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

Year Number of Results
1948 1
1949 2
1950 1
1952 1
1954 1
1955 1
1965 1
1966 1
1967 3
1968 8
1969 7
1970 12
1971 18
1972 15
1973 9
1974 15
1975 23
1976 22
1977 13
1978 15
1979 17
1980 15
1981 11
1982 22
1983 9
1984 6
1985 18
1986 21
1987 31
1988 24
1989 31
1990 35
1991 31
1992 29
1993 43
1994 38
1995 31
1996 47
1997 46
1998 52
1999 41
2000 48
2001 35
2002 35
2003 37
2004 41
2005 37
2006 62
2007 34
2008 45
2009 42
2010 46
2011 48
2012 52
2013 44
2014 60
2015 39
2016 35
2017 41
2018 33
2019 33
2020 47
2021 67
2022 66
2023 43
2024 23

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1,727 results

Results by year

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Page 1
Welcome and farewell.
Rees L, Baum M, Flynn J. Rees L, et al. Among authors: baum m. Pediatr Nephrol. 2021 Feb;36(2):217. doi: 10.1007/s00467-020-04868-x. Epub 2020 Dec 21. Pediatr Nephrol. 2021. PMID: 33346876 No abstract available.
Prevalence and Correlates of Long COVID Symptoms Among US Adults.
Perlis RH, Santillana M, Ognyanova K, Safarpour A, Lunz Trujillo K, Simonson MD, Green J, Quintana A, Druckman J, Baum MA, Lazer D. Perlis RH, et al. Among authors: baum ma. JAMA Netw Open. 2022 Oct 3;5(10):e2238804. doi: 10.1001/jamanetworkopen.2022.38804. JAMA Netw Open. 2022. PMID: 36301542 Free PMC article.
Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.
Warejko JK, Tan W, Daga A, Schapiro D, Lawson JA, Shril S, Lovric S, Ashraf S, Rao J, Hermle T, Jobst-Schwan T, Widmeier E, Majmundar AJ, Schneider R, Gee HY, Schmidt JM, Vivante A, van der Ven AT, Ityel H, Chen J, Sadowski CE, Kohl S, Pabst WL, Nakayama M, Somers MJG, Rodig NM, Daouk G, Baum M, Stein DR, Ferguson MA, Traum AZ, Soliman NA, Kari JA, El Desoky S, Fathy H, Zenker M, Bakkaloglu SA, Müller D, Noyan A, Ozaltin F, Cadnapaphornchai MA, Hashmi S, Hopcian J, Kopp JB, Benador N, Bockenhauer D, Bogdanovic R, Stajić N, Chernin G, Ettenger R, Fehrenbach H, Kemper M, Munarriz RL, Podracka L, Büscher R, Serdaroglu E, Tasic V, Mane S, Lifton RP, Braun DA, Hildebrandt F. Warejko JK, et al. Among authors: baum m. Clin J Am Soc Nephrol. 2018 Jan 6;13(1):53-62. doi: 10.2215/CJN.04120417. Epub 2017 Nov 10. Clin J Am Soc Nephrol. 2018. PMID: 29127259 Free PMC article.
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: baum ma. 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.
Editorial: Accelerating Genetic Gains in Pulses.
Pratap A, Kumar S, Polowick PL, Blair MW, Baum M. Pratap A, et al. Among authors: baum m. Front Plant Sci. 2022 Apr 7;13:879377. doi: 10.3389/fpls.2022.879377. eCollection 2022. Front Plant Sci. 2022. PMID: 35463449 Free PMC article. No abstract available.
Editorial: Pediatric nephrolithiasis.
Baum M. Baum M. Curr Opin Pediatr. 2020 Apr;32(2):261-264. doi: 10.1097/MOP.0000000000000874. Curr Opin Pediatr. 2020. PMID: 31876622 No abstract available.
Neonatal nephrology.
Baum M. Baum M. Curr Opin Pediatr. 2012 Apr;24(2):181-3. doi: 10.1097/MOP.0b013e3283504e77. Curr Opin Pediatr. 2012. PMID: 22327949 No abstract available.
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
van der Ven AT, Connaughton DM, Ityel H, Mann N, Nakayama M, Chen J, Vivante A, Hwang DY, Schulz J, Braun DA, Schmidt JM, Schapiro D, Schneider R, Warejko JK, Daga A, Majmundar AJ, Tan W, Jobst-Schwan T, Hermle T, Widmeier E, Ashraf S, Amar A, Hoogstraaten CA, Hugo H, Kitzler TM, Kause F, Kolvenbach CM, Dai R, Spaneas L, Amann K, Stein DR, Baum MA, Somers MJG, Rodig NM, Ferguson MA, Traum AZ, Daouk GH, Bogdanović R, Stajić N, Soliman NA, Kari JA, El Desoky S, Fathy HM, Milosevic D, Al-Saffar M, Awad HS, Eid LA, Selvin A, Senguttuvan P, Sanna-Cherchi S, Rehm HL, MacArthur DG, Lek M, Laricchia KM, Wilson MW, Mane SM, Lifton RP, Lee RS, Bauer SB, Lu W, Reutter HM, Tasic V, Shril S, Hildebrandt F. van der Ven AT, et al. Among authors: baum ma. J Am Soc Nephrol. 2018 Sep;29(9):2348-2361. doi: 10.1681/ASN.2017121265. Epub 2018 Aug 24. J Am Soc Nephrol. 2018. PMID: 30143558 Free PMC article.
PHYOX2: a pivotal randomized study of nedosiran in primary hyperoxaluria type 1 or 2.
Baum MA, Langman C, Cochat P, Lieske JC, Moochhala SH, Hamamoto S, Satoh H, Mourani C, Ariceta G, Torres A, Wolley M, Belostotsky V, Forbes TA, Groothoff J, Hayes W, Tönshoff B, Takayama T, Rosskamp R, Russell K, Zhou J, Amrite A, Hoppe B; PHYOX2 study investigators. Baum MA, et al. Kidney Int. 2023 Jan;103(1):207-217. doi: 10.1016/j.kint.2022.07.025. Epub 2022 Aug 22. Kidney Int. 2023. PMID: 36007597 Free article. Clinical Trial.
Editorial: Intensive care unit nephrology.
Baum M. Baum M. Curr Opin Pediatr. 2023 Apr 1;35(2):231-233. doi: 10.1097/MOP.0000000000001211. Epub 2022 Nov 24. Curr Opin Pediatr. 2023. PMID: 36855944 No abstract available.
1,727 results