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Year Number of Results
1953 1
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1960 1
1969 1
1970 2
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1972 2
1973 2
1974 2
1975 25
1976 46
1977 26
1978 47
1979 31
1980 41
1981 40
1982 42
1983 30
1984 48
1985 37
1986 40
1987 40
1988 60
1989 37
1990 49
1991 62
1992 55
1993 57
1994 71
1995 68
1996 93
1997 95
1998 102
1999 79
2000 89
2001 77
2002 98
2003 131
2004 108
2005 144
2006 98
2007 98
2008 139
2009 140
2010 136
2011 195
2012 210
2013 202
2014 203
2015 220
2016 198
2017 190
2018 214
2019 232
2020 230
2021 293
2022 242
2023 222
2024 209
2025 22

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5,159 results

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Page 1
Angiography after Out-of-Hospital Cardiac Arrest without ST-Segment Elevation.
Desch S, Freund A, Akin I, Behnes M, Preusch MR, Zelniker TA, Skurk C, Landmesser U, Graf T, Eitel I, Fuernau G, Haake H, Nordbeck P, Hammer F, Felix SB, Hassager C, Engstrøm T, Fichtlscherer S, Ledwoch J, Lenk K, Joner M, Steiner S, Liebetrau C, Voigt I, Zeymer U, Brand M, Schmitz R, Horstkotte J, Jacobshagen C, Pöss J, Abdel-Wahab M, Lurz P, Jobs A, de Waha-Thiele S, Olbrich D, Sandig F, König IR, Brett S, Vens M, Klinge K, Thiele H; TOMAHAWK Investigators. Desch S, et al. N Engl J Med. 2021 Dec 30;385(27):2544-2553. doi: 10.1056/NEJMoa2101909. Epub 2021 Aug 29. N Engl J Med. 2021. PMID: 34459570 Free article. Clinical Trial.
At 30 days, 143 of 265 patients (54.0%) in the immediate-angiography group and 122 of 265 patients (46.0%) in the delayed-angiography group had died (hazard ratio, 1.28; 95% confidence interval [CI], 1.00 to 1.63; P = 0.06). The composite of death or severe neurologic defi …
At 30 days, 143 of 265 patients (54.0%) in the immediate-angiography group and 122 of 265 patients (46.0%) in the delayed-angiography group …
Rethinking adherence.
Steiner JF. Steiner JF. Ann Intern Med. 2012 Oct 16;157(8):580-5. doi: 10.7326/0003-4819-157-8-201210160-00013. Ann Intern Med. 2012. PMID: 23070491
A novel de novo mutation (p.Pro1310Glnfs*46) in KMT2A caused Wiedemann-Steiner Syndrome in a Chinese boy with postnatal growth retardation: a case report.
Chen M, Liu R, Wu C, Li X, Wang Y. Chen M, et al. Mol Biol Rep. 2019 Oct;46(5):5555-5559. doi: 10.1007/s11033-019-04936-y. Epub 2019 Jun 27. Mol Biol Rep. 2019. PMID: 31250358
Wiedemann-Steiner Syndrome (WSS) is a very rare autosomal dominant disease. Mutations in the KMT2A gene have been shown to cause this disease. ...Whole-exome sequencing showed a novel de novo mutation (p.Pro1310Glnfs*46) in KMT2A, which confirmed the diagnosis of WS …
Wiedemann-Steiner Syndrome (WSS) is a very rare autosomal dominant disease. Mutations in the KMT2A gene have been shown to cause this …
Steiner 3-Wiener Index of Zigzag Polyhex Nanotubes.
Huilgol MI, HShobha PH, Udupa HJ, Cangul IN. Huilgol MI, et al. Comb Chem High Throughput Screen. 2024 Oct 15. doi: 10.2174/0113862073329237240929214731. Online ahead of print. Comb Chem High Throughput Screen. 2024. PMID: 39411966
BACKGROUND: Let G be a connected graph and S be a k element subset of the vertex set V(G) of G. Steiner distance is a natural generalization of the usual graph distance. The Steiner-k distance dG(S) between the vertices of S is the minimum size among all connected s …
BACKGROUND: Let G be a connected graph and S be a k element subset of the vertex set V(G) of G. Steiner distance is a natural general …
Lords and ladies leapin' on leptin.
Steiner RA. Steiner RA. Endocrinology. 1996 Nov;137(11):4533-5. doi: 10.1210/endo.137.11.8895313. Endocrinology. 1996. PMID: 8895313 Review. No abstract available.
A Physarum-inspired approach to the Euclidean Steiner tree problem.
Hsu S, Massolo FIS, Schaposnik LP. Hsu S, et al. Sci Rep. 2022 Aug 25;12(1):14536. doi: 10.1038/s41598-022-18316-3. Sci Rep. 2022. PMID: 36008426 Free PMC article.
The inspiration comes from Physarum, a unicellular slime mold capable of solving the traveling salesman and Steiner tree problems. Besides exhibiting individual intelligence, Physarum can also share information with other Physarum organisms through fusion. ...We demonstrat …
The inspiration comes from Physarum, a unicellular slime mold capable of solving the traveling salesman and Steiner tree problems. Be …
Wiedemann-Steiner Syndrome With 2 Novel KMT2A Mutations.
Min Ko J, Cho JS, Yoo Y, Seo J, Choi M, Chae JH, Lee HR, Cho TJ. Min Ko J, et al. J Child Neurol. 2017 Feb;32(2):237-242. doi: 10.1177/0883073816674095. Epub 2016 Oct 24. J Child Neurol. 2017. PMID: 27777327
Wiedemann-Steiner syndrome is a rare genetic disorder characterized by short stature, hairy elbows, facial dysmorphism, and developmental delay. ...Exome sequencing analysis of these patients and their parents revealed a de novo nonsense mutation, p.Gln1978*, of KMT …
Wiedemann-Steiner syndrome is a rare genetic disorder characterized by short stature, hairy elbows, facial dysmorphism, and developme …
Wiedemann-Steiner Syndrome: A Rare Differential Diagnosis of Neurodevelopmental Delay and Dysmorphic Features.
Carman KB, Kaplan E, Aslan CN, Kocagil S, Cilinigr O, Yarar C. Carman KB, et al. J Pediatr Genet. 2020 Sep 23;11(2):162-164. doi: 10.1055/s-0040-1716709. eCollection 2022 Jun. J Pediatr Genet. 2020. PMID: 35769955 Free PMC article.
Wiedemann-Steiner syndrome (WSS) is a rare genetic disorder characterized by dysmorphic features, neurodevelopmental delay, growth retardation, and hypertrichosis cubiti. ...Genetic analysis revealed a heterozygous c.2312dupC (p.Ser774Valfs*11) variant at the KMT2A …
Wiedemann-Steiner syndrome (WSS) is a rare genetic disorder characterized by dysmorphic features, neurodevelopmental delay, growth re …
Unique profile of academic learning difficulties in Wiedemann-Steiner syndrome.
Ng R, Bjornsson HT, Fahrner JA, Harris J. Ng R, et al. J Intellect Disabil Res. 2023 Feb;67(2):101-111. doi: 10.1111/jir.12993. Epub 2022 Nov 27. J Intellect Disabil Res. 2023. PMID: 36437529 Free PMC article.
BACKGROUND: Wiedemann-Steiner syndrome (WSS) is a rare genetic disorder caused by heterozygous variants in KMT2A. ...RESULTS: On average, parent ratings on the Math (mean Z = -3.08, SD = 0.87) and Spatial scales (mean Z = -2.52, SD = 0.85) were significantly more elevated …
BACKGROUND: Wiedemann-Steiner syndrome (WSS) is a rare genetic disorder caused by heterozygous variants in KMT2A. ...RESULTS: On aver …
Wiedemann-Steiner Syndrome with a Pathogenic Variant in KMT2A from Taiwan.
Lee CL, Chuang CK, Chiu HC, Tu RY, Lo YT, Chang YH, Lin HY, Lin SP. Lee CL, et al. Children (Basel). 2021 Oct 22;8(11):952. doi: 10.3390/children8110952. Children (Basel). 2021. PMID: 34828665 Free PMC article.
Wiedemann-Steiner syndrome (WSS) is a rare genetic disorder. Patients with WSS have characteristics of growth retardation, facial dysmorphism, hypertrichosis cubiti (HC), and neurodevelopmental delays. ...Trio-WES showed a de novo mutation of the KMT2A gene (NM_001197104.2 …
Wiedemann-Steiner syndrome (WSS) is a rare genetic disorder. Patients with WSS have characteristics of growth retardation, facial dys …
5,159 results