300::aid-ajmg7>3.0.co;2-3. Am J Med Genet. 2000. PMID: 11038443 Review.
37 results