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

Year Number of Results
1964 1
1965 1
1966 2
1972 2
1973 1
1974 1
1975 1
1976 1
1977 1
1980 2
1984 1
1987 1
1988 1
1989 1
1990 1
1992 2
1994 1
2013 1
2014 2
2016 1
2018 2
2019 1
2021 1
2023 2
2024 1

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31 results

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Page 1
Limb girdle muscular disease caused by HMGCR mutation and statin myopathy treatable with mevalonolactone.
Yogev Y, Shorer Z, Koifman A, Wormser O, Drabkin M, Halperin D, Dolgin V, Proskorovski-Ohayon R, Hadar N, Davidov G, Nudelman H, Zarivach R, Shelef I, Perez Y, Birk OS. Yogev Y, et al. Among authors: nudelman h. Proc Natl Acad Sci U S A. 2023 Feb 14;120(7):e2217831120. doi: 10.1073/pnas.2217831120. Epub 2023 Feb 6. Proc Natl Acad Sci U S A. 2023. PMID: 36745799 Free PMC article.
CDH2 mutation affecting N-cadherin function causes attention-deficit hyperactivity disorder in humans and mice.
Halperin D, Stavsky A, Kadir R, Drabkin M, Wormser O, Yogev Y, Dolgin V, Proskorovski-Ohayon R, Perez Y, Nudelman H, Stoler O, Rotblat B, Lifschytz T, Lotan A, Meiri G, Gitler D, Birk OS. Halperin D, et al. Among authors: nudelman h. Nat Commun. 2021 Oct 26;12(1):6187. doi: 10.1038/s41467-021-26426-1. Nat Commun. 2021. PMID: 34702855 Free PMC article.
Neurologic aspects of spasmodic dysphonia.
Rosenfield DB, Donovan DT, Sulek M, Viswanath NS, Inbody GP, Nudelman HB. Rosenfield DB, et al. Among authors: nudelman hb. J Otolaryngol. 1990 Aug;19(4):231-6. J Otolaryngol. 1990. PMID: 2213994
31 results