Zobrazeno 1 - 10
of 115
pro vyhledávání: '"Huda B Al-Kouatly"'
Autor:
Michail Spiliopoulos, Andrew Haddad, Huda B Al-Kouatly, Haleema Saeed, Michael J Paidas, Sara N Iqbal, Robert I Glazer
Publikováno v:
PLoS ONE, Vol 19, Iss 12, p e0315225 (2024)
[This corrects the article DOI: 10.1371/journal.pone.0277098.].
Externí odkaz:
https://doaj.org/article/fab271e9c9c745fab375d3b0af56b076
Autor:
Michail Spiliopoulos, Andrew Haddad, Huda B Al-Kouatly, Saeed Haleema, Michael J Paidas, Sara N Iqbal, Robert I Glazer
Publikováno v:
PLoS ONE, Vol 17, Iss 11, p e0277098 (2022)
ObjectiveTo determine the expression profile of microRNAs in the peripheral blood of pregnant women with preterm premature rupture of membranes (PPROM) compared to that of healthy pregnant women.Study designThis was a pilot study with case-control de
Externí odkaz:
https://doaj.org/article/aef26f223e1a4c70afa63014857d5a83
Autor:
Oluwatobi Adegboyega, Suhita Gayen nee’ Betal, Pedro Urday, Rachel Huang, Katherine Bodycot, Huda B. Al-Kouatly, Kolawole Solarin, Joanna S. Y. Chan, Sankar Addya, Rupsa C. Boelig, Zubair H. Aghai
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-12 (2024)
Abstract Methadone maintenance treatment for opioid dependent mothers is standard of care. Infants of methadone maintained opioid dependent (MMOD) mothers have better outcomes compared to infants of opioid dependent mothers without treatment. However
Externí odkaz:
https://doaj.org/article/5bc756145518432c9f258c3cdf9038d5
Autor:
Neel S. Iyer, Matthew H. Mossayebi, Tracy J. Gao, Lylach Haizler‐Cohen, Daniele Di Mascio, Rodney A. McLaren Jr, Huda B. Al‐Kouatly
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 7, Pp n/a-n/a (2024)
Abstract Background Glucose‐6‐phosphate dehydrogenase (G6PD) deficiency is an X‐linked recessive disorder that predisposes individuals to hemolysis due to an inborn error of metabolism. We performed a systematic literature review to evaluate G6
Externí odkaz:
https://doaj.org/article/1fa8478b3e704473b401189bfd8c3811
Publikováno v:
Clinical Case Reports, Vol 8, Iss 10, Pp 1993-1996 (2020)
Abstract Extracorporeal membrane oxygenation (ECMO) is used to provide acute respiratory and/or hemodynamic support to patients with severe, refractory respiratory failure. Phrenic nerve injury with subsequent hemidiaphragm paralysis should be includ
Externí odkaz:
https://doaj.org/article/e48823f6e5654a39a1de817e5b490263
Publikováno v:
Clinical Case Reports, Vol 7, Iss 12, Pp 2495-2499 (2019)
Abstract As the field of neurogenetics is expanding rapidly and variant classification criteria evolve, genetic variants in databases are re‐evaluated overtime allowing updated classifications of pathogenicity predication. When caring for patients
Externí odkaz:
https://doaj.org/article/4e8403e7fbcc4766a3a6be752b2c5379
Autor:
Huda B. Al‐Kouatly, Kavya Shivashankar, Matthew H. Mossayebi, Mona Makhamreh, Elizabeth Critchlow, Zimeng Gao, Luther‐King Fasehun, Fowzan S. Alkuraya, Erin E. Ryan, Madhuri Hegde, Sascha Wodoslawsky, Joel Hughes, Seth I. Berger
Publikováno v:
Clinical Genetics. 103:503-512
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f955db7ff12d89e401a68e73c1aa7e4
https://doi.org/10.1111/cge.14309
https://doi.org/10.1111/cge.14309
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 8, Pp n/a-n/a (2020)
Abstract Background Stickler syndrome is a collagen disorder that can affect multiple organ systems. It is characterized by ocular abnormalities, hearing loss, midfacial hypoplasia, hypermobility, and joint abnormalities. The phenotypic expression of
Externí odkaz:
https://doaj.org/article/42abc258385d45b887737d7c4636f9c3
Autor:
Megan B. Raymond, Julie P. Barbera, Sarah Boudova, Kavita Vinekar, Rebecca Horgan, Rodney McLaren, Huda B. Al-Kouatly
Publikováno v:
Obstetrics & Gynecology. 141:445-454
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03d0e9983acde761493df25d35bb997d
https://doi.org/10.1097/aog.0000000000005094
https://doi.org/10.1097/aog.0000000000005094
Autor:
Megan Raymond, Elizabeth Critchlow, Stephanie M. Rice, Sascha Wodoslawsky, Seth I. Berger, Madhuri Hegde, Philip E. Empey, Huda B. Al-Kouatly
Publikováno v:
Molecular Genetics and Metabolism. 137:140-145
Pharmacogenomics (PGx) characterizes genetic variation in medication response. 85-95% of the population carries actionable PGx variants. No prior studies have demonstrated the application and feasibility of PGx in prenatal testing. We assessed parent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c5beaeec49126865b88555098ad0f62
https://doi.org/10.1016/j.ymgme.2022.08.002
https://doi.org/10.1016/j.ymgme.2022.08.002