ABSTRACT Renal impairment (RI), defined as estimated glomerular filtration rate less than 60 mL/min with or without the need for dialysis, is a frequent and severe complication in patients with relapsed/refractory multiple myeloma (RRMM), as it can affect patient prognosis, drug metabolism and treatment options.
Ioannis Ntanasis‐Stathopoulos +7 more
wiley +1 more source
Integration of detection and tracking networks for automated rib multiplanar reconstruction: a feasibility study for fracture diagnosis. [PDF]
Wen D +7 more
europepmc +1 more source
Hepatic Glycogen Storage Diseases in Brazil: A Multicenter Study
ABSTRACT To describe clinical and laboratory characteristics, emphasizing the evolution of patients with hepatic glycogen storage diseases (GSDs) followed in Brazilian reference centers. Multicenter, retrospective study involving 13 centers, using RedCap platform. 132 patients were included: 63 (47.8%) GSD type I (56 Ia, 7 Ib), 13 (9.8%) with type III (
Mariana Pena Costa +23 more
wiley +1 more source
Asymptomatic Rare Rib Anomalies: Bifid Rib and Rib Fusion
openaire +2 more sources
Isogeometric analysis of wing structures using multipatch parametrization and penalty-based coupling method. [PDF]
Wang D, Cao X, Xue Y, Wang W, Du X.
europepmc +1 more source
ABSTRACT People with Phelan–McDermid syndrome (PMS) have reduced speech and language abilities, yet little research has profiled the communication abilities in this population. The purpose of this study was threefold: identifying the language and communication profiles of school‐aged children with PMS, identifying genetic contributions to language and ...
Sarah Quadri‐Valverde +12 more
wiley +1 more source
<i>Bicharracosaurus dionidei,</i> gen. et sp. nov., a new macronarian (Dinosauria, Sauropoda) from the Late Jurassic Cañadón Calcáreo Formation of Argentina and the problematic early evolution of macronarians. [PDF]
Reutter A +4 more
europepmc +1 more source
Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet +10 more
wiley +1 more source
Congenital first and second rib fusion causing neurogenic thoracic outlet syndrome in an adolescent. [PDF]
Sharma DS, Negmadjanov U, Chang KZ.
europepmc +1 more source
On a New Exogyra from the Del Rio Clay and some Observations on the Evolution of Exogyra in the Texas Cretaceous [PDF]
University of Texas at Austin
core +1 more source

