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

Year Number of Results
1952 1
1953 1
1957 1
1958 3
1959 3
1960 1
1961 2
1962 1
1963 1
1964 1
1965 1
1966 4
1967 3
1968 2
1969 1
1971 4
1973 2
1977 1
1978 1
1979 1
1992 2
1993 2
1994 1
1996 1
1997 4
1998 1
1999 1
2000 1
2001 1
2002 1
2003 3
2004 4
2005 2
2006 4
2007 9
2008 3
2009 3
2010 4
2011 4
2012 3
2013 1
2014 4
2015 3
2016 2
2017 3
2018 4
2019 6
2020 9
2021 17
2022 4
2023 5
2024 2

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140 results

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Page 1
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.
Connaughton DM, Dai R, Owen DJ, Marquez J, Mann N, Graham-Paquin AL, Nakayama M, Coyaud E, Laurent EMN, St-Germain JR, Blok LS, Vino A, Klämbt V, Deutsch K, Wu CW, Kolvenbach CM, Kause F, Ottlewski I, Schneider R, Kitzler TM, Majmundar AJ, Buerger F, Onuchic-Whitford AC, Youying M, Kolb A, Salmanullah D, Chen E, van der Ven AT, Rao J, Ityel H, Seltzsam S, Rieke JM, Chen J, Vivante A, Hwang DY, Kohl S, Dworschak GC, Hermle T, Alders M, Bartolomaeus T, Bauer SB, Baum MA, Brilstra EH, Challman TD, Zyskind J, Costin CE, Dipple KM, Duijkers FA, Ferguson M, Fitzpatrick DR, Fick R, Glass IA, Hulick PJ, Kline AD, Krey I, Kumar S, Lu W, Marco EJ, Wentzensen IM, Mefford HC, Platzer K, Povolotskaya IS, Savatt JM, Shcherbakova NV, Senguttuvan P, Squire AE, Stein DR, Thiffault I, Voinova VY, Somers MJG, Ferguson MA, Traum AZ, Daouk GH, Daga A, Rodig NM, Terhal PA, van Binsbergen E, Eid LA, Tasic V, Rasouly HM, Lim TY, Ahram DF, Gharavi AG, Reutter HM, Rehm HL, MacArthur DG, Lek M, Laricchia KM, Lifton RP, Xu H, Mane SM, Sanna-Cherchi S, Sharrocks AD, Raught B, Fisher SE, Bouchard M, Khokha MK, Shril S, Hildebrandt F. Connaughton DM, et al. Among authors: deutsch k. Am J Hum Genet. 2020 Oct 1;107(4):727-742. doi: 10.1016/j.ajhg.2020.08.013. Epub 2020 Sep 4. Am J Hum Genet. 2020. PMID: 32891193 Free PMC article.
The placebo effect.
Heeg MJ, Deutsch KF, Deutsch E. Heeg MJ, et al. Among authors: deutsch kf. Eur J Nucl Med. 1997 Nov;24(11):1433-40. doi: 10.1007/s002590050173. Eur J Nucl Med. 1997. PMID: 9371880 Review.
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT.
Seltzsam S, Wang C, Zheng B, Mann N, Connaughton DM, Wu CW, Schneider S, Schierbaum L, Kause F, Kolvenbach CM, Nakayama M, Dai R, Ottlewski I, Schneider R, Deutsch K, Buerger F, Klämbt V, Mao Y, Onuchic-Whitford AC, Nicolas-Frank C, Yousef K, Pantel D, Lai EW, Salmanullah D, Majmundar AJ, Bauer SB, Rodig NM, Somers MJG, Traum AZ, Stein DR, Daga A, Baum MA, Daouk GH, Tasic V, Awad HS, Eid LA, El Desoky S, Shalaby M, Kari JA, Fathy HM, Soliman NA, Mane SM, Shril S, Ferguson MA, Hildebrandt F. Seltzsam S, et al. Among authors: deutsch k. Genet Med. 2022 Feb;24(2):307-318. doi: 10.1016/j.gim.2021.09.010. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906515 Free PMC article.
Radiation synovectomy revisited.
Deutsch E, Brodack JW, Deutsch KF. Deutsch E, et al. Among authors: deutsch kf. Eur J Nucl Med. 1993 Nov;20(11):1113-27. doi: 10.1007/BF00173494. Eur J Nucl Med. 1993. PMID: 8287881 Review.
Health Literacy in Early Childhood: A Systematic Review of Empirical Studies.
Bánfai-Csonka H, Betlehem J, Deutsch K, Derzsi-Horváth M, Bánfai B, Fináncz J, Podráczky J, Csima M. Bánfai-Csonka H, et al. Among authors: deutsch k. Children (Basel). 2022 Jul 28;9(8):1131. doi: 10.3390/children9081131. Children (Basel). 2022. PMID: 36010022 Free PMC article. Review.
[Changes of first-aid attitude during the COVID–19 pandemic].
Betlehem J, Bánfai-Csonka H, Musch J, Deutsch K, Sánta E, Bánfai B. Betlehem J, et al. Among authors: deutsch k. Orv Hetil. 2021 Apr 2;162(15):571-578. doi: 10.1556/650.2021.32167. Orv Hetil. 2021. PMID: 33798102 Review. Hungarian.
DAAM2 Variants Cause Nephrotic Syndrome via Actin Dysregulation.
Schneider R, Deutsch K, Hoeprich GJ, Marquez J, Hermle T, Braun DA, Seltzsam S, Kitzler TM, Mao Y, Buerger F, Majmundar AJ, Onuchic-Whitford AC, Kolvenbach CM, Schierbaum L, Schneider S, Halawi AA, Nakayama M, Mann N, Connaughton DM, Klämbt V, Wagner M, Riedhammer KM, Renders L, Katsura Y, Thumkeo D, Soliman NA, Mane S, Lifton RP, Shril S, Khokha MK, Hoefele J, Goode BL, Hildebrandt F. Schneider R, et al. Among authors: deutsch k. Am J Hum Genet. 2020 Dec 3;107(6):1113-1128. doi: 10.1016/j.ajhg.2020.11.008. Epub 2020 Nov 23. Am J Hum Genet. 2020. PMID: 33232676 Free PMC article.
Letters.
Deutsch KW, Platt J, Senghaas D. Deutsch KW, et al. Science. 1971 Jun 18;172(3989):1191-2. doi: 10.1126/science.172.3989.1191-b. Science. 1971. PMID: 17747340 No abstract available.
Loss of Kynurenine 3-Mono-oxygenase Causes Proteinuria.
Korstanje R, Deutsch K, Bolanos-Palmieri P, Hanke N, Schroder P, Staggs L, Bräsen JH, Roberts IS, Sheehan S, Savage H, Haller H, Schiffer M. Korstanje R, et al. Among authors: deutsch k. J Am Soc Nephrol. 2016 Nov;27(11):3271-3277. doi: 10.1681/ASN.2015070835. Epub 2016 Mar 28. J Am Soc Nephrol. 2016. PMID: 27020856 Free PMC article.
140 results