Publications by authors named "L Neuman"

Background: Arginase 1 Deficiency (ARG1-D) is a rare debilitating, progressive, inherited, metabolic disease characterized by marked increases in plasma arginine (pArg) and its metabolites, with increased morbidity, substantial reductions in quality of life, and premature mortality. Effective treatments that can lower arginine and improve clinical outcomes is currently lacking. Pegzilarginase is a novel human arginase 1 enzyme therapy.

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Article Synopsis
  • The study examines the prevalence and predictors of cerebral lesions in patients with immune thrombotic thrombocytopenic purpura (iTTP) and hemolytic uremic syndrome (HUS) during their acute phases.
  • One-third of the 73 patients analyzed showed acute ischemic lesions on MRI, and neurological symptoms were not significantly different between iTTP and HUS cases.
  • Key factors predicting these lesions included the presence of old infarcts, elevated blood pulse pressure, and a diagnosis of iTTP, indicating potential areas for enhanced treatment approaches.*
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Marzeptacog alfa (activated) (MarzAA) is an activated recombinant human rFVII variant intended for subcutaneous (s.c.) administration to treat or prevent bleeding in individuals with hemophilia A (HA) or B (HB) with inhibitors, and other rare bleeding disorders.

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Marzeptacog alfa (activated) (MarzAA) is an activated recombinant human FVII (rFVIIa) variant developed as subcutaneous (s.c.) administration for the treatment or prevention of bleeding episodes in patients with hemophilia A (HA) or hemophilia B (HB) with inhibitors and other rare bleeding disorders.

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