Results 81 to 90 of about 54,905 (262)

Primary biliary cirrhosis in early childhood - A rare case report. [PDF]

Int J Surg Case Rep, 2021
Ullah K, Uddin S, Dogar AW, Jan ZU, Abbas SH.   +4 more
europepmc   +1 more source

Primary biliary cirrhosis: an epidemiological study. [PDF]

, 1980

openalex   +1 more source

Hepatopulmonary syndrome in children and adolescents with portal hypertension in Brazil: A multicenter study

Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives To describe the clinical and laboratory characteristics and outcomes of pediatric hepatopulmonary syndrome (HPS) secondary to portal hypertension (PH) in Brazil. Methods Fifty‐four pediatric patients diagnosed with PH and HPS according to the European Respiratory Society criteria were included in this multicenter retrospective study.
Leticia Drumond Alberto, Eleonora Druve Tavares Fagundes, Adriana Teixeira Rodrigues, Thaís Costa Nascentes Queiroz, Gustavo Valverde de Castro, Carlos Oscar Kieling, Sandra Maria Gonçalves Vieira, Natália Lamounier dos Martires Guerra, Natascha Silva Sandy, Gilda Porta, Irene Kazue Miura, Maria Ângela Bellomo Brandão, Gabriel Hessel, Adriana Maria Alves de Tommaso, Alexandre Rodrigues Ferreira   +14 more
wiley   +1 more source

AMA production in primary biliary cirrhosis is promoted by the TLR9 ligand CpG and suppressed by potassium channel blockers [PDF]

, 2007
Yuki Moritoki, Zhe‐Xiong Lian, Heike Wulff, Guo–Xiang Yang, Ya‐Hui Chuang, Ruth Y. Lan, Yoshiyuki Ueno, Aftab A. Ansari, Ross L. Coppel, Ian R. Mackay, Eric M. Gershwin   +10 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

Toll-Like Receptors in Secondary Obstructive Cholangiopathy

Gastroenterology Research and Practice, 2011
Secondary obstructive cholangiopathy is characterized by intra- or extrahepatic bile tract obstruction. Liver inflammation and structural alterations develop due to progressive bile stagnation.
A. G. Miranda-Díaz, H. Alonso-Martínez, J. Hernández-Ojeda, O. Arias-Carvajal, A. D. Rodríguez-Carrizalez, L. M. Román-Pintos   +5 more
doaj   +1 more source

An uncommon case of primary biliary cirrhosis and Hashimoto thyroiditis followed by the concurrent onset of multiple sclerosis and Sjögren syndrome. [PDF]

Turk J Phys Med Rehabil, 2022
Güzel Ş, Özen S.
europepmc   +1 more source

Autoantibody signatures in children with celiac disease, juvenile idiopathic arthritis, and polyautoimmunity

JPGN Reports, EarlyView.
Abstract Objective To determine if multiplex autoantibody arrays can identify novel biomarker signatures in children with one or multiple autoimmune diseases (polyautoimmunity). Methods Plasma collected from children (18 years or younger) in the Boston Children's Hospital Precision Link Biobank for Health Discovery between January 2007 and June 2021 ...
Nan Du, Denis Chang, Madison Wong, Jay R. Thiagarajah, Erin Janssen, Lauren A. Henderson, Krishnan Raghunathan, Jocelyn A. Silvester   +7 more
wiley   +1 more source

Primary biliary cirrhosis associated with myasthenia gravis after postpartum: a case report. [PDF]

J Med Case Rep, 2021
Zhang L, Ding D, Yu L, Qi H, Han C, Jiang J, Jiang J.   +6 more
europepmc   +1 more source

The X-factor in primary biliary cirrhosis: monosomy X and xenobiotics [PDF]

, 2012
Ilaria Bianchi, Ana Lleó, Francesca Bernuzzi, Lisa Caliari, Dan S. Smyk, Pietro Invernizzi   +5 more
openalex   +1 more source