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

Year Number of Results
1965 1
1976 1
1977 1
1978 1
1979 4
1980 3
1981 1
1985 1
1993 1
1995 1
1996 3
1997 3
1998 3
2000 1
2001 1
2002 2
2003 4
2004 3
2005 1
2006 2
2008 1
2009 2
2010 8
2011 4
2012 6
2013 6
2014 11
2015 7
2016 2
2017 3
2018 4
2019 4
2020 3
2021 4
2022 5
2023 5
2024 7

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105 results

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Page 1
Preventing Cardiac Arrest in the Pediatric Cardiac Intensive Care Unit Through Multicenter Collaboration.
Alten J, Cooper DS, Klugman D, Raymond TT, Wooton S, Garza J, Clarke-Myers K, Anderson J, Pasquali SK, Absi M, Affolter JT, Bailly DK, Bertrandt RA, Borasino S, Dewan M, Domnina Y, Lane J, McCammond AN, Mueller DM, Olive MK, Ortmann L, Prodhan P, Sasaki J, Scahill C, Schroeder LW, Werho DK, Zaccagni H, Zhang W, Banerjee M, Gaies M; PC4 CAP Collaborators. Alten J, et al. JAMA Pediatr. 2022 Oct 1;176(10):1027-1036. doi: 10.1001/jamapediatrics.2022.2238. JAMA Pediatr. 2022. PMID: 35788631 Free PMC article.
Transdisciplinary Perspectives on Precision Medicine.
Myers HF, Fair AM, Villalta F, Walz K, Beech BM, Scott WK, Haas DW. Myers HF, et al. Among authors: walz k. Health Equity. 2021 May 13;5(1):288-298. doi: 10.1089/heq.2020.0131. eCollection 2021. Health Equity. 2021. PMID: 34036211 Free PMC article.
Mutations in DNAJC19 cause altered mitochondrial structure and increased mitochondrial respiration in human iPSC-derived cardiomyocytes.
Janz A, Walz K, Cirnu A, Surjanto J, Urlaub D, Leskien M, Kohlhaas M, Nickel A, Brand T, Nose N, Wörsdörfer P, Wagner N, Higuchi T, Maack C, Dudek J, Lorenz K, Klopocki E, Ergün S, Duff HJ, Gerull B. Janz A, et al. Among authors: walz k. Mol Metab. 2024 Jan;79:101859. doi: 10.1016/j.molmet.2023.101859. Epub 2023 Dec 23. Mol Metab. 2024. PMID: 38142971 Free PMC article.
Arnold-Chiari type 1 malformation in Potocki-Lupski syndrome.
Varon A, Whitt Z, Kalika PM, Potocki L, Barbouth DS, Walz K. Varon A, et al. Among authors: walz k. Am J Med Genet A. 2019 Jul;179(7):1366-1370. doi: 10.1002/ajmg.a.61187. Epub 2019 May 8. Am J Med Genet A. 2019. PMID: 31066191
FOXF2 is required for cochlear development in humans and mice.
Bademci G, Abad C, Incesulu A, Elian F, Reyahi A, Diaz-Horta O, Cengiz FB, Sineni CJ, Seyhan S, Atli EI, Basmak H, Demir S, Nik AM, Footz T, Guo S, Duman D, Fitoz S, Gurkan H, Blanton SH, Walter MA, Carlsson P, Walz K, Tekin M. Bademci G, et al. Among authors: walz k. Hum Mol Genet. 2019 Apr 15;28(8):1286-1297. doi: 10.1093/hmg/ddy431. Hum Mol Genet. 2019. PMID: 30561639 Free PMC article.
105 results