Sandra Jackson
Dresden, SN, Germany
Last Updated: 09/26/2026
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Found 11 publications
Serum Neurofilament Light Chain: A Marker of Nervous System Damage in Myopathies.
Journal: Frontiers in neuroscience
Published: October 08, 2021
Myogenic tremor - a novel tremor entity.
Journal: Current opinion in neurology
Published: July 22, 2021
ADCK2 Haploinsufficiency Reduces Mitochondrial Lipid Oxidation and Causes Myopathy Associated with CoQ Deficiency.
Journal: Journal of clinical medicine
Published: August 03, 2019
Novel mutations in MYBPC1 are associated with myogenic tremor and mild myopathy.
Journal: Annals of neurology
Published: September 26, 2018
Variable clinical course in acute necrotizing encephalopathy and identification of a novel RANBP2 mutation.
Journal: Brain & development
Published: November 30, 2015
Expanded phenotypic spectrum of the m.8344A>G "MERRF" mutation: data from the German mitoNET registry.
Journal: Journal of neurology
Published: November 16, 2015
Mitochondrial abnormalities in the myofibrillar myopathies.
Journal: European journal of neurology
Published: June 15, 2015
Critical role of AMP-activated protein kinase in the balance between mitophagy and mitochondrial biogenesis in MELAS disease.
Journal: Biochimica et biophysica acta
Published: April 21, 2015
Autosomal dominant mutations in POLG and C10orf2: association with late onset chronic progressive external ophthalmoplegia and Parkinsonism in two patients.
Journal: Journal of neurology
Published: December 14, 2012
Screening of effective pharmacological treatments for MELAS syndrome using yeasts, fibroblasts and cybrid models of the disease.
Journal: British journal of pharmacology
Published: July 04, 2012
Recovery of MERRF fibroblasts and cybrids pathophysiology by coenzyme Q10.
Journal: Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics
Published: February 23, 2012
Showing 1-11 of 11
Last Updated: 09/26/2026