Mutation in the factor V gene associated with inferior vena cava thrombosis in newborns

Reproducibility and workflow efficiency of a novel software for quantitative coronary plaque characterization using photon-counting and energy-integrating detector computed tomography.

European journal of radiology·2026

Fast neutron generation with few-cycle, relativistic laser pulses at 1 Hz repetition rate.

Scientific reports·2024

The investigation of post-thaw chilled storage and the applicability of large-scale cryopreservation in chub (Squalius cephalus) sperm.

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Application of hydroxypropyl methylcellulose as a protective agent against magnesium stearate induced crystallization of amorphous itraconazole.

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences·2018

Note: 4-bounce neutron polarizer for reflectometry applications.

The Review of scientific instruments·2018

Investigation of Deteriorated Dissolution of Amorphous Itraconazole: Description of Incompatibility with Magnesium Stearate and Possible Solutions.

Molecular pharmaceutics·2017

Pathogenicity of NUSAP1 Variants Is Defined by NMD-Escape: Evidence From Two Novel Cases and Systematic Population-Based Variant Analysis.

Clinical genetics·2026

Biallelic ABCA13 Loss-of-Function Variants in a Child With Neurodevelopmental Delay: A Case Report.

Clinical genetics·2026

Variants in the Imprinted IGF2 Gene: A Review and Phasing of De Novo Variants Using Long-Read Sequencing.

Clinical genetics·2026

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Clinical genetics·2026

Recurrent Sterile Polyserositis Reveals an Underrecognized Autoinflammatory Phenotype in MECP2 Duplication Syndrome.

Clinical genetics·2026

Identification of Copy Number Variants as a Suspected Cause of Cerebral Small Vessel Disease.

Clinical genetics·2026

Cryptic and Overt Acute Kidney Injury Share Biomarker Characteristics in Pediatric Acute Respiratory Distress Syndrome.

Critical care explorations·2026

Admission blood gas, platelet, and inflammatory parameters associated with intraventricular hemorrhage in preterm infants: a retrospective case-control study.

Open medicine (Warsaw, Poland)·2026

Case Report: Successful hematopoietic stem cell transplantation in pediatric pyruvate kinase deficiency: a single-center Asian case series demonstrating favorable outcomes.

Frontiers in immunology·2026

Perinatal, socioenvironmental, and neurological factors to predict motor delay in infants born preterm.

Developmental medicine and child neurology·2026

Patient-Derived iPSC-MSC Modelling Reveals Reversible GSK3-Mediated Suppression of Mesenchymal Lineage Differentiation in Legg-Calvé-Perthes Disease.

Journal of cellular and molecular medicine·2026

The Establishment of a Simplified Clinical Scoring System for Neurodevelopmental Follow-Up and Its Application in Very Preterm Infants.

Child: care, health and development·2026

Related Experiment Videos

Mutation in the factor V gene associated with inferior vena cava thrombosis in newborns

Related Concept Videos

Reproducibility and workflow efficiency of a novel software for quantitative coronary plaque characterization using photon-counting and energy-integrating detector computed tomography.

Fast neutron generation with few-cycle, relativistic laser pulses at 1 Hz repetition rate.

The investigation of post-thaw chilled storage and the applicability of large-scale cryopreservation in chub (Squalius cephalus) sperm.

Application of hydroxypropyl methylcellulose as a protective agent against magnesium stearate induced crystallization of amorphous itraconazole.

Note: 4-bounce neutron polarizer for reflectometry applications.

Investigation of Deteriorated Dissolution of Amorphous Itraconazole: Description of Incompatibility with Magnesium Stearate and Possible Solutions.

Pathogenicity of NUSAP1 Variants Is Defined by NMD-Escape: Evidence From Two Novel Cases and Systematic Population-Based Variant Analysis.

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Mutation in the factor V gene associated with inferior vena cava thrombosis in newborns

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