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Results 21 - 40 of 84,676  for All Library Resources

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21
Congenital diseases caused by defective O -glycosylation of Notch receptors
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Congenital diseases caused by defective O -glycosylation of Notch receptors

Nagoya journal of medical science, 2018-08, Vol.80 (3), p.299-307

ISSN: 0027-7622 ;EISSN: 2186-3326 ;DOI: 10.18999/nagjms.80.3.299 ;PMID: 30214079

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22
Unexplained stillbirth versus SIDS: common congenital diseases of the autonomic nervous system--pathology and nosology
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Unexplained stillbirth versus SIDS: common congenital diseases of the autonomic nervous system--pathology and nosology

Early human development, 2011-03, Vol.87 (3), p.209 [Peer Reviewed Journal]

Copyright © 2010 Elsevier Ireland Ltd. All rights reserved. ;EISSN: 1872-6232 ;DOI: 10.1016/j.earlhumdev.2010.12.009 ;PMID: 21262556

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23
New insights into the roles for DYRK family in mammalian development and congenital diseases
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New insights into the roles for DYRK family in mammalian development and congenital diseases

Genes & 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: 37396550

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24
Epigenetic deregulation of imprinting in congenital diseases of aberrant growth
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Epigenetic deregulation of imprinting in congenital diseases of aberrant growth

BioEssays, 2006-05, Vol.28 (5), p.453-459 [Peer Reviewed Journal]

Copyright © 2006 Wiley Periodicals, Inc. ;2006 Wiley Periodicals, Inc. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0265-9247 ;EISSN: 1521-1878 ;DOI: 10.1002/bies.20407 ;PMID: 16615080

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25
Unveiling Mysteries in Congenital Diseases: A Case Report of Williams-Beuren Syndrome
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Unveiling Mysteries in Congenital Diseases: A Case Report of Williams-Beuren Syndrome

Cardiovascular innovations and applications, 2024-01, Vol.9 (1), p.984 [Peer Reviewed Journal]

ISSN: 2009-8618 ;EISSN: 2009-8782 ;DOI: 10.15212/CVIA.2024.0005

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26
The impact of neighborhood to industrial areas on health in Uzbekistan: an ecological analysis of congenital diseases, infant mortality, and lung cancer
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The impact of neighborhood to industrial areas on health in Uzbekistan: an ecological analysis of congenital diseases, infant mortality, and lung cancer

Environmental science and pollution research international, 2020-05, Vol.27 (14), p.17243-17249 [Peer Reviewed Journal]

Springer-Verlag GmbH Germany, part of Springer Nature 2020 ;Springer-Verlag GmbH Germany, part of Springer Nature 2020. ;ISSN: 0944-1344 ;EISSN: 1614-7499 ;DOI: 10.1007/s11356-020-08190-9 ;PMID: 32152854

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27
S1936 A Not so Common Case of Recurrent Acute Pancreatitis and Its Implications
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S1936 A Not so Common Case of Recurrent Acute Pancreatitis and Its Implications

The American journal of gastroenterology, 2023-10, Vol.118 (10S), p.S1433-S1434 [Peer Reviewed Journal]

2023 by The American College of Gastroenterology ;ISSN: 0002-9270 ;EISSN: 1572-0241 ;DOI: 10.14309/01.ajg.0000957384.25902.0f

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28
Klinefelterʼs Syndrome-Associated Alpha-1 Antitrypsin Cholestatic Phenotype: A Genetic Linkage Between Two Congenital Diseases: 2005
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Klinefelterʼs Syndrome-Associated Alpha-1 Antitrypsin Cholestatic Phenotype: A Genetic Linkage Between Two Congenital Diseases: 2005

The American journal of gastroenterology, 2016-10, Vol.111, p.S955-S956 [Peer Reviewed Journal]

ISSN: 0002-9270 ;EISSN: 1572-0241 ;DOI: 10.14309/00000434-201610001-02005

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29
Correlation of Folic Acid Metabolism Gene Polymorphism with Maternal Delivery Outcomes and Neonatal Congenital Diseases During Pregnancy
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Article
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Correlation of Folic Acid Metabolism Gene Polymorphism with Maternal Delivery Outcomes and Neonatal Congenital Diseases During Pregnancy

International journal of pharmacology, 2022-05, Vol.18 (5), p.869-876

ISSN: 1811-7775 ;EISSN: 1812-5700 ;DOI: 10.3923/ijp.2022.869.876

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30
S2676 Abnormal Liver Enzymes Secondary to Congenital Hepatic Fibrosis with Multiple Biliary Cysts
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S2676 Abnormal Liver Enzymes Secondary to Congenital Hepatic Fibrosis with Multiple Biliary Cysts

The American journal of gastroenterology, 2021-10, Vol.116 (1), p.S1122-S1122 [Peer Reviewed Journal]

2021 by The American College of Gastroenterology ;ISSN: 0002-9270 ;EISSN: 1572-0241 ;DOI: 10.14309/01.ajg.0000784236.02409.43

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31
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 outcomes
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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 outcomes

Journal 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.2024.100216

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32
1017 Unusual clinical course of congenital central hypoventilation syndrome: is outgrowing the syndrome possible?
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1017 Unusual clinical course of congenital central hypoventilation syndrome: is outgrowing the syndrome possible?

Sleep (New York, N.Y.), 2019-04, Vol.42 (Supplement_1), p.A409-A410 [Peer Reviewed Journal]

Sleep Research Society 2019. Published by Oxford University Press on behalf of the Sleep Research Society. All rights reserved. For permissions, please e-mail journals.permissions@oup.com. ;ISSN: 0161-8105 ;EISSN: 1550-9109 ;DOI: 10.1093/sleep/zsz069.1014

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33
C Identification of the major genetic contributors to tetralogy of fallot
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Article
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C Identification of the major genetic contributors to tetralogy of fallot

Heart (British Cardiac Society), 2019-05, Vol.105 (Suppl 6), p.A182 [Peer Reviewed Journal]

2019, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;2019 2019, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2019-BCS.226

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34
139 Identification of the major genetic contributors to tetralogy of fallot
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139 Identification of the major genetic contributors to tetralogy of fallot

Heart (British Cardiac Society), 2019-05, Vol.105 (Suppl 6), p.A114 [Peer Reviewed Journal]

2019, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;2019 2019, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2019-BCS.136

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35
Comparison of Intramedullary Magnetic Nail, Monolateral External Distractor, and Spatial External Fixator in Femur Lengthening in Adolescents with Congenital Diseases
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Comparison of Intramedullary Magnetic Nail, Monolateral External Distractor, and Spatial External Fixator in Femur Lengthening in Adolescents with Congenital Diseases

Journal 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: 34945254

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36
Molecular genetic and clinical aspects of socially relevant viruses underlying congenital diseases
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Article
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Molecular genetic and clinical aspects of socially relevant viruses underlying congenital diseases

Infekt͡s︡ii͡a︡ 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-1729

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37
S2094 A Late Diagnosis of Caroli Syndrome
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Article
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S2094 A Late Diagnosis of Caroli Syndrome

The American journal of gastroenterology, 2023-10, Vol.118 (10S), p.S1520-S1520 [Peer Reviewed Journal]

2023 by The American College of Gastroenterology ;ISSN: 0002-9270 ;EISSN: 1572-0241 ;DOI: 10.14309/01.ajg.0000958016.55460.bd

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38
Cirrhosis a Long Term Consequence of Congenital Tricuspid Atresia After Fontan Procedure: 2327
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Cirrhosis a Long Term Consequence of Congenital Tricuspid Atresia After Fontan Procedure: 2327

The American journal of gastroenterology, 2018-10, Vol.113 (Supplement), p.S1306-S1307 [Peer Reviewed Journal]

Copyright Wolters Kluwer Health Medical Research, Lippincott Williams & Wilkins Oct 2018 ;ISSN: 0002-9270 ;EISSN: 1572-0241 ;DOI: 10.14309/00000434-201810001-02326

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39
Echocardiographic arterial measurements in complex congenital diseases before bidirectional Glenn: comparison with cardiovascular magnetic resonance imaging
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Article
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Echocardiographic arterial measurements in complex congenital diseases before bidirectional Glenn: comparison with cardiovascular magnetic resonance imaging

European heart journal cardiovascular imaging, 2017-03, Vol.18 (3), p.332-341 [Peer Reviewed Journal]

Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2016. For permissions please email: journals.permissions@oup.com. 2016 ;Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2016. For permissions please email: journals.permissions@oup.com. ;ISSN: 2047-2404 ;EISSN: 2047-2412 ;DOI: 10.1093/ehjci/jew069 ;PMID: 27099275

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40
Cardiac Manifestations in a Western Moyamoya Disease Population: A Single Center Descriptive Study and Review
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Article
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Cardiac Manifestations in a Western Moyamoya Disease Population: A Single Center Descriptive Study and Review

Neurosurgery, 2020-12, Vol.67 (Supplement_1) [Peer Reviewed Journal]

Copyright © 2020 by the Congress of Neurological Surgeons 2020 ;Copyright © 2020 by the Congress of Neurological Surgeons ;ISSN: 0148-396X ;EISSN: 1524-4040 ;DOI: 10.1093/neuros/nyaa447_304

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