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1
Balancing the fat: lipid droplets and human disease
Balancing the fat: lipid droplets and human disease
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Balancing the fat: lipid droplets and human disease

EMBO molecular medicine, 2013-07, Vol.5 (7), p.973-983 [Peer Reviewed Journal]

Copyright © 2013 The Authors. Published by John Wiley and Sons, Ltd on behalf of EMBO ;2013 The Authors. Published by John Wiley and Sons, Ltd on behalf of EMBO. ;2013. This work is published under http://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. ;2013 The Authors. Published by John Wiley and Sons, Ltd on behalf of EMBO 2013 ;ISSN: 1757-4676 ;EISSN: 1757-4684 ;DOI: 10.1002/emmm.201100671 ;PMID: 23740690

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2
Congenital anomalies and maternal age: A systematic review and meta‐analysis of observational studies
Congenital anomalies and maternal age: A systematic review and meta‐analysis of observational studies
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Congenital anomalies and maternal age: A systematic review and meta‐analysis of observational studies

Acta obstetricia et gynecologica Scandinavica, 2022-05, Vol.101 (5), p.484-498 [Peer Reviewed Journal]

2022 The Authors. published by John Wiley & Sons Ltd on behalf of Nordic Federation of Societies of Obstetrics and Gynecology (NFOG). ;2022 The Authors. Acta Obstetricia et Gynecologica Scandinavica published by John Wiley & Sons Ltd on behalf of Nordic Federation of Societies of Obstetrics and Gynecology (NFOG). ;2022. This article 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: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1111/aogs.14339 ;PMID: 35288928

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3
Hippocampal alterations and functional correlates in adolescents and young adults with congenital heart disease
Hippocampal alterations and functional correlates in adolescents and young adults with congenital heart disease
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Hippocampal alterations and functional correlates in adolescents and young adults with congenital heart disease

Human brain mapping, 2019-08, Vol.40 (12), p.3548-3560 [Peer Reviewed Journal]

2019 Wiley Periodicals, Inc. ;ISSN: 1065-9471 ;EISSN: 1097-0193 ;DOI: 10.1002/hbm.24615 ;PMID: 31070841

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4
Guidance for the prevention and emergency management of adult patients with adrenal insufficiency
Guidance for the prevention and emergency management of adult patients with adrenal insufficiency
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Guidance for the prevention and emergency management of adult patients with adrenal insufficiency

Clinical medicine (London, England), 2020-07, Vol.20 (4), p.371-378 [Peer Reviewed Journal]

2020 © 2020 THE AUTHORS. Published by Elsevier Limited on behalf of the Royal College of Physicians. ;Royal College of Physicians 2020. All rights reserved. ;Copyright Royal College of Physicians Jul 2020 ;Royal College of Physicians 2020. All rights reserved. 2020 ;ISSN: 1470-2118 ;EISSN: 1473-4893 ;DOI: 10.7861/clinmed.2019-0324 ;PMID: 32675141

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5
Adrenal insufficiency – recognition and management
Adrenal insufficiency – recognition and management
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Adrenal insufficiency – recognition and management

Clinical medicine (London, England), 2017-06, Vol.17 (3), p.258-262 [Peer Reviewed Journal]

2017 © 2017 THE AUTHORS. Published by Elsevier Limited on behalf of the Royal College of Physicians. ;Royal College of Physicians 2017. All rights reserved. ;Copyright Royal College of Physicians Jun 2017 ;Royal College of Physicians 2017. All rights reserved. 2017 ;ISSN: 1470-2118 ;EISSN: 1473-4893 ;DOI: 10.7861/clinmedicine.17-3-258 ;PMID: 28572228

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6
The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings
The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings
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The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings

Acta obstetricia et gynecologica Scandinavica, 2021-02, Vol.100 (2), p.235-243 [Peer Reviewed Journal]

2020 Nordic Federation of Societies of Obstetrics and Gynecology ;2020 Nordic Federation of Societies of Obstetrics and Gynecology. ;Copyright © 2021 Acta Obstetricia et Gynecologica Scandinavica ;ISSN: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1111/aogs.14003 ;PMID: 32981064

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7
Autosomal recessive non‐syndromic hearing loss genes in Pakistan during the previous three decades
Autosomal recessive non‐syndromic hearing loss genes in Pakistan during the previous three decades
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Autosomal recessive non‐syndromic hearing loss genes in Pakistan during the previous three decades

Journal of cellular and molecular medicine, 2024-04, Vol.28 (8), p.e18119-n/a [Peer Reviewed Journal]

2024 The Authors. published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. ;2024 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. ;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: 1582-1838 ;EISSN: 1582-4934 ;DOI: 10.1111/jcmm.18119 ;PMID: 38534090

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8
Accuracy of fetal echocardiography diagnosis and anticipated perinatal and early postnatal care in congenital heart disease in mid‐gestation
Accuracy of fetal echocardiography diagnosis and anticipated perinatal and early postnatal care in congenital heart disease in mid‐gestation
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Accuracy of fetal echocardiography diagnosis and anticipated perinatal and early postnatal care in congenital heart disease in mid‐gestation

Acta obstetricia et gynecologica Scandinavica, 2022-10, Vol.101 (10), p.1112-1119 [Peer Reviewed Journal]

2022 The Authors. published by John Wiley & Sons Ltd on behalf of Nordic Federation of Societies of Obstetrics and Gynecology (NFOG). ;2022 The Authors. Acta Obstetricia et Gynecologica Scandinavica published by John Wiley & Sons Ltd on behalf of Nordic Federation of Societies of Obstetrics and Gynecology (NFOG). ;2022. This article 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: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1111/aogs.14423 ;PMID: 35818931

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9
Emerging roles of non‐coding RNAs in scoliosis
Emerging roles of non‐coding RNAs in scoliosis
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Emerging roles of non‐coding RNAs in scoliosis

Cell proliferation, 2020-02, Vol.53 (2), p.e12736-n/a [Peer Reviewed Journal]

2019 The Authors. Published by John Wiley & Sons Ltd. ;2019 The Authors. Cell Proliferation Published by John Wiley & Sons Ltd. ;2020. 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: 0960-7722 ;EISSN: 1365-2184 ;DOI: 10.1111/cpr.12736 ;PMID: 31828859

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10
Leukocyte – endothelial interactions in inflammation
Leukocyte – endothelial interactions in inflammation
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Leukocyte – endothelial interactions in inflammation

Journal of cellular and molecular medicine, 2009-07, Vol.13 (7), p.1211-1220 [Peer Reviewed Journal]

2009 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd No claim to US government works ;Copyright Blackwell Publishing Ltd. Jul 2009 ;Copyright John Wiley & Sons, Inc. Jul 2009 ;2009 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd No claim to US government works 2009 ;ISSN: 1582-1838 ;EISSN: 1582-4934 ;DOI: 10.1111/j.1582-4934.2009.00811.x ;PMID: 19538472

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11
A new hERG allosteric modulator rescues genetic and drug‐induced long‐QT syndrome phenotypes in cardiomyocytes from isogenic pairs of patient induced pluripotent stem cells
A new hERG allosteric modulator rescues genetic and drug‐induced long‐QT syndrome phenotypes in cardiomyocytes from isogenic pairs of patient induced pluripotent stem cells
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A new hERG allosteric modulator rescues genetic and drug‐induced long‐QT syndrome phenotypes in cardiomyocytes from isogenic pairs of patient induced pluripotent stem cells

EMBO molecular medicine, 2016-09, Vol.8 (9), p.1065-1081 [Peer Reviewed Journal]

2016 The Authors. Published under the terms of the CC BY 4.0 license ;2016 The Authors. Published under the terms of the CC BY 4.0 license. ;COPYRIGHT 2016 John Wiley & Sons, Inc. ;2016. 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: 1757-4676 ;EISSN: 1757-4684 ;DOI: 10.15252/emmm.201606260 ;PMID: 27470144

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12
Telocytes and putative stem cells in ageing human heart
Telocytes and putative stem cells in ageing human heart
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Telocytes and putative stem cells in ageing human heart

Journal of cellular and molecular medicine, 2015-01, Vol.19 (1), p.31-45 [Peer Reviewed Journal]

2014 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. ;Copyright © 2015 John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine ;2015. 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. ;2014 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. 2014 ;ISSN: 1582-1838 ;EISSN: 1582-4934 ;DOI: 10.1111/jcmm.12509 ;PMID: 25545142

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13
Healthcare professionals’ attitudes towards termination of pregnancy at viable stage
Healthcare professionals’ attitudes towards termination of pregnancy at viable stage
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Healthcare professionals’ attitudes towards termination of pregnancy at viable stage

Acta obstetricia et gynecologica Scandinavica, 2021-01, Vol.100 (1), p.74-83 [Peer Reviewed Journal]

2020 Nordic Federation of Societies of Obstetrics and Gynecology ;2020 Nordic Federation of Societies of Obstetrics and Gynecology. ;Copyright © 2021 Acta Obstetricia et Gynecologica Scandinavica ;ISSN: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1111/aogs.13967 ;PMID: 32740906

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14
Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim
Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim
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Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim

EMBO molecular medicine, 2018-01, Vol.10 (1), p.63-75 [Peer Reviewed Journal]

2017 The Authors. Published under the terms of the CC BY 4.0 license ;2017 The Authors. Published under the terms of the CC BY 4.0 license. ;2018. 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: 1757-4676 ;EISSN: 1757-4684 ;DOI: 10.15252/emmm.201708168 ;PMID: 29191945

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15
Structural network topology correlates of microstructural brain dysmaturation in term infants with congenital heart disease
Structural network topology correlates of microstructural brain dysmaturation in term infants with congenital heart disease
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Structural network topology correlates of microstructural brain dysmaturation in term infants with congenital heart disease

Human brain mapping, 2018-11, Vol.39 (11), p.4593-4610 [Peer Reviewed Journal]

2018 Wiley Periodicals, Inc. ;ISSN: 1065-9471 ;EISSN: 1097-0193 ;DOI: 10.1002/hbm.24308 ;PMID: 30076775

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16
Congenital human cytomegalovirus infection and neurologic diseases in newborns
Congenital human cytomegalovirus infection and neurologic diseases in newborns
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Congenital human cytomegalovirus infection and neurologic diseases in newborns

Chinese medical journal, 2019-09, Vol.132 (17), p.2109-2118 [Peer Reviewed Journal]

Copyright © 2019 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. 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. ;Copyright © Wanfang Data Co. Ltd. All Rights Reserved. ;Copyright © 2019 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. 2019 ;ISSN: 0366-6999 ;EISSN: 2542-5641 ;DOI: 10.1097/cm9.0000000000000404 ;PMID: 31433331

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17
Hypermethylation‐mediated down‐regulation of lncRNA TBX5‐AS1:2 in Tetralogy of Fallot inhibits cell proliferation by reducing TBX5 expression
Hypermethylation‐mediated down‐regulation of lncRNA TBX5‐AS1:2 in Tetralogy of Fallot inhibits cell proliferation by reducing TBX5 expression
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Hypermethylation‐mediated down‐regulation of lncRNA TBX5‐AS1:2 in Tetralogy of Fallot inhibits cell proliferation by reducing TBX5 expression

Journal of cellular and molecular medicine, 2020-06, Vol.24 (11), p.6472-6484 [Peer Reviewed Journal]

2020 The Authors. published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. ;2020 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. ;2020. 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: 1582-1838 ;EISSN: 1582-4934 ;DOI: 10.1111/jcmm.15298 ;PMID: 32368852

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18
BET1 variants establish impaired vesicular transport as a cause for muscular dystrophy with epilepsy
BET1 variants establish impaired vesicular transport as a cause for muscular dystrophy with epilepsy
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BET1 variants establish impaired vesicular transport as a cause for muscular dystrophy with epilepsy

EMBO molecular medicine, 2021-12, Vol.13 (12), p.e13787-n/a [Peer Reviewed Journal]

2021 The Authors. Published under the terms of the CC BY 4.0 license ;2021 The Authors. Published under the terms of the CC BY 4.0 license. ;2021. 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. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1757-4676 ;EISSN: 1757-4684 ;DOI: 10.15252/emmm.202013787 ;PMID: 34779586

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19
ALX1‐related frontonasal dysplasia results from defective neural crest cell development and migration
ALX1‐related frontonasal dysplasia results from defective neural crest cell development and migration
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ALX1‐related frontonasal dysplasia results from defective neural crest cell development and migration

EMBO molecular medicine, 2020-10, Vol.12 (10), p.e12013-n/a [Peer Reviewed Journal]

2020 The Authors. Published under the terms of the CC BY 4.0 license ;2020 The Authors. Published under the terms of the CC BY 4.0 license. ;2020. 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: 1757-4676 ;EISSN: 1757-4684 ;DOI: 10.15252/emmm.202012013 ;PMID: 32914578

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20
Protein tyrosine phosphatase receptor type Q in cerebrospinal fluid reflects ependymal cell dysfunction and is a potential biomarker for adult chronic hydrocephalus
Protein tyrosine phosphatase receptor type Q in cerebrospinal fluid reflects ependymal cell dysfunction and is a potential biomarker for adult chronic hydrocephalus
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Protein tyrosine phosphatase receptor type Q in cerebrospinal fluid reflects ependymal cell dysfunction and is a potential biomarker for adult chronic hydrocephalus

European journal of neurology, 2021-02, Vol.28 (2), p.389-400 [Peer Reviewed Journal]

2020 The Authors. published by John Wiley & Sons Ltd on behalf of European Academy of Neurology ;2020 The Authors. European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology. ;2020. This article 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: 1351-5101 ;EISSN: 1468-1331 ;DOI: 10.1111/ene.14575 ;PMID: 33035386

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