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The Journal of Dermatology|October 13, 2023
Clinically relevant improvements in adults and adolescents with atopic dermatitis who did not achieve Investigator's Global Assessment treatment success following 8 weeks of ruxolitinib cream monotherapyEric L Simpson, Leon Kircik, Andrew Blauvelt, et al.
Clinicoeconomics and Outcomes Research : CEOR|April 20, 2026
Real-World Treatment Patterns in Patients with Atopic Dermatitis Initiating Ruxolitinib Cream: A 12-Month Follow-Up Analysis of a US Payer Claims DatabaseJinan Liu, Karishma Desai, Hung-Yuan P Chen, et al.
The Journal of Dermatological Treatment|February 1, 2024
Ruxolitinib cream monotherapy demonstrates rapid improvement in the extent and signs of mild to moderate atopic dermatitis across head and neck and other anatomic regions in adolescents and adults: pooled results from 2 phase 3 studiesEric L Simpson, Robert Bissonnette, Zelma C Chiesa Fuxench, et al.
Molecular Genetics and Metabolism|April 12, 2026
Truncated N-glycans destabilize POMT1 and POMT2 but do not limit cellular O-mannosylation in HEK293 cellsDaniel Sturm, Christina Hölscher, Ivan Andújar Martínez, et al.
American Journal of Clinical Dermatology|November 15, 2024
Ruxolitinib Cream Monotherapy Improved Symptoms and Quality of Life in Adults and Adolescents with Mild-to-Moderate Atopic Dermatitis: Patient-Reported Outcomes from Two Phase III StudiesEric L Simpson, Matthias Augustin, Diamant Thaçi, et al.
Dermatology and Therapy|February 12, 2026
Ruxolitinib Cream As-Needed Monotherapy Demonstrates Sustained Disease and Symptom Control in Patients with Mild to Moderate Atopic Dermatitis: Pooled Analysis from Two Phase 3 StudiesAndrew Blauvelt, Leon Kircik, Eric L Simpson, et al.
Human Molecular Genetics|August 23, 2022
Expression and subcellular localization of USH1C/harmonin in human retina provides insights into pathomechanisms and therapyKerstin Nagel-Wolfrum, Benjamin R Fadl, Mirjana M Becker, et al.
Journal of Neurology|December 12, 2024
Regional distribution of polymorphisms associated to the disease-causing gene of spinocerebellar ataxia type 3Tim Lukas Elter, Daniel Sturm, Magda M Santana, et al.
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