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

Year Number of Results
1993 1
2003 2
2004 1
2006 2
2008 3
2009 5
2010 3
2011 2
2012 3
2013 2
2014 2
2016 1
2017 4
2018 5
2019 2
2020 5
2021 4
2022 6
2023 4
2024 4

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49 results

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Page 1
Hereditary orotic aciduria identified by newborn screening.
Staretz-Chacham O, Damseh NS, Daas S, Abu Salah N, Anikster Y, Barel O, Dumin E, Fattal-Valevski A, Falik-Zaccai TC, Hershkovitz E, Josefsberg S, Landau Y, Lerman-Sagie T, Mandel H, Rock R, Rostami N, Saraf-Levy T, Shaul Lotan N, Spiegel R, Tal G, Ulanovsky I, Wilnai Y, Korman SH, Almashanu S. Staretz-Chacham O, et al. Among authors: falik zaccai tc. Front Genet. 2023 Mar 14;14:1135267. doi: 10.3389/fgene.2023.1135267. eCollection 2023. Front Genet. 2023. PMID: 36999056 Free PMC article.
Clinical utility gene card for: Xeroderma pigmentosum.
Schubert S, Lehmann J, Kalfon L, Slor H, Falik-Zaccai TC, Emmert S. Schubert S, et al. Among authors: falik zaccai tc. Eur J Hum Genet. 2014 Jul;22(7). doi: 10.1038/ejhg.2013.233. Epub 2013 Oct 9. Eur J Hum Genet. 2014. PMID: 24105368 Free PMC article. Review. No abstract available.
INSR-Related Severe Insulin Resistance Syndrome.
Mesika A, Klar A, Falik Zaccai TC. Mesika A, et al. Among authors: falik zaccai tc. 2018 Jan 25 [updated 2024 Apr 25]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2018 Jan 25 [updated 2024 Apr 25]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 29369573 Free Books & Documents. Review.
Mammalian Homologue NME3 of DYNAMO1 Regulates Peroxisome Division.
Honsho M, Abe Y, Imoto Y, Chang ZF, Mandel H, Falik-Zaccai TC, Fujiki Y. Honsho M, et al. Among authors: falik zaccai tc. Int J Mol Sci. 2020 Oct 28;21(21):8040. doi: 10.3390/ijms21218040. Int J Mol Sci. 2020. PMID: 33126676 Free PMC article.
Addition of galactose-1-phosphate measurement enhances newborn screening for classical galactosemia.
Daas S, Abu Salah N, Anikster Y, Barel O, Damseh NS, Dumin E, Fattal-Valevski A, Falik-Zaccai TC, Habib C, Josefsberg S, Korman SH, Kneller K, Landau Y, Lerman-Sagie T, Mandel H, Manor Y, Moady Abdalla T, Rock R, Rostami N, Saada A, Saraf-Levy T, Shaul Lotan N, Spiegel R, Staretz-Chacham O, Tal G, Ulanovsky I, Vaisid T, Wilnai Y, Almashanu S. Daas S, et al. Among authors: falik zaccai tc. J Inherit Metab Dis. 2023 Mar;46(2):232-242. doi: 10.1002/jimd.12580. Epub 2022 Dec 20. J Inherit Metab Dis. 2023. PMID: 36515074
National Rapid Genome Sequencing in Neonatal Intensive Care.
Marom D, Mory A, Reytan-Miron S, Amir Y, Kurolap A, Cohen JG, Morhi Y, Smolkin T, Cohen L, Zangen S, Shalata A, Riskin A, Peleg A, Lavie-Nevo K, Mandel D, Chervinsky E, Fisch CF, Fleisher Sheffer V, Falik-Zaccai TC, Rips J, Shlomai NO, Friedman SE, Shporen CH, Ben-Yehoshua SJ, Simmonds A, Yaacobi RG, Bauer-Rusek S, Omari H, Weiss K, Hochwald O, Koifman A, Globus O, Batzir NA, Yaron N, Segel R, Morag I, Reish O, Eliyahu A, Leibovitch L, Schwartz ME, Abramsky R, Hochberg A, Oron A, Banne E, Portnov I, Samra NN, Singer A, Baris Feldman H. Marom D, et al. Among authors: falik zaccai tc. JAMA Netw Open. 2024 Feb 5;7(2):e240146. doi: 10.1001/jamanetworkopen.2024.0146. JAMA Netw Open. 2024. PMID: 38386321 Free PMC article.
Concomitant congenital CMV infection and inherited liver diseases.
Swed-Tobia R, Kassis I, Weiss K, Tal G, Shaoul R, Falik-Zaccai TC, Mandel H, Meir M. Swed-Tobia R, et al. Among authors: falik zaccai tc. Eur J Med Genet. 2021 Aug;64(8):104249. doi: 10.1016/j.ejmg.2021.104249. Epub 2021 May 20. Eur J Med Genet. 2021. PMID: 34023521
49 results