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2009 1
2010 1
2019 1
2020 2
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Page 1
Applications of Nanomaterials in Leishmaniasis: A Focus on Recent Advances and Challenges.
Saleem K, Khursheed Z, Hano C, Anjum I, Anjum S. Saleem K, et al. Among authors: anjum i. Nanomaterials (Basel). 2019 Dec 9;9(12):1749. doi: 10.3390/nano9121749. Nanomaterials (Basel). 2019. PMID: 31818029 Free PMC article. Review.
An Overview of the Applications of Nanomaterials and Nanodevices in the Food Industry.
Shafiq M, Anjum S, Hano C, Anjum I, Abbasi BH. Shafiq M, et al. Among authors: anjum i. Foods. 2020 Feb 3;9(2):148. doi: 10.3390/foods9020148. Foods. 2020. PMID: 32028580 Free PMC article. Review.
Comprehensive mutational screening in a cohort of Danish families with hereditary congenital cataract.
Hansen L, Mikkelsen A, Nürnberg P, Nürnberg G, Anjum I, Eiberg H, Rosenberg T. Hansen L, et al. Among authors: anjum i. Invest Ophthalmol Vis Sci. 2009 Jul;50(7):3291-303. doi: 10.1167/iovs.08-3149. Epub 2009 Jan 31. Invest Ophthalmol Vis Sci. 2009. PMID: 19182255
A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family.
Anjum I, Eiberg H, Baig SM, Tommerup N, Hansen L. Anjum I, et al. Mol Vis. 2010 Mar 30;16:549-55. Mol Vis. 2010. PMID: 20361012 Free PMC article.
An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan.
Rasool S, Baig JM, Moawia A, Ahmad I, Iqbal M, Waseem SS, Asif M, Abdullah U, Makhdoom EUH, Kaygusuz E, Zakaria M, Ramzan S, Haque SU, Mir A, Anjum I, Fiaz M, Ali Z, Tariq M, Saba N, Hussain W, Budde B, Irshad S, Noegel AA, Höning S, Baig SM, Nürnberg P, Hussain MS. Rasool S, et al. Among authors: anjum i. Mol Genet Genomic Med. 2020 Sep;8(9):e1408. doi: 10.1002/mgg3.1408. Epub 2020 Jul 17. Mol Genet Genomic Med. 2020. PMID: 32677750 Free PMC article.