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The American Journal of Case Reports|November 25, 2020
Phenotypic Heterogeneity in 5 Family Members with the Mitochondrial Variant m.3243A>GJosef Finsterer, Franco LacconeNeurologia I Neurochirurgia Polska|May 8, 2016
Fatal consequences of climbing a ladder under apixaban and drunkenClaudia Stöllberger, Josef FinstererPediatric Neurology|September 20, 2015
Abnormalities of Skin and Cutaneous Appendages in Neuromuscular DisordersJosef Finsterer, Salma WakilJournal of the Neurological Sciences|July 19, 2014
CNS-disease affecting the heart: brain-heart disordersJosef Finsterer, Karim WahbiActa Neurologica Belgica|July 31, 2014
Fasciculations in human hereditary diseaseJosef Finsterer, Rahim AliyevKorean Circulation Journal|March 26, 2016
Heart Disease in Disorders of Muscle, Neuromuscular Transmission, and the NervesJosef Finsterer, Claudia StöllbergerActa Medica Iranica|November 30, 2015
Diagnosing Mitochondrial Disorder without Sophisticated MeansJosef Finsterer, Marlies FrankMitochondrion|May 17, 2016
Prevalence of neoplasms in definite and probable mitochondrial disordersJosef Finsterer, Marlies FrankWiener Medizinische Wochenschrift (1946)|October 25, 2013
Unclassified cardiomyopathies in neuromuscular disordersJosef Finsterer, Claudia StöllbergerMolecular Genetics and Metabolism Reports|November 22, 2017
Only some patients with bulbar and spinal muscular atrophy may develop cardiac diseaseJosef Finsterer, Claudia StöllbergerPageof 69