skip to main content
Language:
Search Limited to: Search Limited to: Resource type Show Results with: Show Results with: Search type Index

Results 1 - 20 of 65,599  for All Library Resources

Results 1 2 3 4 5 next page
Refined by: subject: Life Sciences & Biomedicine remove
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Pedicle subtraction osteotomy in patient with congenital kyphosis
Material Type:
Article
Add to My Research

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

Full text available

2
Can placental shear wave elastography predict preeclampsia in high-risk pregnant women during second trimester? Insights from a prospective cohort study
Material Type:
Article
Add to My Research

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

Full text available

3
Predictors of mortality in critically ill children hospitalized with laboratory- confirmed COVID-19 pneumonia
Material Type:
Article
Add to My Research

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

Full text available

4
Novel mutation as a cause of anterior segment dysgenesis leading to blindness in progeny: the genetics decoded
Material Type:
Article
Add to My Research

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

Full text available

5
Mowat-Wilson syndrome: unraveling the complexities of diagnosis, treatment, and symptom management
Material Type:
Article
Add to My Research

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

Full text available

6
Congenital cardiac surgery and diaphragmatic paralysis: efficacy of diaphragm plication
Material Type:
Article
Add to My Research

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

Full text available

7
Novel and deleterious nucleotide variations in the HAND1 gene probably affect miRNA target sites and protein function in pediatric patients with congenital heart disease
Material Type:
Article
Add to My Research

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

Digital Resources/Online E-Resources

8
Predictors of mortality among children at a tertiary hospital in Tanzania: a cohort study
Material Type:
Article
Add to My Research

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

Full text available

9
Screening of GHSR, GHRHR, GH1 genes in isolated growth hormone deficiency disease in Egyptian patients
Material Type:
Article
Add to My Research

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

Full text available

10
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
Material Type:
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

Digital Resources/Online E-Resources

11
Unusual coexistence of restrictive heart disease and Kallmann syndrome: a case report
Material Type:
Article
Add to My Research

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

Full text available

12
Trisomy 21-driven metabolite alterations are linked to cellular injuries in Down syndrome
Material Type:
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

Digital Resources/Online E-Resources

13
An unknown wide persistent ductus arteriosus debuting with atrial fibrillation in older adult: a case report
Material Type:
Article
Add to My Research

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

Full text available

14
Conventional and molecular cytogenetic characterization of a Moroccan patient with WAGR syndrome
Material Type:
Article
Add to My Research

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

Full text available

15
Genome-wide analysis identifies MYH11 compound heterozygous variants leading to visceral myopathy corresponding to late-onset form of megacystis-microcolon-intestinal hypoperistalsis syndrome
Material Type:
Article
Add to My Research

Genome-wide analysis identifies MYH11 compound heterozygous variants leading to visceral myopathy corresponding to late-onset form of megacystis-microcolon-intestinal hypoperistalsis syndrome

Molecular 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: 38625590

Digital Resources/Online E-Resources

16
Consanguinity, complex diseases and congenital disabilities in the Souss population (Southern Morocco): a cross-sectional survey
Material Type:
Article
Add to My Research

Consanguinity, complex diseases and congenital disabilities in the Souss population (Southern Morocco): a cross-sectional survey

Egyptian 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-w

Full text available

17
Efficacy of inhaled iloprost in children with pulmonary hypertension after pediatric cardiac surgery: a case series
Material Type:
Article
Add to My Research

Efficacy of inhaled iloprost in children with pulmonary hypertension after pediatric cardiac surgery: a case series

Cardiothoracic 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/s43057-024-00125-1

Full text available

18
Scaffold-free bone-like 3D structure established through osteogenic differentiation from human gingiva-derived stem cells
Material Type:
Article
Add to My Research

Scaffold-free bone-like 3D structure established through osteogenic differentiation from human gingiva-derived stem cells

Biochemistry 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: 38379857

Full text available

19
Risk Factors and Outcomes Associated with Gaps in Care in Children with Congenital Heart Disease
Material Type:
Article
Add to My Research

Risk Factors and Outcomes Associated with Gaps in Care in Children with Congenital Heart Disease

Pediatric 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: 38485760

Digital Resources/Online E-Resources

20
Compound Heterozygous ROBO3 Mutation in Two Siblings Presenting with Horizontal Gaze Palsy without Scoliosis: Case-Based Review
Material Type:
Article
Add to My Research

Compound Heterozygous ROBO3 Mutation in Two Siblings Presenting with Horizontal Gaze Palsy without Scoliosis: Case-Based Review

Journal 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: 38721573

Digital Resources/Online E-Resources

Results 1 - 20 of 65,599  for All Library Resources

Results 1 2 3 4 5 next page

Personalize your results

  1. Edit

Refine Search Results

Expand My Results

  1.   

Refine My Results

New Records 

  1. New From Last Month  (17)
  2. New From Last 3 Month  (375)
  3. More options open sub menu

Subject 

  1. Humans  (50,017)
  2. Biological And Medical Sciences  (36,834)
  3. Medical Sciences  (36,290)
  4. Female  (31,433)
  5. Male  (27,962)
  6. Congenital Diseases  (21,242)
  7. Adult  (15,531)
  8. Pediatrics  (13,741)
  9. Surgery  (13,549)
  10. Child  (12,861)
  11. Infant  (11,298)
  12. Infant, Newborn  (10,369)
  13. Cardiovascular System & Cardiology  (10,188)
  14. Adolescent  (10,132)
  15. Child, Preschool  (10,047)
  16. Cardiac & Cardiovascular Systems  (9,520)
  17. Heart  (8,512)
  18. Pregnancy  (8,073)
  19. More options open sub menu

Language 

  1. English  (65,527)
  2. Japanese  (7,816)
  3. Portuguese  (210)
  4. German  (67)
  5. Turkish  (65)
  6. French  (45)
  7. Spanish  (44)
  8. Polish  (22)
  9. Chinese  (21)
  10. Norwegian  (20)
  11. Russian  (10)
  12. Italian  (5)
  13. Korean  (2)
  14. Swedish  (2)
  15. Hungarian  (1)
  16. Dutch  (1)
  17. Ukrainian  (1)
  18. Persian  (1)
  19. Danish  (1)
  20. More options open sub menu

Searching Remote Databases, Please Wait