Eurorad
brought to you by the ESR
Brought to you by the
myESR
Login
Home
Advanced Search
Teaching Cases
Quizzes
FAQs
Contact Us
History
Submit a Case
About Us
Home
Advanced Search
Teaching Cases
Quizzes
FAQs
Contact Us
History
Submit a Case
About Us
Home
Advanced Search
Abdominal imaging
Neuroradiology
Paediatric radiology
Area of interest
0 selected
Clear all
Liver
(1)
Neuroradiology brain
(4)
Imaging Technique
1 selected
Clear all
Conventional radiography
(12)
CT
(26)
CT-High Resolution
(1)
Digital radiography
(4)
Experimental
(1)
Image manipulation / Reconstruction
(2)
Lymphography
(1)
Mammography
(2)
MR
(57)
MR-Angiography
(1)
MR-Diffusion/Perfusion
(8)
MR-Functional imaging
(1)
MR-Spectroscopy
(5)
Nuclear medicine conventional
(4)
Percutaneous
(2)
PET-CT
(1)
RIS
(2)
SPECT
(2)
Ultrasound
(9)
Procedure
0 selected
Clear all
Complications
(1)
Diagnostic procedure
(3)
Imaging sequences
(1)
Molecular imaging
(1)
Technical aspects
(1)
Teleradiology
(1)
Special Focus
1 selected
Clear all
Abscess
(2)
Acute
(4)
Congenital
(2)
Dilatation
(1)
Dysplasias
(1)
Genetic defects
(3)
Haemodynamics / Flow dynamics
(1)
Infection
(1)
Inflammation
(4)
Ischaemia / Infarction
(2)
Metabolic disorders
(5)
Neoplasia
(12)
Seizure disorders
(1)
Tissue characterisation
(1)
Trauma
(1)
Case Type
1 selected
Clear all
Clinical Cases
(5)
Editors Selection
0 selected
Clear all
No
(5)
Yes
(0)
Search options
Reset Search
Show filters
Sort cases by:
Section
Publishing date
Fulltext search
Sort by
Published on
Section
Order
Asc
Desc
Apply
5 Items
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke (melas) syndrome: a 2 year follow-up
# 15941
22.07.2018
Clinical Cases
Magnetic Resonace Imaging findings in a case of infantile Refsum disease
# 13640
06.07.2016
Clinical Cases
Maple syrup urine disease
# 11483
23.01.2014
Clinical Cases
A case of noninvasive diagnosis and evaluation of treatment in patient with non-alcoholic fatty liver disease (NAFLD) using localised proton MRI spectroscopy
# 10683
08.02.2013
Clinical Cases
Fatal infantile encephalopathy due to complex 1 deficiency – a mitochondrial DNA mutation disorder.
# 9584
16.07.2012
Clinical Cases
5 Items