Results 131 to 140 of about 55,562 (305)

VP43.07: Prevalence of single umbilical artery in monochorionic twins with selective growth restriction [PDF]

, 2020
Sofia Amylidi‐Mohr, C. Hecht, Beatrice Mosimann, Jarmila A. Zdanowicz, Daniel Surbek, David Baud, Luigi Raio   +6 more
openalex   +1 more source

Non‐Histone Lactylation: A New Frontier in Cerebral Ischemia‐Reperfusion Injury

Med Research, EarlyView.
ABSTRACT Reperfusion therapy is the mainstay of treatment for ischemic stroke (IS) but frequently exacerbates secondary injury. Following cerebral ischemia and hypoxia, lactate accumulates markedly. Traditionally regarded as a metabolic byproduct, lactate has gained new significance with the discovery of protein lactylation. In addition to experimental
Minghui Tang, Yuying Mo, Zhishan Ling, Yuting Zeng, Qi Zhang, Shuqi Zheng, Shuyang Wen, Yupeng Xiao, Siying Long, Tingting Yang, Qianru Li, Wenjie Shi, Guozhi Huang, Qing Zeng   +13 more
wiley   +1 more source

Risks of Funipuncture in Fetuses With Single Umbilical Arteries [PDF]

, 2000
Waldo Sepúlveda, V. Dezerega, Eduardo Carstens, Jorge Gutiérrez, Carlos Schnapp   +4 more
openalex   +1 more source

Stillbirth in pregnancies with flat OGTT: Placental clues to occult maternal dysmetabolism

International Journal of Gynecology &Obstetrics, EarlyView.
Emma Bertucci, Alessandra Danieli, Francesco Ricciardiello, Isabella Neri, Francesca Monari, Alessandro D. Genazzani, Gaetano Bulfamante, Antonio La Marca, Laura Botticelli, Fabio Facchinetti, Laura Avagliano   +10 more
wiley   +1 more source

Prenatal 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 more
wiley   +1 more source

Diagnosis and Management of Prenatal Hereditary Pyropoikilocytosis

Prenatal Diagnosis, EarlyView.
ABSTRACT Hereditary pyropoikilocytosis (HPP) is a severe hemolytic anemia caused by variants in SPTA1, SPTB, and EPB41. These weaken horizontal interactions in the erythrocyte cytoskeleton, causing membrane fragmentation and splenic sequestration. It will readily cause fetal anemia and often hydrops fetalis. Prenatal diagnosis requires first ruling out
Connor Hartzell, Samantha Stover, Nora Gibson, Timothy Olson, James Connelly, Matthew Grace, Jennifer Andrews   +6 more
wiley   +1 more source

From dual to single umbilical artery: a case of umbilical artery thrombosis with hypercoiling and literature review. [PDF]

Front Med (Lausanne)
Ding W, Yan J, Lin X, Yan L, Tao E.
europepmc   +1 more source

Correction: Is uterine growth retardation with normal umbilical artery blood flow a benign condition? [PDF]

, 1990
B Wexler, J Mcmurtry, G I'ibblin, J Larsen, P, S Ljunghall, H Hedstrand, Wjc Currie, P Turner, C Johnson, Dmn1 Wilson, O' Fallon, Wvm, C Bcngtsson, J Lennartsson, Lindqvist, D Churchill, C Maloney, J Bear, W Ritz, F Haslback, M, R Hiatt, L Dales, G Friedman, Gi), E Vahlensieck, D Bach, A Hesse, W Robertson, M Peacock, M Baker, 1p Strazzullo, V Nunziata, M Cirillo, C Pak, B Lewis, A Chait, G Sigurdsson, P Strazztillo, I 'rcvisan, M Farinaro, E, P Strazzullo, Cappuccio Fl, ' Macgregor, G Strazzullo 1', 1p Strazzulllo, I Cappucco, M Itresisan, J Miorris, \ij Gardner, Cirillo Al, M Latiretizi, ( Dollerv, Ct7, H Duncan, B Schumcr, A Breckeitridge, P Strazzullo, F Cappuccio, M Trevisan, D Alccarron, P Pingree, R Rubin, S Gaucher, Motlitch Al, S Krutzik, Cirillo Al, A Siani, V Nunziata, F Cappucico, P Amattioli, P Strazzullo   +73 more
openalex   +1 more source

The Expanding Role of Gene Sequencing in Shaping Fetal Therapies: Clinical and Ethical Considerations

Prenatal Diagnosis, EarlyView.
ABSTRACT In utero interventions are transformative in addressing genetic and anatomic conditions during fetal development. Next generation sequencing enables early genetic testing, playing a pivotal role in prenatal decision‐making by supporting risk stratification, precise and timely diagnosis, which directly informs eligibility for fetal surgical and
Matthew A. Shear, Beltran Borges, Billie R. Lianoglou, Tony Lum, Emma Canepa, Jennifer L. Cohen, Julia E. H. Brown, Akos Herzeg   +7 more
wiley   +1 more source

Hematuria in a 3-month-old filly with an internal umbilical abscess and internal iliac artery aneurysm.

, 2021
Luiza S. Zakia, Sarah Shaw, Natacha Bonomelli, Siobhán O’Sullivan, Alex zur Linden, Marie Dubois, John Scott Baird, Bruce Guest   +7 more
openalex   +1 more source