P
Pontus Harten
Researcher at University of Kiel
Publications - 14
Citations - 2048
Pontus Harten is an academic researcher from University of Kiel. The author has contributed to research in topics: Histoplasmosis & Lupus erythematosus. The author has an hindex of 6, co-authored 14 publications receiving 1856 citations.
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Journal ArticleDOI
The American College of Rheumatology nomenclature and case definitions for neuropsychiatric lupus syndromes
Matthew H. Liang,Michael Corzillius,Sang Cheol Bae,Robert A. Lew,Paul R. Fortin,Caroline Gordon,David A. Isenberg,Graciela S. Alarcón,Karin V. Straaton,Judah A. Denburg,Susan D. Denburg,John M. Esdaile,Bonnie I. Glanz,Elizabeth W. Karlson,Shahram Khoshbin,Malcolm P. Rogers,Peter H. Schur,John G. Hanly,Elizabeth Kozora,Sterling G. West,Robert G. Lahita,Michael D. Lockshin,Joseph M. McCune,Patricia M. Moore,Michelle Petri,W. Neal Roberts,Jorge Sánchez-Guerrero,Martin Veilleux,Robin L. Brey,Wayne D. Cornblath,Christopher M. Filley,John D. Fisk,Pontus Harten,Elaine M. Hay,Grant L. Iverson,Steven R. Levine,Elizabeth Waterhouse,Daniel J. Wallace,John B. Winer +38 more
TL;DR: The American College of Rheumatology Nomenclature for NPSLE provides case definitions for 19 neuropsychiatric syndromes seen in SLE, with reporting standards and recommendations for laboratory and imaging tests.
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Treatment-free remission in severe systemic lupus erythematosus following synchronization of plasmapheresis with subsequent pulse cyclophosphamide.
TL;DR: The results demonstrate that treatment-free clinical remission can be achieved in some patients with severe SLE.
Journal ArticleDOI
Multiple Organ Manifestations in Thromboangiitis Obliterans (Buerger's Disease) A Case Report:
TL;DR: A case of TAO with multiple organ involvement, including myocardial, splenic, and cerebral infarctions; pulmonary embolisms; and probable intestinal ischemia during a twenty-three-year course is reported.
Journal ArticleDOI
Disseminated histoplasmosis in a non-immunocompromised host.
TL;DR: A case of acute disseminated histoplasmosis in a young, nonimmunocompromised European woman who was severely ill with fever, lymphadenopathy, anemia, thrombocytopenia, hepatosplenomegaly, and polyserositis is described.
Journal ArticleDOI
FabryScan: a screening tool for early detection of Fabry disease
Kathrin Arning,Dennis Naleschinski,R. Maag,Marieke Biegstraaten,Peter Kropp,Jürgen Lorenzen,Carla E. M. Hollak,Ivo N. van Schaik,Pontus Harten,R Zeuner,Andreas Binder,Ralf Baron +11 more
TL;DR: The FabryScan is a combination of a brief and simple questionnaire with three simple bedside tests with good discriminative value for the identification of Fabry patients in patients with chronic extremity pain.