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The immunogenicity and efficacy of acommercially available Infectious Bovine Rhinotracheitis (IBR) virus vaccine against a Pakistani field IBR strain.
Vet Ital. 2023 Mar 31;59(1):65-70. doi: 10.12834/VetIt.2922.19929.3.
Vet Ital. 2023.
PMID: 37994637
Free article.
Thiourea-Capped Nanoapatites Amplify Osmotic Stress Tolerance in Zea mays L. by Conserving Photosynthetic Pigments, Osmolytes Biosynthesis and Antioxidant Biosystems.
Faryal S, Ullah R, Khan MN, Ali B, Hafeez A, Jaremko M, Qureshi KA.
Faryal S, et al.
Molecules. 2022 Sep 6;27(18):5744. doi: 10.3390/molecules27185744.
Molecules. 2022.
PMID: 36144480
Free PMC article.
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A GDF5 frameshift mutation segregating with Grebe type chondrodysplasia and brachydactyly type C+ in a 6 generations family: Clinical report and mini review.
Faryal S, Farooq M, Abdullah U, Ali Z, Saadi SM, Ullah F, Khan K, Sarwar Y, Sher M, Chopra AA, Tommerup N, Baig SM.
Faryal S, et al.
Eur J Med Genet. 2021 Jul;64(7):104226. doi: 10.1016/j.ejmg.2021.104226. Epub 2021 Apr 16.
Eur J Med Genet. 2021.
PMID: 33872773
Review.
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Role of the DECAF Score in Predicting In-hospital Mortality in Acute Exacerbation of Chronic Obstructive Pulmonary Disease.
Memon MA, Faryal S, Brohi N, Kumar B.
Memon MA, et al. Among authors: faryal s.
Cureus. 2019 Jun 4;11(6):e4826. doi: 10.7759/cureus.4826.
Cureus. 2019.
PMID: 31403014
Free PMC article.
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A novel in-frame mutation in CLN3 leads to Juvenile neuronal ceroid lipofuscinosis in a large Pakistani family.
Sher M, Farooq M, Abdullah U, Ali Z, Faryal S, Zakaria M, Ullah F, Bukhari H, Møller RS, Tommerup N, Baig SM.
Sher M, et al. Among authors: faryal s.
Int J Neurosci. 2019 Sep;129(9):890-895. doi: 10.1080/00207454.2019.1586686. Epub 2019 Mar 20.
Int J Neurosci. 2019.
PMID: 30892110
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A novel mutation in CDK5RAP2 gene causes primary microcephaly with speech impairment and sparse eyebrows in a consanguineous Pakistani family.
Abdullah U, Farooq M, Mang Y, Marriam Bakhtiar S, Fatima A, Hansen L, Kjaer KW, Larsen LA, Faryal S, Tommerup N, Mahmood Baig S.
Abdullah U, et al. Among authors: faryal s.
Eur J Med Genet. 2017 Dec;60(12):627-630. doi: 10.1016/j.ejmg.2017.07.017. Epub 2017 Aug 2.
Eur J Med Genet. 2017.
PMID: 28778786
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A missense variant in ITPR1 provides evidence for autosomal recessive SCA29 with asymptomatic cerebellar hypoplasia in carriers.
Klar J, Ali Z, Farooq M, Khan K, Wikström J, Iqbal M, Zulfiqar S, Faryal S, Baig SM, Dahl N.
Klar J, et al. Among authors: faryal s.
Eur J Hum Genet. 2017 Jun;25(7):848-853. doi: 10.1038/ejhg.2017.54. Epub 2017 May 10.
Eur J Hum Genet. 2017.
PMID: 28488678
Free PMC article.
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