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Cureus|November 11, 2024
Leigh Syndrome Caused by Compound Heterozygous Variants c.1162A_C and c.1138G_C in the NDUFV1 Gene: A Case ReportJosef FinstererPediatric Neurology|October 14, 2020
Clinical Therapeutic Management of Human Mitochondrial DisordersJosef FinstererCase Reports in Neurological Medicine|October 16, 2020
Photosensitive Epilepsy and Polycystic Ovary Syndrome as Manifestations of MERRFJosef FinstererPediatric Endocrinology, Diabetes, and Metabolism|February 4, 2022
MELAS or Leigh syndrome, that's the questionJosef FinstererCureus|February 1, 2022
Atheromatosis of the Scalp: A Novel Feature of Chronic Progressive External Ophthalmoplegia Plus Due to a Single Mitochondrial DNA DeletionJosef FinstererWorld Journal of Clinical Cases|June 29, 2023
Symmetric DWI hyperintensities in CMT1X patients after SARS-CoV-2 vaccination should not be classified as stroke-like lesionsJosef FinstererMedicine|February 7, 2020
Variant m.1555A>G in MT-RNR1 causes hearing loss and multiorgan mitochondrial disorderJosef FinstererPolish Journal of Pathology : Official Journal of the Polish Society of Pathologists|October 28, 2020
Diagnosing MERRF requires clinical and genetic evidenceJosef FinstererEpilepsy & Behavior Reports|January 14, 2022
SUDEP cases require thorough post-mortem work-up to eventually detect an underlying causeJosef FinstererThe International Journal of Neuroscience|April 6, 2005
Lactate stress testing in sporadic amyotrophic lateral sclerosisJosef FinstererPageof 69