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Dermatology Research and Practice|June 30, 2010
Diagnostic pitfalls in newborns and babies with blisters and erosionsElke Nischler, Alfred Klausegger, Clemens Hüttner, et al.Movement Disorders : Official Journal of the Movement Disorder Society|December 3, 2014
Mortality in Parkinson's disease: a 38-year follow-up studyBernadette Pinter, Anja Diem-Zangerl, Gregor Karl Wenning, et al.Journal of the Neurological Sciences|June 13, 2006
Parkinson's disease and arithmetics: the role of executive functionsLaura Zamarian, Pamela Visani, Margarete Delazer, et al.Orphanet Journal of Rare Diseases|July 12, 2020
Profiling trial burden and patients' attitudes to improve clinical research in epidermolysis bullosaChristine Prodinger, Anja Diem, Katherina Ude-Schoder, et al.Pediatric Dermatology|August 23, 2011
Diffuse cutaneous mastocytosis masquerading as epidermolysis bullosaKristin Kleewein, Roland Lang, Anja Diem, et al.Journal of Neurology|January 18, 2005
Progression of parkinsonism in multiple system atrophyKlaus Seppi, Farid Yekhlef, Anja Diem, et al.Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|December 24, 2005
[Dental alterations in junctional epidermolysis bullosa--report of a patient with a mutation in the LAMB3-gene]Elke Sadler, Martin Laimer, Anja Diem, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Comparison of diffusion-weighted imaging and [123I]IBZM-SPECT for the differentiation of patients with the Parkinson variant of multiple system atrophy from those with Parkinson's diseaseKlaus Seppi, Michael F H Schocke, Eveline Donnemiller, et al.Orphanet Journal of Rare Diseases|November 2, 2018
Basal pharmacokinetic parameters of topically applied diacerein in pediatric patients with generalized severe epidermolysis bullosa simplexMichael Ablinger, Thomas K Felder, Monika Wimmer, et al.Diagnostics (Basel, Switzerland)|October 27, 2022
Recessive Dystrophic Epidermolysis bullosa due to Hemizygous 40 kb Deletion of COL7A1 and the Proximate PFKFB4 Gene Focusing on the Mutation c.425A>G Mimicking Homozygous StatusAlfred Klausegger, Niklas Jeschko, Markus Grammer, et al.Pageof 3