Correlated bursts of activity in the neonatal hippocampus in vivo.
Leinekugel X, Khazipov R, Cannon R, Hirase H, Ben-Ari Y, Buzsáki G - Science (New York, N.Y.) - Jun 2002
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Clinical and genetic analysis of a new multigenerational pedigree with GEFS+ (Generalized Epilepsy with Febrile Seizures Plus).
Gérard F, Pereira S, Robaglia-Schlupp A, Genton P, Szepetowski P - Epilepsia - Jun 2002
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Chronic morphine treatment alters endogenous opioid control of hippocampal mossy fiber synaptic transmission.
Harrison JM, Allen RG, Pellegrino MJ, Williams JT, Manzoni OJ - Journal of neurophysiology - Mai 2002
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Correlative fluorescence and electron microscopy of biocytin-filled neurons with a preservation of the postsynaptic ultrastructure.
Morozov Y, Khalilov I, Ben-Ari Y, Represa A - Journal of neuroscience methods - Mai 2002
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A locus for bilateral perisylvian polymicrogyria maps to Xq28.
Villard L, Nguyen K, Cardoso C, Martin CL, Weiss AM, Sifry-Platt M, Grix AW, Graham JM, Winter RM, Leventer RJ, Dobyns WB - American journal of human genetics - Avr 2002
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Discharge patterns of hypoglossal motoneurons during fictive breathing, coughing, and swallowing.
Roda F, Gestreau C, Bianchi AL - Journal of neurophysiology - Avr 2002
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Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation.
Rio M, Molinari F, Heuertz S, Ozilou C, Gosset P, Raoul O, Cormier-Daire V, Amiel J, Lyonnet S, Le Merrer M, Turleau C, de Blois MC, Prieur M, Romana S, Vekemans M, Munnich A, Colleaux L - Journal of medical genetics - Avr 2002
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Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse.
De Sandre-Giovannoli A, Chaouch M, Kozlov S, Vallat JM, Tazir M, Kassouri N, Szepetowski P, Hammadouche T, Vandenberghe A, Stewart CL, Grid D, Lévy N - American journal of human genetics - Mar 2002
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