Results 41 to 50 of about 222,722 (307)

Outcomes of 38 patients with PFIC3: Impact of genotype and of response to ursodeoxycholic acid therapy

open access: yesJHEP Reports, 2023
Background & Aims: Progressive familial intrahepatic cholestasis type 3 (PFIC3) is a rare liver disease caused by biallelic variations in ABCB4. Data reporting on the impact of genotype and of response to ursodeoxycholic acid (UDCA) therapy on long ...
Emmanuel Gonzales   +18 more
doaj  

Colonic Atresia Associated with Biliary Atresia

open access: yesJournal of Indian Association of Pediatric Surgeons, 2023
Colonic atresia (CA) is an uncommon type of intestinal atresia commonly associated with other anomalies, while biliary atresia (BA) is also rare but usually an isolated anomaly. The pathogenesis for either of the anomalies is unclear. The co-occurrence of both pathologies has not been mentioned in the literature.
Shailesh Solanki   +3 more
openaire   +3 more sources

Indications for pediatric liver transplantation [PDF]

open access: yes, 1987
Two hundred fifty pediatric (
Andreas G. Tzakis   +21 more
core   +1 more source

Pediatric Liver Transplantation: Then and Now [PDF]

open access: yes, 2020
This paper reviews the past 50 years of liver transplantation in children from the perspective of patient demographics, perioperative patient management, surgical techniques, immunosuppression and patient ...
Banh, DPT   +4 more
core   +1 more source

Role of high-frequency linear probe in ultrasound diagnosis of biliary atresia

open access: yesMedical Journal of Dr. D.Y. Patil University, 2014
Cause of cholestatic jaundice in early infancy continues to be a diagnostic dilemma, with biliary atresia being the most common cause. Increasing age is a negative prognostic factor for biliary atresia.
Sanjay Khaladkar   +3 more
doaj   +1 more source

Biliary Atresia

open access: yesSeminars in Pediatric Surgery, 2000
Although the prognosis of biliary atresia has been dramatically improved in the era of liver transplantation, the Kasai operation is still the first line of surgical treatment. Successful hepatic portoenterostomy depends on early diagnosis and surgery, adequate surgical technique, prevention of cholangitis, and precise postoperative management.
M, Nio, R, Ohi
openaire   +2 more sources

Diagnostic Imaging of Biliary Atresia

open access: yes대한영상의학회지, 2022
Biliary atresia is a rare but significant cause of neonatal cholestasis. An early and accurate diagnosis is important for proper management and prognosis.
Haesung Yoon   +3 more
doaj   +1 more source

Effects of cytomegalovirus infection on the differential diagnosis between biliary atresia and intrahepatic cholestasis in a Chinese large cohort study

open access: yesAnnals of Hepatology, 2021
Introduction and objectives: Differentiating biliary atresia from other causes of neonatal cholestasis is challenging, particularly when cytomegalovirus (CMV) and biliary atresia occur simultaneously.
Dongying Zhao   +6 more
doaj  

ATRESIA BILIER

open access: yesMajalah Kedokteran Andalas, 2009
AbstrakAtresia bilier merupakan penyakit yang jarang terjadi dan penyababnya belum diketahui secara pasti. Karakteristik dari penyakit ini adalah terjadinya inflamasi progresif pada duktus bilier sehingga terjadi obstruksi ekstrahepatal yang akhirnya ...
Julinar Julinar   +2 more
doaj   +1 more source

The Current Status of Liver Transplantation. [PDF]

open access: yes, 1971
More than thirty patients have now undergone liver transplantation in Denver, some more than once, and survivals of up to two and a half years have been achieved. Through this and other experience it has been learned that graft viability is more critical
Starzl, Thomas E
core   +1 more source

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