René Stevens

Mutations in APOPT1, Encoding a Mitochondrial Protein, Cause Cavitating Leukoencephalopathy with Cytochrome c Oxidase Deficiency

Laura Melchionda, Tobias B. Haack, Steven Hardy et al. · The American Journal of Human Genetics · 2014 · 77 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Blepharophimosis‐mental retardation (BMR) syndromes: A proposed clinical classification of the so‐called Ohdo syndrome, and delineation of two new BMR syndromes, one X‐linked and one autosomal recessive

Alain Verloès, Dominique Brémond‐Gignac, Bertrand Isidor et al. · American Journal of Medical Genetics Part A · 2006 · 74 citations

Medicine, Endocrinology, Genetics +17

Mutation of the iron‐sulfur cluster assembly gene <i>IBA57</i> causes fatal infantile leukodystrophy

François‐Guillaume Debray, Claudia Stümpfig, Arnaud Vanlander et al. · Journal of Inherited Metabolic Disease · 2015 · 52 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Incorporating Photography as a Therapeutic Tool in Counseling

René Stevens, Evans Spears · Journal of Creativity in Mental Health · 2009 · 32 citations

Education, Counseling, Photography +8

Polymerase gamma deficiency (POLG): Clinical course in a child with a two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh’s encephalopathy

Emmanuel Scalais, Baudouin François, Patrick Schlesser et al. · European Journal of Paediatric Neurology · 2012 · 26 citations

Medicine, Neurology, Pediatrics +11