Most DLBCL cases fall into the DLBCL, NOS category. Within this category, researchers have identified 2 main cell-of-origin (COO) molecular subtypes using gene expression profiling: germinal center ...
Areas of angioedema tend to be pale and painful ... Skin conditions to be considered for differential diagnosis are summarized in Table 2. Mast cells are the primary effector cell of urticaria.
Bhavin, who brings over 27 years of experience as a technology professional with domain expertise in Fashion, Home & Grocery Retail, Manufacturing, will be addressing DDX Asia Business Conference on ...
Angioedema is a well-known side effect of treatment with an angiotensin-converting enzyme (ACE) inhibitor and one that we have been willing to accept in view of the incidence of the problem and ...
Taking cognizance of this emerging need, Thoughtshows & Events (formerly VJ Media Works), organiser of the digital display expo DDX Asia, will be conducting a 2-day industry conference entitled ‘DDX ...
To be organized in Mumbai on February 20 & 21, 2025 at Nesco Exhibition Centre, Goregaon, Mumbai, along with DDX Asia 2025 Expo, the conference will have industry leaders sharing their observations ...
The DSM-5, otherwise known as the "Diagnostic and Statistical Manual of Mental Disorders," Fifth Edition, is a book published by the American Psychiatric Association (APA) to help mental health ...
The diagnosis of the so-called “disease X” in the Democratic Republic of the Congo is “leaning more toward malaria,” an official from the Africa Centers for Disease Control and Prevention ...
Summary: Researchers identified variants in the DDX53 gene, located on the X chromosome, as contributors to autism spectrum disorder (ASD). These genetic variants, found predominantly in males, ...
Using a blood pressure chart by age can help you interpret your results to see how they compare to the normal ranges across groups, and within your own age cohort. A chart can help as you monitor your ...
Hereditary angioedema (HAE) is an autosomal dominant disease caused mostly by deleterious mutations in the gene encoding the C1-inhibitor (C1-INH) (C1-INH-HAE). It occurs in quantitative and ...