Results 31 to 40 of about 28,352 (224)

Liver Cirrhosis in a Patient with Sickle Cell Trait (Hb Sβ+ Thalassemia) without Other Known Causes of Hepatic Disease

open access: yesCase Reports in Gastroenterology, 2009
Liver involvement in patients with sickle cell anemia/trait includes a wide range of alterations, from mild liver function test abnormalities to cirrhosis and acute liver failure. Approximately 15–30% of patients with sickle cell anemia present cirrhosis
Luca Santi   +7 more
doaj   +1 more source

Geographic Modelling of Sickle cell Trait in four US Regions

open access: yesJournal of the Georgia Public Health Association, 2017
Background: Many studies have been done concerning the prevalence of sickle cell trait, its incidence and screening techniques. It is most commonly observed in the Black and Hispanic population in the United States.
Marian Tabi, Anunay Bhattacharya
doaj   +1 more source

Hypoxic Stress in Athletes With Sickle Cell Trait

open access: yes, 2016
The purpose of this study was to examine various changes of blood measures in select athletes with sickle cell trait due (SCT) to exercise at different simulated altitudes (n=2).
Reynolds, Samantha Elizabeth
core   +1 more source

Prevalence of sickle cell trait in blood donors in the Midwest region of the State of Minas Gerais

open access: yesRevista Médica de Minas Gerais, 2022
Introduction: Although sickle cell trait is considered a benign condition, there are studies showing that it presents relevant clinical manifestations, which makes it important to carry out studies to know its prevalence.
Ladeira, Valéria Sutana   +2 more
doaj   +1 more source

Hemarthrosis and sickle cell trait [PDF]

open access: yesArthritis & Rheumatism, 1970
AbstractA case of sickle cell trait associated with hemarthrosis in several joints is presented. It is suggested that coincidental acute inflammation of the synovial membrane enhanced the sickling phenomenon and produced the resultant bleeding disturbance.
D F, Casey, E S, Cathcart
openaire   +2 more sources

Comparative cranial biomechanics reveal macroevolutionary trends in theropod dinosaurs, with emphasis on Tyrannosauroidea

open access: yesThe Anatomical Record, EarlyView.
Abstract Tyrannosaurus is viewed as a model organism in vertebrate paleontology, with numerous studies analyzing its feeding biomechanics. Nonetheless, the evolution of this feeding performance has been under‐addressed in Tyrannosauroidea, especially in basal tyrannosauroids. Here we used muscle‐force reconstruction and finite element analysis (FEA) to
Evan Johnson‐Ransom   +4 more
wiley   +1 more source

Sickle cell trait: not as benign as once thought [PDF]

open access: yesJournal of Community Hospital Internal Medicine Perspectives, 2014
We describe a case of renal papillary necrosis in a middle-aged female with sickle cell trait who presented with gross hematuria. We wish to highlight this case for several reasons. Sickle cell trait is often viewed as a benign condition despite the fact
Uqba Khan   +4 more
doaj   +1 more source

Studies on the Hemoglobin of Cooley's Anemia and Cooley's Trait [PDF]

open access: yes, 1952
The diseases sickle cell anemia and Cooley's anemia (also known as thalassemia or Mediterranean anemia) have associated with them "minor" or "trait" forms of the disease in which the symptomatology is minimal, and the abnormalities in the red cells are ...
Rich, Alexander
core  

Diet of bird‐like troodontid dinosaurs: synthesis of a contentious clade

open access: yesBiological Reviews, EarlyView.
ABSTRACT Troodontidae is a clade of small‐to medium‐sized maniraptoran theropods that mainly lived in Laurasia (modern Asia, North America and Europe) during the Jurassic and Cretaceous periods and are believed to have had a variety of diets. The uniqueness of troodontid teeth suggests that they diverged from the typical flesh‐based diet of non‐avian ...
Yui Chi Fan   +2 more
wiley   +1 more source

The Virginia Sickle Cell Anemia Awareness Program: Education, Screening, and Counseling [PDF]

open access: yes, 1977
In 1968, a program of screening for sickle trait carriers was begun as part of the work of the Hematology Division, Department of Medicine, at the Medical College of Virginia.
Cooper, Florence N., Scott, Robert B.
core   +1 more source

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