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

Year Number of Results
1998 1
1999 1
2000 2
2001 1
2003 1
2004 3
2005 6
2006 5
2007 5
2008 3
2009 3
2010 2
2011 1
2012 2
2013 4
2014 4
2015 1
2016 6
2017 7
2018 5
2019 10
2020 9
2021 12
2022 8
2023 0
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Search Results

85 results
Results by year
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Page 1
Fetal Brain Volume Predicts Neurodevelopment in Congenital Heart Disease.
Sadhwani A, Wypij D, Rofeberg V, Gholipour A, Mittleman M, Rohde J, Velasco-Annis C, Calderon J, Friedman KG, Tworetzky W, Grant PE, Soul JS, Warfield SK, Newburger JW, Ortinau CM, Rollins CK. Sadhwani A, et al. Among authors: soul js. Circulation. 2022 Apr 12;145(15):1108-1119. doi: 10.1161/CIRCULATIONAHA.121.056305. Epub 2022 Feb 10. Circulation. 2022. PMID: 35143287
Management of seizures in neonates with neonatal encephalopathy treated with hypothermia.
DeLaGarza-Pineda O, Mailo JA, Boylan G, Chau V, Glass HC, Mathur AM, Shellhaas RA, Soul JS, Wusthoff CJ, Chang T; Newborn Brain Society Guidelines and Publications Committee. DeLaGarza-Pineda O, et al. Among authors: soul js. Semin Fetal Neonatal Med. 2021 Aug;26(4):101279. doi: 10.1016/j.siny.2021.101279. Epub 2021 Sep 15. Semin Fetal Neonatal Med. 2021. PMID: 34563467 Review.
A Pilot Randomized, Controlled, Double-Blind Trial of Bumetanide to Treat Neonatal Seizures.
Soul JS, Bergin AM, Stopp C, Hayes B, Singh A, Fortuno CR, O'Reilly D, Krishnamoorthy K, Jensen FE, Rofeberg V, Dong M, Vinks AA, Wypij D, Staley KJ; Boston Bumetanide Trial Group. Soul JS, et al. Ann Neurol. 2021 Feb;89(2):327-340. doi: 10.1002/ana.25959. Epub 2020 Dec 3. Ann Neurol. 2021. PMID: 33201535 Free PMC article. Clinical Trial.
De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome.
Vetrini F, McKee S, Rosenfeld JA, Suri M, Lewis AM, Nugent KM, Roeder E, Littlejohn RO, Holder S, Zhu W, Alaimo JT, Graham B, Harris JM, Gibson JB, Pastore M, McBride KL, Komara M, Al-Gazali L, Al Shamsi A, Fanning EA, Wierenga KJ, Scott DA, Ben-Neriah Z, Meiner V, Cassuto H, Elpeleg O, Holder JL Jr, Burrage LC, Seaver LH, Van Maldergem L, Mahida S, Soul JS, Marlatt M, Matyakhina L, Vogt J, Gold JA, Park SM, Varghese V, Lampe AK, Kumar A, Lees M, Holder-Espinasse M, McConnell V, Bernhard B, Blair E, Harrison V; DDD study; Muzny DM, Gibbs RA, Elsea SH, Posey JE, Bi W, Lalani S, Xia F, Yang Y, Eng CM, Lupski JR, Liu P. Vetrini F, et al. Among authors: soul js. Genome Med. 2019 Feb 28;11(1):12. doi: 10.1186/s13073-019-0623-0. Genome Med. 2019. PMID: 30819258 Free PMC article.
85 results