Results 61 to 70 of about 308,468 (256)

Evan syndrome as initial presentation of COVID-19 infection

open access: yesThe Egyptian Journal of Bronchology, 2022
Background Evans’ syndrome (ES) is a rare and chronic autoimmune disease characterized by the concomitant or sequential association of auto-immune hemolytic anemia (AIHA) with immune thrombocytopenia (ITP), and less frequently autoimmune neutropenia with
Hamdy A. Mohammadien   +2 more
doaj   +1 more source

Creating the Poor Law Legacy: Institutional Care for Older People Before the Welfare State

open access: yes, 2012
Why, despite the universalist aspiration of the British welfare state, was institutional care for poor older people so frequently condemned as inferior?
Gorsky, Martin
core   +1 more source

Cardiac manifestations of PRKAG2 mutation. [PDF]

open access: yes, 2018
BACKGROUND:The Protein Kinase AMP-Activated Non-Catalytic Subunit Gamma 2 (PRKAG2) cardiac syndrome is characterized by glycogen accumulation in the cardiac tissue.
Ardehali, Reza   +3 more
core   +1 more source

Histopathologic Analysis of the Morpho‐Functional Zones of the Human Acetabular Labrum

open access: yesClinical Anatomy, EarlyView.
ABSTRACT The structural and functional adaptation of soft tissues to mechanical load controls their ability to withstand injury and influences their capacity for healing. Similar to the knee meniscus, the acetabular labrum exhibits zonal differences in mechanical load distribution, resulting in distinct regions with unique structural and functional ...
Abdulaziz A. Alomiery   +4 more
wiley   +1 more source

A rare case of calvarial tuberculosis in post-COVID-19 scenario

open access: yesInternational Journal of Mycobacteriology, 2022
Isolated calvarial involvement with tuberculosis (TB) is a very rare entity, with the incidence of only 0.01% of all patients with mycobacterial infections.
Abhijit Acharya   +2 more
doaj   +1 more source

The spectrum of Evans' syndrome [PDF]

open access: yesArchives of Disease in Childhood, 1997
Eleven patients (10 boys, one girl) with Evans' syndrome with a median follow up time of 8.0 years were evaluated retrospectively. Six patients had either persistent hepatosplenomegaly or generalised lymphadenopathy, or both. In five patients, an increase in lymph node and/or spleen size was observed during the exacerbations of cytopenias.
S, Savaşan, I, Warrier, Y, Ravindranath
openaire   +2 more sources

Sleep Problems in Children With Autism Spectrum Disorder [PDF]

open access: yes, 2020
The purpose of the current study was to examine the effect of restricted and repetitive behaviors (RRBs) on the relationship between sleep problems and externalizing behaviors in young children with autism spectrum disorder (ASD).
Alba, Laura A
core  

Endothelium in the pharyngeal arches 3, 4 and 6 is derived from the second heart field. [PDF]

open access: yes, 2017
Oxygenated blood from the heart is directed into the systemic circulation through the aortic arch arteries (AAAs). The AAAs arise by remodeling of three symmetrical pairs of pharyngeal arch arteries (PAAs), which connect the heart with the paired dorsal ...
Astrof, Sophie   +5 more
core   +2 more sources

A Novel Patient‐Specific Landmark‐Guided Approach for Intramuscular Botulinum Neurotoxin Injections Into the Rotator Cuff: A Cadaveric Study

open access: yesClinical Anatomy, EarlyView.
ABSTRACT Myofascial pain syndrome (MFPS) causes chronic shoulder pain. Supraspinatus and infraspinatus, rotator cuff muscles innervated by the suprascapular nerve, are commonly affected. Intramuscular botulinum neurotoxin (BoNT) injections near motor points (i.e., visible nerve branch entry sites used as a proxy for motor endplates) are an effective ...
Dave Osinachukwu Duru   +5 more
wiley   +1 more source

A strange case of Evans syndrome

open access: yesItalian Journal of Medicine, 2013
Evans syndrome is a rare autoimmune disease presenting hemolytic anemia, thrombocytopenia and/or neutropenia. It may be associated with other autoimmune or lymphoproliferative diseases.
Manuel Monti   +5 more
doaj   +1 more source

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