Results 1 to 10 of about 6,798,096 (355)

Ternary Syndrome Decoding with Large Weight [PDF]

arXiv, 2019
The Syndrome Decoding problem is at the core of many code-based cryptosystems. In this paper, we study ternary Syndrome Decoding in large weight. This problem has been introduced in the Wave signature scheme but has never been thoroughly studied. We perform an algorithmic study of this problem which results in an update of the Wave parameters.
A Becker, A Becker, A May, AD Flaxman, C Peters, CT Gueye, D Wagner, E Berlekamp, E Prange, J Stern, JT Coffey, M Chaimovich, N Howgrave-Graham, N Sendrier, NT Courtois, S Hirose, T Johansson, Z Galil   +17 more
arxiv   +6 more sources

Syndrome In Question [PDF]

Anais Brasileiros de Dermatologia, 2014
The authors present a male 40-year-old patient with established diagnosis of Behçet's disease which had evolved to recurrent bilateral auricular polychondritis crises. MAGIC syndrome (mouth and genital ulcers with inflamed cartilage) is rare and groups together patients with this clinical picture without necessarily fulfilling the clinical criteria for
Nascimento, Ana Claudia Mendes do, Gaspardo, Daniela Barros Cortez, Cortez, Tatiana Mimura, Miot, Helio Amante   +3 more
  +28 more sources

Decoding of Quantum Data-Syndrome Codes via Belief Propagation [PDF]

in Proc. IEEE International Symposium on Information Theory (ISIT), 2021, pp. 1552--1557, 2021
Quantum error correction is necessary to protect logical quantum states and operations. However, no meaningful data protection can be made when the syndrome extraction is erroneous due to faulty measurement gates. Quantum data-syndrome (DS) codes are designed to protect the data qubits and syndrome bits concurrently.
arxiv   +1 more source

Myelodysplastic syndromes with nephrotic syndrome [PDF]

American Journal of Hematology, 1999
It is sometimes reported that the immunological abnormalities in myelodysplastic syndromes (MDS) induce autoimmune disease (i.e., acute systemic vasculitic syndrome, chronic cutaneous vasculitis, polyneuropathy, relapsing polychondritis, and steroid-responsive pulmonary disorders).
Tadashi Maehara, Takayuki Saitoh, Takafumi Matsushima, Hideki Uchiumi, Jun Tsuchiya, Masamitsu Karasawa, Takuji Naruse, Hirokazu Murakami, Kazuaki Moridaira, Norifumi Tsukamoto, Jun'ichi Tamura   +10 more
openaire   +3 more sources

Diagnosis and Management of the Metabolic Syndrome: An American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement

Current Opinion in Cardiology, 2005
The metabolic syndrome has received increased attention in the past few years. This statement from the American Heart Association (AHA) and the National Heart, Lung, and Blood Institute (NHLBI) is intended to provide up-to-date guidance for professionals
S. Grundy, J. Cleeman, S. Daniels, K. Donato, R. Eckel, B. Franklin, D. Gordon, R. Krauss, P. Savage, Sidney C. Smith, J. Spertus, F. Costa   +11 more
semanticscholar   +2 more sources

Corticobasal syndrome: neuroimaging and neurophysiological advances [PDF]

, 2019
Corticobasal degeneration (CBD) is a neurodegenerative condition characterized by 4R-tau protein deposition in several brain regions that clinically manifests itself as a heterogeneous atypical parkinsonism typically expressing in the adulthood.
Asci, Francesco, Berardelli, Alfredo, Bologna, Matteo, Colosimo, Carlo, Di Stasio, Flavio, Fabbrini, Giovanni, Marsili, Luca, Pantano, Patrizia, Suppa, Antonio, Upadhyay, Neeraj   +9 more
core   +1 more source

Syndrome in question [PDF]

Anais Brasileiros de Dermatologia, 2016
Neurofibromatosis is extremely variable in its presentation. Segmental neurofibromatosis (SNF), which corresponds to NF-type 5 in the Riccardi classification, is a rare disorder. It may go unrecognized if few lesions are observed. We present a case of segmental neurofibromatosis in a 28 year-old patient who presented with multiple papules and nodules ...
Rosmaninho, Aristóteles, Carvalho, Sandrina, Oujo, Elena, Horta, Miguel   +3 more
openaire   +14 more sources

Parent and self-report health-related quality of life measures in young patients with Tourette syndrome [PDF]

, 2012
Tourette syndrome is a neurodevelopmental disorder characterized by tics and comorbid behavioral problems. This study compared child- and parent-reported quality of life and everyday functioning.
Balottin, U, Blangiardo, R, Cali', PV, Cardona, F, Cavanna, AE, Eddy, CM, Gagliardi, E, Luoni, C, Rizzo, R, Selvini, C, Silvestri, PR, Termine, C   +11 more
core   +1 more source

Multisystem Inflammatory Syndrome in U.S. Children and Adolescents

New England Journal of Medicine, 2020
Background Understanding the epidemiology and clinical course of multisystem inflammatory syndrome in children (MIS-C) and its temporal association with coronavirus disease 2019 (Covid-19) is important, given the clinical and public health implications ...
Leora R. Feldstein, E. B. Rose, S. Horwitz, J. Collins, M. Newhams, M. Son, J. Newburger, L. Kleinman, S. Heidemann, Amarilis Martin, Aalok R. Singh, Simon Li, Keiko M. Tarquinio, P. Jaggi, M. Oster, Sheemon P. Zackai, Jennifer K. Gillen, A. Ratner, R. Walsh, J. Fitzgerald, M. Keenaghan, Hussam Alharash, S. Doymaz, K. Clouser, John S. Giuliano, Anjali Gupta, R. Parker, A. Maddux, Vinod Havalad, S. Ramsingh, H. Bukulmez, T. Bradford, L. Smith, M. Tenforde, C. Carroll, Becky J. Riggs, S. Gertz, A. Daube, Amanda N Lansell, Alvaro J Coronado Munoz, C. Hobbs, K. Marohn, N. Halasa, Manish M Patel, A. Randolph   +44 more
semanticscholar   +1 more source

Hypereosinophilic syndromes [PDF]

Orphanet Journal of Rare Diseases, 2007
Hypereosinophilic syndromes (HES) constitute a rare and heterogeneous group of disorders, defined as persistent and marked blood eosinophilia (1.5 x 10(9)/L for more than six consecutive months) associated with evidence of eosinophil-induced organ damage, where other causes of hypereosinophilia such as allergic, parasitic, and malignant disorders have ...
Roufosse, Florence, Goldman, Michel, Cogan, Elie   +2 more
openaire   +5 more sources