Fouad Mitri
University Hospital Heidelberg
11 Papers
16 Citations
Fouad Mitri is an academic researcher from University Hospital Heidelberg. The author has contributed to research in topics: Medicine & Cancer. The author has an hindex of 2, co-authored 7 publications.
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Papers
Cytokine release syndrome-like serum responses after COVID-19 vaccination are frequent and clinically inapparent under cancer immunotherapy
Thomas Walle,Sunanjay Bajaj,Joscha A. Kraske,T. Rösner,Christiane S Cussigh,Katharina A. Kälber,L. J. Müller,S.B. Strobel,Jana Burghaus,Stefan M. Kallenberger,Christoph Stein-Thöringer,Maximilian Jenzer,Antonia Schubert,Steffen Kahle,Anja Williams,Birgit Hoyler,Lin Zielske,Renate Skatula,Stefanie Sawall,Mathias F. Leber,Russell Kunes,Johannes Krisam,Carlo Fremd,Andreas Schneeweiss,Jürgen Krauss,Leonidas Apostolidis,Anne Berger,Georg Martin Haag,Stefanie Zschäbitz,Niels Halama,Christoph Springfeld,Jessica C. Hassel,Dirk Jäger,Omar Abdelrahim,Elena Busch,Patrick Derigs,Katharina Dischinger,Fouad Mitri,Kerstin Schmidt,Irfan A. Bhatti,Barbara Grün,Nicolas Hohmann,Lena Woydack,Xin-Wen Zhang,Dyke Ferber,Andreas Mock,Tillmann Pompecki,Timo Schank,Guy Ungerechts +48 more
TL;DR: In this paper , adverse events and serum cytokines in patients with 23 different tumors undergoing or not undergoing COVID-19 vaccination under ICI therapy in a prospectively planned German single-center cohort study (n = 220).
A case of PAPASH syndrome in a young man carrying a novel heterozygote missense variant in PSTPIP1.
TL;DR: A 19-year-old man with recurrent ulcerated nodules on the lower extremities, neck, and torso was found to have multiple acne scars and pustules on his face and neck.
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Livedo racemosa in neurological diseases: an update on the differential diagnoses
TL;DR: The present review summarizes the most important central and peripheral neurological diseases in pediatric and adult age groups associated with livedo, providing physicians with an overview of the clinical presentation, etiology, diagnosis and management of these conditions.
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Cutaneous manifestations in Moyamoya angiopathy: A review.
TL;DR: Moyamoya angiopathy (MA) is a progressive cerebrovascular disease with a poorly understood pathophysiology as mentioned in this paper, it is mainly characterized by progressive bilateral stenosis of the terminal intracranial part of the supraclinoid internal carotid arteries and the proximal parts of the middle and anterior cerebral arteries, as well as the development of a fragile collateral network at the base of the brain.
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