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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2009 4
2010 1
2012 1
2015 3
2016 2
2017 2
2018 2
2019 1
2020 2
2021 4
2022 6
2023 1
2024 1

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27 results

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Page 1
"You Have to Find a Way for This Child to Be at the Center": Pediatric Cardiologists' Views on Triadic Communication in Consultations on Congenital Heart Defects.
Karni-Visel Y, Dekel R, Sadeh Y, Sherman L, Katz U. Karni-Visel Y, et al. Among authors: katz u. Health Commun. 2024 Apr 1:1-12. doi: 10.1080/10410236.2024.2329422. Online ahead of print. Health Commun. 2024. PMID: 38557305
Communication in pediatric medicine is especially challenging because it includes children and their parent(s), and children's cognitive and communication skills are still developing. ...The grounded theory approach was used to identify three main categories: (1) th …
Communication in pediatric medicine is especially challenging because it includes children and their parent(s), and children's …
Comparison of Speckle Tracking Echocardiography During Different Pacing Modalities for Cardiac Resynchronization Therapy Response Prediction.
Tejman-Yarden S, Barzilai DH, Ertracht O, Bachner-Heinenzon N, Bogdan S, Katz U, Chatterji S, Dray EM, Bolkier Y, Glikson M, Beinart R. Tejman-Yarden S, et al. Among authors: katz u. Heart Int. 2022 Jun 1;16(1):64-70. doi: 10.17925/HI.2022.16.1.64. eCollection 2022. Heart Int. 2022. PMID: 36275354 Free PMC article. Review.
Background: The aim of this study was to evaluate left ventricular mechanical activation pattern by speckle tracking echocardiography (STE) as a predictor of response to cardiac resynchronization therapy (CRT) in patients with heart failure. Methods: Echocardiography was p …
Background: The aim of this study was to evaluate left ventricular mechanical activation pattern by speckle tracking echocardiography (STE) …
Vici syndrome in Israel: Clinical and molecular insights.
Chorin O, Hirsch Y, Rock R, Salzer Sheelo L, Goldberg Y, Mandel H, Hershkovitz T, Fleischer N, Greenbaum L, Katz U, Barel O, Hamed N, Ben-Zeev B, Greenberger S, Nasser Samra N, Stern Zimmer M, Raas-Rothschild A, Pode-Shakked B. Chorin O, et al. Among authors: katz u. Front Genet. 2022 Sep 20;13:991721. doi: 10.3389/fgene.2022.991721. eCollection 2022. Front Genet. 2022. PMID: 36204321 Free PMC article.
Finally, based on two-dimensional facial photographs of individuals with Vici syndrome (n = 19), a composite facial mask was created using the DeepGestalt algorithm, illustrating facial features typical of this disorder. Conclusion: We report on ten children and one fetus …
Finally, based on two-dimensional facial photographs of individuals with Vici syndrome (n = 19), a composite facial mask was created using t …
Differences in severity of cardiovascular anomalies in children with Noonan syndrome based on the causative gene.
Shehade-Awwad N, Yeshayahu Y, Pinhas-Hamiel O, Katz U. Shehade-Awwad N, et al. Among authors: katz u. Front Pediatr. 2022 Sep 8;10:946071. doi: 10.3389/fped.2022.946071. eCollection 2022. Front Pediatr. 2022. PMID: 36160796 Free PMC article.
We analyzed molecular genetics and the severity of cardiac malformations. RESULTS: The cohort comprised 74 children with NS. Consistent with previous studies, pathogenic variants in PTPN11 were the most common (62%). Cardiovascular anomalies presented in 57%; pulmonary ste …
We analyzed molecular genetics and the severity of cardiac malformations. RESULTS: The cohort comprised 74 children with NS. Consiste …
Clinical Features in a Large Cohort of Patients With 22q11.2 Deletion Syndrome.
Nissan E, Katz U, Levy-Shraga Y, Frizinsky S, Carmel E, Gothelf D, Somech R. Nissan E, et al. Among authors: katz u. J Pediatr. 2021 Nov;238:215-220.e5. doi: 10.1016/j.jpeds.2021.07.020. Epub 2021 Jul 17. J Pediatr. 2021. PMID: 34284033
The most common symptoms that led to diagnosis were congenital heart defect, speech delay, palate anomalies, and developmental delay. Common clinical features included recurrent infections (76 patients), congenital heart diseases (61 patients), and otorhinolaryngolo …
The most common symptoms that led to diagnosis were congenital heart defect, speech delay, palate anomalies, and developmental delay. …
Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects.
Bolkier Y, Barel O, Marek-Yagel D, Atias-Varon D, Kagan M, Vardi A, Mishali D, Katz U, Salem Y, Tirosh-Wagner T, Jacobson JM, Raas-Rothschild A, Chorin O, Eliyahu A, Sarouf Y, Shlomovitz O, Veber A, Shalva N, Javasky E, Ben Moshe Y, Staretz-Chacham O, Rechavi G, Mane S, Anikster Y, Vivante A, Pode-Shakked B. Bolkier Y, et al. Among authors: katz u. J Med Genet. 2022 Jul;59(7):691-696. doi: 10.1136/jmedgenet-2021-107775. Epub 2021 Jul 2. J Med Genet. 2022. PMID: 34215651
BACKGROUND: The molecular basis of heterotaxy and congenital heart malformations associated with disruption of left-right asymmetry is broad and heterogenous, with over 25 genes implicated in its pathogenesis thus far. OBJECTIVE: We sought to elucidate the molecular basis …
BACKGROUND: The molecular basis of heterotaxy and congenital heart malformations associated with disruption of left-right asymmetry i …
Immune and TRG repertoire signature of the thymus in Down syndrome patients.
Rabinowicz S, Lev A, Lee YN, Machnes-Maayan D, Katz U, Vardi A, Mishali D, Somech R. Rabinowicz S, et al. Among authors: katz u. Pediatr Res. 2021 Jan;89(1):102-109. doi: 10.1038/s41390-020-0857-y. Epub 2020 Mar 31. Pediatr Res. 2021. PMID: 32231346
METHODS: Genomic DNA was extracted from thymuses of pediatric patients who underwent heart surgery, where six were with DS and six were non-syndromic patients. ...
METHODS: Genomic DNA was extracted from thymuses of pediatric patients who underwent heart surgery, where six were with DS and six we …
27 results