scispace - formally typeset
J

John W. Earl

Researcher at Children's Hospital at Westmead

Publications -  43
Citations -  1400

John W. Earl is an academic researcher from Children's Hospital at Westmead. The author has contributed to research in topics: Melphalan & Population. The author has an hindex of 24, co-authored 43 publications receiving 1266 citations. Previous affiliations of John W. Earl include Boston Children's Hospital & Alexandra Hospital.

Papers
More filters
Journal ArticleDOI

Cerebrospinal fluid neopterin in paediatric neurology: a marker of active central nervous system inflammation

TL;DR: Cerebrospinal fluid neopterin production is increased by interferon‐gamma stimulation and appears to act as a marker of intrathecal immune activation and may be a biological marker of central nervous system (CNS) inflammation.
Journal ArticleDOI

Population Pharmacokinetics of Liposomal Amphotericin B in Pediatric Patients with Malignant Diseases

TL;DR: The model has been evaluated and can be used in the design of rational dosing strategies for L-AmB antifungal therapy in this special population of pediatric patients with malignant diseases.
Journal ArticleDOI

Perinatal hypophosphatasia presenting as neonatal epileptic encephalopathy with abnormal neurotransmitter metabolism secondary to reduced co-factor pyridoxal-5′-phosphate availability

TL;DR: Two neonates presenting with perinatal hypophosphatasia and severe epileptic encephalopathy resulting in death had increased levels of urinary vanillactate, indicating functional deficiency of aromatic amino acid decarboxylase, a pyridoxal-5-phosphate (PLP)-dependent enzyme required for dopamine and serotonin biosynthesis.
Journal ArticleDOI

B Cell, Th17, and Neutrophil Related Cerebrospinal Fluid Cytokine/Chemokines Are Elevated in MOG Antibody Associated Demyelination

TL;DR: The findings suggest that MOG Ab POS patients have a more pronounced CNS inflammatory response with elevation of predominant humoral associated cytokines/chemokines, as well as some Th 17 and neutrophil related cytokines and chemokines suggesting a differential inflammatory pathogenesis associated with MOG antibody seropositivity.