biliary atresia/albumin

Lyen an sove nan clipboard la

Chwazi kalite sòt

Paj 1 soti nan 109 rezilta yo

Clinical significance of 99mTc-DTPA-galactosyl human serum albumin liver scintigraphy in follow-up patients with biliary atresia.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

OBJECTIVE Technetium 99m DTPA-galactosyl human serum albumin (GSA) liver scintigraphy was performed in follow-up patients with biliary atresia, and its clinical significance was investigated. METHODS Between 1994 and 2001, GSA liver scintigraphy was performed 153 times in 57 follow-up patients.

Using 99mTc-DTPA galactosyl human serum albumin liver scintigraphy as a prognostic indicator in jaundice-free patients with biliary atresia.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

BACKGROUND We evaluated the clinical significance of follow-up data, including 99mTc-DTPA galactosyl human serum albumin (99mTc-GSA) liver scintigraphy data, as prognostic indicators for jaundice-free patients with biliary atresia (BA). METHODS Of 87 patients who underwent Kasai portoenterostomy

Role of plasma thrombopoietin level in thrombocytopenia of postoperative biliary atresia patients.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

OBJECTIVE To evaluate if thrombocytopenia may be related to plasma thrombopoietin level (P-TPO) in postoperative biliary atresia (BA). METHODS Forty-three postoperative BA patients aged 1 to 20 years were included. P-TPO was measured by enzyme immunoassay. P-TPO was compared with platelet counts

Role of hepatic portocholecystostomy ('gallbladder Kasai') in treating infants with biliary atresia.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

The aim of this study is to compare liver function and cholangitis episodes during the first year postoperatively between patients who undergo hepatic portocholecystostomy (HPC) and patients who undergo hepatic portoenterostomy (HPE). Records of six patients who underwent HPC for biliary atresia

Liver transplantation in Japanese and Australian/New Zealand children with biliary atresia: a 10-year comparative study.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

OBJECTIVE To compare Japanese with Australian/New Zealand (ANZ) children with biliary atresia who were treated by liver transplantation, and evaluate the indications for and timing of transplantation. METHODS Retrospective study. METHODS Queensland Liver Transplant Service (QLTS),

Shear wave elastography for evaluation of the urgency of liver transplantation in pediatric patients with biliary atresia

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Background: To investigate the role of two-dimensional shear wave elastography (2D-SWE) in the preoperative evaluation of pediatric patients with biliary atresia awaiting liver transplantation. Methods:

Portal hypertensive gastropathy after surgery for biliary atresia.
Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo
Log In / Enskri

OBJECTIVE To clarify the correlation between portal hypertensive gastropathy (PHG) and clinical features after surgery for biliary atresia (BA). METHODS Routine upper gastrointestinal endoscopies were done over 3 years in 27 children who underwent surgery for BA. We reviewed the recorded endoscopic

Rapid progression of intrapulmonary arteriovenous shunting in polysplenia syndrome associated with biliary atresia.
Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo
Log In / Enskri

This report describes a patient with biliary atresia (BA) associated with polysplenia syndrome who showed a rapid progression of intrapulmonary arteriovenous shunting (IPS), resulting in a fatal outcome. Intrauterine ultrasonography at 36 weeks of gestation revealed fetal abnormalities, including

Long-term native liver fibrosis in biliary atresia: development of a novel scoring system using histology and standard liver tests.
Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo
Log In / Enskri

OBJECTIVE Although liver fibrosis is an important predictor of outcomes for biliary atresia (BA), postsurgical native liver histology has not been well reported. Here, we retrospectively evaluated postsurgical native liver histology, and developed and assessed a novel scoring system - the BA liver

Prediction of survival in extrahepatic biliary atresia by hepatic duplex sonography.
Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo
Log In / Enskri

BACKGROUND The clinical course of biliary atresia patients is extremely variable. To optimize conservative treatment and correctly schedule liver transplantation, noninvasive investigations that are predictive of individual survival and that can be performed regularly are needed. In this study, the

Portal vein dynamics in biliary atresia.
Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo
Log In / Enskri

A prospective sonographic investigation of portal vein caliber was done in 40 children with biliary atresia (n = 37) and biliary hypoplasia (n = 3) from 1 to 135 months old. The patients were divided into two groups according to hepatobiliary function (HBF). HBF was determined by serum bilirubin

Clinical benefit of liver stiffness measurement at 3 months after Kasai hepatoportoenterostomy to predict the liver related events in biliary atresia.
Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo
Log In / Enskri

BACKGROUND The progression of hepatic fibrosis may result in decompensated hepatic failure with cirrhosis, liver related events (LRE) such as ascites, variceal bleeding, and death after successful and timely Kasai hepatoportoenterostomy (HPE) in biliary atresia. The aim of this study is to suggest

Hepatocytes buried in the cirrhotic livers of patients with biliary atresia proliferate and function in the livers of urokinase-type plasminogen activator-NOG mice.
Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo
Log In / Enskri

The pathogenesis of biliary atresia (BA), which leads to end-stage cirrhosis in most patients, has been thought to inflame and obstruct the intrahepatic and extrahepatic bile ducts. BA is not believed to be caused by abnormalities in parenchymal hepatocytes. However, there has been no report of a

Plasma endothelin-1 level as a marker reflecting the severity of portal hypertension in biliary atresia.
Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo
Log In / Enskri

OBJECTIVE The aim of this study was to examine if the plasma endothelin-1 (ET-1), a potent vasoconstrictor, level may reflect the severity of portal hypertension associated with liver cirrhosis in biliary atresia (BA). METHODS Forty-eight postoperative BA patients aged 6 months to 20 years were

Association of serum levels of tissue inhibitors of metalloproteinase-1 with clinical outcome in children with biliary atresia.
Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo
Log In / Enskri

The purpose of this study was to determine the possible role of serum levels of tissue inhibitors of metalloproteinase-1 (TIMP-1) in the pathogenesis of the progressive inflammation and fibrosis in biliary atresia (BA). Serum concentrations of TIMP-1 were measured in 57 BA patients and 15 healthy

Previous
1
2
3
4
5
6
7
8
Next

Antre nan paj
facebook nou an
Herbal & Natural Medicine
Baz done ki pi konplè remèd fèy medsin te apiye nan syans
Travay nan 55 lang
Geri èrbal te apiye nan syans
Remèd fèy rekonesans pa imaj
Kat entèaktif GPS - tag zèb sou kote (vini byento)
Li piblikasyon syantifik ki gen rapò ak rechèch ou an
Search remèd fèy medsin pa efè yo
Izeganize enterè ou yo ak rete kanpe fè dat ak rechèch la nouvèl, esè klinik ak rive
Tape yon sentòm oswa yon maladi epi li sou remèd fèy ki ta ka ede, tape yon zèb ak wè maladi ak sentòm li itilize kont.
* Tout enfòmasyon baze sou rechèch syantifik pibliye

biliary atresia/albumin

Clinical significance of 99mTc-DTPA-galactosyl human serum albumin liver scintigraphy in follow-up patients with biliary atresia.

Using 99mTc-DTPA galactosyl human serum albumin liver scintigraphy as a prognostic indicator in jaundice-free patients with biliary atresia.

Role of plasma thrombopoietin level in thrombocytopenia of postoperative biliary atresia patients.

Role of hepatic portocholecystostomy ('gallbladder Kasai') in treating infants with biliary atresia.

Liver transplantation in Japanese and Australian/New Zealand children with biliary atresia: a 10-year comparative study.

Shear wave elastography for evaluation of the urgency of liver transplantation in pediatric patients with biliary atresia

Portal hypertensive gastropathy after surgery for biliary atresia.

Rapid progression of intrapulmonary arteriovenous shunting in polysplenia syndrome associated with biliary atresia.

Long-term native liver fibrosis in biliary atresia: development of a novel scoring system using histology and standard liver tests.

Prediction of survival in extrahepatic biliary atresia by hepatic duplex sonography.

Portal vein dynamics in biliary atresia.

Clinical benefit of liver stiffness measurement at 3 months after Kasai hepatoportoenterostomy to predict the liver related events in biliary atresia.

Hepatocytes buried in the cirrhotic livers of patients with biliary atresia proliferate and function in the livers of urokinase-type plasminogen activator-NOG mice.

Plasma endothelin-1 level as a marker reflecting the severity of portal hypertension in biliary atresia.

Association of serum levels of tissue inhibitors of metalloproteinase-1 with clinical outcome in children with biliary atresia.

Baz done ki pi konplè remèd fèy medsin te apiye nan syans