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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
|---|---|---|---|
| 1 |
Material Type: Article
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Emanuel syndrome due to unusual patternEgyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.21-6 [Peer Reviewed Journal]The Author(s) 2024 ;COPYRIGHT 2024 Springer ;The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-024-00494-6Full text available |
| 2 |
Material Type: Article
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The detailed profile of congenital heart diseases in 254 children with Down syndrome in Saudi ArabiaCardiothoracic Surgeon, 2024-12, Vol.32 (1), p.1-6, Article 1 [Peer Reviewed Journal]The Author(s) 2024 ;COPYRIGHT 2024 Springer ;The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2662-2203 ;ISSN: 2636-333X ;EISSN: 2662-2203 ;DOI: 10.1186/s43057-023-00121-xFull text available |
| 3 |
Material Type: Article
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Left atrial vortex flow and its relationship with left atrial functions in patients with congenital heart diseaseThe Egyptian heart journal, 2024-12, Vol.76 (1), p.53-53 [Peer Reviewed Journal]The Author(s) 2024 ;2024. The Author(s). ;COPYRIGHT 2024 Springer ;The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-2608 ;EISSN: 2090-911X ;DOI: 10.1186/s43044-024-00486-2 ;PMID: 38696068Full text available |
| 4 |
Material Type: Article
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An alternative surgical approach for isolated pulmonary valve infective endocarditis secondary to restrictive ventricular septal defect: a case reportCardiothoracic Surgeon, 2024-12, Vol.32 (1), p.4-5 [Peer Reviewed Journal]The Author(s) 2024. corrected publication 2024 ;COPYRIGHT 2024 Springer ;The Author(s) 2024. corrected publication 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2636-333X ;EISSN: 2662-2203 ;DOI: 10.1186/s43057-024-00123-3Full text available |
| 5 |
Material Type: Article
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Diagnostic yield of the chromosomal microarray analysis in turkish patients with unexplained development delay/ıntellectual disability(ID), autism spectrum disorders and/or multiple congenital anomalies and new clinical findingsMolecular biology reports, 2024-12, Vol.51 (1), p.577-577 [Peer Reviewed Journal]The Author(s), under exclusive licence to Springer Nature B.V. 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. ;2024. The Author(s), under exclusive licence to Springer Nature B.V. ;ISSN: 0301-4851 ;EISSN: 1573-4978 ;DOI: 10.1007/s11033-024-09545-y ;PMID: 38664339Digital Resources/Online E-Resources |
| 6 |
Material Type: Article
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Mowat-Wilson syndrome: unraveling the complexities of diagnosis, treatment, and symptom managementEgyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.40-10 [Peer Reviewed Journal]The Author(s) 2024 ;COPYRIGHT 2024 Springer ;The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-024-00517-2Full text available |
| 7 |
Material Type: Article
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Novel and deleterious nucleotide variations in the HAND1 gene probably affect miRNA target sites and protein function in pediatric patients with congenital heart diseaseMolecular biology reports, 2024-12, Vol.51 (1), p.468-468 [Peer Reviewed Journal]The Author(s), under exclusive licence to Springer Nature B.V. 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. ;2024. The Author(s), under exclusive licence to Springer Nature B.V. ;ISSN: 0301-4851 ;EISSN: 1573-4978 ;DOI: 10.1007/s11033-024-09410-y ;PMID: 38551686Digital Resources/Online E-Resources |
| 8 |
Material Type: Article
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Roles of cardiac neural crest cells in cardiovascular development and associated congenital defects-an integrated reviewTranslational research in anatomy, 2024-09, Vol.36, p.100304, Article 100304 [Peer Reviewed Journal]2024 ;ISSN: 2214-854X ;EISSN: 2214-854X ;DOI: 10.1016/j.tria.2024.100304Full text available |
| 9 |
Material Type: Article
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Combined genetic-pharmacologic inactivation of tightly linked ADAMTS proteases in temporally specific windows uncovers distinct roles for versican proteolysis and glypican-6 in cardiac developmentMatrix biology, 2024-08, Vol.131, p.1 [Peer Reviewed Journal]ISSN: 0945-053X ;EISSN: 1569-1802 ;DOI: 10.1016/j.matbio.2024.05.003Digital Resources/Online E-Resources |
| 10 |
Material Type: Article
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Mechanical thrombectomy for cerebrovascular occlusion in a patient with situs inversusRadiology case reports, 2024-08, Vol.19 (8), p.3488-3491 [Peer Reviewed Journal]EISSN: 1930-0433Full text available |
| 11 |
Material Type: Reports
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DiGeorge syndrome (22q11.2 deletion syndrome)Mayo Clinic Health Information Library : Diseases and Conditions, 20242024 Mayo Foundation for Medical Education and Research (MRMER). All rights reserved.Digital Resources/Online E-Resources |
| 12 |
Material Type: Reports
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DiGeorge syndrome (22q11.2 deletion syndrome)Mayo Clinic Health Information Library : Diseases and Conditions, 20242024 Mayo Foundation for Medical Education and Research (MRMER). All rights reserved.Digital Resources/Online E-Resources |
| 13 |
Material Type: Reports
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Tetralogy of FallotMayo Clinic Health Information Library : Diseases and Conditions, 20242024 Mayo Foundation for Medical Education and Research (MRMER). All rights reserved.Digital Resources/Online E-Resources |
| 14 |
Material Type: Article
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Effects of antibiotics, hospitalisation and surgical complications on self-reported immunological vulnerability following paediatric open-heart surgery and thymectomy: a single-centre retrospective cohort studyBMJ paediatrics open, 2024-06, Vol.8 (1), p.e002651 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. ;2024 Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2024 ;EISSN: 2399-9772 ;DOI: 10.1136/bmjpo-2024-002651 ;PMID: 38830724Full text available |
| 15 |
Material Type: Reports
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Tetralogy of FallotMayo Clinic Health Information Library : Diseases and Conditions, 20242024 Mayo Foundation for Medical Education and Research (MRMER). All rights reserved.Digital Resources/Online E-Resources |
| 16 |
Material Type: Newsletter Article
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Clinical Electrophysiology Journal Issues Research Articles in May 1, 2024 EditionTargeted News Service, 2024Targeted News ServiceDigital Resources/Online E-Resources |
| 17 |
Material Type: Reports
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Tetralogy of FallotMayo Clinic Health Information Library : Diseases and Conditions, 20242024 Mayo Foundation for Medical Education and Research (MRMER). All rights reserved.Digital Resources/Online E-Resources |
| 18 |
Material Type: Article
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Parents seeking treatment overseasArchives of disease in childhood, 2024-06, Vol.109 (6), p.456-457 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;2024 Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0003-9888 ;EISSN: 1468-2044 ;DOI: 10.1136/archdischild-2023-326729 ;PMID: 38182268Full text available |
| 19 |
Material Type: Article
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Flow pattern analysis of right ventricular outflow tract in repaired tetralogy of Fallot through 4D flow MRIHeart and vessels, 2024-06, Vol.39 (6), p.556-562 [Peer Reviewed Journal]Springer Nature Japan KK, part of Springer Nature 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. ;2024. Springer Nature Japan KK, part of Springer Nature. ;ISSN: 0910-8327 ;EISSN: 1615-2573 ;DOI: 10.1007/s00380-024-02361-1 ;PMID: 38368576Digital Resources/Online E-Resources |
| 20 |
Material Type: Article
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Severity Scoring Cutoff for MLPA and Its Diagnostic Yield in 332 North Indian Children with Developmental DelayJournal of pediatric genetics (Birmingham, Ala.), 2024-06, Vol.13 (2), p.81-89 [Peer Reviewed Journal]Thieme. All rights reserved. ;Thieme. All rights reserved. 2022 Georg Thieme Verlag KG ;ISSN: 2146-4596 ;EISSN: 2146-460X ;DOI: 10.1055/s-0042-1757194 ;PMID: 38721576Digital Resources/Online E-Resources |
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