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2022 EIP abstract book
2022 EIP abstract book
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2022 EIP abstract book

Cogent public health, 2022-12, Vol.9 (1) [Peer Reviewed Journal]

2022 The Author(s). This open access article is distributed under a Creative Commons Attribution (CC-BY) 4.0 license. This work is licensed under the Creative Commons Attribution License 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: 2770-7571 ;EISSN: 2770-7571 ;DOI: 10.1080/27707571.2022.2138037

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2
22q11 deletion syndrome: current perspective
22q11 deletion syndrome: current perspective
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22q11 deletion syndrome: current perspective

Application of clinical genetics, 2015-01, Vol.8 (default), p.123-132 [Peer Reviewed Journal]

COPYRIGHT 2015 Dove Medical Press Limited ;COPYRIGHT 2015 Dove Medical Press Limited ;2015. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2015 Hacıhamdioğlu et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License 2015 ;ISSN: 1178-704X ;EISSN: 1178-704X ;DOI: 10.2147/TACG.S82105 ;PMID: 26056486

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3
3D-printed scaffolds of mesoporous bioglass/gliadin/polycaprolactone ternary composite for enhancement of compressive strength, degradability, cell responses and new bone tissue ingrowth
3D-printed scaffolds of mesoporous bioglass/gliadin/polycaprolactone ternary composite for enhancement of compressive strength, degradability, cell responses and new bone tissue ingrowth
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3D-printed scaffolds of mesoporous bioglass/gliadin/polycaprolactone ternary composite for enhancement of compressive strength, degradability, cell responses and new bone tissue ingrowth

International journal of nanomedicine, 2018-01, Vol.13, p.5433-5447 [Peer Reviewed Journal]

COPYRIGHT 2018 Dove Medical Press Limited ;2018. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2018 Zhang et al. This work is published and licensed by Dove Medical Press Limited 2018 ;ISSN: 1178-2013 ;ISSN: 1176-9114 ;EISSN: 1178-2013 ;DOI: 10.2147/IJN.S164869 ;PMID: 30271139

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4
3D printing approaches for cardiac tissue engineering and role of immune modulation in tissue regeneration
3D printing approaches for cardiac tissue engineering and role of immune modulation in tissue regeneration
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3D printing approaches for cardiac tissue engineering and role of immune modulation in tissue regeneration

International journal of nanomedicine, 2019-01, Vol.14, p.1311-1333 [Peer Reviewed Journal]

COPYRIGHT 2019 Dove Medical Press Limited ;2019. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2019 Qasim et al. This work is published and licensed by Dove Medical Press Limited 2019 ;ISSN: 1178-2013 ;ISSN: 1176-9114 ;EISSN: 1178-2013 ;DOI: 10.2147/IJN.S189587 ;PMID: 30863063

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5
46,XY agonadism associated with adrenal adenoma myelolipoma: report of a case analyzing Y-chromosome-specific sequences
46,XY agonadism associated with adrenal adenoma myelolipoma: report of a case analyzing Y-chromosome-specific sequences
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46,XY agonadism associated with adrenal adenoma myelolipoma: report of a case analyzing Y-chromosome-specific sequences

Gynecological endocrinology, 2003-10, Vol.17 (5), p.429-432 [Peer Reviewed Journal]

2003 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2003 ;2004 INIST-CNRS ;ISSN: 0951-3590 ;EISSN: 1473-0766 ;DOI: 10.1080/09513590312331290348 ;PMID: 14710593 ;CODEN: GYENER

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6
A 5-year follow-up study of neonates with Hirschsprung's disease undergoing transanal Soave or Swenson surgery
A 5-year follow-up study of neonates with Hirschsprung's disease undergoing transanal Soave or Swenson surgery
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A 5-year follow-up study of neonates with Hirschsprung's disease undergoing transanal Soave or Swenson surgery

Patient preference and adherence, 2017-01, Vol.11, p.1957-1961 [Peer Reviewed Journal]

COPYRIGHT 2017 Dove Medical Press Limited ;COPYRIGHT 2020 Dove Medical Press Limited ;COPYRIGHT 2017 Dove Medical Press Limited ;COPYRIGHT 2020 Dove Medical Press Limited ;2017 Zhang et al. This work is published and licensed by Dove Medical Press Limited 2017 ;ISSN: 1177-889X ;EISSN: 1177-889X ;DOI: 10.2147/PPA.S149722 ;PMID: 29238171

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7
AB Blood Group Confers Higher Risk for Primary Brain Tumors in Pediatrics
AB Blood Group Confers Higher Risk for Primary Brain Tumors in Pediatrics
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AB Blood Group Confers Higher Risk for Primary Brain Tumors in Pediatrics

Risk management and healthcare policy, 2021-01, Vol.14, p.4031-4035 [Peer Reviewed Journal]

2021 Al Shudifat et al. ;COPYRIGHT 2021 Dove Medical Press Limited ;2021. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 Al Shudifat et al. 2021 Al Shudifat et al. ;ISSN: 1179-1594 ;EISSN: 1179-1594 ;DOI: 10.2147/RMHP.S322546 ;PMID: 34611451

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8
Abnormalities of Cytokine Receptor Signalling Contributing to Diseases of Red Blood Cell Production
Abnormalities of Cytokine Receptor Signalling Contributing to Diseases of Red Blood Cell Production
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Abnormalities of Cytokine Receptor Signalling Contributing to Diseases of Red Blood Cell Production

Annals of medicine (Helsinki), 1999, Vol.31 (3), p.208-216 [Peer Reviewed Journal]

1999 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 1999 ;1999 INIST-CNRS ;ISSN: 0785-3890 ;EISSN: 1365-2060 ;DOI: 10.3109/07853899909115980 ;PMID: 10442676

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9
Absence epilepsy and the CHD2 gene: an adolescent male with moderate intellectual disability, short-lasting psychoses, and an interstitial deletion in 15q26.1-q26.2
Absence epilepsy and the CHD2 gene: an adolescent male with moderate intellectual disability, short-lasting psychoses, and an interstitial deletion in 15q26.1-q26.2
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Absence epilepsy and the CHD2 gene: an adolescent male with moderate intellectual disability, short-lasting psychoses, and an interstitial deletion in 15q26.1-q26.2

Neuropsychiatric disease and treatment, 2016-05, Vol.12 (Issue 1), p.1135-1139 [Peer Reviewed Journal]

2016. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2016 Verhoeven et al. This work is published and licensed by Dove Medical Press Limited 2016 ;ISSN: 1176-6328 ;ISSN: 1178-2021 ;EISSN: 1178-2021 ;DOI: 10.2147/NDT.S102272 ;PMID: 27274247

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10
Abstracts of Poster Presentations
Abstracts of Poster Presentations
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Abstracts of Poster Presentations

The journal of maternal-fetal & neonatal medicine, 2004-10, Vol.16, p.133 [Peer Reviewed Journal]

Copyright CRC Press Oct 2004 ;ISSN: 1476-7058 ;EISSN: 1476-4954 ;CODEN: JMNMAE

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11
Accuracy of the hypospadias diagnoses and surgical treatment registrations in the Danish National Patient Register
Accuracy of the hypospadias diagnoses and surgical treatment registrations in the Danish National Patient Register
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Accuracy of the hypospadias diagnoses and surgical treatment registrations in the Danish National Patient Register

Clinical epidemiology, 2017-01, Vol.9, p.483-489 [Peer Reviewed Journal]

COPYRIGHT 2017 Dove Medical Press Limited ;COPYRIGHT 2017 Dove Medical Press Limited ;2017. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2017 Arendt et al. This work is published and licensed by Dove Medical Press Limited 2017 ;ISSN: 1179-1349 ;EISSN: 1179-1349 ;DOI: 10.2147/CLEP.S143118 ;PMID: 29042817

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12
Acne in Apert's syndrome: treatment with isotretinoin
Acne in Apert's syndrome: treatment with isotretinoin
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Acne in Apert's syndrome: treatment with isotretinoin

The Journal of dermatological treatment, 2003, Vol.14 (1), p.43-45 [Peer Reviewed Journal]

2003 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2003 ;2003 INIST-CNRS ;ISSN: 0954-6634 ;EISSN: 1471-1753 ;DOI: 10.1080/09546630305549 ;PMID: 12745854

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13
Acquired Factor XIII Deficiency Inducing Recurrent and Fatal Bleeding, Description of a Case
Acquired Factor XIII Deficiency Inducing Recurrent and Fatal Bleeding, Description of a Case
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Acquired Factor XIII Deficiency Inducing Recurrent and Fatal Bleeding, Description of a Case

Journal of blood medicine, 2020-01, Vol.11, p.43-45 [Peer Reviewed Journal]

2020 Di Micco et al. ;COPYRIGHT 2020 Dove Medical Press Limited ;COPYRIGHT 2020 Dove Medical Press Limited ;2020. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2020 Di Micco et al. 2020 Di Micco et al. ;ISSN: 1179-2736 ;EISSN: 1179-2736 ;DOI: 10.2147/JBM.S232115 ;PMID: 32099500

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14
Acquired hemophilia A: emerging treatment options
Acquired hemophilia A: emerging treatment options
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Acquired hemophilia A: emerging treatment options

Journal of Blood Medicine, 2015-01, Vol.6 (default), p.143-150 [Peer Reviewed Journal]

COPYRIGHT 2015 Dove Medical Press Limited ;COPYRIGHT 2015 Dove Medical Press Limited ;2015. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2015 Janbain et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License 2015 ;ISSN: 1179-2736 ;EISSN: 1179-2736 ;DOI: 10.2147/JBM.S77332 ;PMID: 26056504

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15
Acquired hypofibrinogenemia: current perspectives
Acquired hypofibrinogenemia: current perspectives
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Acquired hypofibrinogenemia: current perspectives

Journal of Blood Medicine, 2016-01, Vol.7, p.217-225 [Peer Reviewed Journal]

COPYRIGHT 2016 Dove Medical Press Limited ;2016. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2016 Besser and MacDonald. This work is published and licensed by Dove Medical Press Limited 2016 ;ISSN: 1179-2736 ;EISSN: 1179-2736 ;DOI: 10.2147/JBM.S90693 ;PMID: 27713652

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16
Acquired von Willebrand syndrome in multiple myeloma
Acquired von Willebrand syndrome in multiple myeloma
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Acquired von Willebrand syndrome in multiple myeloma

Hematology (Luxembourg), 2011-07, Vol.16 (4), p.209-212 [Peer Reviewed Journal]

W. S. Maney & Son Ltd 2011 2011 ;ISSN: 1607-8454 ;EISSN: 1607-8454 ;DOI: 10.1179/102453311X12953015767617 ;PMID: 21756536

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17
Acute forearm compartment syndrome in the setting of acquired hemophilia A
Acute forearm compartment syndrome in the setting of acquired hemophilia A
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Acute forearm compartment syndrome in the setting of acquired hemophilia A

Case reports in plastic surgery and hand surgery, 2022-12, Vol.9 (1), p.140-144 [Peer Reviewed Journal]

2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. ;2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This work is licensed under the Creative Commons Attribution License 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. ;2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2022 The Author(s) ;ISSN: 2332-0885 ;EISSN: 2332-0885 ;DOI: 10.1080/23320885.2022.2071274 ;PMID: 35601981

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18
Acute leukemia in congenital methehemoglobinemia - an enigma to explore
Acute leukemia in congenital methehemoglobinemia - an enigma to explore
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Acute leukemia in congenital methehemoglobinemia - an enigma to explore

Journal of community hospital internal medicine perspectives, 2019, Vol.9 (1), p.55-58 [Peer Reviewed Journal]

2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of Greater Baltimore Medical Center. This work is licensed under the Creative Commons Attribution – Non-Commercial License 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. ;2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of Greater Baltimore Medical Center. 2019 The Author(s) ;ISSN: 2000-9666 ;EISSN: 2000-9666 ;DOI: 10.1080/20009666.2018.1555431 ;PMID: 30788079

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19
Acute leukemia in congenital methehemoglobinemia - an enigma to explore
Acute leukemia in congenital methehemoglobinemia - an enigma to explore
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Acute leukemia in congenital methehemoglobinemia - an enigma to explore

Journal of Community Hospital Internal Medicine Perspectives, 2019, Vol.9 (1), p.55-58

2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of Greater Baltimore Medical Center. 2019 ;EISSN: 2000-9666 ;DOI: 10.1080/20009666.2018.1555431

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20
Acute renal failure in critically ill newborns increases the risk of death: a prospective observational study from India
Acute renal failure in critically ill newborns increases the risk of death: a prospective observational study from India
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Acute renal failure in critically ill newborns increases the risk of death: a prospective observational study from India

The journal of maternal-fetal & neonatal medicine, 2016-09, Vol.29 (17), p.2878-2882 [Peer Reviewed Journal]

2015 Taylor & Francis. 2015 ;ISSN: 1476-7058 ;EISSN: 1476-4954 ;DOI: 10.3109/14767058.2015.1107900 ;PMID: 26479450

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