Results 211 to 220 of about 738,318 (352)

Bezlotoxumab as Treatment for Recurrent/Chronic Clostridioides difficile Infection in Pediatric Stem Cell Transplant Recipients: A Multi‐Institutional Experience

open access: yesPediatric Blood &Cancer, EarlyView.
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]

open access: yesToxicol Rep
Monfared A   +5 more
europepmc   +1 more source

Genetic Diagnosis and Clinical Features of Fetuses With Congenital Diaphragmatic Hernia

open access: yesPrenatal Diagnosis, EarlyView.
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]

open access: yesInt J Surg Case Rep
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]

open access: bronze, 1988
C. Richard Parker   +5 more
openalex   +1 more source

Prenatal Exome Sequencing Identifies Dual Maternal‐Fetal Diagnosis of HbF Mission Bay, a Novel HBG2 Variant Associated With Methemoglobinemia, Hypoxia and Hemolytic Anemia

open access: yesPrenatal Diagnosis, EarlyView.
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]

open access: yesFront Immunol
Kikuta K   +7 more
europepmc   +1 more source

Human umbilical cord plasma proteins revitalize hippocampal function in aged mice

open access: yesNature, 2017
Joseph M. Castellano   +12 more
semanticscholar   +1 more source

Hemophilia A: An Ideal Disease for Prenatal Therapy

open access: yesPrenatal Diagnosis, EarlyView.
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

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