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1
Left atrial vortex flow and its relationship with left atrial functions in patients with congenital heart disease
Left atrial vortex flow and its relationship with left atrial functions in patients with congenital heart disease
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Left atrial vortex flow and its relationship with left atrial functions in patients with congenital heart disease

The 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: 38696068

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2
Pedicle subtraction osteotomy in patient with congenital kyphosis
Pedicle subtraction osteotomy in patient with congenital kyphosis
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Pedicle subtraction osteotomy in patient with congenital kyphosis

Egyptian 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/s41984-024-00283-8

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3
Can placental shear wave elastography predict preeclampsia in high-risk pregnant women during second trimester? Insights from a prospective cohort study
Can placental shear wave elastography predict preeclampsia in high-risk pregnant women during second trimester? Insights from a prospective cohort study
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Can placental shear wave elastography predict preeclampsia in high-risk pregnant women during second trimester? Insights from a prospective cohort study

Egyptian 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/s43055-024-01205-2

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4
Predictors of mortality in critically ill children hospitalized with laboratory- confirmed COVID-19 pneumonia
Predictors of mortality in critically ill children hospitalized with laboratory- confirmed COVID-19 pneumonia
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Predictors of mortality in critically ill children hospitalized with laboratory- confirmed COVID-19 pneumonia

The 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-x

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5
An alternative surgical approach for isolated pulmonary valve infective endocarditis secondary to restrictive ventricular septal defect: a case report
An alternative surgical approach for isolated pulmonary valve infective endocarditis secondary to restrictive ventricular septal defect: a case report
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An alternative surgical approach for isolated pulmonary valve infective endocarditis secondary to restrictive ventricular septal defect: a case report

Cardiothoracic 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/s43057-024-00123-3

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6
Novel mutation as a cause of anterior segment dysgenesis leading to blindness in progeny: the genetics decoded
Novel mutation as a cause of anterior segment dysgenesis leading to blindness in progeny: the genetics decoded
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Novel mutation as a cause of anterior segment dysgenesis leading to blindness in progeny: the genetics decoded

Egyptian 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/s43042-024-00493-7

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7
Mowat-Wilson syndrome: unraveling the complexities of diagnosis, treatment, and symptom management
Mowat-Wilson syndrome: unraveling the complexities of diagnosis, treatment, and symptom management
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Mowat-Wilson syndrome: unraveling the complexities of diagnosis, treatment, and symptom management

Egyptian 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/s43042-024-00517-2

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8
Congenital cardiac surgery and diaphragmatic paralysis: efficacy of diaphragm plication
Congenital cardiac surgery and diaphragmatic paralysis: efficacy of diaphragm plication
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Congenital cardiac surgery and diaphragmatic paralysis: efficacy of diaphragm plication

Cardiothoracic 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/s43057-024-00126-0

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9
Novel and deleterious nucleotide variations in the HAND1 gene probably affect miRNA target sites and protein function in pediatric patients with congenital heart disease
Novel and deleterious nucleotide variations in the HAND1 gene probably affect miRNA target sites and protein function in pediatric patients with congenital heart disease
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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 disease

Molecular 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: 38551686

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10
A formative mixed methods evaluation of a new Ross program: why context matters
A formative mixed methods evaluation of a new Ross program: why context matters
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A formative mixed methods evaluation of a new Ross program: why context matters

Cardiothoracic Surgeon, 2024-12, Vol.32 (1), p.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: 2636-333X ;EISSN: 2662-2203 ;DOI: 10.1186/s43057-024-00128-y

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11
Predictors of mortality among children at a tertiary hospital in Tanzania: a cohort study
Predictors of mortality among children at a tertiary hospital in Tanzania: a cohort study
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Predictors of mortality among children at a tertiary hospital in Tanzania: a cohort study

The 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/s43054-024-00271-5

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12
Screening of GHSR, GHRHR, GH1 genes in isolated growth hormone deficiency disease in Egyptian patients
Screening of GHSR, GHRHR, GH1 genes in isolated growth hormone deficiency disease in Egyptian patients
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Screening of GHSR, GHRHR, GH1 genes in isolated growth hormone deficiency disease in Egyptian patients

Egyptian 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-y

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13
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 findings
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 findings
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Article 		Add to My Research

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 findings

Molecular 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: 38664339

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14
The detailed profile of congenital heart diseases in 254 children with Down syndrome in Saudi Arabia
The detailed profile of congenital heart diseases in 254 children with Down syndrome in Saudi Arabia
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The detailed profile of congenital heart diseases in 254 children with Down syndrome in Saudi Arabia

Cardiothoracic 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-x

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15
Unusual coexistence of restrictive heart disease and Kallmann syndrome: a case report
Unusual coexistence of restrictive heart disease and Kallmann syndrome: a case report
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Unusual coexistence of restrictive heart disease and Kallmann syndrome: a case report

The 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: 38635120

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16
Trisomy 21-driven metabolite alterations are linked to cellular injuries in Down syndrome
Trisomy 21-driven metabolite alterations are linked to cellular injuries in Down syndrome
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Article 		Add to My Research

Trisomy 21-driven metabolite alterations are linked to cellular injuries in Down syndrome

Cellular 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: 38433139

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17
Appropriate timing of veno-arterial extracorporeal membrane oxygenation initiation after cardiac surgery
Appropriate timing of veno-arterial extracorporeal membrane oxygenation initiation after cardiac surgery
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Appropriate timing of veno-arterial extracorporeal membrane oxygenation initiation after cardiac surgery

Cardiothoracic Surgeon, 2024-12, Vol.32 (1), p.2-9, Article 2 [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/s43057-023-00120-y

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18
An unknown wide persistent ductus arteriosus debuting with atrial fibrillation in older adult: a case report
An unknown wide persistent ductus arteriosus debuting with atrial fibrillation in older adult: a case report
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An unknown wide persistent ductus arteriosus debuting with atrial fibrillation in older adult: a case report

Egyptian 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/s43055-024-01239-6

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19
Engineered platforms for mimicking cardiac development and drug screening
Engineered platforms for mimicking cardiac development and drug screening
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Engineered platforms for mimicking cardiac development and drug screening

Cellular and molecular life sciences : CMLS, 2024-12, Vol.81 (1), p.197-197 [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/s00018-024-05231-1 ;PMID: 38664263

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20
Conventional and molecular cytogenetic characterization of a Moroccan patient with WAGR syndrome
Conventional and molecular cytogenetic characterization of a Moroccan patient with WAGR syndrome
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Conventional and molecular cytogenetic characterization of a Moroccan patient with WAGR syndrome

Egyptian 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/s43042-024-00514-5

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