Results 191 to 200 of about 8,404,331 (252)
Few Caregivers of Older Adults With Dementia Have Shared Access to Their Care Recipients' Electronic Health Record Portal. [PDF]
Southerland LT +4 more
europepmc +1 more source
ABSTRACT Asparaginase is a critical treatment component for patients with acute lymphoblastic leukemia/lymphoblastic lymphoma (ALL/LBL). However, the successful delivery of asparaginase‐based therapy remains challenging across care settings due to its complex administration, distinct toxicity profile, prolonged treatment duration, and the need for ...
Amir Ali +8 more
wiley +1 more source
Walled-off necrosis with portal vein fistula and arterial bleeding successfully treated without collection drainage: A case report. [PDF]
Marques LC +10 more
europepmc +1 more source
More Liver Volume Is Necessary for High Risk Living Donor Liver Transplantation Candidates
Annals of Gastroenterological Surgery, EarlyView.
Haruka Kobayashi +3 more
wiley +1 more source
ABSTRACT Background Exposures to human pathogens and toxins in licensed facilities in Canada have been monitored by a federal surveillance system since 2015, yet the affected persons (APs) in these incidents remain uncharacterized. This study comprehensively describes APs, highlighting sector‐specific patterns and trends over time.
Emily F. Tran +4 more
wiley +1 more source
Outcomes of a Modified Portal Venovenous Bypass Technique During Liver Transplantation in High-MELD Recipients. [PDF]
Megaly MG +10 more
europepmc +1 more source
ABSTRACT Progressive familial intrahepatic cholestasis (PFIC) is classically caused by biallelic pathogenic variants, yet monoallelic variants of uncertain significance (VUS) in PFIC‐associated genes are increasingly identified in children with cholestasis, creating diagnostic uncertainty.
Brett J. Hoskins +9 more
wiley +1 more source
Left-sided gallbladder associated with an accessory liver lobe and portal vein trifurcation encountered during laparoscopic cholecystectomy: a case report. [PDF]
Alamri H, Almowllad R, Alqahtani R.
europepmc +1 more source
ABSTRACT Biallelic variants in NSMCE2 (MMS21), which encodes the SUMO E3 ligase subunit of the SMC5/6 chromatin‐maintenance complex, have recently been implicated in microcephalic primordial dwarfism (MPD), corresponding to Seckel syndrome type 10 (OMIM #617246).
Cristina Peduto +5 more
wiley +1 more source

