Results 171 to 180 of about 2,165,687 (231)

Geographic Diversity in the Incidence of Human Prion Diseases - China, 2006-2019. [PDF]

China CDC Wkly, 2023
Shi Q, Xiao K, Gao L, Wu Y, Zhou W, Liang D, Chen C, Dong X.   +7 more
europepmc   +1 more source

EUS‐Guided Choledochoduodenostomy Versus Hepaticogastrostomy in Case of Concomitant Gastric Outlet Obstruction Treated by EUS‐Guided Gastroenterostomy: A Systematic Review and Meta‐Analysis

United European Gastroenterology Journal, Volume 14, Issue 7, September 2026.
ABSTRACT Background Biliary (BO) and gastric outlet obstruction (GOO) frequently complicate pancreatic cancer, often delaying treatment. While EUS‐guided gastroenterostomy (EUS‐GE) is preferred over duodenal stenting for GOO, the optimal approach for biliary drainage (BD) between EUS‐guided choledochoduodenostomy (EUS‐CDS) and hepaticogastrostomy (EUS ...
Marco Spadaccini, Yen‐I Chen, Roberto Leone, Antonella Durante, Maria Margherita Massaro, Giuseppe Vanella, Maria Terrin, Matteo Colombo, Carlo Fabbri, Shannon Melissa Chan, Alessandro Fugazza, Roberto De Sire, Jeremie Albouys, Silvia Carrara, Jeremie Jacques, Daryl Ramai, Andrea Anderloni, Cesare Hassan, Paolo Giorgio Arcidiacono, Anthony Yuen Bun Teoh, Alessandro Repici, the BRIDGE study group   +21 more
wiley   +1 more source

Letter to the Editor Regarding Kortazar-Zubizarreta et al. 'The Risk of Transmission of Genetic Prion Diseases Is Greater Than 50%'. [PDF]

Eur J Neurol
Nihat A, Mok TH, Minikel EV, Collinge J, Mead S.   +4 more
europepmc   +1 more source

EUS‐Guided Gallbladder Drainage for Acute Cholecystitis in the Western World: Heterogeneity in Current Practice and the Relation With Patient Outcome

United European Gastroenterology Journal, Volume 14, Issue 7, September 2026.
ABSTRACT Background Laparoscopic cholecystectomy is the standard treatment for acute cholecystitis (AC), but some patients are unfit for (immediate) surgery. Endoscopic ultrasound‐guided gallbladder drainage (EUS‐GBD) using a lumen‐apposing metal stent (LAMS) is increasingly used in this population.
Louis De Wispelaere, Eva Hufkens, Hannah van Malenstein, Wim Laleman, Michiel Bronswijk, Schalk van der Merwe, Roberto Di Mitri, Michele Amata, Daniela Scimeca, Niels G. Venneman, Koen R. Beukema, Alberto Larghi, Antonio Pelegrino, Felice Molinario, Dominiek De Wulf, Elise Devolder, Dennis Yang, Mustafa Arain, Natalie Cosgrove, Muhammad K. Hasan, Maham Hayat, Kambiz Kadkhodayan, Christophe Snauwaert, Roberto Trasolini, Cynthuja Thilakanathan, Shirley Jiang, Douglas G. Adler, Lionel S. D'Souza, Rogier P. Voermans, Anouk G. Overdevest, Roy L. J. Van Wanrooij, Enrique Pérez‐Cuadrado‐Robles, Willem J. Lammers, Pieter Jan de Jonge, Marco J. Bruno, Helena Degroote, Thomas Billiet, Alexander Arlt, Sebastian Stefanovic, Emine Gökce, Ellen Deschepper, Pieter Hindryckx   +41 more
wiley   +1 more source

Prion Diseases-When Proteins Turn Lethal: Creutzfeldt-Jakob Disease (CJD) and the Quest for Classification, Diagnosis, Therapeutic Approaches, and Emerging Research. [PDF]

Molecules
Ramesh TS, Bartusik-Aebisher D, Dynarowicz K, Aebisher D.   +3 more
europepmc   +1 more source

Harmonized Acquisition of Connectome MRI and Clinical Data for Stroke, Parkinson's Disease and Glioma: Delphi‐Derived Protocol Recommendations by the European Academy of Neurology

European Journal of Neurology, Volume 33, Issue 9, September 2026.
In the context of the Horizon Europe EBRAINS 2.0 research consortium, Delphi‐derived, consented protocol recommendations from European Academy of Neurology Scientific Panel experts provide a pragmatic framework for harmonizing multi‐scale data acquisition for connectome analyses in stroke, Parkinson's Disease, and glioma.
Thomas Berger, Lorenzo Pini, Alessandro Salvalaggio, Simone Cauzzo, Christine Klein, Maria Lolich, Alberto Picca, Dauren Ramankulov, Maria A. Rocca, Roberta Rudà, Alessandro Sodero, Alessandro Tessitore, Thomas Truelsen, Roland Wiest, Gereon R. Fink, Elena Moro, Philippe Ryvlin, Maurizio Corbetta   +17 more
wiley   +1 more source

The Evolution of Experimental Rodent Models for Prion Diseases. [PDF]

J Neurochem
DeFranco JP, Telling GC.
europepmc   +1 more source

Etiology matters: genetic and acquired prion diseases engage different mechanisms at a presymptomatic stage. [PDF]

Neural Regen Res, 2023
Jackson WS.
europepmc   +1 more source

Proteostasis of organelles in aging and disease

The FEBS Journal, Volume 293, Issue 18, Page 5600-5626, September 2026.
Cells rely on regulated proteostasis mechanisms to keep their internal compartments functioning properly. When these mechanisms fail, damaged proteins accumulate, disrupting organelles, such as the nucleus, mitochondria, endoplasmic reticulum, Golgi, and lysosomes, as well as membraneless organelles, such as stress granules, processing bodies, the ...
Yara Nabawi, Cansu Doğan, Dunja Petrović, Gülce Perçin, Seda Koyuncu, David Vilchez   +5 more
wiley   +1 more source

Enhanced Sensitivity of a Modified Quaking-Induced Conversion Diagnostic Test for the Broad Detection of Sporadic and Inherited Prion Diseases: A Retrospective Study. [PDF]

Ann Neurol
Myskiw J, Fox R, Kielich DMS, Lamoureux L, Leonhardt M, Nykvist O, Slota JA, Avery K, Phillipson C, Frost K, Simon S, Appleby BS, Bailey-Elkin BA, Booth SA.   +13 more
europepmc   +1 more source