Stela Lefter
Dublin, L, Ireland
Last Updated: 09/26/2026
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Found 18 publications
Adult presentation of a rare mitochondrial tRNA Val gene mutation-an expanding clinical phenotype.
Journal: European journal of neurology
Published: May 07, 2024
Late-onset Tay-Sachs disease presenting with a neuromuscular phenotype-a case series.
Journal: European journal of neurology
Published: April 22, 2023
Late-Onset Tay-Sachs Disease - expanding the clinical phenotype.
Journal: Tremor and other hyperkinetic movements (New York, N.Y.)
Published: January 10, 2023
The Diagnostic Yield of Electromyography at Detecting Abnormalities on Muscle Biopsy: A Single Center Experience.
Journal: The Neurodiagnostic journal
Published: June 14, 2021
Late-Onset Tay-Sachs Disease in an Irish Family.
Journal: Movement disorders clinical practice
Published: June 19, 2020
Papillitis, a Rare Cytomegalovirus Manifestation in an Immunocompetent Host.
Journal: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society
Published: April 03, 2020
Acute severe sensory ganglionopathy in systemic lupus erythematous.
Journal: Neuromuscular disorders : NMD
Published: March 11, 2020
A population-based epidemiologic study of adult neuromuscular disease in the Republic of Ireland.
Journal: Neurology
Published: July 12, 2016
Andersen-Tawil syndrome with early fixed myopathy.
Journal: Journal of clinical neuromuscular disease
Published: November 22, 2014
A novel MYH7 Leu1453pro mutation resulting in Laing distal myopathy in an Irish family.
Journal: Neuromuscular disorders : NMD
Published: July 01, 2014
Last Updated: 09/26/2026