Mathieu Milh - Publications
2010
Posterior glucose hypometabolism in Lafora disease: early and late FDG-PET assessment.
Jennesson M, Milh M, Villeneuve N, Guedj E, Marie PY, Vignal JP, Raffo E, Vespignani H, Mancini J, Maillard L.
Epilepsia, 2010, 51:708-711.
Neuromyelitis optica in France: a multicenter study of 125 patients.
Collongues N, Marignier R, Zéphir H, Papeix C, Blanc F, Ritleng C, Tchikviladzé M, Outteryck O, Vukusic S, Fleury M, Fontaine B, Brassat D, Clanet M, Milh M, Pelletier J, Audoin B, Ruet A, Lebrun-Frenay C, Thouvenot E, Camu W, Debouverie M, Créange A, Moreau T, Labauge P, Castelnovo G, Edan G, Le Page E, Defer G, Barroso B, Heinzlef O, Gout O, Rodriguez D, Wiertlewski S, Laplaud D, Borgel F, Tourniaire P, Grimaud J, Brochet B, Vermersch P, Confavreux C, de Seze J.
Neurology, 2010, 74:736-742.
Language disorders in children with morphologic abnormalities of the hippocampus.
Agostini G, Mancini J, Chabrol B, Villeneuve N, Milh M, George F, Maurel B B, Girard N.
Archives de Pédiatrie, 2010, sous presse.
Deletion of YWHAE in a patient with periventricular heterotopias and marked corpus callosum hypoplasia.
Mignon-Ravix C, Cacciagli P, El-Waly B, Moncla A, Milh M, Girard N, Chabrol B, Philip N, Villard L.
Journal of Medical Genetics, 2010, 47:132-136.
2009
Inhibitory actions of the gamma-aminobutyric acid in pediatric Sturge-Weber syndrome.
Tyzio R, Khalilov I, Represa A, Crepel V, Zilberter Y, Rheims S, Aniksztejn L, Cossart R, Nardou R, Mukhtarov M, Minlebaev M, Epsztein J, Milh M, Becq H, Jorquera I, Bulteau C, Fohlen M, Oliver V, Dulac O, Dorfmüller G, Delalande O, Ben-Ari Y, Khazipov R.
Annals of Neurology, 2009, 66:209-218.
LIS1-related isolated lissencephaly: spectrum of mutations and relationships with malformation severity.
Saillour Y, Carion N, Quelin C, Leger PL, Boddaert N, Elie C, Toutain A, Mercier S, Barthez MA, Milh M, Joriot S, des Portes V, Philip N, Broglin D, Roubertie A, Pitelet G, Moutard ML, Pinard JM, Cances C, Kaminska A, Chelly J, Beldjord C, Bahi-Buisson N.
Archives of Neurology, 2009, 66:1007-1015.
Transient brain magnetic resonance imaging hyperintensity in basal ganglia and brain stem of epileptic infants treated with vigabatrin.
Milh M, Villeneuve N, Chapon F, Pineau S, Lamoureux S, Livet MO, Bartoli C, Hugonenq C, Mancini J, Chabrol B, Girard N.
Journal of Child Neurology, 2009, 24:305-315.
Treatment of childhood convulsive status epilepticus: an update.
Milh M, Villeneuve N, Chabrol B.
Archives de Pédiatrie, 2009, 16:790-792.
Handicap: definition and classification.
Chabrol B, Halbert C, Milh M, Mancini J.
Archives de Pédiatrie, 2009, 16:912-914.
Epilepsy in the child.
Milh M, Chabrol B.
Revue du Praticien, 2009, 59:689-693.
2008
GLUT-1 deficiency syndrome or De Vivo disease: a case report.
Ticus I, Cano A, Villeneuve N, Milh M, Mancini J, Chabrol B.
Archives de Pédiatrie, 2008, 15:1296-1299.
Epileptic seizures in childhood: from seizure type to diagnosis.
Milh M, Ticus I, Villeneuve N, Hugonencq C, Mancini J, Chabrol B.
Archives de Pédiatrie, 2008, 15:216-222.
Key clinical features to identify girls with CDKL5 mutations.
Bahi-Buisson N, Nectoux J, Rosas-Vargas H, Milh M, Boddaert N, Girard B, Cances C, Ville D, Afenjar A, Rio M, Héron D, N'guyen Morel MA, Arzimanoglou A, Philippe C, Jonveaux P, Chelly J, Bienvenu T.
Brain, 2008, 131:2647-2661.
[GLUT-1 deficiency syndrome or De Vivo disease: a case report]
Ticus I, Cano A, Villeneuve N, Milh M, Mancini J, Chabrol B.
Archives de Pediatrie, 2008, 15:1296-1299.
2007
Inhibition of glutamate transporters results in a "suppression-burst" pattern and partial seizures in the newborn rat.
Milh M, Becq H, Villeneuve N, Ben-Ari Y, Aniksztejn L.
Epilepsia, 2007, 48:169-174.
Cell domain-dependent changes in the glutamatergic and GABAergic drives during epileptogenesis in the rat CA1 region.
El-Hassar L, Milh M, Wendling F, Ferrand N, Esclapez M, Bernard C.
The Journal of Physiology, 2007, 578:193-211.
Rapid cortical oscillations and early motor activity in premature human neonate.
Milh M, Kaminska A, Huon C, Lapillonne A, Ben-Ari Y, Khazipov R.
Cerebral Cortex, 2007, 17:1582-1594.
2006
Ongoing epileptiform activity in the post-ischemic hippocampus is associated with a permanent shift of the excitatory-inhibitory synaptic balance in CA3 pyramidal neurons.
Epsztein J, Milh M, Bihi RI, Jorquera I, Ben-Ari Y, Represa A, Crépel V.
Journal of Neuroscience, 2006, 26:7082-7092.
2005
Altering cannabinoid signaling during development disrupts neuronal activity.
Bernard C, Milh M, Morozov YM, Ben-Ari Y, Freund TF, Gozlan H.
Proc Natl Acad Sci U S A, 2005, 102:9388-9393.
2003
Effects of antiepileptic drugs on refractory seizures in the intact immature corticohippocampal formation in vitro.
Quilichini PP, Diabira D, Chiron C, Milh M, Ben-Ari Y, Gozlan H.
Epilepsia, 2003, 44:1365-1374.
Werner mesomelic dysplasia with Hirschsprung disease.
Goldenberg A, Milh M, de Lagausie P, Mesnage R, Benarif F, de Blois MC, Munnich A, Lyonnet S, Cormier-Daire V.
American Journal of Medical Genetics, 2003, 123:186-189.