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1 |
Material Type: Article
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Congenital Diseases of DNA Replication: Clinical Phenotypes and Molecular MechanismsInternational journal of molecular sciences, 2021-01, Vol.22 (2), p.911 [Peer Reviewed Journal]2021. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms22020911 ;PMID: 33477564Full text available |
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2 |
Material Type: Article
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Pre-Ribosomal RNA Processing in Human Cells: From Mechanisms to Congenital DiseasesBiomolecules (Basel, Switzerland), 2018-10, Vol.8 (4), p.123 [Peer Reviewed Journal]2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Distributed under a Creative Commons Attribution 4.0 International License ;2018 by the authors. 2018 ;ISSN: 2218-273X ;EISSN: 2218-273X ;DOI: 10.3390/biom8040123 ;PMID: 30356013Full text available |
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3 |
Material Type: Article
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Infants with Congenital Diseases Identified through Newborn Screening-United States, 2018-2020International journal of neonatal screening, 2023-04, Vol.9 (2), p.23 [Peer Reviewed Journal]COPYRIGHT 2023 MDPI AG ;2023 by the authors. 2023 ;ISSN: 2409-515X ;EISSN: 2409-515X ;DOI: 10.3390/ijns9020023 ;PMID: 37092517Full text available |
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4 |
Material Type: Article
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Bone fragility in patients affected by congenital diseases non skeletal in originOrphanet journal of rare diseases, 2021-01, Vol.16 (1), p.11-11, Article 11 [Peer Reviewed Journal]COPYRIGHT 2021 BioMed Central Ltd. ;2021. This work is licensed 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. ;The Author(s) 2021 ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/s13023-020-01611-5 ;PMID: 33407701Full text available |
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5 |
Material Type: Article
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New insights into the roles for DYRK family in mammalian development and congenital diseasesGenes & diseases, 2023-05, Vol.10 (3), p.758-770 [Peer Reviewed Journal]2022 Chongqing Medical University ;2022 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. ;2022 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. 2022 Chongqing Medical University ;ISSN: 2352-3042 ;ISSN: 2352-4820 ;EISSN: 2352-3042 ;DOI: 10.1016/j.gendis.2021.12.004 ;PMID: 37396550Full text available |
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6 |
Material Type: Article
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Unveiling Mysteries in Congenital Diseases: A Case Report of Williams-Beuren SyndromeCardiovascular innovations and applications, 2024-01, Vol.9 (1), p.984 [Peer Reviewed Journal]ISSN: 2009-8618 ;EISSN: 2009-8782 ;DOI: 10.15212/CVIA.2024.0005Full text available |
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7 |
Material Type: Article
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Congenital diseases with multi-organ expression as an indication for liver transplantation in children during the first years of life: Integrative approach to improve the outcomesJournal of liver transplantation, 2024-05, Vol.14, Article 100216 [Peer Reviewed Journal]2024 The Author(s) ;ISSN: 2666-9676 ;EISSN: 2666-9676 ;DOI: 10.1016/j.liver.2024.100216Full text available |
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8 |
Material Type: Article
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Comparison of Intramedullary Magnetic Nail, Monolateral External Distractor, and Spatial External Fixator in Femur Lengthening in Adolescents with Congenital DiseasesJournal of clinical medicine, 2021-12, Vol.10 (24), p.5957 [Peer Reviewed Journal]2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 2077-0383 ;EISSN: 2077-0383 ;DOI: 10.3390/jcm10245957 ;PMID: 34945254Full text available |
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9 |
Material Type: Article
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Molecular genetic and clinical aspects of socially relevant viruses underlying congenital diseasesInfekt͡s︡ii͡a︡ i immunitet, 2021-09, Vol.11 (4), p.635-648 [Peer Reviewed Journal]ISSN: 2220-7619 ;EISSN: 2313-7398 ;DOI: 10.15789/2220-7619-MGA-1729Full text available |
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10 |
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]2019 ;ISSN: 2341-2879 ;EISSN: 2341-2879 ;DOI: 10.1016/j.anpede.2018.11.012Full text available |
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11 |
Material Type: Article
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Oral manifestations of genetic and congenital diseasesRevista română de stomatologie (Bucharest, Romania : 2004), 2015-03, Vol.61 (1), p.107-111 [Peer Reviewed Journal]ISSN: 1843-0805 ;EISSN: 2069-6078 ;DOI: 10.37897/RJS.2015.1.21Full text available |
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12 |
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 |
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13 |
Material Type: Article
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Single-cell analysis of developing and azoospermia human testicles reveals central role of Sertoli cellsNature communications, 2020-11, Vol.11 (1), p.5683-5683, Article 5683 [Peer Reviewed Journal]The Author(s) 2020. corrected publication 2021. 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. ;The Author(s) 2020, corrected publication 2021 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-020-19414-4 ;PMID: 33173058Full text available |
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14 |
Material Type: Article
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Molecular screening of the human parvoviruses B19 and bocavirus 1 in the study of congenital diseases as applied to symptomatic pregnant women and childrenAccess microbiology, 2019, Vol.1 (5), p.e000037-e000037 [Peer Reviewed Journal]2019 The Authors. ;2019 The Authors 2019 ;ISSN: 2516-8290 ;EISSN: 2516-8290 ;DOI: 10.1099/acmi.0.000037 ;PMID: 32974527Full text available |
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15 |
Material Type: Article
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Underlying Medical Conditions Associated With Severe COVID-19 Illness Among ChildrenJAMA Network Open, 2021-06, Vol.4 (6), p.e2111182-e2111182 [Peer Reviewed Journal]2021. 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. ;Copyright 2021 Kompaniyets L et al. . ;ISSN: 2574-3805 ;EISSN: 2574-3805 ;DOI: 10.1001/jamanetworkopen.2021.11182 ;PMID: 34097050Full text available |
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16 |
Material Type: Article
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Probable congenital SARS-CoV-2 infection in a neonate born to a woman with active SARS-CoV-2 infectionCanadian Medical Association journal (CMAJ), 2020-06, Vol.192 (24), p.E647-E650 [Peer Reviewed Journal]COPYRIGHT 2020 Joule Inc. ;Copyright Joule Inc Jun 15, 2020 ;2020 Joule Inc. or its licensors 2020 ;ISSN: 0820-3946 ;EISSN: 1488-2329 ;DOI: 10.1503/cmaj.200821 ;PMID: 32409520Full text available |
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17 |
Material Type: Article
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Self-assembling human heart organoids for the modeling of cardiac development and congenital heart diseaseNature communications, 2021-08, Vol.12 (1), p.5142-5142, Article 5142 [Peer Reviewed Journal]2021. The Author(s). ;The Author(s) 2021. 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. ;The Author(s) 2021 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-021-25329-5 ;PMID: 34446706Full text available |
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18 |
Material Type: Article
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Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implicationsScientific reports, 2021-01, Vol.11 (1), p.1526-1526, Article 1526 [Peer Reviewed Journal]The Author(s) 2021. 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. ;The Author(s) 2021 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-81093-y ;PMID: 33452396Full text available |
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Material Type: Article
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SCMR Position Paper (2020) on clinical indications for cardiovascular magnetic resonanceJournal of cardiovascular magnetic resonance, 2020-11, Vol.22 (1), p.76-76, Article 76 [Peer Reviewed Journal]COPYRIGHT 2020 BioMed Central Ltd. ;COPYRIGHT 2020 BioMed Central Ltd. ;2020. This work is licensed 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. ;The Author(s) 2020 ;ISSN: 1532-429X ;ISSN: 1097-6647 ;EISSN: 1532-429X ;DOI: 10.1186/s12968-020-00682-4 ;PMID: 33161900Full text available |
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20 |
Material Type: Article
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Global epidemiology of Duchenne muscular dystrophy: an updated systematic review and meta-analysisOrphanet journal of rare diseases, 2020-06, Vol.15 (1), p.1-141, Article 141 [Peer Reviewed Journal]COPYRIGHT 2020 BioMed Central Ltd. ;2020. This work is licensed 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. ;Attribution ;The Author(s) 2020 ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/s13023-020-01430-8 ;PMID: 32503598Full text available |