Cranial magnetic resonance imaging of Wolfram (DIDMOAD) syndrome
Author:
Publisher
Wiley
Subject
Radiology Nuclear Medicine and imaging
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1440-1673.2005.01420.x/fullpdf
Reference18 articles.
1. MRI of Wolfram syndrome (DIDMOAD)
2. Mitochondrial mutation commonly associated with Leber's hereditary optic neuropathy observed in a patient with Wolfram syndrome (DIDMOAD).
3. Growth hormone deficiency and empty sella in DIDMOAD syndrome: an endocrine study.
4. Juvenile Diabetes Mellitus and Optic Atrophy
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