Results 61 to 70 of about 29,360 (257)

Rotman lens-based two-tier hybrid beamforming for wideband mmWave MIMO-OFDM system with beam squint

EURASIP Journal on Wireless Communications and Networking, 2018
In this paper, we study the hybrid beamforming for the wideband mmWave multiuser MIMO-OFDM system. We characterize the frequency-dependent beam angle problem, i.e., beam squint effect. Firstly, we extend the mmWave channel model from the Saleh-Valenzuela
Bin Liu, Hongbo Zhu
doaj   +1 more source

High‐Resolution Genomic Characterization of WAGR Spectrum Disorder: Insights From a Novel Cohort and Literature Synthesis, and Validation of Patient‐Reported Data

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT WAGR spectrum disorder (WAGRSD) is an ultra‐rare congenital disorder caused by heterozygous deletion of chromosome 11p13. While classically associated with Wilms tumor, Aniridia, Genitourinary anomalies, and a Range of developmental delays, accurate delineation of the deletion is critical for prognosis because the phenotypic spectrum extends ...
Andrew M. George, Bamelak T. Duki, Zoe S. Katz, Aravind Viswanathan, Suzanne P. MacFarland, Evan R. Hathaway, Caitlin Monahan, John Morris, Kelly L. Trout, Shari M. Krantz, Arupa Ganguly, Jennifer M. Kalish   +11 more
wiley   +1 more source

Rewind: Good Morning to the Night [PDF]

, 2013
Today is a special day, a momentous day. It\u27s a day I\u27ve thought about for a long time. A day for beginnings and a day for looking back. So I\u27m looking back for today\u27s blog, to one of my favorite posts.
Rudy, John M.
core   +1 more source

Clinical, Behavioral and Neuroradiological Phenotype in an Italian Cohort of Patients With Xia Gibbs Syndrome: A Multicenter Cross‐Sectional Study and Systematic Literature Review

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Heterozygous variants in the AHDC1 gene are associated with Xia Gibbs Syndrome (XGS), a genetic disorder with a highly variable phenotype. Cognitive impairment, motor delay, language delay, neonatal hypotonia, and sleep apnea are considered “cardinal” signs of the disease.
Giulia Cinelli, Stefania Della Vecchia, Patrizia Bergonzini, Elisa Caramaschi, Elisabetta Spezia, Claudia Parenti, Simona Filomena Madeo, Laura Lucaccioni, Cavalleri Francesca, Marisa Pugliese, Federico Raviglione, Clara Colonna, Olga Calabrese, Ilaria Stanghellini, Maria Carmen Marongiu, Enrico Biagioni, Anna Rita Ferrari, Roberta Battini, Lorenzo Iughetti   +18 more
wiley   +1 more source

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young, Armelle Pindon, Maggie R. Brand, Kate Wears, Katherine H. Young, Alyssa Mendel, Michael J. Lyons   +6 more
wiley   +1 more source

Safety and Perioperative Outcomes of Immediate Versus Delayed Sequential Bilateral Cataract Surgery in the Pediatric Population: A Systematic Review and Meta‐Analysis

Eye &ENT Research, EarlyView.
ABSTRACT Background Bilateral congenital cataracts are a major cause of preventable childhood blindness. Although delayed sequential bilateral cataract surgery (DSBCS) has traditionally been the preferred approach, immediate sequential bilateral cataract surgery (ISBCS) is increasingly being considered to reduce anesthesia exposure and healthcare ...
Mehreen Akram, Zarwa Rashid, Hafiz Aqib Ilyas, Danyal Bakht, Muhammad Arham, Syed Ali Ahsan, Sheraz Ali, Faryal Bakht, Zubaida Hanif   +8 more
wiley   +1 more source

Two-Dimensional Autofocus for Ultra-High-Resolution Squint Spotlight Airborne SAR Based on Improved Spectrum Modification

Remote Sensing
For ultra-high-resolution (UHR) squint spotlight airborne synthetic aperture radar (SAR), the severe range-azimuth coupling caused by squint mode and the spatial and frequency dependence of the motion error brought by ultra-wide bandwidth both make it ...
Min Chen, Xiaolan Qiu, Yao Cheng, Mingyang Shang, Ruoming Li, Wangzhe Li   +5 more
doaj   +1 more source

Gender differences and delay in presentation of childhood squint [PDF]

, 2009
Objective: To assess gender differences and delay in presentation of childhood squint in a tertiary care hospital.Methods: It was a series of children presenting with squint at the Aga Khan University Hospital, Karachi, Pakistan.
Ahmad, Khabir, Chaudhry, Tanveer Anjum, Khan, Aziz, Khan, Muhammad Bilal Salman   +3 more
core   +1 more source

On the infrared scaling solution of SU(N) Yang-Mills theories in the maximally Abelian gauge

, 2010
An improved method for extracting infrared exponents from functional equations is presented. The generalizations introduced allow for an analysis of quite complicated systems such as Yang-Mills theory in the maximally Abelian gauge.
A. Cucchieri, A. Cucchieri, A. Cucchieri, A. Cucchieri, A. Cucchieri, A. Cucchieri, A. Maas, A. Maas, A. Maas, A. Maas, A. Sternbeck, A. Sternbeck, A.C. Aguilar, A.I. Davydychev, A.R. Fazio, A.S. Kronfeld, A.S. Kronfeld, C. Anastasiou, C. Kellermann, C. Lerche, C.S. Fischer, C.S. Fischer, C.S. Fischer, C.S. Fischer, C.S. Fischer, D. Dudal, D. Dudal, D. Dudal, D. Zwanziger, D. Zwanziger, D. Zwanziger, D. Zwanziger, D. Zwanziger, D. Zwanziger, D. Zwanziger, D. Zwanziger, E.M. Ilgenfritz, G. ’t Hooft, G.V. Dunne, G.V. Dunne, H. Min, I.G. Halliday, I.L. Bogolubsky, J. Berges, J. Braun, J. Greensite, J. Thierry-Mieg, J.A. Gracey, J.C. Taylor, J.M. Pawlowski, J.M. Pawlowski, J.M. Pawlowski, K. Amemiya, K. Schwenzer, K. Schwenzer, L. Baulieu, L. Fister, L. Smekal von, L. Smekal von, M. Q. Huber, M.A.L. Capri, M.A.L. Capri, M.A.L. Capri, M.A.L. Capri, M.A.L. Capri, M.Q. Huber, M.Q. Huber, M.Q. Huber, P. Baal van, P. Boucaud, R. Alkofer, R. Alkofer, R. Alkofer, R. Alkofer, R. Alkofer, R. Alkofer, R. Alkofer, R. Alkofer, R. Alkofer, R. Alkofer, S. Mandelstam, T. Shinohara, T. Suzuki, T.A. DeGrand, V.G. Bornyakov, V.G. Bornyakov, V.N. Gribov, W. Schleifenbaum, Z.F. Ezawa   +88 more
core   +1 more source

Spontaneous resorption of sub-retinal cortical lens material

Indian Journal of Ophthalmology, 2014
We report a rare case of retained sub-retinal cortical material, which underwent spontaneous resorption. Patient presented with a left eye traumatic retinal detachment with a large retinal tear and posteriorly dislocated cataractous lens.
Salil S Gadkari, Sucheta R Kulkarni, Kuldeep Dole   +2 more
doaj   +1 more source