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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.
The Quarterly Journal of Nuclear Medicine and Molecular Imaging : Official Publication of the Italian Association of Nuclear Medicine (AIMN) [And] the International Association of Radiopharmacology (IAR), [And] Section of the Society Of|February 20, 2010
(131)I-MIBG treatment of pheochromocytoma: low versus intermediate activity regimens of therapyM R Castellani, S Seghezzi, C Chiesa, et al.
The British Journal of Dermatology|July 7, 2023
Malignancy risk in patients with atopic dermatitis: a population-based cohort studyJoy Wan, Daniel B Shin, Maha N Syed, et al.
Journal (Canadian Dental Association)|January 1, 1996
Effects of a chlorhexidine varnish on the gingival status of adolescentsM I Valente, G Seabra, C Chiesa, et al.
Medical Physics|October 5, 2013
Molecular radiotherapy: the NUKFIT software for calculating the time-integrated activity coefficientP Kletting, S Schimmel, H A Kestler, et al.
International Journal of Oncology|May 3, 2011
Effect of specific activity on organ uptake of iodine-123-meta-iodobenzylguanidine in humansJ Farahati, M Lassmann, M Scheubeck, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|March 1, 1997
Effect of specific activity on cardiac uptake of iodine-123-MIBGJ Farahati, D Bier, M Scheubeck, et al.
Nuklearmedizin. Nuclear Medicine|October 17, 2007
[Procedure guidelines for radioiodine therapy of differentiated thyroid cancer (version 3)]M Dietlein, J Dressler, W Eschner, et al.
Anticancer Research|July 23, 1998
A simple and semi-automated system for increasing the recovery of aqueous [18F] fluoride from targetC Pascali, A Bogni, D Decise, et al.
Journal of Medical Genetics|August 19, 2008
A novel mutation in the sulfate transporter gene SLC26A2 (DTDST) specific to the Finnish population causes de la Chapelle dysplasiaL Bonafé, J Hästbacka, A de la Chapelle, et al.
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