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Cureus|March 10, 2025
Presentation, Treatment, and Outcome of a First Stroke-like Episode in a Carrier of the Compound Heterozygous Variants c.695G_A and c.2209G_C in POLG: A Case ReportDominik Zieglgänsberger, Josef FinstererCureus|September 25, 2023
Progressive Mitochondrial Encephalopathy Due to the Novel Compound Heterozygous Variants c.182C>T and c.446A>AG in NARS2: A Case ReportJosef Finsterer, Sounira MehriEuropean Journal of Internal Medicine|August 4, 2023
Cannabidiol's impact on drug-metabolizationClaudia Stöllberger, Josef FinstererCureus|June 12, 2023
Novel Phenotype of LMNA Variant c.154C>G Affecting Heart, Liver, and Lipid and Iron Metabolism: A Case ReportJosef Finsterer, Gerhard PölzlAmerican Journal of Translational Research|February 10, 2018
Polycystic ovary syndrome in mitochondrial disorders due mtDNA or nDNA variantsJosef Finsterer, Sinda Zarrouk-MahjoubClinical Nephrology. Case Studies|February 20, 2018
Comment to: Focal segmental glomerulosclerosis associated with mitochondrial disease by Lim et al. in Clin Nephrol Case Stud. 2017; 5: 20-25Josef Finsterer, Sinda Zarrouk-MahjoubMetabolic Brain Disease|October 20, 2017
Correction to: Contribution of the MRPS22 variant and a Down mosaic to the phenotypeJosef Finsterer, Sinda Zarrouk-MahjoubClinical Neurology and Neurosurgery|December 3, 2014
Anterocollis and anterocaputJosef Finsterer, Gonzalo J RevueltaBiomedical Reports|May 19, 2017
Renal manifestations of primary mitochondrial disordersJosef Finsterer, Fulvio Alexandre ScorzaPageof 70