Results 161 to 170 of about 68,021 (347)
ABSTRACT This retrospective study aimed to explore the value of DAT‐FAT serological profiles confirmed by AET in classifying neonatal jaundice, evaluating its severity, and guiding clinical management. A total of 915 jaundiced newborns (584 pathological, 331 physiological) admitted from July 2018 to August 2021 were included.
Tian‐Ge Wu +7 more
wiley +1 more source
SkinDB: A Curated Resource for Dermatological Data Warehousing and Bioinformatics Exploration
SkinDB is an open‐access transcriptomic database integrating 220 datasets and 11,283 samples across six major skin diseases. Its code‐free interface supports cross‐disease analyses, visualizations, and data downloads for dermatological research. ABSTRACT Dermatology lacks a centralized analysis‐ready transcriptomic resource, leaving publicly available ...
Haoxue Zhang +8 more
wiley +1 more source
Petrozzi, John W, Kligman, Albert M
openaire +2 more sources
ABSTRACT Aim In this article, we present two cases of severe fetal hemolytic anemia based on a beta‐thalassaemia trait inherited from a single parent. Results These cases, presented at 20 and 28 weeks' gestation, necessitated intra‐uterine blood transfusions.
Eva van der Meij +11 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
Evaluation of efficacy and complication between three mode of phototherapy
Background: Even though phototherapy has been used for more than 30 years, reports of significant toxicity are rare. Phototherapy is highly effective method for preventing and treating hyperbilirubinemia. Methods: A prospective study was performed in 200
Ghotbi, H, Behjati, Sh
core
Diagnosis and Management of Prenatal Hereditary Pyropoikilocytosis
ABSTRACT Hereditary pyropoikilocytosis (HPP) is a severe hemolytic anemia caused by variants in SPTA1, SPTB, and EPB41. These weaken horizontal interactions in the erythrocyte cytoskeleton, causing membrane fragmentation and splenic sequestration. It will readily cause fetal anemia and often hydrops fetalis. Prenatal diagnosis requires first ruling out
Connor Hartzell +6 more
wiley +1 more source
The Diagnosis and Prenatal Management of Non‐RHD Alloimmunizations
ABSTRACT Red blood cell (RBC) alloimmunization remains a relevant cause of hemolytic disease of the fetus and newborn (HDFN). Although RhD immunization has significantly decreased since the implementation of systematic prophylaxis, it is still the main cause of alloimmunization in pregnancy.
Mar Bennasar, Antoni Borrell
wiley +1 more source

