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11. Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy. (7th June 2016)

12. Development of a Mitochondrial Myopathy‐Composite Assessment Tool. Issue 4 (30th August 2021)

13. Diagnosis of 'possible' mitochondrial disease: an existential crisis. Issue 3 (25th January 2019)

14. Erratum to: Common data elements for clinical research in mitochondrial disease: a National Institute for Neurological Disorders and Stroke project. Issue 1 (4th October 2017)

15. Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann‐Steiner syndrome. Issue 6 (30th March 2021)

18. Mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3′‐end processing. Issue 10 (18th June 2019)

20. Pediatric Leigh Syndrome: Neuroimaging Features and Genetic Correlations. Issue 2 (13th June 2020)