Cranial Magnetic Resonance Imaging Mistakenly Suggests Prenatal Ischaemia in PEHO-Like Syndrome «
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12868478 | | Longman , tolmie , mcwilliam and maclennan describe two sisters with a peho-like syndrome , for the eldest of whom cranial magnetic resonance imaging revealed periventricular white matter changes , whilst cerebellar hypoplasia , characteristic of true peho syn |
Infantile Cerebello-Optic Atrophy «
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=8460530 | | Haltia and somer describe eight cases of the progressive encephalopathy syndrome with edema , hypsarrhythmia and optic atrophy (peho syndrome). |
Online Mendelian Inheritance in Man «
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=260565 | | Summarizes the current understanding of progressive encephalopathy with edema , hypsarrhythmia , and optic atrophy (peho syndrome). |
PEHO syndrome «
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=8301648 | | Somer describes a number of finnish cases. |
Progressive Encephalopathy with Edema, Hypsarrhythmia, and Optic Atrophy (PEHO syndrome) in Two Japanese Siblings «
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=8552220 | | Fujimoto et al report on two japanese siblings with peho syndrome (progressive encephalopathy with edema , hypsarrhythmia , and optic atrophy) , the first case report of peho syndrome outside finland. |
