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Journal of the Neurological Sciences|May 5, 2012
Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritanceJosef Finsterer, Wolfgang Löscher, Stefan Quasthoff, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|February 14, 2014
Presumed mitochondrial disease manifesting with recurrent syncopesJosef Finsterer, Romana Höftberger, Boris Rolinski, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|June 6, 2003
Influence of tiapride on platelet counts in healthy volunteers and patients with movement disordersNicole Kotzailias, Josef Finsterer, Susanne Aull, et al.
Journal of Medical Cases|November 22, 2021
Dilated Cardiomyopathy due to the Novel MT-CYB Missense Mutation m.14757T>CSinda Zarrouk, Josef Finsterer, Sounira Mehri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 24, 2008
Recovery from acute paraplegia due to spontaneous spinal, epidural hematoma under minimal-dose acetyl-salicylic acidJosef Finsterer, Stefanie Seywald, Claudia Stöllberger, et al.
Journal of Medical Case Reports|October 13, 2016
Takotsubo-like syndrome triggered by fludrocortisone overdose for Addison's disease: a case reportRadu Campean, Matthias Hasun, Claudia Stöllberger, et al.
Texas Heart Institute Journal|May 28, 2024
Coronary Angiography in Patients With Left Ventricular Hypertrabeculation/NoncompactionNicolas de Cillia, Josef Finsterer, Radu Campean, et al.
Journal of the Renin-Angiotensin-Aldosterone System : JRAAS|February 19, 2011
The CC genotype of the angiotensin II type I receptor gene independently associates with acute myocardial infarction in a Tunisian populationSounira Mehri, Sinda Mahjoub, Josef Finsterer, et al.
International Journal of Cardiology|November 5, 2013
Pathomorphologic findings in left ventricular hypertrabeculation/noncompaction of adults in relation to neuromuscular disordersDaniel Gerger, Claudia Stöllberger, Martin Grassberger, et al.
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