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Stenotic bridging bronchus: A very rare entity

Salih Topcu, Serife Tuba Liman, Hasan Tahsin Sarisoy, Abdulkadir Babaoglu, Emre Ozker
2006 Journal of Thoracic and Cardiovascular Surgery  
bronchus was seen between the trachea and residual carina. b and c, Appearance after divided stenotic bridging bronchus. Its diameter was 2 mm, and primary end-to-end anastomosis was present.  ...  MR and echocardiography are usually sufficient for evaluation of additional cardiovascular anomalies. CPB might be needed if there are additional cardiac anomalies.  ...  B ridging bronchus (BB) is one of the rarely seen congenital anomalies. BB is generally associated with other congenital anomalies, especially vascular anomalies.  ... 
doi:10.1016/j.jtcvs.2006.01.011 pmid:16678624 fatcat:ktqkiwghzzdgthghqr4iymixb4

Evaluation of coronary artery abnormalities in Williams syndrome patients using myocardial perfusion scintigraphy and CT angiography

Yakup Ergul, Kemal Nisli, Hulya Kayserili, Birsen Karaman, Seher Basaran, Memduh Dursun, Ebru Yilmaz, Nurhan Ergul, Seher Nilgun Unal, Aygun Dindar
2012 Cardiology Journal  
CT angiography and dipyridamole 99m Tc-sestamibi SPECT MPS seem to be less invasive methods of detecting coronary artery anomalies and myocardial perfusion defects in WS patients.  ...  This study aims to detect coronary artery anomalies and myocardial perfusion defects in WS patients using noninvasive diagnostic methods. Methods: This study features 38 patients diagnosed with WS.  ...  Thus, there is a need for less invasive imaging methods that would allow to detect coronary lesions.  ... 
doi:10.5603/cj.2012.0053 fatcat:74hf6wxxqfcxnpr25m4dp2jupu

Surgical Outcome of Aortopulmonary Window Repair in Early Infancy

Chun-An Chen, Shuenn-Nan Chiu, En-Ting Wu, Ming-Tai Lin, Jou-Kou Wang, Mei-Hwan Wu, Chung-I Chang, Ing-Sh Chiu
2006 Journal of the Formosan Medical Association  
With recent advances, echocardiography has become the principal diagnostic modality for A APW and associated cardiovascular anomalies. 5, 14 However, it is not uncommon that these structural anomalies  ...  and coronary artery anomalies. 2, 3, 5, 19, 20 In the largest review of the current literature, Kutsche and Van Mierop 2 reported that 52% of patients with APW had associated cardiovascular anomalies  ... 
doi:10.1016/s0929-6646(09)60268-0 pmid:17000454 fatcat:kzhsjsnpuzh57dmm7xpaaikawu

A quadricuspid aortic valve in an asymptomatic 40-year-old man: a case report

Giovanni Pasanisi, Gaia Mazzanti, Biagio Sassone
2018 Journal of Medical Case Reports  
Transesophageal echocardiography detected a quadricuspid aortic valve characterized by four cusps of equal size and severe aortic valvular regurgitation, without any further anomalies.  ...  Integrated transthoracic and transesophageal echocardiography enables identification and characterization of a quadricuspid aortic valve anomaly.  ...  At 6-month follow-up visit he was asymptomatic and echocardiography detected only mild residual aortic regurgitation; he did not receive ongoing therapy.  ... 
doi:10.1186/s13256-018-1755-3 pmid:30111367 pmcid:PMC6094910 fatcat:czkud4gh3vf63ckeh2nxavh7ce

Ambient backscatter communication-based smart 5G IoT network

Qiang Liu, Songlin Sun, Xueguang Yuan, Yang'an Zhang
2021 EURASIP Journal on Wireless Communications and Networking  
shallow neural network and the deep neural network can greatly reduce the pressure caused by the frequent deep neural network calculations of the MEC and greatly reduce the energy consumed by the MEC for  ...  Alarm generation: When anomaly detection detects that the user is attacked by a disease, an alarm message will be generated.  ...  For example, when detecting abnormalities in cardiovascular diseases, if abnormalities are detected in the MEC layer, alarm information is generated.  ... 
doi:10.1186/s13638-021-01917-3 fatcat:ujgrym7aqvgi7aenc6jso6p6py

One-Class Conditional Anomaly Detection Algorithm (OCCADA) for Multiple Linear and Logistic Regression

Ivy Kim D
2020 International Journal of Advanced Trends in Computer Science and Engineering  
The study used six (6) models for evaluation of the One-Class Conditional Anomaly Detection Algorithm (OCCADA) and its application to MLR & LR.  ...  The results show that the use of the new one-class conditional anomaly detection algorithm using semi-supervised learning was effective in producing a highly accurate model for classifying conditional  ...  However, there are no existing algorithms for semi-supervised learning for a one-class dataset for conditional anomaly detection to date.  ... 
doi:10.30534/ijatcse/2020/66912020 fatcat:e4qa6beomfb6bcdadndlplpe2i

Association Between fetal Lymphedema and Congenital Cardiovascular Defects in Turner Syndrome

M.L. Loscalzo, P.L. Van, V.B. Ho
2005 ACC Current Journal Review  
The presence of BAV and/or COARC was detected by magnetic resonance imaging combined with echocardiography, and renal anomalies were determined by ultrasound. Results.  ...  Turner syndrome (TS) is associated with congenital cardiovascular defects (CCVDs), most commonly bicuspid aortic valve (BAV) and aortic coarctation (COARC), congenital renal anomalies, and fetal lymphedema  ...  ACKNOWLEDGMENTS We are grateful to Eileen Lange, RN, and the nurses of the National Institutes of Health Clinical Center for excellent care of our patients.  ... 
doi:10.1016/j.accreview.2005.04.011 fatcat:zbvnvsipvrakxglevtas7fzqzu

A Pathogenic Homozygous Mutation in The Pleckstrin Homology Domain of RASA1 Is Responsible for Familial Tricuspid Atresia in An Iranian Consanguineous Family

Ahoura Nozari, Ehsan Aghaei-Moghadam, Aliakbar Zeinaloo, Afagh Alavi, Saghar Ghasemi Firouzabdi, Shohre Minaee, Marzieh Eskandari Hesari, Farkhondeh Behjati
2018 Cell journal  
Patients were carefully assessed to exclude extra-cardiac anomalies. We identified a homozygous RASA1 germline mutation, c.1583A>G (p.Tyr528Cys) in the family.  ...  This could be responsible for the TA pathogenesis in our patients. We strongly suggest that parents with CM/AVM should be investigated for RASA1 heterozygous mutations.  ...  Acknowledgments We would like to thank the patients and their families for contributing to this study.  ... 
doi:10.22074/cellj.2019.5734 pmid:30507091 pmcid:PMC6275424 fatcat:enshgtn6krblxbveutkih5jfta

Undiagnosed Double Aortic Arch in an Adult With Repaired Tetralogy of Fallot

Anita Sadeghpour, Nakisa Khansari, Marziyeh Pakbaz, Kiara Rezaei Kalantari, Hamidreza Pouraliakbar, Maziar Gholampour Dehaki
2019 JACC Case Reports  
A double aortic arch was detected incidentally by echocardiography and cardiac computed tomography. (Level of Difficulty: Intermediate.)  ...  This report describes a young woman with a history of totally corrected tetralogy of Fallot who was a candidate for pulmonic valve replacement.  ...  Many diagnostic modalities may help in detecting this anomaly.  ... 
doi:10.1016/j.jaccas.2019.08.022 fatcat:pkut5kmcv5gmlo3wd5zzsckane

Mutations in the Sarcomere Gene MYH7 in Ebstein Anomaly

A. V. Postma, K. van Engelen, J. van de Meerakker, T. Rahman, S. Probst, M. J. H. Baars, U. Bauer, T. Pickardt, S. R. Sperling, F. Berger, A. F. M. Moorman, B. J. M. Mulder (+4 others)
2010 Circulation: Cardiovascular Genetics  
Methods and Results-Mutational analysis in a cohort of 141 unrelated probands with Ebstein anomaly was performed by next-generation sequencing and direct DNA sequencing of MYH7.  ...  An association between Ebstein anomaly with left ventricular noncompaction (LVNC) and mutations in MYH7 encoding ␤-myosin heavy chain has been shown; in this report, we have screened for MYH7 mutations  ...  Sylva for technical assistance and A. Schalinski for assistance with recruitment of patients. Sources of Funding Disclosures None.  ... 
doi:10.1161/circgenetics.110.957985 pmid:21127202 fatcat:r3vzc3ksvzbjxfdrmlxwq7dmme

Prevalence of structural birth defects in IVF-ICSI pregnancies resulting from autologous and donor oocytes in Indian sub-continent: Results from 2444 births

Manish Banker, Parul Arora, Jwal Banker, Hetal Benani, Sandeep Shah, Parmeswaran Grace Luther Lalitkumar
2019 Acta Obstetricia et Gynecologica Scandinavica  
Seven babies underwent surgery: three for gastrointestinal malformations, one for mild hydrocephalus and three for cardiovascular defects.  ...  Therefore, the chances of detection of birth defects in the antenatal period is higher when compared with general population.  ... 
doi:10.1111/aogs.13541 pmid:30663773 fatcat:eijapgkg7vg4hjr5xr7dgbfchy

Page 277 of Birth Defects Research. Part B, Developmental and Reproductive Toxicology 2006 Vol. 77, Issue 4 [page]

2006 Birth Defects Research. Part B, Developmental and Reproductive Toxicology 2006  
As was evident with the outcome for anomalies of the respiratory system, diagnoses may be grouped under certain general codes.  ...  did not, were similar, and there was no association detected between filling prescriptions for NSAIDs in the first trimester and anomalies of the musculoskeletal system.  ... 

Sertraline use in the first trimester and risk of congenital anomalies: a systemic review and meta-analysis of cohort studies

Zi-Qi Shen, Shan-Yan Gao, Shawn Xiang Li, Tie-Ning Zhang, Cai-Xia Liu, Hai-Chen Lv, Yuan Zhang, Ting-Ting Gong, Xin Xu, Chao Ji, Qi-Jun Wu, Da Li
2016 British Journal of Clinical Pharmacology  
Fluvoxamine Sertraline Fluoxetine These Tables list key protein targets and ligands in this article that are hyperlinked to corresponding entries in, the common portal for  ...  Pregnant women who used sertraline in the first trimester had a statistically significant increased risk of infant cardiovascular-related malformations (OR = 1.36; 95% CI = 1.06-1.74; I 2 = 64.4%; n =  ...  confounders in order to rule out residual confounders.  ... 
doi:10.1111/bcp.13161 pmid:27770542 pmcid:PMC5346877 fatcat:gul2mkoeqfempgnag7ofethgie

Birth Defects Are Preventable

Andrew E. Czeizel
2005 International Journal of Medical Sciences  
Secondary prevention: early detection followed by effective early treatment, e.g. neonatal orthopedic screening is very effective for the early detection and treatment of deformities such as congenital  ...  Birth defects -or by according to the World Health Organization's (WHO) term: congenital anomalies -are structural, functional and/or biochemical-molecular defects present at birth whether detected at  ... 
doi:10.7150/ijms.2.91 pmid:16007259 pmcid:PMC1168872 fatcat:l2o7zfpah5dezljmg25ricbuiq

HOXA1 mutations are not a common cause of Duane anomaly

Max A. Tischfield, Wai-Man Chan, Jann-Frederik Grunert, Caroline Andrews, Elizabeth C. Engle
2006 American Journal of Medical Genetics. Part A  
The HOXA1-related syndrome Acknowledgments We thank the many clinicians who referred patients for this study, and the patients and their families for their participation.  ...  , cardiovascular anomalies, and/or malformed kidneys.  ...  No mutations were detected in HOXA1 in any of the 131 probands.  ... 
doi:10.1002/ajmg.a.31167 pmid:16528738 pmcid:PMC2553396 fatcat:eakzvyejwne43ivztgekozkvze
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