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Handbook of Clinical Neurology|April 30, 2013
Respiratory chain deficienciesPascale Delonlay, Agnes Rötig, Harvey B Sarnat
Molecular Genetics and Metabolism|October 3, 2002
Coenzyme Q(10) and idebenone in the therapy of respiratory chain diseases: rationale and comparative benefitsVanna Geromel, Niklas Darin, Dominique Chrétien, et al.
Developmental Medicine and Child Neurology|January 19, 2008
Transient magnetic resonance diffusion abnormalities in West syndrome: the radiological expression of non-convulsive status epilepticus?Isabelle Desguerre, Ixtasu Marti, Vassili Valayannopoulos, et al.
Molecular Genetics and Metabolism|March 23, 2005
Pyruvate carboxylase deficiency: clinical and biochemical response to anaplerotic diet therapyFanny Mochel, Pascale DeLonlay, Guy Touati, et al.
The Journal of Clinical Endocrinology and Metabolism|March 24, 2005
Respiratory chain defects may present only with hypoglycemiaFanny Mochel, Abdelhamid Slama, Guy Touati, et al.
Developmental Medicine and Child Neurology|August 23, 2014
Seizures and epilepsy in hypoglycaemia caused by inborn errors of metabolismSvetlana Gataullina, Pascale Delonlay, Eric Lemaire, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|December 17, 2002
Massive subdural haematomas in Menkes disease mimicking shaken baby syndromeMarie-Cécile Nassogne, Mark Sharrard, Lucie Hertz-Pannier, et al.
Epilepsia|March 4, 2010
Epileptic phenotypes in children with respiratory chain disordersSandra El Sabbagh, Anne-Sophie Lebre, Nadia Bahi-Buisson, et al.
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