Search Results - "RAOUL, O"

Miniaturization of Patch Antennas Using a Metamaterial-Inspired Technique by Ouedraogo, R. O., Rothwell, E. J., Diaz, A. R., Fuchi, K., Temme, A.

“…A new design methodology for producing highly miniaturized patch antennas is introduced. The methodology uses complementary split-ring resonators placed…”
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A Reconfigurable Microstrip Leaky-Wave Antenna With a Broadly Steerable Beam by Ouedraogo, R. O., Rothwell, E. J., Greetis, B. J.

“…A half-width microstrip leaky-wave antenna with an electronically steerable main beam is introduced. Lumped capacitors are connected between the free edge of…”
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Electro-clinical features in epileptic children with chromosome 15q duplication syndrome by Dangles, M.-T., Malan, V., Dumas, G., Romana, S., Raoul, O., Coste-Zeitoun, D., Soufflet, C., Vignolo-Diard, P., Bahi-Buisson, N., Barnérias, C., Chemaly, N., Desguerre, I., Gitiaux, C., Hully, M., Bourgeois, M., Guimier, A., Rio, M., Munnich, A., Nabbout, R., Kaminska, A., Eisermann, M.

“…•West or Lennox-Gastaut syndrome often occur in isodicentric chromosome 15q duplication.•Focal epilepsy often occurs in interstitial chromosome 15q…”
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Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders by Jacquemont, M-L, Sanlaville, D, Redon, R, Raoul, O, Cormier-Daire, V, Lyonnet, S, Amiel, J, Le Merrer, M, Heron, D, de Blois, M-C, Prieur, M, Vekemans, M, Carter, N P, Munnich, A, Colleaux, L, Philippe, A

“…Background: Autism spectrum disorders (ASD) refer to a broader group of neurobiological conditions, pervasive developmental disorders. They are characterised…”
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A Tunable Dual-Band Miniaturized Monopole Antenna for Compact Wireless Devices by Ouedraogo, Raoul O., Tang, Junyan, Fuchi, Kazuko, Rothwell, Edward J., Diaz, Alejandro R., Chahal, Prem

“…A technique for producing miniaturized tunable planar monopole antennas for wireless communication applications is introduced. Miniaturization is achieved by…”
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A Continuously Tunable Miniaturized Patch Antenna by Junyan Tang, Ouedraogo, Raoul O., Rothwell, Edward J., Diaz, Alejandro R., Fuchi, Kazuko

“…A tunable miniaturized patch antenna is introduced. Miniaturization is achieved by placing a layer of complementary split-ring resonators horizontally between…”
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19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation by Malan, V, Raoul, O, Firth, H V, Royer, G, Turleau, C, Bernheim, A, Willatt, L, Munnich, A, Vekemans, M, Lyonnet, S, Cormier-Daire, V, Colleaux, L

“…Deletions of chromosome 19 have rarely been reported, with the exception of some patients with deletion 19q13.2 and Blackfan-Diamond syndrome due to…”
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Mid-trimester maternal ADAM12 levels differ according to fetal gender in pregnancies complicated by preeclampsia by Myers, Jenny E, Thomas, Grégoire, Tuytten, Robin, Van Herrewege, Yven, Djiokep, Raoul O, Roberts, Claire T, Kenny, Louise C, Simpson, Nigel A B, North, Robyn A, Baker, Philip N

“…An overrepresentation of adverse pregnancy outcomes has been observed in pregnancies associated with a male fetus. We investigated the association between…”
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In Situ Optimization of Metamaterial-Inspired Loop Antennas by Ouedraogo, R.O., Rothwell, E.J., Diaz, A., Shih-Yuan Chen, Temme, A., Fuchi, K.

“…A new methodology for designing metamaterial-inspired antennas using an in situ optimization technique is introduced. Through this approach, an optimization…”
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Waveguide band-stop filter design using optimized pixelated inserts by Ouedraogo, Raoul O., Rothwell, Edward J., Diaz, Alejandro R., Fuchi, Kazuko, Tang, Junyan

“…A technique is introduced for designing band‐stop waveguide filters by optimizing a grid of metallic pixels on a dielectric sheet placed longitudinal to the…”
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A Self-Structuring Electromagnetic Scatterer by Yen-Sheng Chen, Yao-Chia Chan, Hsueh-Jyh Li, Rothwell, E. J., Ouedraogo, R. O., Shih-Yuan Chen

“…A novel self-structuring electromagnetic scatterer (SSES) is proposed. The SSES can alter its electrical shape to fulfill various operational objectives, such…”
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Spectrum of NSD1 mutations in Sotos and Weaver syndromes by Rio, M, Clech, L, Amiel, J, Faivre, L, Lyonnet, S, Le Merrer, M, Odent, S, Lacombe, D, Edery, P, Brauner, R, Raoul, O, Gosset, P, Prieur, M, Vekemans, M, Munnich, A, Colleaux, L, Cormier-Daire, V

“…Sotos syndrome is an overgrowth syndrome characterised by pre- and postnatal overgrowth, macrocephaly, advanced bone age, and typical facial features. Weaver…”
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An Automatically Tunable Cavity Resonator System by Ouedraogo, Raoul O, Rothwell, Edward J, Shih-Yuan Chen, Greetis, Brian J

“…A tunable cavity resonator is described that uses a feedback control system to alter its resonant characteristics in response to changes in its environment,…”
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Paternal deletion of the GNAS imprinted locus (including ) in two girls presenting with severe pre- and post-natal growth retardation and intractable feeding difficulties by GENEVIEVE, David, SANLAVILLE, Damien, MUNNICH, Arnold, ROMANA, Serge, RAOUL, Odile, CORMIER-DAIRE, Valérie, VEKEMANS, Michel, FAIVRE, Laurence, KOTTLER, Marie-Laure, JAMBOU, Marguerite, GOSSET, Philippe, BOUSTANI-SAMARA, Dinane, PINTO, Graziella, OZILOU, Catherine, ABEGUILE, Geneviève

“…Deletions of the long arm of chromosome 20 are rare. Here, we report on two girls with a very small interstitial deletion of the long arm of chromosome 20…”
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A Self-Tuning Electromagnetic Shutter by Ouedraogo, R O, Rothwell, E J, Shih-Yuan Chen, Temme, A

“…A self-tuning electromagnetic shutter is introduced, consisting of a slotted metallic surface with computer controlled switches placed across the slots. By…”
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Cryptic terminal deletion of chromosome 9q34: a novel cause of syndromic obesity in childhood? by Cormier-Daire, V, Molinari, F, Rio, M, Raoul, O, de Blois, M-C, Romana, S, Vekemans, M, Munnich, A, Colleaux, L

“…[...]obesity is a frequent feature in several other chromosome anomalies including fragile X, trisomy 21, and Turner syndrome. [...]while obesity and mental…”
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Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation by 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, M-C, Prieur, M, Romana, S, Vekemans, M, Munnich, A, Colleaux, L

“…Recent studies have shown that cryptic unbalanced subtelomeric rearrangements contribute to a significant proportion of idiopathic syndromic mental retardation…”
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Molecular cytogenetic analysis of five 2q37 deletions: refining the brachydactyly candidate region by Chaabouni, M., Le Merrer, M., Raoul, O., Prieur, M., de Blois, M.C., Philippe, A., Vekemans, M., Romana, S.P.

“…Deletions of the 2q37 region are associated with a recognizable pattern of MCA/MR so-called the AHO-like syndrome. Brachydactyly is a variable but…”
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Antenna miniaturization: definitions, concepts, and a review with emphasis on metamaterials by Rothwell, Edward J., Ouedraogo, Raoul O.

“…The ability to shrink the physical dimensions of an antenna without significant performance degradation has been of great interest for over half a century…”
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Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype by Joly, G, Lapierre, J-M, Ozilou, C, Gosset, P, Aurias, A, De Blois, M-C, Prieur, M, Raoul, O, Colleaux, L, Munnich, A, Romana, SP, Vekemans, M, Turleau, C

“…Segmental aneusomy for small chromosomal regions has been shown to be a common cause of mental retardation and multiple congenital anomalies. A screening…”
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