Results 141 to 150 of about 27,764 (256)

RASGRP1 Deficiency Manifesting as Severe Vasculopathy and Fatal Autoimmune Hemolytic Anemia

open access: yeseJHaem, Volume 7, Issue 3, June 2026.
ABSTRACT Background RASGRP1 deficiency is a rare inborn error of immunity characterized by immunodeficiency, autoimmunity, and lymphoproliferation. Results We report a 5‐year‐old male with novel homozygous splice‐donor mutations in RASGRP1(c.1720+1G>A and c.1720+2T>C) who presented with severe vasculopathy (ischemic stroke and thrombosis), secondary ...
Kosar Asna Ashari   +5 more
wiley   +1 more source

Antiphospholipid Antibodies and Methods of their Determination [PDF]

open access: yes, 2018
Tato bakalářská práce popisuje problematiku antifosfolipidových protilátek jako intenzivně zkoumanou skupinu protilátek způsobujících různorodé klinické projevy jako: antifosfolipidový syndrom, trombózy a komplikace v těhotenství.
Bulay Juta
core  

Antiphospholipid antibodies and subclinical interstitial lung disease in the MESA cohort

open access: yesRespiratory Research
Background Interstitial lung disease (ILD) is a rare complication of antiphospholipid syndrome (APS), but circulating antiphospholipid antibodies have been detected in patients with ILD without APS. Whether antiphospholipid antibodies are associated with
Claire F. McGroder   +12 more
doaj   +1 more source

Long‐Term Dermoscopic Evolution of Reticular Erythematous Mucinosis: Case Report

open access: yesJEADV Clinical Practice, Volume 5, Issue 2, Page 637-639, June 2026.
ABSTRACT Reticular erythematous mucinosis is a rare dermatosis with a challenging diagnosis. To date, its dermoscopic features have not been well characterised in the literature. Only a limited number of case reports have described dermoscopic findings that may be indicative of the disorder, including the presence of dotted and linear vessels, as well ...
Grażyna Kamińska‐Winciorek   +4 more
wiley   +1 more source

The Role of Neutrophils and NETosis in Diseases: The Implications for Therapy

open access: yesMedComm, Volume 7, Issue 6, June 2026.
Neutrophils secrete cytokines, express specific surface proteins, increase or decrease in cell count, and their ratio to lymphocyte count can be used as biomarkers to characterize collective status and disease progression. Neutrophils can monitor and track the body's health status, “Wei Bing” status, disease status, and different times of disease ...
Zhen Ma   +6 more
wiley   +1 more source

Clinical Utility of Stillbirth Investigations in Australia: A Cohort Study

open access: yesAustralian and New Zealand Journal of Obstetrics and Gynaecology, Volume 66, Issue 3, June 2026.
ABSTRACT Background Stillbirths impact over two million parents globally every year. Despite current knowledge, technology, and investigations, many stillbirths remain unexplained and are not fully investigated. An important step forward in addressing this gap is determining which investigations produce the highest utility in identifying the cause of ...
Tania Marsden   +22 more
wiley   +1 more source

Immunomodulatory Role of Natural Progesterone in Pregnancy: A Review

open access: yesJournal of Obstetrics and Gynaecology Research, Volume 52, Issue 6, June 2026.
ABSTRACT Aim Pregnancy complications such as miscarriage, preterm birth (PTB), and luteal phase defects (LPD) are significant reproductive health issues globally, with both physical and psychological implications. This review aims to examine the role of natural progesterone in pregnancy‐related disorders, specifically threatened and recurrent ...
Prakash Mehta   +8 more
wiley   +1 more source

Frequency of antiphospholipid antibodies and antiphospholipid syndrome in women with recurrent miscarriages

open access: yes, 1970
Summary Objectives: The aim of the study was to evaluate antiphospholipid antibodies and antiphospholipid syndrome frequency (according to current criteria) in women with recurrent miscarriages.
Skrzypczak, Jana, Rajewski, Marcin
core  

Antiphospholipid Syndrome Novel Therapies

open access: yes, 2014
Antiphospholipid syndrome (APS) is an autoimmune disease characterised by arterial and/or venous thrombosis, recurrent pregnancy loss, and persistently positive antiphospholipid antibodies (aPLs).
Mohamad Bittar, Imad Uthman
core  

CLINICAL IMPORTANCE OF ANTIPHOSPHOLIPID ANTIBODIES IN HEMODIALYSIS PATIENTS WITH VASCULAR ACCESS THROMBOSIS

open access: yesTurkish Journal of Nephrology, 2019
Antiphospholipid antibodies can cause recurrent thrombotic attacks in some patients. Antiphospholipid antibodies are detected in patients with autoimmune disease especially systemic lupus erythematosus, infectious, malignant and drug-induced disorders ...
Ali Rıza ODABAŞ   +2 more
doaj  

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