Results 131 to 140 of about 64,247 (285)
Impact of heparin‐aspirin therapy in patients with recurrent pregnancy loss characterized by thrombophilia resistant to low‐dose aspirin therapy: A retrospective study [PDF]
Tomoko Ichikawa +12 more
openalex +1 more source
Recurrent pregnancy loss in food deserts in the mid-south using geographic information system analysis [PDF]
N. Van De Velde +6 more
openalex +1 more source
Rangewide responses of Mimulus cardinalis to an extreme heat event
Abstract Premise Extreme events are an understudied aspect of ongoing anthropogenic climate change that could play a disproportionate role in the threat that rapid environmental shifts pose to natural populations. Methods We exposed plants originating from seeds that were harvested before (ancestors) and after (descendants) multiple extreme heat events
Lucas J. Albano +6 more
wiley +1 more source
ABSTRACT Postpartum hemorrhage (PPH) remains the leading cause of preventable maternal mortality despite standard interventions. Recent fibrinogen trials failed to improve outcomes, prompting interest in coagulation factor XIII (FXIII). FXIII functions as “molecular cement,” cross‐linking fibrin and stabilizing clots.
Jeremy W. Jacobs +8 more
wiley +1 more source
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim +9 more
wiley +1 more source
Ruthenium and recurrent pregnancy loss: insights into oxidative and genotoxic effects. [PDF]
Alrashed M.
europepmc +1 more source
Chromosomal Abnormalities in Recurrent Pregnancy Loss at a Tertiary Care Center. [PDF]
Sinha MB, Thakur P, Verma R.
europepmc +1 more source
Gestational Aging on Fast Forward: The Epigenetic Link to Recurrent Pregnancy Loss [PDF]
Anam Farooqui, Susan Idicula‐Thomas
openalex +1 more source
ABSTRACT Hypoparathyroidism, sensorineural deafness, and renal dysplasia (HDR) syndrome is caused by pathogenic variants in the GATA3 gene located on chromosome 10p14. Here we present a 10‐year‐old girl with HDR syndrome who also has oligoarticular juvenile idiopathic arthritis (JIA).
Lauren N. Meiss +8 more
wiley +1 more source
Deficiencia combinada de proteínas c y s
Las trombofilias son un grupo de enfermedades que favorecen la formación de trombosis, tanto arteriales como venosas, que han sido asociadas con diferentes complicaciones durante el embarazo, como: aborto recurrente, preclampsia, crecimiento intrauterino
Yaneth Zamora-González +3 more
doaj

