Results 41 to 50 of about 1,160,128 (185)
Caroli′s syndrome with autosomal recessive polycystic kidney disease
Caroli′s syndrome (CS) is a rare congenital disorder characterized by multiple segmental cystic or saccular dilatations of the intrahepatic bile ducts and congenital hepatic fibrosis.
Prithi Shenoy +3 more
doaj +1 more source
Cholestatic liver diseases are a significant cause of morbidity and mortality and the leading indication for pediatric liver transplant. These include diseases such as biliary atresia, Alagille syndrome, progressive intrahepatic cholestasis entities ...
Alyssa Kriegermeier, Richard Green
doaj +1 more source
ABSTRACT Background and Aims Primary sclerosing cholangitis (PSC) and inflammatory bowel disease (IBD) represent a unique clinical syndrome affecting up to 80% of PSC patients, characterised by distinct epidemiological patterns, pathophysiological mechanisms and clinical outcomes that differ substantially from either condition occurring independently ...
Luisa Bertin +7 more
wiley +1 more source
A 40 years old woman with monolobar Caroli’s syndrome treated by left hepatic lobectomy
Caroli’s disease (CD) is a rare congenital abnormality characterized by dilatation of intra hepatic bile ducts, which causes stone formation, recurrent cholangitis and higher risk for biliary malignancy.
Hamid Tavakkoli +5 more
doaj
ABSTRACT Noonan syndrome (NS) is a rare multisystemic condition among the RASopathy group, characterized by a broad phenotypic spectrum and genetic variability. It results from pathogenic variants in genes regulating the RAS/MAPK pathway, affecting cell proliferation and differentiation.
Romain Martineau +10 more
wiley +1 more source
Water in Edo-Tokyo’s urban space
Issue 169/2021 di "Storia urbana" su "Water in Edo-Tokyo’s urban space" con contributi di: Rosa CAROLI, Inventing Edo, Rethinking Edo-Tokyo: Water and the City; Yuko TANAKA, Waterside Culture in Edo; Fumiko KOBAYASHI, Representations of Edo-Tōkyo ...
Caroli Rosa, Caroli, Rosa
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Right Hemithorax Empyema in a Known Case of Caroli Syndrome
Introduction: Caroli disease is a rare congenital disorder characterized by segmental, nonob-structive dilatation of intrahepatic bile ducts. The term Caroli syndrome is used for the asso-ciation of Caroli disease with congenital hepatic fibrosis.
Ramin Ebrahimian +2 more
doaj
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 +14 more
wiley +1 more source
Abstract The rapid evolution of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) has compromised the efficacy of many authorized monoclonal antibody products. This highlights the need for alternative strategies, especially for vulnerable populations such as immunocompromised individuals.
Ferran Abancó +16 more
wiley +1 more source
Maladie et syndrome de Caroli : Deux entités rares (à propos de 5 cas) [PDF]
La maladie de Caroli (MC) et le Syndrome de Caroli sont deux affections rares caractérisées par une ectasie canalaire congénitale segmentaire des voies biliaires intra-hépatiques (VBIH) :- Le syndrome de Caroli étant plus fréquent, souvent diffus ...
Ouazzani, Houria +4 more
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