Gabriel T. Doctor
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 9 publications
Quantifying APOL1, Human Leukocyte Antigen, and Other Genetic Contributions to Unexplained Kidney Failure.
Journal: American journal of kidney diseases : the official journal of the National Kidney Foundation
Published: October 23, 2024
Multiethnic prevalence of the APOL1 G1 and G2 variants among the Israeli dialysis population.
Journal: Clinical kidney journal
Published: October 08, 2024
Granulomatous Tubulointerstitial Nephritis in a Kidney Allograft: Treatment with Interleukin-6 Receptor Antagonist Stabilises Kidney Function.
Journal: Journal of clinical medicine
Published: April 08, 2024
Quantifying variant contributions in cystic kidney disease using national-scale whole-genome sequencing.
Journal: The Journal of clinical investigation
Published: March 27, 2024
Cladribine: Off-label disease modification for people with multiple sclerosis in resource-poor settings?
Journal: Multiple sclerosis journal - experimental, translational and clinical
Published: January 17, 2018
Guillain-Barré syndrome with exaggerated pleocytosis and anti-GM1 ganglioside antibodies.
Journal: BMJ case reports
Published: January 08, 2018
DNA methylation analysis of paediatric low-grade astrocytomas identifies a tumour-specific hypomethylation signature in pilocytic astrocytomas.
Journal: Acta neuropathologica communications
Published: February 12, 2016
Molecular analysis of pediatric brain tumors identifies microRNAs in pilocytic astrocytomas that target the MAPK and NF-κB pathways.
Journal: Acta neuropathologica communications
Published: November 28, 2015
Showing 1-9 of 9
Last Updated: 09/26/2026