Results 71 to 80 of about 28,167 (192)

Hughes syndrome antiphospholipid syndrome

open access: yesHamdan Medical Journal, 2008
An increasingly important link between aPL antibodies and a clinical syndrome is becoming recognized worldwide. This syndrome, known as the antiphospholipid syndrome (APS) or Hughes syndrome, is a prothrombotic disorder leading to both arterial and venous thrombosis and, in pregnancy, recurrent abortion and pregnancy loss (Figure 13.1).
openaire   +2 more sources

Obstetric antiphospholipid syndrome

open access: yesAutoimmunity Reviews, 2012
Antiphospholipid syndrome (APS) in pregnancy has a serious impact on maternal and fetal morbidity. It causes recurrent pregnancy miscarriage and it is associated with other adverse obstetric findings like preterm delivery, intrauterine growth restriction, preeclampsia, HELLP syndrome and others.
Galarza-Maldonado, Claudio   +6 more
openaire   +3 more sources

Retrospective analysis of the tolerability and effectiveness of rimegepant for the acute treatment of migraine in adolescents

open access: yesHeadache: The Journal of Head and Face Pain, EarlyView.
Abstract Objective This study aims to evaluate the tolerability and effectiveness of the off‐label use of rimegepant as acute migraine treatment in adolescents. Background Calcitonin gene‐related peptide (CGRP) levels are elevated during migraine attacks.
Konstantinos Tourlas   +4 more
wiley   +1 more source

Neonatal Antiphospholipid Syndrome

open access: yesNeoReviews, 2014
Antiphospholipid antibody syndrome (APS) during pregnancy may result in pregnancy morbidity and passive transfer of antibodies to the fetus, resulting in an increased risk of prematurity, intrauterine growth restriction, thrombocytopenia, and developmental delay.
Magalhães, Claudia Saad   +2 more
openaire   +2 more sources

Apoptosis, annexin A5 and anti-annexin A5 antibodies in the antiphospholipid syndrome [PDF]

open access: yesJournal of Medical Biochemistry, 2013
It has been proposed that apoptosis is one of the mechanisms involved in the generation of antiphospholipid antibodies. The presence of antiphospholipid antibodies is the main laboratory criterion for a definite diagnosis of the antiphospholipid syndrome.
Bećarević Mirjana   +2 more
doaj  

Immunomodulation in the Treatment of Refractory Catastrophic Antiphospholipid Syndrome

open access: yesCase Reports in Hematology, 2018
Catastrophic antiphospholipid syndrome is a rare condition with high morbidity and mortality. We present a refractory case of catastrophic antiphospholipid syndrome with a view to highlight the importance of early identification and aggressive treatment ...
Karthik Nath, Andrew McCann
doaj   +1 more source

Time‐dependent association between prenatal hair glucocorticoid levels and child behavior problems

open access: yesJournal of Child Psychology and Psychiatry, EarlyView.
Background Child internalizing and externalizing behavioral problems are highly prevalent psychiatric symptoms worldwide, for which maternal prenatal stress is a known risk factor. However, underlying neuroendocrine mechanisms remain largely unclear. We investigated whether maternal hair cortisol (HCC) and cortisone concentration (HCNC) are associated ...
Richard G. Künzel   +11 more
wiley   +1 more source

Adenosine receptor agonism protects against NETosis and thrombosis in antiphospholipid syndrome

open access: yesNature Communications, 2019
Antiphospholipid syndrome is characterised by increased neutrophil extracellular trap formation (NETosis) and, consequently, increased thrombotic events. Here Ali et al.
Ramadan A. Ali   +12 more
doaj   +1 more source

Huntington's Disease‐like Syndrome as a Rare Presentation of CACNA1A‐Related Disorder

open access: yes
Movement Disorders Clinical Practice, EarlyView.
Petros Boumis   +14 more
wiley   +1 more source

Oral Microbiome in Systemic Autoimmune Diseases: A Systematic Review

open access: yesOral Diseases, EarlyView.
ABSTRACT Objective The oral cavity represents a key but underexplored interface between host immunity and microbial communities. The aim of this systematic review was to synthesize current literature on oral microbiota alterations in systemic autoimmune diseases.
Sophie Jung   +2 more
wiley   +1 more source

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