Condition: ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3


rs1060499624 in RANBP2 gene and ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 PMID 19118815 2009 Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2.

PMID 2759111 1989 Haemorheologic studies in patients with reduced coronary vasodilator capacity but normal coronary angiogram (syndrome X).

PMID 21945312 2012 Immunomodulatory therapy in recurrent acute necrotizing encephalopathy ANE1: is it useful?

PMID 19811512 2010 Recurrent acute necrotizing encephalopathy following influenza A in a genetically predisposed family.

PMID 25522933 2015 RANBP2 mutation and acute necrotizing encephalopathy: 2 cases and a literature review of the expanding clinico-radiological phenotype.

PMID 26923722 2016 Variable clinical course in acute necrotizing encephalopathy and identification of a novel RANBP2 mutation.

PMID 27591117 2016 RANBP2 mutation in an Indian child with recurrent acute necrotizing encephalopathy.

PMID 20473521 2010 Untreated recurrent acute necrotising encephalopathy associated with RANBP2 mutation, and normal outcome in a Caucasian boy.

PMID 25128471 2014 Familial acute necrotizing encephalopathy due to mutation in the RANBP2 gene.

PMID 21205700 2011 Dominant encephalopathy mimicking mitochondrial disease.