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Author/Creator Mignon-Ravix, Cécile

1. Deletion of YWHAE in a patient with periventricular heterotopias and pronounced corpus callosum hypoplasia. Issue 2 (26th July 2009)

Authors:
Mignon-Ravix, Cécile; Cacciagli, Pierre; El-Waly, Bilal; Moncla, Anne; Milh, Mathieu; Girard, Nadine; Chabrol, Brigitte; Philip, Nicole; Villard, Laurent
Journal:
Journal of medical genetics
Issue:
Volume 47:Issue 2(2010)
Page Start:
132
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Heterogeneity of FHF1 related phenotype: Novel case with early onset severe attacks of apnea, partial mitochondrial respiratory chain complex II deficiency, neonatal onset seizures without neurodegeneration. (September 2017)

Authors:
Villeneuve, Nathalie; Abidi, Affef; Cacciagli, Pierre; Mignon-Ravix, Cécile; Chabrol, Brigitte; Villard, Laurent; Milh, Mathieu
Journal:
European journal of paediatric neurology
Issue:
Volume 21:Number 5(2017:Sep.)
Page Start:
783
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗