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Results 1 - 20 of 17,524  for All Library Resources

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1
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
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
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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

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2
Genome-wide analysis identifies MYH11 compound heterozygous variants leading to visceral myopathy corresponding to late-onset form of megacystis-microcolon-intestinal hypoperistalsis syndrome
Genome-wide analysis identifies MYH11 compound heterozygous variants leading to visceral myopathy corresponding to late-onset form of megacystis-microcolon-intestinal hypoperistalsis syndrome
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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

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3
Impact of Habitual Yogurt Intake in Mother–Child Dyads on Incidence of Childhood Otitis Media: The Japan Environment and Children’s Study (JECS)
Impact of Habitual Yogurt Intake in Mother–Child Dyads on Incidence of Childhood Otitis Media: The Japan Environment and Children’s Study (JECS)
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Impact of Habitual Yogurt Intake in Mother–Child Dyads on Incidence of Childhood Otitis Media: The Japan Environment and Children’s Study (JECS)

Probiotics and antimicrobial proteins, 2024-06, Vol.16 (3), p.884-893 [Peer Reviewed Journal]

The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2023. 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. ;2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature. ;ISSN: 1867-1306 ;EISSN: 1867-1314 ;DOI: 10.1007/s12602-023-10086-2 ;PMID: 37195509

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4
Maternal antenatal mental health and its associations with perinatal outcomes and the use of healthcare services in children from the NINFEA birth cohort study
Maternal antenatal mental health and its associations with perinatal outcomes and the use of healthcare services in children from the NINFEA birth cohort study
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Maternal antenatal mental health and its associations with perinatal outcomes and the use of healthcare services in children from the NINFEA birth cohort study

European journal of pediatrics, 2024-06, Vol.183 (6), p.2769-2781 [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. ;ISSN: 0340-6199 ;EISSN: 1432-1076 ;DOI: 10.1007/s00431-024-05525-3 ;PMID: 38564067

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5
Disease activity and neonatal outcomes after exposure to natalizumab throughout pregnancy
Disease activity and neonatal outcomes after exposure to natalizumab throughout pregnancy
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Disease activity and neonatal outcomes after exposure to natalizumab throughout pregnancy

Journal of neurology, neurosurgery and psychiatry, 2024-06, Vol.95 (6), p.561-570 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. ;2024 Author(s) (or their employer(s)) 2024. 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. ;Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2024 ;ISSN: 0022-3050 ;EISSN: 1468-330X ;DOI: 10.1136/jnnp-2023-332804 ;PMID: 38124108

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6
Goldenhar Syndrome: Quality-of-Life Analysis of 43 Consecutive Patients
Goldenhar Syndrome: Quality-of-Life Analysis of 43 Consecutive Patients
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Goldenhar Syndrome: Quality-of-Life Analysis of 43 Consecutive Patients

The Journal of craniofacial surgery, 2024-06, Vol.35 (4), p.1170 [Peer Reviewed Journal]

Copyright © 2024 by Mutaz B. Habal, MD. ;EISSN: 1536-3732 ;DOI: 10.1097/SCS.0000000000010057 ;PMID: 38385678

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7
CPAK classification cannot be used to determine segmental coronal extra‐articular knee deformity
CPAK classification cannot be used to determine segmental coronal extra‐articular knee deformity
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CPAK classification cannot be used to determine segmental coronal extra‐articular knee deformity

Knee surgery, sports traumatology, arthroscopy : official journal of the ESSKA, 2024-06, Vol.32 (6), p.1557-1570 [Peer Reviewed Journal]

2024 European Society of Sports Traumatology, Knee Surgery and Arthroscopy. ;ISSN: 0942-2056 ;EISSN: 1433-7347 ;DOI: 10.1002/ksa.12168 ;PMID: 38643399

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8
Pregnancy and cardiac maternal outcomes in women with inherited cardiomyopathy: interest of the CARPREG II risk score
Pregnancy and cardiac maternal outcomes in women with inherited cardiomyopathy: interest of the CARPREG II risk score
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Pregnancy and cardiac maternal outcomes in women with inherited cardiomyopathy: interest of the CARPREG II risk score

ESC Heart Failure, 2024-06, Vol.11 (3), p.1506-1514 [Peer Reviewed Journal]

2024 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. ;2024. 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: 2055-5822 ;EISSN: 2055-5822 ;DOI: 10.1002/ehf2.14694 ;PMID: 38361389

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9
Spectrum of congenital anomalies of the kidney and urinary tract (CAKUT) including renal parenchymal malformations during fetal life and the implementation of prenatal exome sequencing (WES)
Spectrum of congenital anomalies of the kidney and urinary tract (CAKUT) including renal parenchymal malformations during fetal life and the implementation of prenatal exome sequencing (WES)
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Spectrum of congenital anomalies of the kidney and urinary tract (CAKUT) including renal parenchymal malformations during fetal life and the implementation of prenatal exome sequencing (WES)

Archives of gynecology and obstetrics, 2024-06, Vol.309 (6), p.2613-2622 [Peer Reviewed Journal]

The Author(s) 2023 ;2023. The Author(s). ;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: 1432-0711 ;ISSN: 0932-0067 ;EISSN: 1432-0711 ;DOI: 10.1007/s00404-023-07165-8 ;PMID: 37535131

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10
Breast size in lactating women and the content of macronutrients in human milk
Breast size in lactating women and the content of macronutrients in human milk
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Breast size in lactating women and the content of macronutrients in human milk

American journal of human biology, 2024-06, Vol.36 (6), p.e24055 [Peer Reviewed Journal]

2024 Wiley Periodicals LLC. ;EISSN: 1520-6300 ;DOI: 10.1002/ajhb.24055 ;PMID: 38420902

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11
Adult idiopathic bilateral occlusion of foramen of Monro: Systematic review with illustrative case
Adult idiopathic bilateral occlusion of foramen of Monro: Systematic review with illustrative case
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Adult idiopathic bilateral occlusion of foramen of Monro: Systematic review with illustrative case

Clinical neurology and neurosurgery, 2024-06, Vol.241, p.108279-108279, Article 108279 [Peer Reviewed Journal]

2024 Elsevier B.V. ;Copyright © 2024 Elsevier B.V. All rights reserved. ;2024. Elsevier B.V. ;ISSN: 0303-8467 ;EISSN: 1872-6968 ;DOI: 10.1016/j.clineuro.2024.108279 ;PMID: 38640777

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12
Potential Association Between COVID-19 Vaccination and Facial Palsy: Three Cases With Neuroimaging Findings
Potential Association Between COVID-19 Vaccination and Facial Palsy: Three Cases With Neuroimaging Findings
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Potential Association Between COVID-19 Vaccination and Facial Palsy: Three Cases With Neuroimaging Findings

Ear, nose, & throat journal, 2024-06, Vol.103 (1_suppl), p.110S-114S [Peer Reviewed Journal]

The Author(s) 2022 ;The Author(s) 2022 2022 SAGE Publications ;ISSN: 0145-5613 ;EISSN: 1942-7522 ;DOI: 10.1177/01455613221113818 ;PMID: 35855585

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13
Parental Perception of Children's Mental Health During the Pandemic: Insights From an Italian Cross‐Sectional Study
Parental Perception of Children's Mental Health During the Pandemic: Insights From an Italian Cross‐Sectional Study
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Parental Perception of Children's Mental Health During the Pandemic: Insights From an Italian Cross‐Sectional Study

The Journal of school health, 2024-06, Vol.94 (6), p.539-550 [Peer Reviewed Journal]

2024 American School Health Association. ;2024, American School Health Association ;ISSN: 0022-4391 ;EISSN: 1746-1561 ;DOI: 10.1111/josh.13449 ;PMID: 38532496

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14
Advanced magnetic resonance imaging detects altered placental development in pregnancies affected by congenital heart disease
Advanced magnetic resonance imaging detects altered placental development in pregnancies affected by congenital heart disease
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Advanced magnetic resonance imaging detects altered placental development in pregnancies affected by congenital heart disease

Scientific reports, 2024-05, Vol.14 (1), p.12357-12357 [Peer Reviewed Journal]

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. ;The Author(s) 2024 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-024-63087-8 ;PMID: 38811636

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15
Early-pregnancy N-terminal pro-brain natriuretic peptide level is inversely associated with hypertensive disorders of pregnancy diagnosed after 35 weeks of gestation
Early-pregnancy N-terminal pro-brain natriuretic peptide level is inversely associated with hypertensive disorders of pregnancy diagnosed after 35 weeks of gestation
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Early-pregnancy N-terminal pro-brain natriuretic peptide level is inversely associated with hypertensive disorders of pregnancy diagnosed after 35 weeks of gestation

Scientific reports, 2024-05, Vol.14 (1), p.12225-12225 [Peer Reviewed Journal]

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. ;The Author(s) 2024 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-024-63206-5 ;PMID: 38806648

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16
Anomalous origin of the coronary artery: prevalence and coronary artery disease in adults undergoing coronary tomographic angiography
Anomalous origin of the coronary artery: prevalence and coronary artery disease in adults undergoing coronary tomographic angiography
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Anomalous origin of the coronary artery: prevalence and coronary artery disease in adults undergoing coronary tomographic angiography

BMC cardiovascular disorders, 2024-05, Vol.24 (1), p.271-271 [Peer Reviewed Journal]

2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;The Author(s) 2024 ;ISSN: 1471-2261 ;EISSN: 1471-2261 ;DOI: 10.1186/s12872-024-03942-8 ;PMID: 38783173

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17
Heart disease in pregnancy and risk of pre-eclampsia: a Swedish register-based study
Heart disease in pregnancy and risk of pre-eclampsia: a Swedish register-based study
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Heart disease in pregnancy and risk of pre-eclampsia: a Swedish register-based study

Open heart, 2024-05, Vol.11 (1), p.e002728 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. ;2024 Author(s) (or their employer(s)) 2024. 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. ;ISSN: 2053-3624 ;ISSN: 2398-595X ;EISSN: 2053-3624 ;DOI: 10.1136/openhrt-2024-002728 ;PMID: 38782544

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18
Previously undiagnosed genetic disease in adult patient with hepatic masses and reported history of congenital hyperinsulinism
Previously undiagnosed genetic disease in adult patient with hepatic masses and reported history of congenital hyperinsulinism
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Previously undiagnosed genetic disease in adult patient with hepatic masses and reported history of congenital hyperinsulinism

BMJ case reports, 2024-05, Vol.17 (5), p.e259355 [Peer Reviewed Journal]

BMJ Publishing Group Limited 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;2024 BMJ Publishing Group Limited 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2023-259355 ;PMID: 38782444

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19
CHD7 Disorder-Not CHARGE Syndrome-Presenting as Isolated Cochleovestibular Dysfunction
CHD7 Disorder-Not CHARGE Syndrome-Presenting as Isolated Cochleovestibular Dysfunction
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CHD7 Disorder-Not CHARGE Syndrome-Presenting as Isolated Cochleovestibular Dysfunction

Genes, 2024-05, Vol.15 (5), p.643 [Peer Reviewed Journal]

2024 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. ;EISSN: 2073-4425 ;DOI: 10.3390/genes15050643 ;PMID: 38790272

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20
A HGF Mutation in the Familial Case of Primary Lymphedema: A Report
A HGF Mutation in the Familial Case of Primary Lymphedema: A Report
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A HGF Mutation in the Familial Case of Primary Lymphedema: A Report

International journal of molecular sciences, 2024-05, Vol.25 (10), p.5464 [Peer Reviewed Journal]

2024 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. ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms25105464 ;PMID: 38791500

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