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Page 1
Age-Specific Cut-off Values of Amino Acids and Acylcarnitines for Diagnosis of Inborn Errors of Metabolism Using Liquid Chromatography Tandem Mass Spectrometry.
Sarker SK, Islam MT, Biswas A, Bhuyan GS, Sultana R, Sultana N, Rakhshanda S, Begum MN, Rahat A, Yeasmin S, Khanam M, Saha AK, Noor FA, Sajib AA, Islam ABMMK, Qadri SK, Shahidullah M, Mannan MA, Muraduzzaman AKM, Shirin T, Rahman SM, Qadri SS, Saha N, Akhteruzzaman S, Qadri F, Mannoor K. Sarker SK, et al. Among authors: qadri sk, qadri ss, qadri f. Biomed Res Int. 2019 Jan 6;2019:3460902. doi: 10.1155/2019/3460902. eCollection 2019. Biomed Res Int. 2019. PMID: 30723736 Free PMC article.
Molecular Analysis of Glucose-6-Phosphate Dehydrogenase Gene Mutations in Bangladeshi Individuals.
Sarker SK, Islam MT, Eckhoff G, Hossain MA, Qadri SK, Muraduzzaman AK, Bhuyan GS, Shahidullah M, Mannan MA, Tahura S, Hussain M, Akhter S, Nahar N, Shirin T, Qadri F, Mannoor K. Sarker SK, et al. Among authors: qadri sk, qadri f. PLoS One. 2016 Nov 23;11(11):e0166977. doi: 10.1371/journal.pone.0166977. eCollection 2016. PLoS One. 2016. PMID: 27880809 Free PMC article. Clinical Trial.
Bacterial and viral pathogen spectra of acute respiratory infections in under-5 children in hospital settings in Dhaka city.
Bhuyan GS, Hossain MA, Sarker SK, Rahat A, Islam MT, Haque TN, Begum N, Qadri SK, Muraduzzaman AK, Islam NN, Islam MS, Sultana N, Jony MH, Khanam F, Mowla G, Matin A, Begum F, Shirin T, Ahmed D, Saha N, Qadri F, Mannoor K. Bhuyan GS, et al. Among authors: qadri sk, qadri f. PLoS One. 2017 Mar 27;12(3):e0174488. doi: 10.1371/journal.pone.0174488. eCollection 2017. PLoS One. 2017. PMID: 28346512 Free PMC article.
High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh.
Islam MT, Sarkar SK, Sultana N, Begum MN, Bhuyan GS, Talukder S, Muraduzzaman AKM, Alauddin M, Islam MS, Biswas PP, Biswas A, Qadri SK, Shirin T, Banu B, Sadya S, Hussain M, Sarwardi G, Khan WA, Mannan MA, Shekhar HU, Chowdhury EK, Sajib AA, Akhteruzzaman S, Qadri SS, Qadri F, Mannoor K. Islam MT, et al. Among authors: qadri sk, qadri ss, qadri f. BMC Genet. 2018 Jan 2;19(1):1. doi: 10.1186/s12863-017-0594-3. BMC Genet. 2018. PMID: 29295702 Free PMC article.
High resolution melting curve analysis enables rapid and reliable detection of G6PD variants in heterozygous females.
Islam MT, Sarker SK, Talukder S, Bhuyan GS, Rahat A, Islam NN, Mahmud H, Hossain MA, Muraduzzaman AKM, Rahman J, Qadri SK, Shahidullah M, Mannan MA, Tahura S, Hussain M, Saha N, Akhter S, Nahar N, Begum F, Shirin T, Akhteruzzaman S, Qadri SS, Qadri F, Mannoor K. Islam MT, et al. Among authors: qadri sk, qadri ss, qadri f. BMC Genet. 2018 Aug 10;19(1):58. doi: 10.1186/s12863-018-0664-1. BMC Genet. 2018. PMID: 30097005 Free PMC article.
Mutation Spectrum in TPO Gene of Bangladeshi Patients with Thyroid Dyshormonogenesis and Analysis of the Effects of Different Mutations on the Structural Features and Functions of TPO Protein through In Silico Approach.
Begum MN, Islam MT, Hossain SR, Bhuyan GS, Halim MA, Shahriar I, Sarker SK, Haque S, Konika TK, Islam MS, Rahat A, Qadri SK, Sultana R, Begum S, Sultana S, Saha N, Hasan M, Hasanat MA, Banu H, Shekhar HU, Chowdhury EK, Sajib AA, Islam ABMMK, Qadri SS, Qadri F, Akhteruzzaman S, Mannoor K. Begum MN, et al. Among authors: qadri sk, qadri ss, qadri f. Biomed Res Int. 2019 Feb 24;2019:9218903. doi: 10.1155/2019/9218903. eCollection 2019. Biomed Res Int. 2019. PMID: 30915365 Free PMC article.
Nationwide carrier detection and molecular characterization of β-thalassemia and hemoglobin E variants in Bangladeshi population.
Noor FA, Sultana N, Bhuyan GS, Islam MT, Hossain M, Sarker SK, Islam K, Khan WA, Rahman M, Qadri SK, Shekhar HU, Qadri F, Qadri SS, Mannoor K. Noor FA, et al. Among authors: qadri sk, qadri ss, qadri f. Orphanet J Rare Dis. 2020 Jan 15;15(1):15. doi: 10.1186/s13023-020-1294-z. Orphanet J Rare Dis. 2020. PMID: 31941534 Free PMC article.
Feeding difficulty in an infant: an unusual cause.
Qadri SK, Logarajah V, Nah SA, Jamuar SS. Qadri SK, et al. BMJ Case Rep. 2018 Aug 23;2018:bcr2018225289. doi: 10.1136/bcr-2018-225289. BMJ Case Rep. 2018. PMID: 30139785 Free PMC article.
29 results