H Syndrome: A Rare Genodermatosis Imaged With 18F-FDG PET/CT. (January 2018)
- Record Type:
- Journal Article
- Title:
- H Syndrome: A Rare Genodermatosis Imaged With 18F-FDG PET/CT. (January 2018)
- Main Title:
- H Syndrome
- Authors:
- Turpin, Sophie
Patey, Natalie
Beaudin, Marianne
Mitchell, Grant
Lambert, Raymond - Abstract:
- Abstract : Abstract: H syndrome (OMIM 612391) is an extremely rare autosomal recessive genodermatosis, characterized by extensive skin infiltration. We report a case imaged with 18 F-FDG PET/CT.
- Is Part Of:
- Clinical nuclear medicine. Volume 43:Number 1(2018)
- Journal:
- Clinical nuclear medicine
- Issue:
- Volume 43:Number 1(2018)
- Issue Display:
- Volume 43, Issue 1 (2018)
- Year:
- 2018
- Volume:
- 43
- Issue:
- 1
- Issue Sort Value:
- 2018-0043-0001-0000
- Page Start:
- Page End:
- Publication Date:
- 2018-01
- Subjects:
- 18F-FDG -- children -- H syndrome -- PET/CT -- Rosai-Dorfman -- SLC29A3 gene
Nuclear medicine -- Periodicals
Radioisotope scanning -- Periodicals
Nuclear Medicine -- Periodicals
616.07575 - Journal URLs:
- http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&NEWS=n&PAGE=toc&D=ovft&AN=00003072-000000000-00000 ↗
http://journals.lww.com/nuclearmed/pages/default.aspx ↗
http://journals.lww.com ↗ - DOI:
- 10.1097/RLU.0000000000001896 ↗
- Languages:
- English
- ISSNs:
- 0363-9762
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.314000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 8723.xml