Results 271 to 280 of about 113,177 (334)
ABSTRACT Background Between 2002 and 2013, we performed pancreatoduodenectomy (PD) with combined resection of the superior mesenteric artery (SMA) (PD‐SMAR) to treat locally advanced pancreatic head cancer (PHC). Since 2011, we have performed PD with circumferential lymph node dissection along the SMA (PD‐CLDS), in which we dissected lymph nodes all ...
Isamu Makino +9 more
wiley +1 more source
Motion Mitigation Techniques for Abdominal and Cardiac MR Imaging
ABSTRACT MRI of the heart and abdominal organs provides unparalleled soft tissue contrast and quantitative biomarkers, yet remains highly susceptible to physiological motion. Contractions of the myocardium, respiratory excursions, peristalsis, vascular pulsatility, and unpredictable bulk patient movement generate artifacts that impair image quality ...
Eric M. Schrauben +3 more
wiley +1 more source
Donor noradrenaline use is associated with better allograft survival in recipients of pancreas transplantation. [PDF]
Shapey IM +6 more
europepmc +1 more source
This case series evaluated the clinical utility of [99mTc]Tc‐MAG3 renal scintigraphy in managing malignant ureteral obstruction (MUO). Renal scintigraphy‐guided decision‐making allowed safe conservative management in selected patients, particularly those with a non‐functional excretion pattern, and helped avoid unnecessary urinary drainage.
Akira Ohtsu +11 more
wiley +1 more source
Abstract Extraintestinal manifestations (EIMs) manifest in 6%‐47% of patients with inflammatory bowel disease (IBD). Here, we characterize the course of EIMs in pediatric patients receiving vedolizumab included in the VedoKids cohort study. This was a subgroup analysis of the pediatric VedoKids cohort, a multicenter, prospective study of children (aged
Giulia D'Arcangelo +11 more
wiley +1 more source
Abstract Dedicator of cytokinesis 8 (DOCK8) deficiency is a rare autosomal recessive primary immunodeficiency. Patients with DOCK8 deficiency typically present at early age with allergic manifestations, cutaneous and respiratory infections, raised immunoglobulin E, and they have an increased risk of developing malignancies.
Natalia Nedelkopoulou +4 more
wiley +1 more source
Expanding the genotypic spectrum of PCSK1 deficiency: A novel mutation in severe neonatal diarrhea
Abstract Among congenital diarrhea and enteropathies (CODEs), proprotein convertase subtilisin/kexin type 1 (PCSK1) deficiency is a rare monogenic disorder, associated with severe neonatal diarrhea and polyendocrinopathies. We report an 18‐day‐old male neonate, born to consanguineous parents, presenting with persistent watery diarrhea, metabolic ...
Eleonora Saraceno +7 more
wiley +1 more source
Bone marrow chimerism and pancreatic islet grafts [PDF]
Ildstad, ST, Ricordi, C, Starzl, TE
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