Results 281 to 290 of about 829,213 (404)

Prolonged bile duct obstruction: a new experimental model for cirrhosis in the rat.

, 1984
J Kountouras, Barbara H. Billing, P. J. Scheuer   +2 more
openalex   +1 more source

DOCK8 deficiency presenting with sclerosing cholangitis, raised immunoglobulin E, and bronchiectasis: A fatal pediatric case report

JPGN Reports, EarlyView.
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, Kelechi Ugonna, Stephen Hughes, Sanjay Rajwal, Marumbo Mtegha   +4 more
wiley   +1 more source

Management of Iatrogenic Bile-Duct Injury After Cholecystectomy, 1995-2025: Systematic Review and Meta-Analysis. [PDF]

Life (Basel)
Piriianu C, Toma EA, Enciu O, Ardelean M, Miron A, Calu V.   +5 more
europepmc   +1 more source

A rare case of pediatric autoimmune pancreatitis and autoimmune hepatitis in a patient with sickle cell disease

JPGN Reports, EarlyView.
Abstract Concurrent pediatric autoimmune pancreatitis (AIP) and autoimmune hepatitis (AIH) are rarely reported, and no established pediatric‐specific guidelines are available to guide the diagnosis and management of these conditions in children. While AIP and AIH share an underlying autoimmune mechanism of injury, marked by chronic inflammatory changes
Sasha‐Jane Abi‐Aad, Michelle Edward, David Germain, Rene Gomez‐Esquivel, Racha Khalaf   +4 more
wiley   +1 more source

Randomized trial of endoscopic sphincterotomy with balloon dilation versus endoscopic sphincterotomy alone for removal of bile duct stones.

Gastroenterology, 2013
A. Teoh, F. Cheung, Bing Hu, Ya-min Pan, L. Lai, P. Chiu, S. Wong, F. Chan, J. Lau   +8 more
semanticscholar   +1 more source

Atezolizumab-induced vanishing bile duct syndrome: a case report. [PDF]

Front Oncol
Noblejas Quiles CT, Macías Cerrolaza JA, Benitez Fuentes JD, López Gómez L, Sánchez Cánovas M, Nevado Rodríguez M, Martín Cascón M, Vigueras Campuzano I, Chaves Benito A, Lázaro Sánchez AD.   +9 more
europepmc   +1 more source

Maralixibat for the treatment of severe xanthomas in two children with Alagille syndrome: Case reports

JPGN Reports, EarlyView.
Abstract Alagille syndrome (ALGS) is a rare, autosomal dominant disorder which presents with a broad range of clinical manifestations, including cholestatic pruritus. A unique manifestation of ALGS is the presence of xanthomas in 24%–42% of patients, which can lead to liver transplantation.
Geetanjali Bora, Ruben E. Quiros‐Tejeira, Bernadette Vitola   +2 more
wiley   +1 more source

Cholangioscopy-guided laser lithotripsy alongside a plastic stent for common bile duct stones after total gastrectomy. [PDF]

Endoscopy
Soma R, Miwa H, Endo K, Oishi R, Suzuki Y, Tsuchiya H, Maeda S.   +6 more
europepmc   +1 more source