Search Results - "Roze, E"

Mixed central and peripheral nervous system disorders in severe SARS-CoV-2 infection by Chaumont, H., San-Galli, A., Martino, F., Couratier, C., Joguet, G., Carles, M., Roze, E., Lannuzel, A.

“…We report four cases of severe COVID-19 in male patients aged 50–70 with the combination of central and peripheral nervous system disorders occurring…”
Get full text

Paroxysmal movement disorders: An update by Méneret, A., Roze, E.

“…Paroxysmal movement disorders comprise both paroxysmal dyskinesia, characterized by attacks of dystonic and/or choreic movements, and episodic ataxia, defined…”
Get full text

PRRT2 mutations and paroxysmal disorders by Méneret, A., Gaudebout, C., Riant, F., Vidailhet, M., Depienne, C., Roze, E.

“…In the past year, mutations in the PRRT2 gene have been identified in patients with paroxysmal kinesigenic dyskinesia and other paroxysmal disorders. We…”
Get full text

Cerebellar processing of sensory inputs primes motor cortex plasticity by Popa, T, Velayudhan, B, Hubsch, C, Pradeep, S, Roze, E, Vidailhet, M, Meunier, S, Kishore, A

“…Plasticity of the human primary motor cortex (M1) has a critical role in motor control and learning. The cerebellum facilitates these functions using sensory…”
Get full text

Central nervous system infections in a tropical area: influence of emerging and rare infections by Chaumont, H., Roze, E., Tressières, B., Lazarini, F., Lannuzel, A.

“…Background and purpose The frequency of infectious encephalitis and the distribution of causative pathogens in tropical areas are poorly known and may be…”
Get full text

Abnormal cerebellar processing of the neck proprioceptive information drives dysfunctions in cervical dystonia by Popa, T., Hubsch, C., James, P., Richard, A., Russo, M., Pradeep, S., Krishan, S., Roze, E., Meunier, S., Kishore, A.

“…The cerebellum can influence the responsiveness of the primary motor cortex (M1) to undergo spike timing-dependent plastic changes through a complex mechanism…”
Get full text

Acute meningoencephalitis in a patient with COVID-19 by Chaumont, H., Etienne, P., Roze, E., Couratier, C., Roger, P.-M., Lannuzel, A.

Get full text

Cerebrospinal fluid biomarkers in SARS-CoV-2 patients with acute neurological syndromes by Chaumont, H., Kaczorowski, F., San-Galli, A., Michel, P.P., Tressières, B., Roze, E., Quadrio, I., Lannuzel, A.

“…Mechanisms underlying acute brain injury in SARS-CoV-2 patients remain poorly understood. A better characterization of such mechanisms remains essential to…”
Get full text

3.3.3 MYOCLONUS: CLINICAL PRESENTATION by Roze, E

Get full text

Late-onset idiopathic focal dystonia of the trunk: A treatable cause of bent spine syndrome by Hainque, E., Apartis, E., Tarrano, C., Karachi, C., Roze, E.

Get full text

Long-term outcomes after NeuroCOVID: A 6-month follow-up study on 60 patients by Chaumont, H., Meppiel, E., Roze, E., Tressières, B., de Broucker, T., Lannuzel, A.

“…Long-term outcomes after neurological manifestations due to COVID-19 are poorly known. The aim of our study was to evaluate the functional outcome and identify…”
Get full text

Neuroinflammatory markers at school age in preterm born children with neurodevelopmental impairments by Van der Zwart, S., Knol, E.F., Gressens, P., Koopman, C., Benders, M., Roze, E.

“…Immune system activation in the neonatal period is associated with white matter injury in preterm infants. In animal studies, neonatal priming of the immune…”
Get full text

Cerebellar rTMS stimulation may induce prolonged clinical benefits in essential tremor, and subjacent changes in functional connectivity: An open label trial by Popa, T, Russo, M, Vidailhet, M, Roze, E, Lehéricy, S, Bonnet, C, Apartis, E, Legrand, A.P, Marais, L, Meunier, S, Gallea, C

“…Abstract Background Cerebello-thalamo-cortical (CTC) pathways dysfunction is involved in pathological oscillations causing tremor in essential tremor (ET)…”
Get full text

Restoration of normal motor control in Parkinson's disease during REM sleep by De Cock, Valérie Cochen, Vidailhet, Marie, Leu, Smaranda, Texeira, Antonio, Apartis, Emmanuelle, Elbaz, Alexis, Roze, Emmanuel, Willer, Jean Claude, Derenne, Jean Philippe, Agid, Yves, Arnulf, Isabelle

“…Although normal subjects do not move during REM sleep, patients with Parkinson's disease may experience REM sleep behaviour disorder (RBD). The characteristics…”
Get full text

SAMCEP Society consensus on the treatment of upper facial lines with botulinum neurotoxin type A: A tailored approach by Braccini, F, Catoni, I, Belfkira, F, Lagier, J, Roze, E, Paris, J, Huth, J, Bronsard, V, Cartier, H, David, M, Galatoire, O, Obadia, D, Sabatier, H, Sarfati, E, Kestemont, P, Winter, C, Redaelli, A

“…The safety and efficacy of botulinum neurotoxin type A (BoNTA) treatments are well established, but injection techniques, target muscles, and toxin doses…”
Get full text

Treatment for dystonia in childhood by Roubertie, A., Mariani, L. L., Fernandez-Alvarez, E., Doummar, D., Roze, E.

“…Management of childhood dystonia differs in certain respects from that of adult dystonia: (i) childhood dystonia is more often secondary than primary; (ii)…”
Get full text

Cerebellar Processing of Sensory Inputs Primes Motor Cortex Plasticity by Popa, T., Velayudhan, B., Hubsch, C., Pradeep, S., Roze, E., Vidailhet, M., Meunier, S., Kishore, A.

Get full text

A novel DCC mutation and genetic heterogeneity in congenital mirror movements by Depienne, C, Cincotta, M, Billot, S, Bouteiller, D, Groppa, S, Brochard, V, Flamand, C, Hubsch, C, Meunier, S, Giovannelli, F, Klebe, S, Corvol, J C, Vidailhet, M, Brice, A, Roze, E

“…DCC is the receptor for netrin, a protein that guides axon migration of developing neurons across the body's midline. Mutations in the DCC gene were recently…”
Get full text

GLUT1 deficiency syndrome: An update by Gras, D., Roze, E., Caillet, S., Méneret, A., Doummar, D., Billette de Villemeur, T., Vidailhet, M., Mochel, F.

“…Glucose transporter type 1 deficiency syndrome is caused by heterozygous, mostly de novo, mutations in the SLC2A1 gene encoding the glucose transporter GLUT1…”
Get full text

Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein by Mariani, L. L., Rivaud-Péchoux, S., Charles, P., Ewenczyk, C., Meneret, A., Monga, B. B., Fleury, M.-C., Hainque, E., Maisonobe, T., Degos, B., Echaniz-Laguna, A., Renaud, M., Wirth, T., Grabli, D., Brice, A., Vidailhet, M., Stoppa-Lyonnet, D., Dubois-d’Enghien, C., Le Ber, I., Koenig, M., Roze, E., Tranchant, C., Durr, A., Gaymard, B., Anheim, M.

“…Whether the recessive ataxias, Ataxia with oculomotor apraxia type 1 (AOA1) and 2 (AOA2) and Ataxia telangiectasia (AT), can be distinguished by…”
Get full text