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1
10-year follow-up of congenital cytomegalovirus infection complicated with severe neurological findings in infancy: a case report
10-year follow-up of congenital cytomegalovirus infection complicated with severe neurological findings in infancy: a case report
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10-year follow-up of congenital cytomegalovirus infection complicated with severe neurological findings in infancy: a case report

BMC pediatrics, 2018-11, Vol.18 (1), p.369-369, Article 369 [Peer Reviewed Journal]

COPYRIGHT 2018 BioMed Central Ltd. ;COPYRIGHT 2018 BioMed Central Ltd. ;Copyright © 2018. 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). 2018 ;ISSN: 1471-2431 ;EISSN: 1471-2431 ;DOI: 10.1186/s12887-018-1348-8 ;PMID: 30470211

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2
10-Year Overview of the Hospital-Based Prevalence and Treatment of Congenital Cataracts: The CCPMOH Experience
10-Year Overview of the Hospital-Based Prevalence and Treatment of Congenital Cataracts: The CCPMOH Experience
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10-Year Overview of the Hospital-Based Prevalence and Treatment of Congenital Cataracts: The CCPMOH Experience

PloS one, 2015-11, Vol.10 (11), p.e0142298-e0142298 [Peer Reviewed Journal]

2015 Lin et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2015 Lin et al 2015 Lin et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0142298 ;PMID: 26540510

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3
100 days outcome of severe wasting in hospitalised infants <6 months of age
100 days outcome of severe wasting in hospitalised infants <6 months of age
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100 days outcome of severe wasting in hospitalised infants <6 months of age

Public health nutrition, 2021-12, Vol.24 (17), p.5847-5856 [Peer Reviewed Journal]

The Author(s), 2021. Published by Cambridge University Press on behalf of The Nutrition Society ;The Authors 2021 2021 The Authors ;ISSN: 1368-9800 ;EISSN: 1475-2727 ;DOI: 10.1017/S1368980021003268 ;PMID: 34353402

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4
1000 Days: The "WeCare Generation" Program-The Ultimate Model for Improving Human Mental Health and Economics: The Study Protocol
1000 Days: The "WeCare Generation" Program-The Ultimate Model for Improving Human Mental Health and Economics: The Study Protocol
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1000 Days: The "WeCare Generation" Program-The Ultimate Model for Improving Human Mental Health and Economics: The Study Protocol

International journal of environmental research and public health, 2022-12, Vol.19 (24), p.16741 [Peer Reviewed Journal]

2022 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. ;2022 by the authors. 2022 ;ISSN: 1660-4601 ;ISSN: 1661-7827 ;EISSN: 1660-4601 ;DOI: 10.3390/ijerph192416741 ;PMID: 36554625

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5
106: REVIEW OF SCREENING PROGRAM EFFECT ON INCIDENCE OF HEMOLYTIC DISEASE DUE TO G6PD DEFICIENCIES
106: REVIEW OF SCREENING PROGRAM EFFECT ON INCIDENCE OF HEMOLYTIC DISEASE DUE TO G6PD DEFICIENCIES
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106: REVIEW OF SCREENING PROGRAM EFFECT ON INCIDENCE OF HEMOLYTIC DISEASE DUE TO G6PD DEFICIENCIES

BMJ open, 2017-02, Vol.7 (Suppl 1), p.bmjopen-2016-015415.106 [Peer Reviewed Journal]

Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ 2017 This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ 2017 ;ISSN: 2044-6055 ;EISSN: 2044-6055 ;DOI: 10.1136/bmjopen-2016-015415.106

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6
11-Keto-testosterone and other androgens of adrenal origin
11-Keto-testosterone and other androgens of adrenal origin
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11-Keto-testosterone and other androgens of adrenal origin

Physiological research, 2020-09, Vol.69 (Suppl 2), p.S187-S192 [Peer Reviewed Journal]

Copyright Institute of Physiology 2020 ;2020 Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic 2020 ;ISSN: 0862-8408 ;EISSN: 1802-9973 ;DOI: 10.33549/physiolres.934516 ;PMID: 33094617

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7
11 Novel Systematic Method for Identifying Congenital Anomaly Cases in Electronic Health Record Databases
11 Novel Systematic Method for Identifying Congenital Anomaly Cases in Electronic Health Record Databases
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11 Novel Systematic Method for Identifying Congenital Anomaly Cases in Electronic Health Record Databases

Journal of clinical and translational science, 2024-04, Vol.8 (s1), p.3-3 [Peer Reviewed Journal]

The Author(s), 2024. The Association for Clinical and Translational Science. This work is licensed under the Creative Commons Attribution – Non-Commercial – No Derivatives License This is an Open Access article, distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is unaltered and is properly cited. The written permission of Cambridge University Press must be obtained for commercial re-use or in order to create a derivative work. (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Association for Clinical and Translational Science 2024 2024 The Association for Clinical and Translational Science ;EISSN: 2059-8661 ;DOI: 10.1017/cts.2024.32

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8
12,13-diHOME and noradrenaline are associated with the occurrence of acute myocardial infarction in patients with type 2 diabetes mellitus
12,13-diHOME and noradrenaline are associated with the occurrence of acute myocardial infarction in patients with type 2 diabetes mellitus
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12,13-diHOME and noradrenaline are associated with the occurrence of acute myocardial infarction in patients with type 2 diabetes mellitus

Diabetology and metabolic syndrome, 2023-06, Vol.15 (1), p.142-142, Article 142 [Peer Reviewed Journal]

2023. The Author(s). ;COPYRIGHT 2023 BioMed Central Ltd. ;2023. 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) 2023 ;ISSN: 1758-5996 ;EISSN: 1758-5996 ;DOI: 10.1186/s13098-023-01115-9 ;PMID: 37386486

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9
15q23 Gain in a Neonate with a Giant Omphalocele and Multiple Co-Occurring Anomalies
15q23 Gain in a Neonate with a Giant Omphalocele and Multiple Co-Occurring Anomalies
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15q23 Gain in a Neonate with a Giant Omphalocele and Multiple Co-Occurring Anomalies

Case reports in pediatrics, 2018-01, Vol.2018, p.8702568-5 [Peer Reviewed Journal]

Copyright © 2018 Hui-Fang Zhou et al. ;Copyright © 2018 Hui-Fang Zhou et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0 ;Copyright © 2018 Hui-Fang Zhou et al. 2018 ;ISSN: 2090-6803 ;EISSN: 2090-6811 ;DOI: 10.1155/2018/8702568 ;PMID: 30538881

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10
15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review
15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review
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15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review

Italian journal of pediatrics, 2021-09, Vol.47 (1), p.188-188, Article 188 [Peer Reviewed Journal]

2021. The Author(s). ;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: 1824-7288 ;ISSN: 1720-8424 ;EISSN: 1824-7288 ;DOI: 10.1186/s13052-021-01121-5 ;PMID: 34530895

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11
17 alpha&#8208;hydroxylase deficiency: A case report of young Chinese woman with a rare gene mutation
17 alpha&#8208;hydroxylase deficiency: A case report of young Chinese woman with a rare gene mutation
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17 alpha‐hydroxylase deficiency: A case report of young Chinese woman with a rare gene mutation

Clinical case reports, 2022-07, Vol.10 (7), p.n/a [Peer Reviewed Journal]

2022 The Authors. published by John Wiley & Sons Ltd. ;2022. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2050-0904 ;EISSN: 2050-0904 ;DOI: 10.1002/ccr3.6109 ;PMID: 35898732

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12
17-hydroxyprogesterone levels in blood from the heels of healthy full-term newborns
17-hydroxyprogesterone levels in blood from the heels of healthy full-term newborns
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17-hydroxyprogesterone levels in blood from the heels of healthy full-term newborns

C.E.S. medicina, 2017, Vol.31 (2), p.127-135 [Peer Reviewed Journal]

Copyright Universidad CES Jul/Dec 2017 ;This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. ;LICENCIA DE USO: Los documentos a texto completo incluidos en Dialnet son de acceso libre y propiedad de sus autores y/o editores. Por tanto, cualquier acto de reproducción, distribución, comunicación pública y/o transformación total o parcial requiere el consentimiento expreso y escrito de aquéllos. Cualquier enlace al texto completo de estos documentos deberá hacerse a través de la URL oficial de éstos en Dialnet. Más información: https://dialnet.unirioja.es/info/derechosOAI | INTELLECTUAL PROPERTY RIGHTS STATEMENT: Full text documents hosted by Dialnet are protected by copyright and/or related rights. This digital object is accessible without charge, but its use is subject to the licensing conditions set by its authors or editors. Unless expressly stated otherwise in the licensing conditions, you are free to linking, browsing, printing and making a copy for your own personal purposes. All other acts of reproduction and communication to the public are subject to the licensing conditions expressed by editors and authors and require consent from them. Any link to this document should be made using its official URL in Dialnet. More info: https://dialnet.unirioja.es/info/derechosOAI ;ISSN: 0120-8705 ;ISSN: 2215-9177 ;EISSN: 2215-9177 ;DOI: 10.21615/cesmedicina.31.2.1

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13
17q23.2q23.3 de novo duplication in association with speech and language disorder, learning difficulties, incoordination, motor skill impairment, and behavioral disturbances: a case report
17q23.2q23.3 de novo duplication in association with speech and language disorder, learning difficulties, incoordination, motor skill impairment, and behavioral disturbances: a case report
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17q23.2q23.3 de novo duplication in association with speech and language disorder, learning difficulties, incoordination, motor skill impairment, and behavioral disturbances: a case report

BMC medical genetics, 2017-10, Vol.18 (1), p.119-119, Article 119 [Peer Reviewed Journal]

COPYRIGHT 2017 BioMed Central Ltd. ;COPYRIGHT 2017 BioMed Central Ltd. ;Copyright BioMed Central 2017 ;The Author(s). 2017 ;ISSN: 1471-2350 ;EISSN: 1471-2350 ;DOI: 10.1186/s12881-017-0479-3 ;PMID: 29070031

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14
17th Annual Southern Hospital Medicine Conference Abstracts
17th Annual Southern Hospital Medicine Conference Abstracts
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17th Annual Southern Hospital Medicine Conference Abstracts

The Ochsner journal, 2017-04, Vol.17 (1), p.e1-e82 [Peer Reviewed Journal]

Copyright © 2017. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the associated terms available at http://www.ochsnerjournal.org/content/permissions ;Academic Division of Ochsner Clinic Foundation 2017 ;ISSN: 1524-5012 ;EISSN: 2831-4107

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15
19&#8197;Management of pregnancy in SLE and APS
19&#8197;Management of pregnancy in SLE and APS
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19 Management of pregnancy in SLE and APS

Lupus science & medicine, 2022-04, Vol.9 (Suppl 1), p.A10-A11 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. ;2022 Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;EISSN: 2053-8790 ;DOI: 10.1136/lupus-2022-la.19

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16
19p13.2 Microdeletion including NFIX associated with overgrowth and intellectual disability suggestive of Malan syndrome
19p13.2 Microdeletion including NFIX associated with overgrowth and intellectual disability suggestive of Malan syndrome
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19p13.2 Microdeletion including NFIX associated with overgrowth and intellectual disability suggestive of Malan syndrome

Molecular cytogenetics, 2016-09, Vol.9 (1), p.71-71, Article 71 [Peer Reviewed Journal]

COPYRIGHT 2016 BioMed Central Ltd. ;Copyright BioMed Central 2016 ;The Author(s). 2016 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-016-0282-4 ;PMID: 27688808

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17
19p13.3 Deletion With Polyotia: A Case Report and Literature Review
19p13.3 Deletion With Polyotia: A Case Report and Literature Review
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19p13.3 Deletion With Polyotia: A Case Report and Literature Review

Curēus (Palo Alto, CA), 2021-11, Vol.13 (11), p.e19661 [Peer Reviewed Journal]

Copyright © 2021, Silvera Redondo et al. ;Copyright © 2021, Silvera Redondo et al. This work is published under https://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. ;Copyright © 2021, Silvera Redondo et al. 2021 Silvera Redondo et al. ;ISSN: 2168-8184 ;EISSN: 2168-8184 ;DOI: 10.7759/cureus.19661 ;PMID: 34976455

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18
1H-NMR Urinary Metabolic Profile, A Promising Tool for the Management of Infants with Human Cytomegalovirus-Infection
1H-NMR Urinary Metabolic Profile, A Promising Tool for the Management of Infants with Human Cytomegalovirus-Infection
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1H-NMR Urinary Metabolic Profile, A Promising Tool for the Management of Infants with Human Cytomegalovirus-Infection

Metabolites, 2019-11, Vol.9 (12), p.288 [Peer Reviewed Journal]

2019 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. ;2019 by the authors. 2019 ;ISSN: 2218-1989 ;EISSN: 2218-1989 ;DOI: 10.3390/metabo9120288 ;PMID: 31775291

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19
2009 H1N1 influenza A in children: a descriptive clinical study
2009 H1N1 influenza A in children: a descriptive clinical study
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2009 H1N1 influenza A in children: a descriptive clinical study

Annals of Saudi medicine, 2012-01, Vol.32 (1), p.59-63 [Peer Reviewed Journal]

COPYRIGHT 2012 Medknow Publications and Media Pvt. Ltd. ;2012. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Copyright © 2012, Annals of Saudi Medicine 2012 ;ISSN: 0256-4947 ;EISSN: 0975-4466 ;DOI: 10.5144/0256-4947.2012.59 ;PMID: 22156647

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20
2019 HRS/EHRA/APHRS/LAHRS expert consensus statement on catheter ablation of ventricular arrhythmias: Executive summary
2019 HRS/EHRA/APHRS/LAHRS expert consensus statement on catheter ablation of ventricular arrhythmias: Executive summary
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2019 HRS/EHRA/APHRS/LAHRS expert consensus statement on catheter ablation of ventricular arrhythmias: Executive summary

Journal of arrhythmia, 2020-02, Vol.36 (1), p.1-58 [Peer Reviewed Journal]

2020 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of the Japanese Heart Rhythm Society. ;2020 The Authors. Journal of Arrhythmia published by John Wiley & Sons Australia, Ltd on behalf of the Japanese Heart Rhythm Society. ;COPYRIGHT 2020 John Wiley & Sons, Inc. ;2020. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1880-4276 ;EISSN: 1883-2148 ;DOI: 10.1002/joa3.12264 ;PMID: 32071620

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