Prenatal diagnosis of hematologic disorders

Diagnosis of very long chain acyl-dehydrogenase deficiency from an infant's newborn screening card.

Pediatrics·2001

Glucose transporter type 1 deficiency: a study of two cases with video-EEG.

European journal of pediatrics·1999

Development of guidelines for treatment of children with phenylketonuria: report of a meeting at the National Institute of Child Health and Human Development held August 15, 1995, National Institutes of Health, Bethesda, Maryland.

Pediatrics·1999

Management of phenylketonuria for optimal outcome: a review of guidelines for phenylketonuria management and a report of surveys of parents, patients, and clinic directors.

Pediatrics·1999

Tandem spectrometry in newborn screening.

Current opinion in pediatrics·1998

Clinical heterogeneity and prognosis in combined methylmalonic aciduria and homocystinuria (cblC).

Journal of inherited metabolic disease·1997

Advancing the science of Staphylococcus aureus infection prevention in the neonatal intensive care unit.

Seminars in perinatology·2026

The uprise of congenital syphilis in the United States: a preventable failure of perinatal systems.

Seminars in perinatology·2026

Does Low-dose Aspirin prevent preeclampsia or merely delay it?

Seminars in perinatology·2026

The impact of gastrointestinal motility on feeding tolerance in the very preterm infant.

Seminars in perinatology·2026

Congenital cytomegalovirus: Screening strategies and diagnostic challenges.

Seminars in perinatology·2026

Enteral nutrition to optimize health and neurodevelopmental outcomes in very preterm infants.

Seminars in perinatology·2026

Tirofiban-Associated Thrombocytopenia: A Case Report.

Cureus·2026

Body weight rather than unfractionated heparin dose predicts periprocedural bleeding during elective PCI.

International journal of cardiology. Cardiovascular risk and prevention·2026

Adjunctive Cerebrolysin therapy following mechanical thrombectomy for acute basilar artery occlusion: a case report.

Journal of medicine and life·2026

Simultaneous detection of thalassemia, hemoglobinopathies, and G6PD variants using long-read nanopore sequencing: genetic complexity and heterogeneity in Thailand.

PeerJ·2026

First Case Report of Triple Recurrent Cholangitis of "Coildocholithiasis," Following Hepatic Artery Pseudoaneurysm Embolization.

DEN open·2026

Preparative leukapheresis impairs autologous donor hemostasis and platelet function.

Research and practice in thrombosis and haemostasis·2026

Related Experiment Videos

Prenatal diagnosis of hematologic disorders

Related Concept Videos

Diagnosis of very long chain acyl-dehydrogenase deficiency from an infant's newborn screening card.

Glucose transporter type 1 deficiency: a study of two cases with video-EEG.

Development of guidelines for treatment of children with phenylketonuria: report of a meeting at the National Institute of Child Health and Human Development held August 15, 1995, National Institutes of Health, Bethesda, Maryland.

Management of phenylketonuria for optimal outcome: a review of guidelines for phenylketonuria management and a report of surveys of parents, patients, and clinic directors.

Tandem spectrometry in newborn screening.

Clinical heterogeneity and prognosis in combined methylmalonic aciduria and homocystinuria (cblC).

Advancing the science of Staphylococcus aureus infection prevention in the neonatal intensive care unit.

The uprise of congenital syphilis in the United States: a preventable failure of perinatal systems.

Does Low-dose Aspirin prevent preeclampsia or merely delay it?

The impact of gastrointestinal motility on feeding tolerance in the very preterm infant.

Congenital cytomegalovirus: Screening strategies and diagnostic challenges.

Enteral nutrition to optimize health and neurodevelopmental outcomes in very preterm infants.

Tirofiban-Associated Thrombocytopenia: A Case Report.

Body weight rather than unfractionated heparin dose predicts periprocedural bleeding during elective PCI.

Adjunctive Cerebrolysin therapy following mechanical thrombectomy for acute basilar artery occlusion: a case report.

Simultaneous detection of thalassemia, hemoglobinopathies, and G6PD variants using long-read nanopore sequencing: genetic complexity and heterogeneity in Thailand.

First Case Report of Triple Recurrent Cholangitis of "Coildocholithiasis," Following Hepatic Artery Pseudoaneurysm Embolization.

Preparative leukapheresis impairs autologous donor hemostasis and platelet function.

Related Experiment Videos

Prenatal diagnosis of hematologic disorders

Related Concept Videos

Related Articles