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International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|November 6, 2010
Lymphadenectomy in uterine low-grade endometrial stromal sarcoma: an analysis of 19 cases and a literature reviewMauro Signorelli, Robert Fruscio, Tiziana Dell'Anna, et al.International Journal of Hyperthermia : the Official Journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group|August 12, 2009
Combination of hyperthermia and bortezomib results in additive killing in mantle cell lymphoma cellsValeria Milani, Monika Lorenz, Marc Weinkauf, et al.BMC Microbiology|May 9, 2020
Bifidobacterium mongoliense genome seems particularly adapted to milk oligosaccharide digestion leading to production of antivirulent metabolitesPauline Bondue, Christian Milani, Emilie Arnould, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|August 18, 2016
Anions as Triggers in Controlled Release Protocols from Mesoporous Silica Nanoparticles Functionalized with Macrocyclic Copper(II) ComplexesSameh El Sayed, Michele Milani, Chiara Milanese, et al.International Journal of Telerehabilitation|August 4, 2021
Telerehabilitation in Italy During the COVID-19 Lockdown: A Feasibility and Acceptability StudyGiada Milani, Giulia Demattè, Matilde Ferioli, et al.AIDS (London, England)|October 6, 1999
Extracellular HIV-1 Tat protein differentially activates the JNK and ERK/MAPK pathways in CD4 T cellsC Mischiati, F Pironi, D Milani, et al.Acta Geneticae Medicae Et Gemellologiae|January 1, 1975
A case of "g 2 deletion syndrome": ring or partial monosomy? (46,XX,22r or 46,XX,22p- ?)M Milani-Comparetti, V Rossolini, D P Pace, et al.Journal of Occupational Rehabilitation|November 18, 2016
Psychometric Properties of the Obstacles to Return-to-Work Questionnaire in a Brazilian contextDaniela Milani, Neusa Maria Costa Alexandre, Juliana Alvares Duarte Bonini Campos, et al.American Journal of Medical Genetics. Part A|December 27, 2016
Is cutis verticis Gyrata-Intellectual Disability syndrome an underdiagnosed condition? A case report and review of 62 casesArianna Tucci, Lidia Pezzani, Giulietta Scuvera, et al.Pediatric Neurology|March 18, 2014
Does the co-occurrence of FGFR3 gene mutation in hypochondroplasia, medial temporal lobe dysgenesis, and focal epilepsy suggest a syndrome?Antonino Romeo, Monica Lodi, Maurizio Viri, et al.Pageof 566