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Non-invasive prenatal testing for autosomal recessive disorders: A new promising approach.
Alyafee Y, Al Tuwaijri A, Umair M, Alharbi M, Haddad S, Ballow M, Alayyar L, Alam Q, Althenayyan S, Al Ghilan N, Al Khaldi A, Faden MS, Al Sufyan H, Alfadhel M. Alyafee Y, et al. Among authors: ballow m. Front Genet. 2022 Nov 3;13:1047474. doi: 10.3389/fgene.2022.1047474. eCollection 2022. Front Genet. 2022. PMID: 36406136 Free PMC article.
Congenital disorder of glycosylation with defective fucosylation 2 (FCSK gene defect): The third report in the literature with a mild phenotype.
Al Tuwaijri A, Alyafee Y, Umair M, Alsubait A, Alharbi M, AlEidi H, Ballow M, Aldrees M, Alam Q, Al Abdulrahman A, Alrifai MT, Alfadhel M. Al Tuwaijri A, et al. Among authors: ballow m. Mol Genet Genomic Med. 2023 Apr;11(4):e2117. doi: 10.1002/mgg3.2117. Epub 2022 Nov 24. Mol Genet Genomic Med. 2023. PMID: 36426412 Free PMC article.
Practical guidance for the diagnosis and management of secondary hypogammaglobulinemia: A Work Group Report of the AAAAI Primary Immunodeficiency and Altered Immune Response Committees.
Otani IM, Lehman HK, Jongco AM, Tsao LR, Azar AE, Tarrant TK, Engel E, Walter JE, Truong TQ, Khan DA, Ballow M, Cunningham-Rundles C, Lu H, Kwan M, Barmettler S. Otani IM, et al. Among authors: ballow m. J Allergy Clin Immunol. 2022 May;149(5):1525-1560. doi: 10.1016/j.jaci.2022.01.025. Epub 2022 Feb 14. J Allergy Clin Immunol. 2022. PMID: 35176351 Free article.
The new quest in CTLA-4 insufficiency: How to immune modulate effectively?
Westermann-Clark E, Ballow M, Walter JE. Westermann-Clark E, et al. Among authors: ballow m. J Allergy Clin Immunol. 2022 Feb;149(2):543-546. doi: 10.1016/j.jaci.2021.11.020. Epub 2021 Dec 13. J Allergy Clin Immunol. 2022. PMID: 34915039 No abstract available.
207 results