Results 211 to 220 of about 738,318 (352)
ABSTRACT Clostridioides difficile infection (CDI) represents a significant health risk to pediatric stem cell transplant (SCT) patients. In these patients, recurrent CDI is common, requiring prolonged antibiotic usage and increased hospitalization. Bezlotoxumab, a monoclonal antibody that targets the toxin responsible for CDI, has demonstrated efficacy
Aaron E. Fan+8 more
wiley +1 more source
Pharmacogenetic exploration of buprenorphine and related metabolites in umbilical cord blood. [PDF]
Monfared A+5 more
europepmc +1 more source
A giant pigmented nevus with invasion into umbilical cord
WB Reed, William H. Snyder, RE. Horowitz
openalex +2 more sources
Genetic Diagnosis and Clinical Features of Fetuses With Congenital Diaphragmatic Hernia
ABSTRACT Objective Congenital diaphragmatic hernia (CDH) is a rare abnormality with highly heterogeneous genetic causes. This study investigated chromosomal and monogenic abnormalities in fetal CDH patients and evaluated the efficacy of chromosomal microarray analysis (CMA) and whole‐exome sequencing (WES) for genetic diagnosis.
Yan Lü+18 more
wiley +1 more source
Rare antenatal diagnosis of an umbilical cord hemangioma: A case report. [PDF]
Kandoussi H+4 more
europepmc +1 more source
Apolipoprotein A-1 in Umbilical Cord Blood of Newborn Infants: Relation to Gestational Age and High-Density Lipoprotein Cholesterol [PDF]
C. Richard Parker+5 more
openalex +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
Immune composition of the mononuclear cell fraction of human umbilical cord blood. [PDF]
Kikuta K+7 more
europepmc +1 more source
Human umbilical cord plasma proteins revitalize hippocampal function in aged mice
Joseph M. Castellano+12 more
semanticscholar +1 more source
Hemophilia A: An Ideal Disease for Prenatal Therapy
ABSTRACT Hemophilia A (HA) is the most common inherited coagulation defect. Current state‐of‐the‐art treatment consists of frequent administration of prophylactic infusions of coagulation factor VIII (FVIII) protein or bispecific antibodies that replace the cofactor function of FVIIIa to maintain hemostasis. However, these treatments are far from ideal,
Christopher D. Porada+2 more
wiley +1 more source