41. Cerebral imaging in paediatric mitochondrial disorders. Issue 6 (December 2018) Authors: Finsterer, Josef; Zarrouk-Mahjoub, Sinda Journal: Neuroradiology journal Issue: Volume 31:Issue 6(2018:Dec.) Page Start: 596 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
42. Cerebral Manifestations of Mitochondrial Disorders. (29th August 2017) Authors: Finsterer, Josef; Carvalho, Elmano Henrique Torres de Journal: Canadian journal of neurological sciences Issue: Volume 44:Number 6(2017) Page Start: 654 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
43. Cerebral tuberculoma are commonly accompanied by other imaging abnormalities. (August 2022) Authors: Finsterer, Josef Journal: Annals of medicine and surgery Issue: Volume 80(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
44. Cerebro‐Spinal‐Fluid Cytokine Profiles Do Not Reliably Delineate Encephalopathy and Inflammation in Neuro‐COVID. Issue 4 (25th August 2021) Authors: Finsterer, Josef; Scorza, Fulvio A. Journal: Annals of neurology Issue: Volume 90:Issue 4(2021) Page Start: 695 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
45. CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder. (September 2018) Authors: Finsterer, Josef; Fiorini, Ana C.; Scorza, Carla A.; Scorza, Fulvio A. Journal: European journal of paediatric neurology Issue: Volume 22:Number 5(2018:Sep.) Page Start: 889 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
46. Comment on "CPEO and Mitochondrial Myopathy in a Patient with DGUOK Compound Heterozygous Pathogenetic Variant and mtDNA Multiple Deletions". (2nd April 2020) Authors: Finsterer, Josef Other Names: Litofsky Norman S. Academic Editor. Journal: Case reports in neurological medicine Issue: Volume 2020(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
47. Comment on "Mitochondrial Neurogastrointestinal Encephalomyopathy: Novel Pathogenic Mutation in Thymidine Phosphorylase Gene in a Patient from Cape Verde Islands". (28th February 2021) Authors: Finsterer, Josef Other Names: Litofsky Norman S. Academic Editor. Journal: Case reports in neurological medicine Issue: Volume 2021(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
48. Comment on "Role of Mitochondrial Genome Mutations in Pathogenesis of Carotid Atherosclerosis". (28th March 2018) Authors: Finsterer, Josef; Zarrouk-Mahjoub, Sinda Other Names: Cirillo Giuseppe Academic Editor. Journal: Oxidative medicine and cellular longevity Issue: Volume 2018(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
49. Comment on "Ventricular non‐compaction cardiomyopathy: prenatal diagnosis and pathology". (February 2016) Authors: Stöllberger, Claudia; Finsterer, Josef Journal: Prenatal diagnosis Issue: Volume 36:Number 2(2016) Page Start: 197 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
50. Comment on 'MOG antibody-associated encephalomyelitis mimicking bacterial meningomyelitis following ChAdOx1 nCoV-19 vaccination: a case report'. (June 2022) Authors: Finsterer, Josef; Scorza, Fulvio A Journal: Therapeutic advances in neurological disorders Issue: Volume 15(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗