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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
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A strange congenital disease, familial megaduodenus: review of the literatureRevista española de enfermedades digestivas, 2024-03, Vol.116 (3), p.163-164 [Peer Reviewed Journal]COPYRIGHT 2024 Sociedad Espanola de Patologia Digestivas ;ISSN: 1130-0108 ;DOI: 10.17235/reed.2023.9614/2023 ;PMID: 37073712Full text available |
| 2 |
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Enfermedades Huérfanas Orphaned DiseasesArchivos venezolanos de farmacología y terapéutica, 2020-01, Vol.39 (5), p.627-634Copyright Sociedad Latinoamericana de Hipertension 2020 ;ISSN: 0798-0264 ;EISSN: 2610-7988 ;DOI: 10.5281/zenodo.4263347Full text available |
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Validation of the instrument "Infant Malnutrition and Feeding Checklist for Congenital Heart Disease", a tool to identify risk of malnutrition and feeding difficulties in infants with congenital heart diseaseNutrición hospitalaria : organo oficial de la Sociedad Española de Nutrición Parenteral y Enteral, 2023-04, Vol.40 (2), p.303-311ISSN: 0212-1611 ;EISSN: 1699-5198 ;DOI: 10.20960/nh.04388 ;PMID: 36880736Full text available |
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Middle-Range Theory of Ineffective Breathing Pattern in children with Congenital Heart DiseaseRevista latino-americana de enfermagem, 2022-01, Vol.30, p.e3783-e3783 [Peer Reviewed Journal]2022. This work is published under https://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. ;This work is licensed under a Creative Commons Attribution 4.0 International License. ;ISSN: 1518-8345 ;ISSN: 0104-1169 ;EISSN: 1518-8345 ;DOI: 10.1590/1518-8345.5826.3783 ;PMID: 36629731Full text available |
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Epidemiology of congenital heart diseases in Bogotá, Colombia, from 2001 to 2014: Improved surveillance or increased prevalence?Biomédica, 2018-05, Vol.38, p.148-155 [Peer Reviewed Journal]ISSN: 0120-4157 ;EISSN: 0120-4157 ;DOI: 10.7705/biomedica.v38i0.3381 ;PMID: 29809331Full text available |
| 6 |
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Congenital CLN8 disease of neuronal ceroid lipofuscinosis: a novel phenotypeRevista de neurologiá, 2019-02, Vol.68 (4), p.155-159 [Peer Reviewed Journal]EISSN: 1576-6578 ;DOI: 10.33588/rn.6804.2018217 ;PMID: 30741402Full text available |
| 7 |
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Osteogenesis imperfecta tipo IV originada en una rara variante de cambio de sentido en COL1A2C.E.S. medicina, 2019-09, Vol.33 (3), p.215-223 [Peer Reviewed Journal]COPYRIGHT 2019 Universidad del CES ;COPYRIGHT 2019 Universidad del CES ;Copyright Universidad CES Sep-Dec 2019 ;This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. ;LICENCIA DE USO: Los documentos a texto completo incluidos en Dialnet son de acceso libre y propiedad de sus autores y/o editores. Por tanto, cualquier acto de reproducción, distribución, comunicación pública y/o transformación total o parcial requiere el consentimiento expreso y escrito de aquéllos. Cualquier enlace al texto completo de estos documentos deberá hacerse a través de la URL oficial de éstos en Dialnet. Más información: https://dialnet.unirioja.es/info/derechosOAI | INTELLECTUAL PROPERTY RIGHTS STATEMENT: Full text documents hosted by Dialnet are protected by copyright and/or related rights. This digital object is accessible without charge, but its use is subject to the licensing conditions set by its authors or editors. Unless expressly stated otherwise in the licensing conditions, you are free to linking, browsing, printing and making a copy for your own personal purposes. All other acts of reproduction and communication to the public are subject to the licensing conditions expressed by editors and authors and require consent from them. Any link to this document should be made using its official URL in Dialnet. More info: https://dialnet.unirioja.es/info/derechosOAI ;ISSN: 0120-8705 ;ISSN: 2215-9177 ;DOI: 10.21615/cesmedicina.33.3.7Full text available |
| 8 |
Material Type: Article
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Medical Eponyms linked to nailsNasza dermatologia online, 2012-10, Vol.3 (4), p.379-381Copyright Our Dermatology Online Oct 2013 ;Copyright Our Dermatology Online Oct 2012 ;ISSN: 2081-9390 ;EISSN: 2081-9390 ;DOI: 10.7241/ourd.20124.91Full text available |
| 9 |
Material Type: Article
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Síndrome de Pfeiffer materno y neonatalArchivos venezolanos de farmacología y terapéutica, 2017-01, Vol.36 (6), p.158-161Copyright Sociedad Latinoamericana de Hipertension 2017 ;ISSN: 0798-0264 ;EISSN: 2610-7988Full text available |
| 10 |
Material Type: Article
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Clinico-pathological conference (CPC): patient with congenital heart malformation and infective endocarditis/Conferencia clinico-patologica (CPC): paciente con malformacion cardiaca congenita y endocarditis infecciosa/Conferencia clinico patologica (CPC): paciente com malformacao cardiaca congenita e endocardites infecciosa.(Conference news)Iatreia (Medellín, Colombia), 2014-10, Vol.27 (4), p.465 [Peer Reviewed Journal]COPYRIGHT 2014 Universidad de Antioquia, Facultad de Medicina ;ISSN: 0121-0793Full text available |
| 11 |
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Manejo clínico de la epidermolisis ampollosa distrófica hereditaria: a propósito de un caso/Clinical handling of hereditary dystrophic epidermolysis bullosa: a case reportActa pediátrica española, 2012-01, Vol.70 (1), p.31 [Peer Reviewed Journal]Copyright Ediciones Mayo Jan 2012 ;ISSN: 0001-6640 ;EISSN: 2014-2986Full text available |
| 12 |
Material Type: Article
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Síndrome de Waardenburg tipo 1 en gemelos monocigóticos y su familiaRevista de la Facultad de Medicina, Universidad Nacional de Colombia, 2016-04, Vol.64 (2), p.365-371 [Peer Reviewed Journal]Copyright Universidad Nacional de Colombia 2016 ;This work is licensed under a Creative Commons Attribution 4.0 International License. ;ISSN: 0120-0011 ;EISSN: 2357-3848 ;DOI: 10.15446/revfacmed.v64n2.50290Full text available |
| 13 |
Material Type: Article
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Congenital heart disease mortality in Spain during a 10 year period (2003–2012)Anales de Pediatría, 2018-05, Vol.88 (5), p.273-279 [Peer Reviewed Journal]2017 Asociación Española de Pediatría ;Copyright © 2017 Asociación Española de Pediatría. Publicado por Elsevier España, S.L.U. All rights reserved. ;ISSN: 2341-2879 ;EISSN: 2341-2879 ;DOI: 10.1016/j.anpede.2017.06.003 ;PMID: 28711428Full text available |
| 14 |
Material Type: Article
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Analysis of the effect of interventional therapy for congenital heart disease complicated with pulmonary artery hypertensionRevista argentina de clínica psicológica, 2020-01, Vol.29 (3), p.498Copyright FUNDACIÓN AIGLÉ 2020 ;ISSN: 0327-6716 ;EISSN: 1851-7951 ;DOI: 10.24205/03276716.2020.748Full text available |
| 15 |
Material Type: Article
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Advances in the knowledge of the molecular and cellular bases of congenital heart diseases. Second of two parts: Congenital heart defectsCorSalud, 2019-12, Vol.11 (4), p.307-316 [Peer Reviewed Journal]EISSN: 2078-7170Full text available |
| 16 |
Material Type: Article
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Central venous-to-arterial CO2 difference as a biomarker of outcome in children who underwent surgery for congenital heart diseaseBoletin medico del Hospital Infantil de Mexico, 2023-07, Vol.80 (4), p.253-259 [Peer Reviewed Journal]This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. ;ISSN: 0539-6115 ;ISSN: 1665-1146 ;EISSN: 1665-1146 ;DOI: 10.24875/BMHIM.23000066Full text available |
| 17 |
Material Type: Article
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Congenital and hereditary nail diseaseActas dermo-sifiliográficas (English ed.), 2024-04 [Peer Reviewed Journal]Copyright © 2024 AEDV. Publicado por Elsevier España, S.L.U. All rights reserved. ;EISSN: 1578-2190 ;DOI: 10.1016/j.ad.2024.04.002 ;PMID: 38663727Full text available |
| 18 |
Material Type: Article
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Fifty years of neonatal screening for congenital diseases in SpainAnales de Pediatría, 2019-04, Vol.90 (4), p.205-206 [Peer Reviewed Journal]ISSN: 2341-2879 ;EISSN: 2341-2879 ;DOI: 10.1016/j.anpedi.2018.11.013 ;PMID: 30583992Full text available |
| 19 |
Material Type: Article
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Fluid overload as a predictor of morbidity and mortality in pediatric patients following congenital heart surgeryBoletin medico del Hospital Infantil de Mexico, 2022-05, Vol.79 (3), p.187-192 [Peer Reviewed Journal]This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. ;ISSN: 0539-6115 ;ISSN: 1665-1146 ;EISSN: 1665-1146 ;DOI: 10.24875/BMHIM.21000183Full text available |
| 20 |
Material Type: Article
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22q11.2 deletion syndrome: 20 years of experience from two pediatric immunology units and review of clues for diagnosis and disease managementAllergologia et immunopathologia, 2021-01, Vol.49 (1), p.95-100 [Peer Reviewed Journal]2021. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0301-0546 ;EISSN: 1578-1267 ;DOI: 10.15586/aei.v49i1.24 ;PMID: 33528935Full text available |
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