Facioscapulohumeral muscular dystrophy is a slowly progressive but devastating myopathy
caused by loss of repression of the transcription factor DUX4; however, DUX4 expression is …

Facioscapulohumeral muscular dystrophy (FSHD) is a genetically dominant myopathy caused
by mutations that disrupt repression of the normally silent DUX4 gene, which encodes a …

… Toso1,2, Olivia O. Recht1,2, Anja Cucak1,2, Abhinav K Jain5, Michelle C. Barton5, and
Michael Kyba1,2 … Dixit, M., Ansseau, E., Tassin, A., Winokur, S., Shi, R., Qian, H., Sauvage, S …

Abstracts FSHD is a genetically dominant myopathy caused by mutations that cause expression
of the normally silent DUX4 gene. This transcription factor has been shown to interfere …

… Darko Bosnakovski, 1, 2, 3 Sunny SK Chan, 1, 2 Olivia O. Recht, 1, 2 Lynn M. Hartweck, 1,
2 Collin J. Gustafson, 1, 2 Laura L. …

Patients with acute myelogenous leukemia (AML) are at risk for thrombotic complications.
Risk to develop thrombosis is closely tied to leukemia subtype, and studies have shown an …

Background Alveolar rhabdomyosarcoma (aRMS) is a myogenic childhood sarcoma
frequently associated with a translocation-mediated fusion gene, Pax3:Foxo1a. Methods We …

Posterior glenohumeral instability and associated posterior labral lesions are less common
compared to anterior instability and lesions. Subluxations, or partial dislocations, occur more …

Purpose: To retrospectively evaluate the appearance of lesions of osseous and soft-tissue
structures of the glenohumeral joint on magnetic resonance (MR) images after first-time …

… Foreword by Olivia O’Leary … Foreword by Olivia O’Leary … Sometimes correspondents will
deliberately turn the tables on us, as Conor O’Clery of the Irish Times did reporting on the war in …