Results 81 to 90 of about 243,277 (388)

Increased plasma von Willebrand factor antigen levels but normal von Willebrand factor cleaving protease (ADAMTS13) activity in preeclampsia. [PDF]

open access: yes, 2009
The activity of ADAMTS13, the von Willebrand factor (VWF) cleaving protease is low in several conditions, including HELLP (haemolysis, elevated liver enzymes, and low platelet count) syndrome.
Bõze, Tamás   +9 more
core   +1 more source

Excess placental soluble fms-like tyrosine kinase 1 (sFlt1) may contribute to endothelial dysfunction, hypertension, and proteinuria in preeclampsia

open access: yes, 2003
Preeclampsia, a syndrome affecting 5% of pregnancies, causes substantial maternal and fetal morbidity and mortality. The pathophysiology of preeclampsia remains largely unknown.
S. Maynard   +12 more
semanticscholar   +1 more source

Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

open access: yesNature Communications, 2020
Preeclampsia is a serious complication of pregnancy, affecting both maternal and fetal health. In genome-wide association meta-analysis of European and Central Asian mothers, we identify sequence variants that associate with preeclampsia in the maternal ...
V. Steinthorsdottir   +96 more
semanticscholar   +1 more source

Preeclampsia

open access: yesRevista Colombiana de Obstetricia y Ginecología, 1969
Las distintas manifestaciones de la toxicosis gravídica que precede a la máxi­ma complicación de ella, conocida con el nombre de eclampsia se ha denominado Preeclampsia. Este término comprende el conocido cuadro de las albuminurias gravidicas. primer eslabón de la cadena tóxica y la entidad de que nos ocupamos, conocida con el nombre Eclampsismo de ...
Rafael Peralta   +2 more
openaire   +3 more sources

The Behavioral Phenotype and Importance of Multidisciplinary Care in Patients With Sotos Syndrome: A Single‐Center Experience

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Sotos syndrome is an autosomal dominant condition caused by pathogenic variants in the NSD1 gene on chromosome 5q35. It is characterized by macrosomia, distinctive facial features, and developmental delays. Patients are also reported to have a behavioral phenotype including autism spectrum disorder, attention deficit/hyperactivity disorder ...
Aravind Viswanathan   +4 more
wiley   +1 more source

Higher Trace Elements and Lower Fatty Acids Levels in Erythrocytes as Predictors of Preeclampsia

open access: yesIndonesian Biomedical Journal
BACKGROUND: Preeclampsia is one of the common causes of maternal death in Indonesia. Many studies only focus on the diagnosis and pharmacological treatment of preeclampsia.
Ruth Widhiati Raharjo Putri   +5 more
doaj   +1 more source

The common variant rs11646213 is associated with preeclampsia in Han Chinese women. [PDF]

open access: yesPLoS ONE, 2013
BACKGROUND: Preeclampsia, characterized by hypertension and proteinuria, is a multifactorial disease caused by complex interactions between environmental and genetic factors.
Ji-peng Wan   +5 more
doaj   +1 more source

Calcium Supplementation Dose and Vegetable Intake Determine Preeclampsia [PDF]

open access: yes, 2019
Preeclampsia is one of the cause of high maternal mortality rates. Risk factors for preeclampsia include a lack of nutrients such as vitamin A, calcium, sodium and potassium.
fitriani, L. (laila)   +2 more
core  

Mouse models for preeclampsia: disruption of redox-regulated signaling [PDF]

open access: yes, 2009
The concept that oxidative stress contributes to the development of human preeclampsia has never been tested in genetically-defined animal models. Homozygous deletion of catechol-Omethyl transferase (Comt-/-) in pregnant mice leads to human preeclampsia ...
A Malassine   +51 more
core   +4 more sources

Regulation of stanniocalcin-1 secretion by BeWo cells and first trimester human placental tissue from normal pregnancies and those at increased risk of developing preeclampsia. [PDF]

open access: yes, 2020
Stanniocalcin-1 (STC-1) is a multi-functional glycosylated peptide present in the plasma of healthy women postpartum and increased further in pregnancies complicated by preeclampsia. Although the STC-1 gene is expressed by the placenta what regulates its
Asma Khalil   +13 more
core   +1 more source

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