Publications

Found 9 results
Filters: Keyword is Diagnosis, Differential  [Clear All Filters]
2019
Patel R, Coulter LLee, Rimmer J, Parkes M, Chinnery PFrancis & Swift O (2019) Mitochondrial neurogastrointestinal encephalopathy: a clinicopathological mimic of Crohn's disease. BMC Gastroenterol 19, 11
2013
Salsano E, Farina L, Lamperti C, Piscosquito G, Salerno F, Morandi L, Carrara F, Lamantea E, Zeviani M, Uziel G, Savoiardo M & Pareyson D (2013) Adult-onset leukodystrophies from respiratory chain disorders: do they exist?. J Neurol 260, 1617-23
2009
Cesaroni E, Scarpelli M, Zamponi N, Polonara G & Zeviani M (2009) Mitochondrial encephalomyopathy lactic acidosis and strokelike episodes mimicking occipital idiopathic epilepsy. Pediatr Neurol 41, 131-4
2008
Okuyaz C, Ezgü FSüheyl, Biberoglu G, Zeviani M, Tiranti V & Yilgör E (2008) Severe infantile hypotonia with ethylmalonic aciduria: case report. J Child Neurol 23, 703-5
2007
Carneiro F, Moutinho C, Pera G, Caldas C, Fenger C, Offerhaus J, Save V, Stenling R, Nesi G, Mahlke U, Bläker H, Torrado J, Roukos DH, Sabourin J-C, Boeing H, Palli D, H Bueno-de-Mesquita B, Overvad K, Bingham S, Clavel-Chapelon F, Lund, iv E, Trichopoulou A, Manjer J, Riboli E & González CA (2007) Pathology findings and validation of gastric and esophageal cancer cases in a European cohort (EPIC/EUR-GAST). Scand J Gastroenterol 42, 618-27
2006
Orcesi S, Gorni K, Termine C, Uggetti C, Veggiotti P, Carrara F, Zeviani M, Berardinelli A & Lanzi G (2006) Bilateral putaminal necrosis associated with the mitochondrial DNA A8344G myoclonus epilepsy with ragged red fibers (MERRF) mutation: an infantile case. J Child Neurol 21, 79-82
2005
Ishihara LS, Khaw K-T, Luben R, Bingham S, Welch A, Day N & Brayne C (2005) Self-reported parkinsonian symptoms in the EPIC-Norfolk cohort. BMC Neurol 5, 15
2000
Uziel G, Carrara F, Granata T, Lamantea E, Mora M & Zeviani M (2000) Neuromuscular syndrome associated with the 3291T-->C mutation of mitochondrial DNA: a second case. Neuromuscul Disord 10, 415-8
1993
Franceschetti S, Antozzi C, Binelli S, Carrara F, Nardocci N, Zeviani M & Avanzini G (1993) Progressive myoclonus epilepsies: an electroclinical, biochemical, morphological and molecular genetic study of 17 cases. Acta Neurol Scand 87, 219-23