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

Year Number of Results
1974 1
1999 1
2001 1
2002 2
2003 1
2005 1
2006 1
2007 2
2008 1
2009 1
2010 5
2011 3
2012 2
2013 2
2014 4
2015 8
2016 4
2017 8
2018 7
2019 8
2020 9
2021 5
2022 5
2023 10
2024 1

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80 results

Results by year

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Page 1
Superimmunity by pan-sarbecovirus nanobodies.
Xiang Y, Huang W, Liu H, Sang Z, Nambulli S, Tubiana J, Williams KL Jr, Duprex WP, Schneidman-Duhovny D, Wilson IA, Taylor DJ, Shi Y. Xiang Y, et al. Cell Rep. 2022 Jun 28;39(13):111004. doi: 10.1016/j.celrep.2022.111004. Epub 2022 Jun 8. Cell Rep. 2022. PMID: 35738279 Free PMC article.
Neuromuscular disease genetics in under-represented populations: increasing data diversity.
Wilson LA, Macken WL, Perry LD, Record CJ, Schon KR, Frezatti RSS, Raga S, Naidu K, Köken ÖY, Polat I, Kapapa MM, Dominik N, Efthymiou S, Morsy H, Nel M, Fassad MR, Gao F, Patel K, Schoonen M, Bisschoff M, Vorster A, Jonvik H, Human R, Lubbe E, Nonyane M, Vengalil S, Nashi S, Srivastava K, Lemmers RJLF, Reyaz A, Mishra R, Töpf A, Trainor CI, Steyn EC, Mahungu AC, van der Vliet PJ, Ceylan AC, Hiz AS, Çavdarlı B, Semerci Gündüz CN, Ceylan GG, Nagappa M, Tallapaka KB, Govindaraj P, van der Maarel SM, Narayanappa G, Nandeesh BN, Wa Somwe S, Bearden DR, Kvalsund MP, Ramdharry GM, Oktay Y, Yiş U, Topaloğlu H, Sarkozy A, Bugiardini E, Henning F, Wilmshurst JM, Heckmann JM, McFarland R, Taylor RW, Smuts I, van der Westhuizen FH, Sobreira CFDR, Tomaselli PJ, Marques W Jr, Bhatia R, Dalal A, Srivastava MVP, Yareeda S, Nalini A, Vishnu VY, Thangaraj K, Straub V, Horvath R, Chinnery PF, Pitceathly RDS, Muntoni F, Houlden H, Vandrovcova J, Reilly MM, Hanna MG. Wilson LA, et al. Brain. 2023 Dec 1;146(12):5098-5109. doi: 10.1093/brain/awad254. Brain. 2023. PMID: 37516995 Free PMC article.
A boy with neck weakness.
Yiş U, Becker K, Çırak S. Yiş U, et al. Neuromuscul Disord. 2018 Mar;28(3):236-237. doi: 10.1016/j.nmd.2017.11.016. Epub 2017 Dec 5. Neuromuscul Disord. 2018. PMID: 29339009 No abstract available.
A phase 1b randomized clinical trial of CT1812 to measure Aβ oligomer displacement in Alzheimer's disease using an indwelling CSF catheter.
LaBarbera KM, Sheline YI, Izzo NJ, Yuede CM, Waybright L, Yurko R, Edwards HM, Gardiner WD, Blennow K, Zetterberg H, Börjesson-Hanson A, Morgan R, Davis CS, Guttendorf RJ, Schneider LS, DeKosky S, LeVine H 3rd, Grundman M, Caggiano AO, Cirrito JR, Catalano SM, Hamby ME. LaBarbera KM, et al. Transl Neurodegener. 2023 May 12;12(1):24. doi: 10.1186/s40035-023-00358-w. Transl Neurodegener. 2023. PMID: 37173791 Free PMC article. Clinical Trial. No abstract available.
PRUNE1: a disease-causing gene for secondary microcephaly.
Karakaya M, Yilmaz S, Storbeck M, Hoelker I, Heller R, Serdaroglu G, Gökben S, Yis U, Wirth B. Karakaya M, et al. Brain. 2017 Oct 1;140(10):e61. doi: 10.1093/brain/awx197. Brain. 2017. PMID: 28969376 No abstract available.
Giant axonal neuropathy: A differential diagnosis of consideration.
Edem P, Karakaya M, Wirth B, Okur TD, Yiş U. Edem P, et al. Turk J Pediatr. 2019;61(2):275-278. doi: 10.24953/turkjped.2019.02.019. Turk J Pediatr. 2019. PMID: 31951341 Free article.
Edem P, Karakaya M, Wirth B, Okur TD, Yis U. Giant axonal neuropathy: A differential diagnosis of consideration. ...
Edem P, Karakaya M, Wirth B, Okur TD, Yis U. Giant axonal neuropathy: A differential diagnosis of consideration. ...
80 results