Results 131 to 140 of about 261,136 (339)
Clinical progress note: Rubella
Abstract Rates of rubella infection and congenital rubella syndrome decreased significantly since the introduction of the rubella vaccine in 1969. Endemic rubella was declared eliminated in the United States in 2004, and since 2012, all rubella cases in the United States have been associated with infections acquired abroad.
Adam E. Gailani +2 more
wiley +1 more source
ABSTRACT Brain age is an emerging concept that reflects complex, time‐dependent changes in brain structure, identifying departures from expected neurodevelopmental patterns. In the developing brain, accurate MRI‐based age estimation is a quantitative biomarker for detecting atypical neurodevelopment, facilitating early diagnosis, guiding clinical ...
Hosna Asma ull +3 more
wiley +1 more source
Background: In-utero phthalate exposure was shown to be associated with shortened anogenital distance (AGD) in male newborns, but findings among female are inconsistent.
Itai Gueta +16 more
doaj +1 more source
Antithrombin: Deficiency, Diversity, and the Future of Diagnostics
ABSTRACT Our healthcare system provides reactive sick‐care, treating patients after symptoms have appeared by prescription of generic and often suboptimal therapy. This strategy brings along high costs and high pressure which is not sustainable.
Mirjam Kruijt +2 more
wiley +1 more source
P01.09 The intellectual development, mental and behavioral disorders in the children from belarus exposed in utero following the chernobyl accident [PDF]
S. Igumnov, V. Drozdovitchl
openalex +1 more source
Abstract Netherton syndrome (NS) is a rare, severe, and often life‐threatening disease for which current therapeutic approaches are limited and show variable effectiveness. NS is characterized by excessive epidermal desquamation that results in a highly defective epidermal barrier, constitutive skin inflammation, allergies, and hair abnormalities.
Eleni Zingkou +3 more
wiley +1 more source
ABSTRACT Prenatal exome sequencing (ES) can establish rare genetic diagnoses in a fetus but may also lead to occult genetic diagnosis in a biological parent. We present a case of dual fetal and maternal diagnosis by prenatal ES, in a fetus with unexplained anemia and in a pregnant patient with sickle cell disease (SCD) and recurrent unexplained hypoxia.
Matthew A. Shear +6 more
wiley +1 more source

