Search Results - "Pedespan, JM"

Clinical Characteristics of Subependymal Giant Cell Astrocytoma in Tuberous Sclerosis Complex by Jansen, Anna C, Belousova, Elena, Benedik, Mirjana P, Carter, Tom, Cottin, Vincent, Curatolo, Paolo, Dahlin, Maria, D'Amato, Lisa, d'Augères, Guillaume Beaure, de Vries, Petrus J, Ferreira, José C, Feucht, Martha, Fladrowski, Carla, Hertzberg, Christoph, Jozwiak, Sergiusz, Lawson, John A, Macaya, Alfons, Marques, Ruben, Nabbout, Rima, O'Callaghan, Finbar, Qin, Jiong, Sander, Valentin, Sauter, Matthias, Shah, Seema, Takahashi, Yukitoshi, Touraine, Renaud, Youroukos, Sotiris, Zonnenberg, Bernard, Kingswood, John C

“…This study evaluated the characteristics of subependymal giant cell astrocytoma (SEGA) in patients with tuberous sclerosis complex (TSC) entered into the…”
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Infantile Alexander Disease: Spectrum of GFAP Mutations and Genotype-Phenotype Correlation by Rodriguez, Diana, Gauthier, Fernande, Bertini, Enrico, Bugiani, Marianna, Brenner, Michael, N'guyen, Sylvie, Goizet, Cyril, Gelot, Antoinette, Surtees, Robert, Pedespan, Jean-Michel, Hernandorena, Xavier, Troncoso, Monica, Uziel, Graziela, Messing, Albee, Ponsot, Gérard, Pham-Dinh, Danielle, Dautigny, André, Boespflug-Tanguy, Odile

“…Heterozygous, de novo mutations in the glial fibrillary acidic protein ( GFAP) gene have recently been reported in 12 patients affected by neuropathologically…”
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Interferon-β treatment in patients with childhood-onset multiple sclerosis by Mikaeloff, Yann, Moreau, Thibault, Debouverie, Marc, Pelletier, Jean, Lebrun, Christine, Gout, Olivier, Pedespan, Jean-Michel, Van Hulle, Catherine, Vermersch, Patrick, Ponsot, Gérard

“…We present a report of the use of interferon-β before 18 years of age in 16 patients with childhood-onset multiple sclerosis. This study demonstrated that the…”
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Topiramate: efficacy and tolerability in children according to epilepsy syndromes by Mikaeloff, Yann, Saint-Martin, Anne de, Mancini, Josette, Peudenier, Sylviane, Pedespan, Jean-Michel, Vallée, Louis, Motte, Jacques, Bourgeois, Marie, Arzimanoglou, Alexis, Dulac, Olivier, Chiron, Catherine

“…To evaluate the efficacy and tolerability of topiramate (TPM) as add-on therapy in children less than 12 years of age with refractory epilepsy, according to…”
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Acceptability and tolerance of sodium valproate, a new sustained-action granule formulation, in monotherapy for epileptic children from 3 years old by Motte, J, Pedespan, J M, Sevestre, M, Chiron, C

“…Sodium valproate (VPA) is an anti-epileptic drug which was until now administered to children as drinkable or injectable form. A new galenic form of this…”
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Absence epilepsies by Loiseau, P, Duché, B, Pédespan, J M

“…Individuals fulfilling diagnostic criteria for childhood absence epilepsy (CAE) and juvenile absence epilepsy (JAE) were selected from a large group of…”
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Schizencephaly: clinical and imaging features in 30 infantile cases by Denis, Delphine, Chateil, Jean-François, Brun, Muriel, Brissaud, Olivier, Lacombe, Didier, Fontan, Daniel, Flurin, Véronique, Pedespan, Jean-Michel

“…Schizencephaly is an uncommon structural disorder of cerebral cortical development, characterized by congenital clefts spanning the cerebral hemispheres from…”
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MRI and clinical differences between optic pathway tumours in children with and without neurofibromatosis by Chateil, J F, Soussotte, C, Pédespan, J M, Brun, M, Le Manh, C, Diard, F

“…The purpose of this study was to evaluate the value of MRI in studying optic pathway tumours associated with neurofibromatosis, and to look for potentially…”
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Pulsed dye laser for Sturge–Weber syndrome by Léauté-Labréze, C, Boralevi, F, Pedespan, J-M, Meymat, Y, Taïeb, A

“…Port wine stain of Sturge–Weber syndrome represents a cosmetic prejudice with social consequences. We have treated eight patients with a 585 nm pulsed dye…”
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Hereditary neuralgic amyotrophy: a paediatric and familial presentation of Parsonage-Turner syndrome by Husson, M, Goizet, C, Rivera, S, Lacombe, D, Pedespan, J M

“…Hereditary neuralgic amyotrophy is a rare disorder, characterized by recurrent attacks of pain in a brachial plexus distribution. We report the case of a…”
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Prenatal diagnosis of schizencephaly by fetal magnetic resonance imaging by Denis, D, Maugey-Laulom, B, Carles, D, Pedespan, J M, Brun, M, Chateil, J F

“…Schizencephaly is a neuronal migration anomaly characterized by gray matter lined clefts extending from the ventricle to the cortical surface leading to…”
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X-linked myopathy with excessive autophagy: a clinicopathological study of five new families by Chabrol, B., Figarella-Branger, D., Coquet, M., Mancini, J., Fontan, D., Pedespan, J.M., Francannet, C., Pouget, J., Beaufrère, A.M., Pellissier, J.F.

“…In 1988, Kalimo et al. (Ann Neurol 23 (1988) 258)described a new type of X-linked myopathy in a Finnish family. The clinical course was characterized by slow…”
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Woolly adolescent moan and neurological disorders by Pedespan, J M

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Angelman syndrome and intracranial aneurysm: fortuitous association or commune genetic predisposition? by Meyer Witte, S, Espil-Taris, C, Cenraud, C, Le Brun, S, Loiseau, H, Chateil, J F, Lacombe, D, Pédespan, J M

“…Although the pathogenesis of cerebral aneurysms has been studied intensively, it is yet poorly understood. However, a genetic predisposition to this pathology…”
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Surgical treatment of an early epileptic encephalopathy with suppression-bursts and focal cortical dysplasia by Pedespan, J M, Loiseau, H, Vital, A, Marchal, C, Fontan, D, Rougier, A

“…A case of early epileptic encephalopathy (EIEE) with suppression-bursts or Ohtahara's syndrome, associated with focal cortical dysplasia is reported. Infantile…”
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Lymphoplasmacyte-rich meningioma in a child by LOISEAU, H, PEDESPAN, J.-M, VITAL, A, MARCHAL, C, VITAL, C, COHADON, F

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Statistical Analysis of Mitochondrial Pathologies in Childhood: Identification of Deficiencies Using Principal Component Analysis by LETELLIER, T, DURRIEU, G, REDONNET-VERNHET, I, MAZAT, J.-P, MALGAT, M, ROSSIGNOL, R, ANTOCH, J, DESHOUILLERS, J.-M, COQUET, M, LACOMBE, D, NETTER, J.-C, PEDESPAN, J.-M

“…Mitochondrial pathologies are a heterogeneous group of metabolic disorders that are frequently characterized by anomalies of oxidative phosphorylation,…”
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Childhood demyelinating diseases with a prolonged remitting course and their relation to Schilder’s disease: report of two cases by LEUZZI, VINCENZO, LYON, GILLES, CILIO, MARIA ROBERTA, PEDESPAN, JEAN MICHEL, FONTAN, DANIEL, CHATEIL, JEAN-FRANÇOIS, VITAL, ANNE

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Glial and neuronoglial malformative lesions associated with medically intractable epilepsy by VITAL, A, MARCHAL, C, LOISEAU, H, ROUGIER, A, PEDESPAN, J. M, RIVEL, J, VITAL, C

“…In a large series of 116 cortical resections for treatment of medically intractable epilepsy, 10 glial hamartomas and 11 neuronoglial malformative lesions were…”
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Cranial aneurysmal bone cysts presenting with raised intracranial pressure : report of two cases by CHATEIL, J. F, DOUSSET, V, MEYER, P, PEDESPAN, J. M, SAN-GALLI, F, RIVEL, J, CAILLE, J. M, DIARD, F

“…Aneurysmal bone cysts in the skull vault are reported in two patients 7 and 9 years old, who presented with vomiting and headaches caused by raised…”
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