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Year | Number of Results |
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2022 | 3 |
2023 | 2 |
2024 | 1 |
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Page 1
Clinical and haematological characteristics of 38 individuals with Hb G-Makassar in Malaysia.
EJHaem. 2023 Aug 10;4(4):940-948. doi: 10.1002/jha2.750. eCollection 2023 Nov.
EJHaem. 2023.
PMID: 38024609
Free PMC article.
Characterization of New Alpha Zero (α0) Thalassaemia Deletion (--GB) among Malays in Malaysian Population.
Yasin NM, Abdul Hamid FS, Hassan S, Mat Yusoff Y, Mohd Sahid EN, Esa E.
Yasin NM, et al.
Diagnostics (Basel). 2023 Oct 23;13(20):3286. doi: 10.3390/diagnostics13203286.
Diagnostics (Basel). 2023.
PMID: 37892108
Free PMC article.
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Evaluation of in silico predictors on short nucleotide variants in HBA1, HBA2, and HBB associated with haemoglobinopathies.
Tamana S, Xenophontos M, Minaidou A, Stephanou C, Harteveld CL, Bento C, Traeger-Synodinos J, Fylaktou I, Yasin NM, Abdul Hamid FS, Esa E, Halim-Fikri H, Zilfalil BA, Kakouri AC; ClinGen Hemoglobinopathy Variant Curation Expert Panel; Kleanthous M, Kountouris P.
Tamana S, et al. Among authors: yasin nm.
Elife. 2022 Dec 1;11:e79713. doi: 10.7554/eLife.79713.
Elife. 2022.
PMID: 36453528
Free PMC article.
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Global Globin Network Consensus Paper: Classification and Stratified Roadmaps for Improved Thalassaemia Care and Prevention in 32 Countries.
Halim-Fikri BH, Lederer CW, Baig AA, Mat-Ghani SNA, Syed-Hassan SR, Yusof W, Abdul Rashid D, Azman NF, Fucharoen S, Panigoro R, Silao CLT, Viprakasit V, Jalil N, Mohd Yasin N, Bahar R, Selvaratnam V, Mohamad N, Nik Hassan NN, Esa E, Krause A, Robinson H, Hasler J, Stephanou C, Raja-Sabudin RZ, Elion J, El-Kamah G, Coviello D, Yusoff N, Abdul Latiff Z, Arnold C, Burn J, Kountouris P, Kleanthous M, Ramesar R, Zilfalil BA, On Behalf Of The Global Globin Network Ggn.
Halim-Fikri BH, et al. Among authors: mohd yasin n.
J Pers Med. 2022 Mar 31;12(4):552. doi: 10.3390/jpm12040552.
J Pers Med. 2022.
PMID: 35455667
Free PMC article.
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Molecular and hematological studies in a cohort of beta zero South East Asia deletion (β°-thal SEA) from Malaysian perspective.
Yasin NM, Abdul Hamid FS, Hassan S, Sudin A, Yassim H, Mohd Sahid EN, Mat Yusoff Y, Esa E, Saleem M.
Yasin NM, et al.
Front Pediatr. 2022 Nov 30;10:974496. doi: 10.3389/fped.2022.974496. eCollection 2022.
Front Pediatr. 2022.
PMID: 36533237
Free PMC article.
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Rare coinheritance of hemoglobin vancleave with severe beta-thalassemia mutation in a patient with secondary erythrocytosis.
Aziz NA, Musa NH, Mathews M, Rajenderan KT, Abdul Hamid FS, Hassan S, Omar SL, Wan Yusoff WNAB, Mohd Din MLB, Jamaludin NAB, Wan Taib WR, Esa E, Mohd Yasin N.
Aziz NA, et al. Among authors: mohd yasin n.
Hum Genome Var. 2024 Apr 23;11(1):19. doi: 10.1038/s41439-024-00275-y.
Hum Genome Var. 2024.
PMID: 38653961
Free PMC article.
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