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

Year Number of Results
1989 1
2000 2
2001 1
2003 1
2004 1
2005 1
2009 1
2013 1
2014 2
2015 4
2016 3
2018 4
2019 7
2020 10
2021 6
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38 results
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Page 1
Hepatic Lipoprotein Export and Remission of Human Type 2 Diabetes after Weight Loss.
Al-Mrabeh A, Zhyzhneuskaya SV, Peters C, Barnes AC, Melhem S, Jesuthasan A, Aribisala B, Hollingsworth KG, Lietz G, Mathers JC, Sattar N, Lean MEJ, Taylor R. Al-Mrabeh A, et al. Among authors: melhem s. Cell Metab. 2020 Feb 4;31(2):233-249.e4. doi: 10.1016/j.cmet.2019.11.018. Epub 2019 Dec 19. Cell Metab. 2020. PMID: 31866441 Free article. Clinical Trial.
Acute Cor Pulmonale in Critically Ill Patients with Covid-19.
Creel-Bulos C, Hockstein M, Amin N, Melhem S, Truong A, Sharifpour M. Creel-Bulos C, et al. Among authors: melhem s. N Engl J Med. 2020 May 21;382(21):e70. doi: 10.1056/NEJMc2010459. Epub 2020 May 6. N Engl J Med. 2020. PMID: 32374956 Free PMC article. No abstract available.
Retraction Note to: A new inducible transgenic mouse model for C9orf72-associated GGGGCC repeat expansion supports a gain-of-function mechanism in C9orf72-associated ALS and FTD.
Hukema RK, Riemslagh FW, Melhem S, van der Linde HC, Severijnen LW, Edbauer D, Maas A, Charlet-Berguerand N, Willemsen R, van Swieten JC. Hukema RK, et al. Among authors: melhem s. Acta Neuropathol Commun. 2016 Dec 9;4(1):129. doi: 10.1186/s40478-016-0401-9. Acta Neuropathol Commun. 2016. PMID: 27938413 Free PMC article. No abstract available.
LRP10 variants in progressive supranuclear palsy.
Vergouw LJM, Melhem S, Donker Kaat L, Chiu WZ, Kuipers DJS, Breedveld G, Boon AJW, Wang LS, Naj AC, Mlynarksi E, Cantwell L, Quadri M, Ross OA, Dickson DW, Schellenberg GD, van Swieten JC, Bonifati V, de Jong FJ. Vergouw LJM, et al. Among authors: melhem s. Neurobiol Aging. 2020 Oct;94:311.e5-311.e10. doi: 10.1016/j.neurobiolaging.2020.04.016. Epub 2020 Apr 30. Neurobiol Aging. 2020. PMID: 32527607
Somatic TARDBP variants as a cause of semantic dementia.
van Rooij J, Mol MO, Melhem S, van der Wal P, Arp P, Paron F, Donker Kaat L, Seelaar H; Netherlands Brain Bank, Miedema SSM, Oshima T, Eggen BJL, Uitterlinden A, van Meurs J, van Kesteren RE, Smit AB, Buratti E, van Swieten JC. van Rooij J, et al. Among authors: melhem s. Brain. 2020 Dec 1;143(12):3827-3841. doi: 10.1093/brain/awaa317. Brain. 2020. PMID: 33155043 Free PMC article.
Clinical and pathologic phenotype of a large family with heterozygous STUB1 mutation.
Mol MO, van Rooij JGJ, Brusse E, Verkerk AJMH, Melhem S, den Dunnen WFA, Rizzu P, Cupidi C, van Swieten JC, Donker Kaat L. Mol MO, et al. Among authors: melhem s. Neurol Genet. 2020 Mar 23;6(3):e417. doi: 10.1212/NXG.0000000000000417. eCollection 2020 Jun. Neurol Genet. 2020. PMID: 32337344 Free PMC article.
Underlying genetic variation in familial frontotemporal dementia: sequencing of 198 patients.
Mol MO, van Rooij JGJ, Wong TH, Melhem S, Verkerk AJMH, Kievit AJA, van Minkelen R, Rademakers R, Pottier C, Kaat LD, Seelaar H, van Swieten JC, Dopper EGP. Mol MO, et al. Among authors: melhem s. Neurobiol Aging. 2021 Jan;97:148.e9-148.e16. doi: 10.1016/j.neurobiolaging.2020.07.014. Epub 2020 Jul 30. Neurobiol Aging. 2021. PMID: 32843152 Free article.
EIF2AK3 variants in Dutch patients with Alzheimer's disease.
Wong TH, van der Lee SJ, van Rooij JGJ, Meeter LHH, Frick P, Melhem S, Seelaar H, Ikram MA, Rozemuller AJ, Holstege H, Hulsman M, Uitterlinden A, Neumann M, Hoozemans JJM, van Duijn CM, Rademakers R, van Swieten JC. Wong TH, et al. Among authors: melhem s. Neurobiol Aging. 2019 Jan;73:229.e11-229.e18. doi: 10.1016/j.neurobiolaging.2018.08.016. Epub 2018 Aug 24. Neurobiol Aging. 2019. PMID: 30314817 Free article.
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