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Budd-Chiari syndrome and liver transplantation

Budd-Chiari syndrome and liver transplantation

http://www.wikidata.org/entity/Q28083380

about

Budd- Chiari Syndrome as an Initial Manifestation of Systemic Lupus Erythematosus.Post-operative hypertension, a surrogate marker of the graft function and predictor of survival in living donor liver transplant recipients: A retrospective study.Living donor liver transplantation for Budd-Chiari syndrome: Overcoming a troublesome situation Budd-Chiari Syndrome: A focus on surgical treatment.An updated systematic review of the evolution of ALPPS and evaluation of its advantages and disadvantages in accordance with current evidence.Diagnosis and treatment guidelines for aberrant portal hemodynamics: The Aberrant Portal Hemodynamics Study Group supported by the Ministry of Health, Labor and Welfare of Japan.Outcomes of endovascular interventional therapy for primary Budd-Chiari syndrome caused by hepatic venous obstruction

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P2860

Budd-Chiari syndrome and liver transplantation

http://www.wikidata.org/entity/Q28083380

description

2015 nî lūn-bûn

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2015 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի փետրվարին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

@zh-hk

2015年論文

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2015年論文

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2015年论文

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name

Budd-Chiari syndrome and liver transplantation

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Budd-Chiari syndrome and liver transplantation

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Budd-Chiari syndrome and liver transplantation

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type

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Budd-Chiari syndrome and liver transplantation

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Budd-Chiari syndrome and liver transplantation

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Budd-Chiari syndrome and liver transplantation

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Budd-Chiari syndrome and liver transplantation

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Budd-Chiari syndrome and liver transplantation

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Budd-Chiari syndrome and liver transplantation

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IRDR.2014.01031

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Intractable & Rare Diseases Research

P1476

Budd-Chiari syndrome and liver transplantation

@en

P2093

Akamatsu N

http://www.w3.org/2001/XMLSchema#string

Kokudo N

http://www.w3.org/2001/XMLSchema#string

Sugawara Y

http://www.w3.org/2001/XMLSchema#string

P2860

A 27-year experience with surgical treatment of Budd-Chiari syndrome

Managing Budd-Chiari syndrome: a retrospective review of percutaneous hepatic vein angioplasty and surgical shunting

A model to predict poor survival in patients undergoing transjugular intrahepatic portosystemic shunts

A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera

Factor V Leiden related Budd-Chiari syndrome

Transection of the oesophagus for bleeding oesophageal varices.

Determinants of survival and the effect of portosystemic shunting in patients with Budd-Chiari syndrome.

Prevalence of inherited antithrombin, protein C, and protein S deficiencies in portal vein system thrombosis and Budd-Chiari syndrome: a systematic review and meta-analysis of observational studies.

Prevalence of the activating JAK2 tyrosine kinase mutation V617F in the Budd-Chiari syndrome.

Membranous obstruction of the inferior vena cava (obliterative hepatocavopathy, Okuda).

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24-32

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scholarly article

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1521905

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10.5582/IRDR.2014.01031

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1

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272188201

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25674385

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liver transplantation

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4322592

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