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  1. 30321
    “…RESULTS: The sensitivity and specificity of the clinical model based on consolidation-to-tumor ratio (CTR), lobulated signs and vascular anomaly signs was 70.0% and 76.7% in the validation group. …”
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    Application of computed tomography-based radiomics combined with clinical factors in the diagnosis of malignant degree of lung adenocarcinoma
  2. 30322
    “…In this work, a novel methodology applies anomaly detection to distinguish male mosquito tracks from females and couples. …”
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    Online Artículo Texto
    Finding a Husband: Using Explainable AI to Define Male Mosquito Flight Differences
  3. 30323
    “…Two regions of interest (ROIs), called the maximum anomaly region (ROI1) and the tumor region (ROI2), were delineated on the patients’ preoperative MRIs utilizing the tool ITK-SNAP, and Pyradiomics 3.0 was applied to execute feature extraction. …”
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    Online Artículo Texto
    Predicting Histopathological Grading of Adult Gliomas Based On Preoperative Conventional Multimodal MRI Radiomics: A Machine Learning Model
  4. 30324
    por Wakoya, Reta, Afework, Mekbeb
    Publicado 2023
    “…BACKGROUND: Neural tube defects are a type of congenital anomaly caused by an abnormality in the development of the brain and spinal cord during embryogenesis. …”
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    Online Artículo Texto
    Burden of Neural Tube Defects and Their Associated Factors in Africa: A Systematic Review and Meta-Analysis
  5. 30325
    “…Nine patients had large intra-cardiac left-to-right shunts (including 3 with fatal trisomy and palliative programs), 2 had borderline left ventricles, 2 had Taussig-Bing anomaly, and one had a hypoplastic left heart. Four patients had concomitant ductal stenting. …”
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    Online Artículo Texto
    Outcomes of manually modified microvascular plugs to pulmonary flow restrictors in various congenital heart lesions
  6. 30326
    “…As a result of the frame shift caused by this deletion, a premature stop codon was found 43bp downstream from the anomaly, potentially rendering this allele null. Possible explanations for the presence of three HLA-A alleles in one patient include partial allele loss during an autoimmune event, a mutation within a chromosomal duplication of the region, or the patient has undergone a hematopoietic stem cell transplant. …”
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    Abstract 22 Anomalous HLA-A Typing Found in Patient Using PacBio Sequencing Technology
  7. 30327
    “…Although the relationship between this anomaly and psychiatric disorders is emphasized, its nature has not fully understood. …”
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    Schizophrenia and Mega cisterna magna: a Case report
  8. 30328
    “…The nuclear magnetic resonance showed an image suggestive of venous development anomaly, with no acute injuries. Her cerebral spinal fluid was widely studied, and all the results were negative, including: the technique of PCR for many virus and bacteria that can cause meningitis or encephalitis; a bacterial culture; a biochemical study; antineuronal antibodies; and a limbic encephalitis antibodies study. …”
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    Early-onset schizophrenia: an adolescent case report
  9. 30329
    “…Malformations and chromosomal abnormalities are common etiologies; therefore, detailed anomaly scans and invasive testing should be offered. …”
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    Online Artículo Texto
    Small‐for‐gestational‐age fetus diagnosed in the second trimester: Possible etiologies and short‐term neonatal outcomes
  10. 30330
    “…Background Supracardiac total anomalous pulmonary communication (TAPVC) constitutes a rare congenital cardiac anomaly. Most babies with supracardiac TAPVC are diagnosed in infancy and undergo complete surgical repair during infancy. …”
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    Supracardiac Total Anomalous Pulmonary Venous Connection in Adolescence
  11. 30331
    por Smith, Thomas A
    Publicado 2008
    “…Micro-heterogeneity may be the reason for this anomaly. It is proposed that the level of micro-heterogeneity can be estimated from statistical models that estimate the amount of variation in transmission most compatible with a mass-action model for the relationship of infection to exposure. …”
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    Estimation of heterogeneity in malaria transmission by stochastic modelling of apparent deviations from mass action kinetics
  12. 30332
    “…The latter was present in a male diagnosed with Peters’ anomaly who subsequently was found to have a known causative mutation for Peters’ plus syndrome in B3GALTL (c.660+1G>A). …”
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    Absence of NR2E1 mutations in patients with aniridia
  13. 30333
    “…METHODS: A case–control study was performed in which 102 patients with CHD characterized by right ventricle pathology or single ventricle physiology (TGA, UVH, Ebstein’s anomaly, ccTGA, Eisenmenger syndrome, DORV, CAT, unoperated ToF) were compared to 45 age- and sex-matched controls. …”
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    Microvolt T wave alternans in adults with congenital heart diseases characterized by right ventricle pathology or single ventricle physiology: a case control study
  14. 30334
    “…The presence of the distorted ice (called “interphase” by us) also explains the debated “drift anomaly” upon melting. These results are compatible with the high-pressure study by Suzuki and Mishima indicating disappearance of polyamorphism at P ≈ 0.03–0.05 GPa at χ (g) ≈ 0.12–0.15 [J. …”
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    Glass polymorphism in glycerol–water mixtures: II. Experimental studies
  15. 30335
    “…BACKGROUND: A study of pregnancy outcomes related to pregnancy in prison in New South Wales, Australia, designed a two stage linkage to add maternal history of incarceration and serious mental health morbidity, neonatal hospital admission and infant congenital anomaly diagnosis to birth data. Linkage was performed by a dedicated state-wide data linkage authority. …”
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    Preparing linked population data for research: cohort study of prisoner perinatal health outcomes
  16. 30336
    “…We divided the cohort into 2 groups, distinguishing between patients without cranial symptoms/signs (i.e., headaches, clinical temporal artery anomaly, jaw claudication, ophthalmologic symptoms) and those with cranial symptoms/signs. …”
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    Giant-cell arteritis without cranial manifestations: Working diagnosis of a distinct disease pattern
  17. 30337
    Publicado 2019
    “…Exclusion criteria were presence of a severe congenital anomaly, anticipated enteral fasting for longer than 14 days, or no realistic prospect of survival. …”
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    Enteral lactoferrin supplementation for very preterm infants: a randomised placebo-controlled trial
  18. 30338
    “…Background: 48,XXYY syndrome is a rare chromosomal anomaly that causes infertility, developmental and behavioral disorders, among other health problems, in males. …”
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    SAT-299 48,xxyy Syndrome: A Case Report
  19. 30339
    “…In addition, a rare congenital Müllerian anomaly known as Herlyn-Werner-Wunderlich syndrome(HWWS), consisting of uterus didelphys, obstructed hemivagina and unilateral renal agenesis was incidentally diagnosed as an underlying condition. …”
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    SAT-292 Superimposed Peripheral Precocious Puberty Caused by Autonomous Ovarian Follicular Cyst in Being Treated Central Precocious Puberty Patient: Underlying Condition of Herlyn-Werner-Wunderlich Syndrome
  20. 30340
    “…We recruited women with intrahepatic cholestasis of pregnancy, who were aged 18 years or older and with a gestational age between 20 weeks and 40 weeks and 6 days, with a singleton or twin pregnancy and no known lethal fetal anomaly. Participants were randomly assigned 1:1 to ursodeoxycholic acid or placebo, given as two oral tablets a day at an equivalent dose of 500 mg twice a day. …”
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    Ursodeoxycholic acid versus placebo in women with intrahepatic cholestasis of pregnancy (PITCHES): a randomised controlled trial
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