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Neurology International|July 27, 2013
Adult mitochondrial DNA depletion syndrome with mild manifestationsJosef Finsterer, Gabor G Kovacs, Uwe AhtingRevista Medica De Chile|April 29, 2009
Down-Syndrome associated with MBL-deficiency, IgG-deficiency, vasculitis and mutated prothrombinHermann M Wolf, Claudia Stöllberger, Josef FinstererMetabolic Brain Disease|August 29, 2009
Malignant hyperthermia susceptibility in a patient with mitochondrial disorderJosef Finsterer, Andrea Michalek-Sauberer, Romana HöftbergerJournal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 10, 2019
Familial, long-term pollakisuria as initial manifestation of HSP4 due to the SPAST variant c.683-2A>CJosef Finsterer, Salma M Wakil, Franco LacconeClinics (Sao Paulo, Brazil)|June 25, 2022
SARS-CoV-2 vaccinations reduce the prevalence of post-COVID Guillain-Barre syndromeJosef Finsterer, Daniel Matovu, Fulvio A ScorzaCardiology|January 29, 2011
Recovery of systolic dysfunction in duchenne muscular dystrophy due to the point mutation c.4213C>TJosef Finsterer, Claudia Stöllberger, Elke Holinski-FederNeurology International|July 27, 2013
Asymptomatic hyper-creatine-kinase-emia as sole manifestation of inclusion body myositisJosef Finsterer, Claudia Stöllberger, Gabor G KovacsThe Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 3, 2018
Cerebral Manifestations of Mitochondrial DisordersJosef Finsterer, Elmano Henrique Torres de CarvalhoRevista Medica De Chile|January 23, 2014
Neurofibromatosis type I and anti-phospholipid antibody syndrome: report of one caseJosef Finsterer, Claudia Stöllberger, Lilian Schäffl-DoweikPediatric Neurology|February 17, 2018
MERRF Classification: Implications for Diagnosis and Clinical TrialsJosef Finsterer, Sinda Zarrouk-Mahjoub, John M ShoffnerPageof 69