Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Article
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Pedicle subtraction osteotomy in patient with congenital kyphosisEgyptian journal of neurosurgery, 2024-12, Vol.39 (1), p.17-5 [Peer Reviewed Journal]The Author(s) 2024 ;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. ;EISSN: 2520-8225 ;DOI: 10.1186/s41984-024-00283-8Full text available |
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2 |
Material Type: Article
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Can placental shear wave elastography predict preeclampsia in high-risk pregnant women during second trimester? Insights from a prospective cohort studyEgyptian Journal of Radiology and Nuclear Medicine, 2024-12, Vol.55 (1), p.45-9 [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: 0378-603X ;EISSN: 2090-4762 ;DOI: 10.1186/s43055-024-01205-2Full text available |
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3 |
Material Type: Article
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Predictors of mortality in critically ill children hospitalized with laboratory- confirmed COVID-19 pneumoniaThe Egyptian Journal of Bronchology, 2024-12, Vol.18 (1), p.2-6, Article 2 [Peer Reviewed Journal]The Author(s) 2023 ;The Author(s) 2023. 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: 2314-8551 ;ISSN: 1687-8426 ;EISSN: 2314-8551 ;DOI: 10.1186/s43168-023-00254-xFull text available |
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4 |
Material Type: Article
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Novel mutation as a cause of anterior segment dysgenesis leading to blindness in progeny: the genetics decodedEgyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.20-5 [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/s43042-024-00493-7Full text available |
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5 |
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 |
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6 |
Material Type: Article
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Congenital cardiac surgery and diaphragmatic paralysis: efficacy of diaphragm plicationCardiothoracic Surgeon, 2024-12, Vol.32 (1), p.5-6 [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: 2636-333X ;EISSN: 2662-2203 ;DOI: 10.1186/s43057-024-00126-0Full text available |
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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 |
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8 |
Material Type: Article
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Predictors of mortality among children at a tertiary hospital in Tanzania: a cohort studyThe Gazette of the Egyptian Paediatric Association, 2024-12, Vol.72 (1), p.30-11 [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: 1110-6638 ;EISSN: 2090-9942 ;DOI: 10.1186/s43054-024-00271-5Full text available |
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9 |
Material Type: Article
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Screening of GHSR, GHRHR, GH1 genes in isolated growth hormone deficiency disease in Egyptian patientsEgyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.16-11 [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/s43042-024-00480-yFull text available |
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10 |
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 |
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11 |
Material Type: Article
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Unusual coexistence of restrictive heart disease and Kallmann syndrome: a case reportThe Egyptian heart journal, 2024-12, Vol.76 (1), p.50-50 [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/s43044-024-00479-1 ;PMID: 38635120Full text available |
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12 |
Material Type: Article
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Trisomy 21-driven metabolite alterations are linked to cellular injuries in Down syndromeCellular and molecular life sciences : CMLS, 2024-12, Vol.81 (1), p.112-112 [Peer Reviewed Journal]The Author(s) 2024 ;2024. The Author(s). ;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: 1420-682X ;EISSN: 1420-9071 ;DOI: 10.1007/s00018-024-05127-0 ;PMID: 38433139Digital Resources/Online E-Resources |
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13 |
Material Type: Article
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An unknown wide persistent ductus arteriosus debuting with atrial fibrillation in older adult: a case reportEgyptian Journal of Radiology and Nuclear Medicine, 2024-12, Vol.55 (1), p.66-4 [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: 0378-603X ;EISSN: 2090-4762 ;DOI: 10.1186/s43055-024-01239-6Full text available |
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14 |
Material Type: Article
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Conventional and molecular cytogenetic characterization of a Moroccan patient with WAGR syndromeEgyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.37-6 [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/s43042-024-00514-5Full text available |
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15 |
Material Type: Article
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Genome-wide analysis identifies MYH11 compound heterozygous variants leading to visceral myopathy corresponding to late-onset form of megacystis-microcolon-intestinal hypoperistalsis syndromeMolecular genetics and genomics : MGG, 2024-12, Vol.299 (1), p.44-44 [Peer Reviewed Journal]The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, 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. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1617-4615 ;EISSN: 1617-4623 ;DOI: 10.1007/s00438-024-02136-3 ;PMID: 38625590Digital Resources/Online E-Resources |
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16 |
Material Type: Article
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Consanguinity, complex diseases and congenital disabilities in the Souss population (Southern Morocco): a cross-sectional surveyEgyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.27-12 [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/s43042-024-00490-wFull text available |
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17 |
Material Type: Article
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Efficacy of inhaled iloprost in children with pulmonary hypertension after pediatric cardiac surgery: a case seriesCardiothoracic Surgeon, 2024-12, Vol.32 (1), p.7-7 [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: 2636-333X ;EISSN: 2662-2203 ;DOI: 10.1186/s43057-024-00125-1Full text available |
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18 |
Material Type: Article
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Scaffold-free bone-like 3D structure established through osteogenic differentiation from human gingiva-derived stem cellsBiochemistry and biophysics reports, 2024-07, Vol.38, p.101656-101656, Article 101656 [Peer Reviewed Journal]2024 The Authors ;2024 The Authors. ;2024 The Authors 2024 ;ISSN: 2405-5808 ;EISSN: 2405-5808 ;DOI: 10.1016/j.bbrep.2024.101656 ;PMID: 38379857Full text available |
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19 |
Material Type: Article
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Risk Factors and Outcomes Associated with Gaps in Care in Children with Congenital Heart DiseasePediatric cardiology, 2024-06, Vol.45 (5), p.976-985 [Peer Reviewed Journal]The Author(s) 2024 ;2024. The Author(s). ;ISSN: 0172-0643 ;EISSN: 1432-1971 ;DOI: 10.1007/s00246-024-03414-y ;PMID: 38485760Digital Resources/Online E-Resources |
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20 |
Material Type: Article
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Compound Heterozygous ROBO3 Mutation in Two Siblings Presenting with Horizontal Gaze Palsy without Scoliosis: Case-Based ReviewJournal of pediatric genetics (Birmingham, Ala.), 2024-06, Vol.13 (2), p.116-122 [Peer Reviewed Journal]Thieme. All rights reserved. ;Thieme. All rights reserved. 2021 Georg Thieme Verlag KG ;ISSN: 2146-4596 ;EISSN: 2146-460X ;DOI: 10.1055/s-0041-1739387 ;PMID: 38721573Digital Resources/Online E-Resources |