Radhika R. Dhamija

Medical Genetics | Neurology | Pediatric Neurology

200 1st St Sw
Rochester, MN 55905

Last Updated: 09/26/2026

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Found 80 publications

Clinical Utility of Rapid Whole-Genome Sequencing in Hospitalized Adults With Unexplained Neurologic Presentations.

Clinical Utility of Rapid Whole-Genome Sequencing in Hospitalized Adults With Unexplained Neurologic Presentations.

Journal: Neurology

Published: June 16, 2026

Long-term real-world safety and effectiveness of arimoclomol in individuals with NPC: Outcomes from the US early access program over a 4-year period.

Long-term real-world safety and effectiveness of arimoclomol in individuals with NPC: Outcomes from the US early access program over a 4-year period.

Journal: Molecular genetics and metabolism

Published: April 13, 2026

Emerging Topics in Neurogenomics: Summary From Inaugural Child Neurology Society Genetics Summit.

Emerging Topics in Neurogenomics: Summary From Inaugural Child Neurology Society Genetics Summit.

Journal: Pediatric neurology

Published: January 17, 2026

Glutathione synthetase deficiency: 10 years later.

Glutathione synthetase deficiency: 10 years later.

Journal: BMJ case reports

Published: January 07, 2026

MSTO1-related mitochondrial myopathy and ataxia syndrome: Case series and literature review.

MSTO1-related mitochondrial myopathy and ataxia syndrome: Case series and literature review.

Journal: Neuromuscular disorders : NMD

Published: October 24, 2025

Movement Disorder Following Hypoglycemic Encephalopathy in Mitochondrial 3-Hydroxy-3-methylglutaryl-CoA Synthase-2 (mHS) Deficiency.

Movement Disorder Following Hypoglycemic Encephalopathy in Mitochondrial 3-Hydroxy-3-methylglutaryl-CoA Synthase-2 (mHS) Deficiency.

Journal: Annals of internal medicine. Clinical cases

Published: August 26, 2025

Comorbid autosomal dominant LDLR- and collagen VI-related disorders.

Comorbid autosomal dominant LDLR- and collagen VI-related disorders.

Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology

Published: July 20, 2025

Ten years of RASGRP2-related platelet disorder: Implications for molecular haematology and diagnostics.

Ten years of RASGRP2-related platelet disorder: Implications for molecular haematology and diagnostics.

Journal: British journal of haematology

Published: June 05, 2025

Heterozygosity in NPC may be associated with neurologic and systemic phenotypes.

Heterozygosity in NPC may be associated with neurologic and systemic phenotypes.

Journal: Frontiers in neurology

Published: April 25, 2025

Lenmeldy (atidarsagene autotemcel) for individuals with early metachromatic leukodystrophy (MLD): A therapeutics bulletin of the American College of Medical Genetics and Genomics (ACMG).

Lenmeldy (atidarsagene autotemcel) for individuals with early metachromatic leukodystrophy (MLD): A therapeutics bulletin of the American College of Medical Genetics and Genomics (ACMG).

Journal: Genetics in medicine open

Published: April 02, 2025

A National Survey on the Neurogenetics Workforce: Practice Models, Evolving Challenges, and Future Directions.

A National Survey on the Neurogenetics Workforce: Practice Models, Evolving Challenges, and Future Directions.

Journal: Pediatric neurology

Published: February 18, 2025

Novel RRAGD Variants in Autosomal Dominant Kidney Hypomagnesemia and Therapeutic Perspectives.

Novel RRAGD Variants in Autosomal Dominant Kidney Hypomagnesemia and Therapeutic Perspectives.

Journal: Kidney international reports

Published: February 03, 2025

Showing 1-12 of 80

Last Updated: 09/26/2026