Mossayebi MH - Search Results

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Glucose-6-phosphate dehydrogenase deficiency as a cause for nonimmune hydrops fetalis and severe fetal anemia: A systematic review.

Iyer NS, Mossayebi MH, Gao TJ, Haizler-Cohen L, Di Mascio D, McLaren RA Jr, Al-Kouatly HB. Iyer NS, et al. Among authors: mossayebi mh. Mol Genet Genomic Med. 2024 Jul;12(7):e2491. doi: 10.1002/mgg3.2491. Mol Genet Genomic Med. 2024. PMID: 39041728 Free PMC article. Review.

Management of a Retained Broken Suture Needle During Cerclage Placement.

Wodoslawsky S, Mossayebi MH, Alleyne G, Al-Kouatly HB. Wodoslawsky S, et al. Among authors: mossayebi mh. Obstet Gynecol. 2023 Nov 1;142(5):1241-1243. doi: 10.1097/AOG.0000000000005316. Epub 2023 Aug 10. Obstet Gynecol. 2023. PMID: 37562036

HELLP syndrome at <23 weeks' gestation: a systematic literature review.

Mossayebi MH, Iyer NS, McLaren RA Jr, Moussa HN, Sibai BM, Al-Kouatly HB. Mossayebi MH, et al. Am J Obstet Gynecol. 2023 Nov;229(5):502-515.e10. doi: 10.1016/j.ajog.2023.04.046. Epub 2023 May 5. Am J Obstet Gynecol. 2023. PMID: 37150281 Review.

Diagnostic yield from prenatal exome sequencing for non-immune hydrops fetalis: A systematic review and meta-analysis.

Al-Kouatly HB, Shivashankar K, Mossayebi MH, Makhamreh M, Critchlow E, Gao Z, Fasehun LK, Alkuraya FS, Ryan EE, Hegde M, Wodoslawsky S, Hughes J, Berger SI. Al-Kouatly HB, et al. Among authors: mossayebi mh. Clin Genet. 2023 May;103(5):503-512. doi: 10.1111/cge.14309. Epub 2023 Feb 26. Clin Genet. 2023. PMID: 36757664 Review.

Considerations of expanded carrier screening: Lessons learned from combined malonic and methylmalonic aciduria.

Gabriel MC, Rice SM, Sloan JL, Mossayebi MH, Venditti CP, Al-Kouatly HB. Gabriel MC, et al. Among authors: mossayebi mh. Mol Genet Genomic Med. 2021 Apr;9(4):e1621. doi: 10.1002/mgg3.1621. Epub 2021 Feb 24. Mol Genet Genomic Med. 2021. PMID: 33625768 Free PMC article.

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