Results 101 to 110 of about 25,999 (245)
Real‐time fetal brain and placental T2* mapping at 0.55T MRI
Magnetic Resonance in Medicine, EarlyView.ABSTRACT Purpose
To provide real‐time, organ‐specific quantitative information — specifically placental and fetal brain T2 * — to optimize and personalize fetal MRI examinations. Methods
A low‐latency setup enables real‐time processing, including segmentation, T2* fitting, and centile calculation.Jordina Aviles Verdera, Sara Neves Silva, Kelly M. Payette, Raphael Tomi‐Tricot, Megan Hall, Lisa Story, Shaihan J. Malik, Joseph V. Hajnal, Mary A. Rutherford, Jana Hutter +9 morewiley +1 more sourceVulnerable newborn types: analysis of subnational, population‐based birth cohorts for 541 285 live births in 23 countries, 2000–2021
BJOG: An International Journal of Obstetrics &Gynaecology, EarlyView., 2023 Abstract Objective
To examine prevalence of novel newborn types among 541 285 live births in 23 countries from 2000 to 2021. Design
Descriptive multi‐country secondary data analysis. Setting
Subnational, population‐based birth cohort studies (n = 45) in 23 low‐ and middle‐income countries (LMICs) spanning 2000–2021.D. J. Erchick, E. A. Hazel, J. Katz, A. C. C. Lee, M. Diaz, L. S. F. Wu, S. Yoshida, R. Bahl, C. Grandi, A. B. Labrique, M. Rashid, S. Ahmed, A. D. Roy, R. Haque, S. Shaikh, A. H. Baqui, S. K. Saha, R. Khanam, S. Rahman, R. Shapiro, R. Zash, M. F. Silveira, R. Buffarini, P. Kolsteren, C. Lachat, L. Huybregts, D. Roberfroid, L. Zeng, Z. Zhu, J. He, X. Qiu, S. H. Gebreyesus, K. Tesfamariam, D. Bekele, G. Chan, E. Baye, F. Workneh, K. P. Asante, E. B. Kaali, S. Adu‐Afarwuah, K. G. Dewey, S. Gyaase, B. J. Wylie, B. R. Kirkwood, A. Manu, R. D. Thulasiraj, J. Tielsch, R. Chowdhury, S. Taneja, G. R. Babu, P. Shriyan, P. Ashorn, K. Maleta, U. Ashorn, C. Mangani, S. Acevedo‐Gallegos, M. J. Rodriguez‐Sibaja, S. K. Khatry, S. C. LeClerq, L. C. Mullany, F. Jehan, M. Ilyas, S. J. Rogerson, H. W. Unger, R. Ghosh, S. Musange, V. Ramokolo, W. Zembe‐Mkabile, M. Lazzerini, M. Rishard, D. Wang, W. W. Fawzi, D. T. R. Minja, C. Schmiegelow, H. Masanja, E. Smith, J. P. A. Lusingu, O. A. Msemo, F. M. Kabole, S. N. Slim, P. Keentupthai, A. Mongkolchati, R. Kajubi, A. Kakuru, P. Waiswa, D. Walker, D. H. Hamer, K. E. A. Semrau, E. B. Chaponda, R. M. Chico, B. Banda, K. Musokotwane, A. Manasyan, J. M. Pry, B. Chasekwa, J. Humphrey, R. E. Black, the Subnational Vulnerable Newborn Prevalence Collaborative Group and Vulnerable Newborn Measurement Core Group, Hasmot Ali, Parul Christian, Rolf D. W. Klemm, Alan B. Massie, Maithili Mitra, Sucheta Mehra, Kerry J. Schulze, Abu Ahmed Shamim, Alfred Sommer, MD. Barkat Ullah, Keith P. West, Nazma Begum, Nabidul Haque Chowdhury, Md. Shafiqul Islam, Dipak Kumar Mitra, Abdul Quaiyum, Modiegi Diseko, Joseph Makhema, Yue Cheng, Yixin Guo, Shanshan Yuan, Meselech Roro, Bilal Shikur, Frederick Goddard, Sebastien Haneuse, Bezawit Hunegnaw, Yemane Berhane, Alemayehu Worku, Seyram Kaali, Charles D. Arnold, Darby Jack, Seeba Amenga‐Etego, Lisa Hurt, Caitlin Shannon, Seyi Soremekun, Nita Bhandari, Jose Martines, Sarmila Mazumder, Yamuna Ana, R Deepa, Lotta Hallamaa, Juha Pyykkö, Mario I. Lumbreras‐Marquez, Claudia E. Mendoza‐Carrera, Atiya Hussain, Muhammad Karim, Farzana Kausar, Usma Mehmood, Naila Nadeem, Muhammad Imran Nisar, Muhammad Sajid, Ivo Mueller, Maria Ome‐Kaius, Elizabeth Butrick, Felix Sayinzoga, Ilaria Mariani, Willy Urassa, Thor Theander, Phillippe Deloron, Birgitte Bruun Nielsen, Alfa Muhihi, Ramadhani Abdallah Noor, Ib Bygbjerg, Sofie Lykke Moeller, Fahad Aftab, Said M. Ali, Pratibha Dhingra, Usha Dhingra, Arup Dutta, Sunil Sazawal, Atifa Suleiman, Mohammed Mohammed, Saikat Deb, Moses R. Kamya, Miriam Nakalembe, Jude Mulowooz, Nicole Santos, Godfrey Biemba, Julie M. Herlihy, Reuben K. Mbewe, Fern Mweena, Kojo Yeboah‐Antwi, Jane Bruce, Daniel Chandramohan, Andrew Prendergast, Joy E. Lawn, Hannah Blencowe, Eric Ohuma, Yemi Okwaraji, Judith Yargawa, Ellen Bradley, Joanne Katz +189 morewiley +1 more sourceHeterozygous Beta‐Thalassaemia in Pregnancy: Two Rare Causes of Severe Fetal Anemia Requiring Intrauterine Blood Transfusions
Prenatal Diagnosis, EarlyView.ABSTRACT Aim
In this article, we present two cases of severe fetal hemolytic anemia based on a beta‐thalassaemia trait inherited from a single parent. Results
These cases, presented at 20 and 28 weeks' gestation, necessitated intra‐uterine blood transfusions.Eva van der Meij, Frans J. W. Smiers, Tamara T. Koopmann, Ingrid Krapels, Kaatje LePoole, Enrico Lopriore, Johanna M. Middeldorp, Claudia S. Ootjers, Volkher Scharnhorst, Hubertina C. J. Scheepers, Cornelis L. Harteveld, E. J. T. (Joanne) Verweij +11 morewiley +1 more sourceNeonatal mortality risk of vulnerable newborns: A descriptive analysis of subnational, population‐based birth cohorts for 238 203 live births in low‐ and middle‐income settings from 2000 to 2017
BJOG: An International Journal of Obstetrics &Gynaecology, EarlyView., 2023 Abstract Objective
We aimed to understand the mortality risks of vulnerable newborns (defined as preterm and/or born weighing smaller or larger compared to a standard population), in low‐ and middle‐income countries (LMICs). Design
Descriptive multi‐country, secondary analysis of individual‐level study data of babies born since 2000.Elizabeth A. Hazel, Daniel J. Erchick, Joanne Katz, Anne C. C. Lee, Michael Diaz, Lee S. F. Wu, Keith P. West Jr, Abu Ahmed Shamim, Parul Christian, Hasmot Ali, Abdullah H. Baqui, Samir K. Saha, Salahuddin Ahmed, Arunangshu Dutta Roy, Mariângela F. Silveira, Romina Buffarini, Roger Shapiro, Rebecca Zash, Patrick Kolsteren, Carl Lachat, Lieven Huybregts, Dominique Roberfroid, Zhonghai Zhu, Lingxia Zeng, Seifu H. Gebreyesus, Kokeb Tesfamariam, Seth Adu‐Afarwuah, Kathryn G. Dewey, Stephaney Gyaase, Kwaku Poku‐Asante, Ellen Boamah Kaali, Darby Jack, Thulasiraj Ravilla, James Tielsch, Sunita Taneja, Ranadip Chowdhury, Per Ashorn, Kenneth Maleta, Ulla Ashorn, Charles Mangani, Luke C. Mullany, Subarna K. Khatry, Vundli Ramokolo, Wanga Zembe‐Mkabile, Wafaie W. Fawzi, Dongqing Wang, Christentze Schmiegelow, Daniel Minja, Omari Abdul Msemo, John P. A. Lusingu, Emily R. Smith, Honorati Masanja, Aroonsri Mongkolchati, Paniya Keentupthai, Abel Kakuru, Richard Kajubi, Katherine Semrau, Davidson H. Hamer, Albert Manasyan, Jake M. Pry, Bernard Chasekwa, Jean Humphrey, Robert E. Black, Subnational Collaborative Group for Vulnerable Newborn Mortality, Vulnerable Newborn Measurement Core Group, Rolf D. W. Klemm, Allan B. Massie, Maithilee Mitra, Sucheta Mehra, Kerry J. Schulze, Alfred Sommer, Md. Barkat Ullah, Alain B. Labrique, Mabhubur Rashid, Saijuddin Shaikh, Nazma Begum, Nabidul Haque Chowdhury, Md. Shafiqul Islam, Rasheda Khanam, Dipak Kumar Mitra, Abdul Quaiyum, Modiegi Diseko, Joseph Makhema, Yue Cheng, Meselech Roro, Bilal Shikur Endris, Charles D. Arnold, Rajiv Bahl, Nita Bhandari, Jose Martines, Sarmila Mazumder, Lotta Hallamaa, Juha Pyykkö, Willy Urassa, Phillippe Deloron, Ib Christian Bygbjerg, Sofie Lykke Moeller, Thor Grundtvig Theander, Alfa Muhihi, Ramadhani Abdallah Noor, Moses R. Kamya, Miriam Nakalembe, Godfrey Biemba, Julie M. Herlihy, Reuben K. Mbewe, Fern Mweena, Kojo Yeboah‐Antwi, Andrew Prendergast, Joy E. Lawn, Hannah Blencowe, Eric Ohuma, Yemi Okwaraji, Judith Yargawa, Ellen Bradley, Lorena Suarez Idueta +114 morewiley +1 more sourceGenetic Diagnosis and Clinical Features of Fetuses With Congenital Diaphragmatic Hernia
Prenatal Diagnosis, EarlyView.ABSTRACT Objective
Congenital diaphragmatic hernia (CDH) is a rare abnormality with highly heterogeneous genetic causes. This study investigated chromosomal and monogenic abnormalities in fetal CDH patients and evaluated the efficacy of chromosomal microarray analysis (CMA) and whole‐exome sequencing (WES) for genetic diagnosis.Yan Lü, Yi Yu, Jiazhen Chang, Mengmeng Li, Xueting Yang, Xiya Zhou, Na Hao, Hua Meng, Zhenghong Li, Lishuang Ma, Hui You, Shan Jian, Ying Wang, Shengjie Li, Yiqing Yu, Kaili Yin, Mingming Wang, Yulin Jiang, Qingwei Qi +18 morewiley +1 more sourceStillbirths: Contribution of preterm birth and size‐for‐gestational age for 125.4 million total births from nationwide records in 13 countries, 2000–2020
BJOG: An International Journal of Obstetrics &Gynaecology, EarlyView., 2023 Abstract Objective
To examine the contribution of preterm birth and size‐for‐gestational age in stillbirths using six ‘newborn types’. Design
Population‐based multi‐country analyses. Setting
Births collected through routine data systems in 13 countries.Yemisrach B. Okwaraji, Lorena Suárez‐Idueta, Eric O. Ohuma, Ellen Bradley, Judith Yargawa, Veronica Pingray, Gabriela Cormick, Adrienne Gordon, Vicki Flenady, Erzsébet Horváth‐Puhó, Henrik Toft Sørensen, Luule Sakkeus, Liili Abuladze, Mohammed Heidarzadeh, Narjes Khalili, Khalid A. Yunis, Ayah Al Bizri, Shamala D. Karalasingam, Ravichandran Jeganathan, Arturo Barranco, Aimée E. van Dijk, Lisa Broeders, Fawzya Alyafei, Mai AlQubaisi, Neda Razaz, Jonas Söderling, Lucy K. Smith, Ruth J. Matthews, Rachael Wood, Kirsten Monteath, Isabel Pereyra, Gabriella Pravia, Sarka Lisonkova, Qi Wen, Joy E. Lawn, Hannah Blencowe, the National Vulnerable Newborn Collaborative Group for Stillbirths, Veronica Pingray, Gabriela Gabriela, José Belizan, Luz Gibbons, Carlos Guevel, Vicki Flenady, Adrienne Gordon, Kara Warrilow, Harriet Lawford, Erzsébet Horváth‐Puhó, Henrik T. Sørensen, Luule Sakkeus, Liili Abuladze, Khalid A. Yunis, Ayah Al Bizri, Pascale Nakad, Shamala Karalasingam, J. Ravichandran, R. Jeganathan, Nurakman Binti Baharum, Lorena Suárez‐Idueta, Arturo Barranco Flores, Jesus Felipe Gonzalez Roldan, Sonia Lopez Alvarez, Lisa Broeders, Aimée E. van Dijk, Fawzia Alyafei, Mai AlQubaisi, Tawa O. Olukade, Hamdy A. Ali, Mohamad Rami Alturk, Neda Razaz, Jonas Söderling, Lucy K. Smith, Bradley N. Manktelow, Ruth J. Matthews, Elizabeth Draper, Alan Fenton, Jennifer J. Kurinczuk, Rachael Wood, Celina Davis, Kirsten Monteath, Samantha Clarke, Isabel Pereyra, Gabriella Pravia, Sarka Lisonkova, Qi Wen, Joy E. Lawn, Hannah Blencowe, Eric Ohuma, Yemi Okwaraji, Judith Yargawa, Ellen Bradley, Robert Black, Joanne Katz, Dan Erchick, Elizabeth Hazel, Mike Diaz, Anne C. C. Lee +95 morewiley +1 more sourcePrenatal Exome Sequencing Identifies Dual Maternal‐Fetal Diagnosis of HbF Mission Bay, a Novel HBG2 Variant Associated With Methemoglobinemia, Hypoxia and Hemolytic Anemia
Prenatal Diagnosis, EarlyView.ABSTRACT
Prenatal exome sequencing (ES) can establish rare genetic diagnoses in a fetus but may also lead to occult genetic diagnosis in a biological parent. We present a case of dual fetal and maternal diagnosis by prenatal ES, in a fetus with unexplained anemia and in a pregnant patient with sickle cell disease (SCD) and recurrent unexplained hypoxia.Matthew A. Shear, Billie Lianoglou, Ugur Hodoglugil, W. Patrick Devine, Ashutosh Lal, Juan Gonzalez, Teresa N. Sparks +6 morewiley +1 more source