Results 51 to 60 of about 21,958 (289)

Drug delivery with carbon nanotubes for in vivo cancer treatment [PDF]

open access: yesCancer Res. 68 (2008) 6652-6660, 2008
Chemically functionalized single-walled carbon nanotubes (SWNTs) have shown promise in tumor targeted accumulation in mice and exhibit biocompatibility, excretion and little toxicity. Here, we demonstrate in-vivo SWNT drug delivery for tumor suppression in mice.
arxiv   +1 more source

Latent class mixed modelling for phenotypic stratification of primary biliary cholangitis patients on first line treatment [PDF]

open access: yesarXiv, 2022
In patients with primary biliary cholangitis (PBC), the serum liver biochemistry measured during treatment with ursodeoxycholic acid (the UDCA response) accurately predicts long-term outcome. In this study we sought to use liver biochemistry, and in particular alkaline phosphatase (ALP), as a surrogate marker of disease activity, for phenotypic ...
arxiv  

Overview of Biliary Atresia

open access: yes대한영상의학회지, 2022
Biliary atresia is a progressive, idiopathic, obliterative disease of the extrahepatic biliary tree that presents with biliary obstruction in the neonatal period. It is the most common indication for liver transplantation in children.
Tae Yeon Jeon
doaj   +1 more source

Cold-atmospheric plasma induces tumor cell death in preclinical in vivo and in vitro models of human cholangiocarcinoma [PDF]

open access: yesCancers, 12, 1280, 2020, 2020
Through the last decade, cold atmospheric plasma (CAP) has emerged as an innovative therapeutic option for cancer treatment. Recently, we have set up a potentially safe atmospheric pressure plasma jet device that displays antitumoral properties in a preclinical model of cholangiocarcinoma (CCA), a rare and very aggressive cancer emerging from the ...
arxiv   +1 more source

Biliary atresia with hyaline cartilage at the porta hepatis: a novel finding of undetermined significance: a case report [PDF]

open access: yes, 2018
Biliary atresia is an important cause of liver disease and morbidity in infants with unknown etiology. To date, only five cases of biliary atresia with hyaline cartilage at the porta hepatis have been described.
Batra, Vineeta V.   +4 more
core   +2 more sources

Biliary atresia.

open access: yesMayo Clinic Proceedings, 1998
Extrahepatic biliary atresia is an obliterative cholangiopathy that involves all or part of the extrahepatic biliary tree and, in many cases, the intrahepatic bile ducts. In the United States, from 400 to 600 new cases of biliary atresia are encountered annually.
openaire   +2 more sources

Novel NIR-II fluorescent probes for biliary atresia imaging

open access: yesActa Pharmaceutica Sinica B, 2023
Biliary atresia is a rare infant disease that predisposes patients to liver transplantation and death if not treated in time. However, early diagnosis is challenging because the clinical manifestations and laboratory tests of biliary atresia overlap with
Xiaodong Zeng   +9 more
doaj  

Obliterative cholangiopathy in acquired cystic biliary atresia type III after cyst perforation: a case report

open access: yesBMC Pediatrics, 2018
Background In biliary atresia, the disease process of obliterative cholangiopathy may begin in the perinatal period; however, no chronological evidence exists on how the cholangiopathy progresses to biliary obliteration.
Tsugumichi Koshinaga   +4 more
doaj   +1 more source

Embryonic Biliary Atresia in a Very-low-birth-weight Premature Infant

open access: yesJournal of the Formosan Medical Association, 2007
Two major forms of biliary atresia, the embryonic and perinatal type, are considered to have different pathogeneses and distinct prognoses. Embryonic biliary atresia is associated with worse prognosis.
Hung-Wen Chen   +6 more
doaj   +1 more source

Transplantation in children [PDF]

open access: yes, 1976
Kidney transplantation in very young children, less than 2 years of age, has usually failed, mainly because of difficulties maintaining these patients on hemodialysis long enough to permit retransplantation after loss of the original graft.
Charles W. Putnam   +15 more
core   +1 more source

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