✦ LIBER ✦

Dissecting pseudoaneurysm of the hepatic artery: A delayed complication of angioplasty in a liver transplant

✍ Scribed by Rubin Sheng; Philip D. Orons; Hector C. Ramos; Albert B Zajko

Publisher: Springer
Year: 1995
Tongue: English
Weight: 641 KB
Volume: 18
Category: Article
ISSN: 1432-086X
DOI: 10.1007/bf02807234

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Duodenal fistula: Complication of a pseu

Duodenal fistula: Complication of a pseudoaneurysm of the common hepatic artery

✍ Aggarwal, Shashi ;Berry, Manorama 📂 Article 📅 1988 🏛 Springer-Verlag 🌐 English ⚖ 634 KB

Color flow Doppler ultrasound diagnosis

Color flow Doppler ultrasound diagnosis of a pseudoaneurysm of the hepatic artery following liver transplantation

✍ Sylvia A. Worthy; Julie F. C. Olliff; Simon P. Olliff; John A. C. Buckels 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 514 KB

Use of a Multilayered Stent for the Trea

Use of a Multilayered Stent for the Treatment of Hepatic Artery Pseudoaneurysm After Liver Transplantation

✍ Ahmed M. Elsharkawy; Gourab Sen; Ralph Jackson; Robin Williams; John Rose; Mark 📂 Article 📅 2011 🏛 Springer 🌐 English ⚖ 357 KB

Hepatic arterial pseudoaneurysm: a rare

Hepatic arterial pseudoaneurysm: a rare complication of blunt abdominal trauma in children

✍ Karen E. Basile; C. J. Sivit; Peter B. Sachs; Anthony Stallion 📂 Article 📅 1999 🏛 Springer-Verlag 🌐 English ⚖ 254 KB

Stent-Graft for the Management of Hepati

Stent-Graft for the Management of Hepatic Artery Rupture Subsequent to Transcatheter Thrombolysis and Angioplasty in a Liver Transplant Recipient

✍ Koichiro Yamakado; Atsuhiro Nakatsuka; Haruyuki Takaki; Masanobu Usui; Hiroyuki 📂 Article 📅 2007 🏛 Springer 🌐 English ⚖ 183 KB

Liver transplantation for acute intermit

Liver transplantation for acute intermittent porphyria is complicated by a high rate of hepatic artery thrombosis

✍ Joanna K. Dowman; Bridget K. Gunson; Darius F. Mirza; Simon R. Bramhall; Mike N. 📂 Article 📅 2012 🏛 John Wiley and Sons 🌐 English ⚖ 379 KB

Acute intermittent porphyria (AIP) is an autosomal-dominant condition resulting from a partial deficiency of the ubiquitously expressed enzyme porphobilinogen deaminase. Although its clinical expression is highly variable, a minority of patients suffer recurrent life-threatening neurovisceral attack