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461
Effectiveness of a Novel Contralaterally Controlled Neuromuscular Electrical Stimulation for Restoring Lower Limb Motor Performance and Activities of Daily Living in Stroke Survivo...
Published 2022-01-01“…Surface electromyography (sEMG) assessments included average electromyography (aEMG), integrated electromyography (iEMG), and root mean square (RMS) of the paretic TA muscle. …”
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462
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463
中国南方三个Hunter综合征家系的病因学研究
Published 2023-05-01“…与正常蛋白相比,突变蛋白的高级结构预测结果存在明显差异。根据ACMG标准,3个家系的变异均为致病性突变。结论先证者所患疾病为Hunter综合征,<italic>IDS</italic>基因的c.615_622del(p.Ile206Valfs<sup>*</sup>18)、c.847_848del(p.Val283Alafs<sup>*</sup>57)和IVS7 ds+1 G>A (p.G336Dfs*12)均是新的致病性突变,它们是引起患儿发病的内在原因。…”
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464
Vesicoureteral Reflux in Children with Accidental Diagnosis of Unilateral Small Size Kidney
Published 2024-07-01“…Vesicoureteral reflux was diagnosed by voiding C\cystourethrography (VCUG) or radionuclide cystography (RNC). All children were followed for at least for 1 year with urine culture and urinalysis every 1-2 months for detection of UTI. …”
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465
Klasik Şiirin Nadide Bahçesi: Şiiristan
Published 2019-12-01“…Sözlük anlamı “açma, ayırma” olan “şerh” en basit tanımıyla bir eseri herkes tarafından anlaşılır hâle getirme işlemidir. …”
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466
Study of CABAC-based digital video encryption in the H.264/AVC standard
Published 2007-01-01“…Several candidate domains were analyzed and summarized to apply encryption to the latest video coding standard H.264/AVC,and a novel digital video encryption scheme based on CABAC(context-based adaptive binary arithmetic coding) was proposed.During the CABAC encoding,two kinds of secure encryption operations including RCME(regular coding mode encryption) and BCME(bypass coding mode encryption) were utilized,in order to encrypt residual coefficient codeword,motion vector difference codeword and intra-prediction mode,respectively.The experimental results show that the scheme has significant advantages on security,coding efficiency,and errors robustness.…”
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467
PARÁMETROS HEMATOLÓGICOS EN POLLUELOS DE PSITÁCIDOS EN CAUTIVERIO DE ORIGEN SILVESTRE
Published 2013-01-01“…En las cuatro especies citadas, el porcentaje del hematocrito fue de 56,4 ± 3,36; 51 ± 6,52; 47,6 ± 6,47 y 53,8 ± 9,26; el VCM en fl fue de 184,6 ± 13,4; 142,0 ± 25,4; 106,3 ± 11,7 y 162,3 ± 71,9; la cuenta eritrocítica fue de 4,7 ± 2,1 x10 6 /μl; 6,1 ± 8,2 x10 6 /μl; 6,9 ± 1,2 x10 6 /μl y 5,4 ± 1,1 x10 6 /μl; y la cuenta leucocitaria de 3,06 ± 0,15 x10 3 /μl; 3,62 ± 0,24 x10 3 /μl; 4,48 ± 0,36 x10 3 /μl y 3,56 ± 0,71 x10 3 /μl respectivamente para P. senilis , A. albifrons , A. autumnalis y A. oratrix . …”
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468
Vancomycin population pharmacokinetic models: Uncovering pharmacodynamic divergence amid clinicobiological resemblance
Published 2025-01-01“…Simulations were performed for a 47 years old man, weighing 70 kg, with an albumin level of 35.5 g/L, a creatinine clearance of 100 mL/min, an eGFR of 106 mL/min/1.73 m2, and receiving an intravenous infusion of 1 g × 2/day of VCM over 1 h for 48 h. Simulations of time–concentration profiles revealed differences, leading us to determine the probability of achieving microbiological efficacy (AUC/MIC ≥ 400) with each model. …”
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469
Le silence et le cri : Salomé, d’Oscar Wilde à Richard Strauss
Published 2013-06-01“…Wilde’s play and Strauss’s opera can be considered as the acme of the literary, pictorial and musical currents that have been exploring the theme of Salome since the Middle Ages. …”
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470
Robot-assisted ureteral reconstruction for managing kidney transplant patients with ureteric complications
Published 2025-01-01“…Postoperative voiding cystourethrogram (VCUG) was performed at 3.2±1.6 months. Seven patients (77.8%) became VUR-free, while two patients (22.2%) had VUR regression from grade IV to I. …”
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471
中国南方一罕见迟发性脊椎骨骺发育不良大家系的表型和基因型的相关性研究
Published 2022-05-01“…结果通过全外测序、Sanger测序验证和生物信息分析,确定<italic>TRAPPC2</italic>基因及其携带的 c.94 del G突变为本病最可能的致病基因突变;通过RT-PCR,排除了IVS as(-1) del G的可能;通过q-PCR检测,证实该突变导致患者和携带者的<italic>TRAPPC2</italic>基因表达量显著低于正常人群(<italic>P</italic><0.01),且蛋白高级结构预测分析显示正常蛋白和突变蛋白的空间结构存在明显差异。根据ACMG的标准,确定为致病性突变。结论先证者所患疾病为XR型迟发性脊椎骨骺发育不良(SEDT),<italic>TRAPPC2</italic>基因的c.94 del G, p.D32T, fsX6是一还未报道的新致病突变,是患者发病的内在原因,其基因型和表型有显著的相关性。…”
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472
Association between vitamin D levels and preserved ratio impaired spirometry: an investigation of mediating roles of systemic inflammation and metabolic indicators
Published 2025-01-01“…Mediation analysis highlighted bilirubin as a positive mediator (ACME = −4.11 × 10−5, p < 0.001), while TyG demonstrated a suppressive mediation effect (ACME = 2.68 × 10−5, p < 0.001). …”
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473
Développement des compétences générales dans la formation initiale des professeurs des écoles
Published 2023-03-01“…Through the analysis and synthesis of scientific and methodical sources, it was found that soft skills are flexible, sometimes non-special, acme competencies for the successful performance of professional duties. …”
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474
Enhancement and Expansion of the Neural Network-Based Compact Model Using a Binning Method
Published 2024-01-01“…The artificial neural network (ANN)-based compact model has significant advantages over physics-based standard compact models such as BSIM-CMG because it can achieve higher accuracy over a wide range of geometric parameters. …”
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475
Well Pattern and Well Spacing Optimization of Large Volume Water Injection in a Low-Permeability Reservoir with Pressure Sensitivity
Published 2022-01-01“…In the paper, the optimal well pattern and well spacing for the large volume water injection scheme to develop a pressure-sensitive low-permeability reservoir is investigated. Firstly, the CMG is employed to build the basic reservoir model developed by fractured vertical wells. …”
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476
Low Frequency of MKRN3 and DLK1 Variants in Chinese Children with Central Precocious Puberty
Published 2019-01-01“…We identified four novel missense variants of MKRN3, c.1138G > A (p.Glu380Lys), c.1420T > A (p.Leu474Met), c.673C > G (p.Leu225Val), and c.1071C > G (p.Ile357Met) in two sporadic cases and three familial cases. According to ACMG standards, two MKRN3 variant (p.Glu380Lys and p.Ile357Met) are likely pathogenic, and two others are of uncertain significance. …”
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477
DNA copy number variations and craniofacial abnormalities in 1,457 children with neurodevelopmental disorders
Published 2025-01-01“…Regarding the pathogenicity of CNVs, 91 (57.96%, 91/157) were identified as pathogenic, 28 (17.83%, 28/157) as variants of uncertain clinical significance (VOUS), and 38 (24.20%, 38/157) as benign according to the American College of Medical Genetics and Genomics (ACMG).Using a specific sign-scoring scale, the proportion of pathogenic CNVs in children graded 1 point or higher (64%, 58/91) was significantly higher than that of non-pathogenic CNVs (43%, 29/66) (P < 0.05). …”
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478
Valores hematológicos del mono choro común (Lagothrix lagotricha) mantenido en cautiverio en la ciudad de Lima (Perú)
Published 2018-01-01“…Se obtuvieron los siguientes resultados: eritrocitos 8,76 x 106/μl (± 2,91); hematocrito 36,46% (± 3,38); hemoglobina 12,32 g/dl (± 1,89); VCM 60,61 fl (± 7,85); HCM 20,37 pg (± 3.07); CMCH 33,85 g/dl (± 4,61); leucocitos 6,12 x 103/μl (± 1,05); abastonados 0,05 x 103/μl (± 0,11); segmentados 5,54 x 103/μl (± 2,23); linfocitos 2,62 x 103/ul (± 1,60); monocitos 0,07 x 103/μl (± 0,02); eosinófilos 0,42 x 103/μl (± 0,23); basófilos 0,13 x 103/μl (± 0,14) y plaquetas 314,39 x 103/μl (± 78,09). …”
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479
Nanopore Confinement Effect on the Phase Behavior of CO2/Hydrocarbons in Tight Oil Reservoirs considering Capillary Pressure, Fluid-Wall Interaction, and Molecule Adsorption
Published 2021-01-01“…The proposed model has been validated with CMG-Winprop and experimental results with bulk and confined fluids. …”
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480
Novel nonsense mutation in gene CHRNA2 identified by whole-genome sequencing in infant with epilepsy disorder: A case report
Published 2025-01-01“…Moreover, according to various prediction tools (MutationTaster, SIFT, CADD, FATHMM-MKL, LRT, DANN, Eigen, and BayesDel), the mutation is characterized as pathogenic, which corresponds to the American College of Medical Genetics and Genomics (ACMG) classification. According to the findings, mutation of the CHRNA2 gene is closely associated with two disorders known as autosomal dominant nocturnal frontal epilepsy (ADNFLE), and benign familial infantile epilepsy (BFIS). …”
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