Results 171 to 180 of about 124,113 (255)

Colchicine in patients with chronic inflammatory cardiomyopathy: rationale and design of the CMP-MYTHiC. [PDF]

ESC Heart Fail
Ammirati E, Cartella I, Ciabatti M, Colombo G, Masetti M, Pieroni M, Gallone G, Peretto G, Potena L, Scacciavillani R, Raineri C, Caputo A, Pedrotti P, Sormani P, Conti N, Merlo M, Imazio M, Pani A, Ciliberti ML, Gentile P, Pontone G, Villatore A, Pezzullo E, Palazzini M, Casella M, Valsecchi MG, Burzotta F, Carmina V, Garascia A, Scarale AF, Bernasconi DP, Loffredo FS, Narducci ML.   +32 more
europepmc   +1 more source

Exercise limitations in amyloid cardiomyopathy assessed by cardiopulmonary exercise testing—A multicentre study

ESC Heart Failure, Volume 12, Issue 2, Page 1326-1335, April 2025.
Abstract Aims Amyloid cardiomyopathy is caused by the deposition of light chain (AL) or transthyretin amyloid (ATTR) fibrils, that leads to a restrictive cardiomyopathy, often resulting in heart failure (HF) with preserved or reduced ejection fraction.
Robin Willixhofer, Mauro Contini, Michele Emdin, Damiano Magrì, Alice Bonomi, Elisabetta Salvioni, Fabrizio Celeste, Alberico Del Torto, Claudio Passino, Christophe D.J. Capelle, Chiara Arzilli, Emiliano Fiori, Nicolò Capra, Christina Kronberger, Nikita Ermolaev, Andreas Kammerlander, Beatrice Musumeci, Giuseppe Vergaro, Vincenzo Castiglione, René Rettl, Giacomo Tini, Andrea Baggiano, Iacopo Fabiani, Susanna Sciomer, Roza Badr Eslam, Piergiuseppe Agostoni   +25 more
wiley   +1 more source

Absence of SARS-CoV-2 in Placental Tissue After Maternal COVID-19.

JAMA Netw Open
Farhadian SF, Orlinick B, Milano KM, Mekael D, Kliman HJ.   +4 more
europepmc   +1 more source

Secondary Intention Healing of Extensive Nasal Defects: A Multimodal Approach to Optimize Esthetic Outcomes. [PDF]

Case Rep Dermatol Med
Ribas DBR, Garretto YTM, Ramos DG, Milano GI, de Oliveira GV.   +4 more
europepmc   +1 more source

A Hoveyda–Grubbs‐Type Olefin Metathesis Catalyst Bearing a Fluorinated Unsymmetrical NHC Ligand

European Journal of Inorganic Chemistry, EarlyView.
A fluorinated unsymmetrical NHC ruthenium complex was synthesised and employed as a catalyst for olefin metathesis reactions. The modification of the steric and electronic properties of the NHC ligand through the introduction of fluorine substituents results in improved activity but lower selectivity compared to the analogous non‐fluorinated NHC ...
Rubina Troiano, Concetta Liguori, Chiara Costabile, Fabia Grisi   +3 more
wiley   +1 more source

Study of prompt gamma and neutron emission for real-time range verification in proton and carbon-ion therapy. [PDF]

Med Phys
Bellotti ES, Mazzucconi D, Bortot D, Pola A, Fiorini C, Urban K, Agosteo S.   +6 more
europepmc   +1 more source

Understanding Online Health Information Consumption Through Web Analytics of the Italian Society of Pharmacology Magazine: 3-Year Descriptive Analysis. [PDF]

JMIR Form Res
Graziosi A, Santoni M, Cari L, Gozzo L, Crucitta S, Di Sotto A, Altamura C, Di Giacomo S, Rizzi L, Ruocco C, Bitto A, Sava G.   +11 more
europepmc   +1 more source

By‐product of heparin extraction as a sustainable alternative to enhance the use of nitrogen in agriculture

Environmental Progress &Sustainable Energy, EarlyView.
Abstract This study evaluates the potential of a new organic fertilizer derived from porcine intestinal mucosa (designated BHE), a by‐product of the heparin extraction process, as a sustainable nitrogen (N) source for agriculture. The work was conducted in two stages: (i) chemical and spectroscopic characterization of BHE compared with poultry litter ...
Aline Zanquetti, Felipe Augusto Bueno Rossi, Jonatas Thiago Piva, Larissa Macedo dos Santos‐Tonial   +3 more
wiley   +1 more source

Bone-marrow edema estimation with a microwave imaging open-ended coaxial probe array in ex vivo bovine long bones: comparison with CT. [PDF]

Eur Radiol Exp
Conti N, Giaccaglia P, Lidoni V, Rosa A, Sconfienza LM.   +4 more
europepmc   +1 more source

Management of ring chromosome 20 syndrome: Narrative review and consensus recommendations

Epilepsia, EarlyView.
Abstract Ring chromosome 20 (ring 20) is a rare genetic condition usually presenting as developmental and epileptic encephalopathy. The disease is caused by fusion of the long and short arms of chromosome 20. Patients are symptomatic even if there is no loss of genetic material.
Asma Khamis, Emilia Ricci, Maria Paola Canevini, Lieven Lagae, Kentaro Tokumoto, Yushi Inoue, Tim Buckinx, Allison Watson, Kenneth A. Myers   +8 more
wiley   +1 more source