Distal intestinal obstruction syndrome in the early postoperative period after lung transplantation in a patient with cystic fibrosis: Morphological findings on computed tomography [5]

K. Nassenstein; B. Schweiger; M. Kamler; J. Stattaus; T. Lauenstein; J. Barkhausen

doi:10.1136/gut.2005.075994

Distal intestinal obstruction syndrome in the early postoperative period after lung transplantation in a patient with cystic fibrosis: Morphological findings on computed tomography [5]

K. Nassenstein^*, B. Schweiger, M. Kamler, J. Stattaus, T. Lauenstein, J. Barkhausen

^*Corresponding author for this work

Clinic of Radiology and Nuclear Medicine

University of Duisburg-Essen

6 Citations (Scopus)

Original language	English
Journal	Gut
Volume	54
Issue number	11
Pages (from-to)	1662-1663
Number of pages	2
ISSN	0017-5749
DOIs	https://doi.org/10.1136/gut.2005.075994
Publication status	Published - 01.11.2005

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10.1136/gut.2005.075994

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title = "Distal intestinal obstruction syndrome in the early postoperative period after lung transplantation in a patient with cystic fibrosis: Morphological findings on computed tomography [5]",

author = "K. Nassenstein and B. Schweiger and M. Kamler and J. Stattaus and T. Lauenstein and J. Barkhausen",

year = "2005",

month = nov,

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doi = "10.1136/gut.2005.075994",

language = "English",

volume = "54",

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T1 - Distal intestinal obstruction syndrome in the early postoperative period after lung transplantation in a patient with cystic fibrosis

T2 - Morphological findings on computed tomography [5]

AU - Nassenstein, K.

AU - Schweiger, B.

AU - Kamler, M.

AU - Stattaus, J.

AU - Lauenstein, T.

AU - Barkhausen, J.

PY - 2005/11/1

Y1 - 2005/11/1

UR - https://www.scopus.com/pages/publications/27444434161

U2 - 10.1136/gut.2005.075994

DO - 10.1136/gut.2005.075994

M3 - Letters

C2 - 16227368

AN - SCOPUS:27444434161

SN - 0017-5749

VL - 54

SP - 1662

EP - 1663

JO - Gut

JF - Gut

IS - 11

ER -

Distal intestinal obstruction syndrome in the early postoperative period after lung transplantation in a patient with cystic fibrosis: Morphological findings on computed tomography [5]

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