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1
CLEFT LIP AND PALATE
CLEFT LIP AND PALATE
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CLEFT LIP AND PALATE

Guident, 2017-06, Vol.10 (7), p.26

Copyright Guident Jun 2017 ;ISSN: 0976-2248

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2
Serious arrhythmia in initiators of citalopram, escitalopram, and other selective serotonin reuptake inhibitors: A population‐based cohort study in older adults
Serious arrhythmia in initiators of citalopram, escitalopram, and other selective serotonin reuptake inhibitors: A population‐based cohort study in older adults
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Serious arrhythmia in initiators of citalopram, escitalopram, and other selective serotonin reuptake inhibitors: A population‐based cohort study in older adults

Clinical and translational science, 2022-09, Vol.15 (9), p.2105-2115 [Peer Reviewed Journal]

2022 The Authors. published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics. ;2022 The Authors. Clinical and Translational Science published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics. ;COPYRIGHT 2022 John Wiley & Sons, Inc. ;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: 1752-8054 ;EISSN: 1752-8062 ;DOI: 10.1111/cts.13319 ;PMID: 35733364

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3
Associations between thyroid dysfunction and developmental status in children with excessive iodine status
Associations between thyroid dysfunction and developmental status in children with excessive iodine status
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Associations between thyroid dysfunction and developmental status in children with excessive iodine status

PloS one, 2017-11, Vol.12 (11), p.e0187241-e0187241 [Peer Reviewed Journal]

COPYRIGHT 2017 Public Library of Science ;COPYRIGHT 2017 Public Library of Science ;2017 Aakre 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. ;2017 Aakre et al 2017 Aakre et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0187241 ;PMID: 29166388

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4
Impact of percutaneous ventricular septal defect closure on left ventricular remodeling and function
Impact of percutaneous ventricular septal defect closure on left ventricular remodeling and function
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Article 		Add to My Research

Impact of percutaneous ventricular septal defect closure on left ventricular remodeling and function

The Egyptian heart journal, 2021-10, Vol.73 (1), p.86-86, Article 86 [Peer Reviewed Journal]

The Author(s) 2021 ;COPYRIGHT 2021 Springer ;The Author(s) 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. ;ISSN: 2090-911X ;ISSN: 1110-2608 ;EISSN: 2090-911X ;DOI: 10.1186/s43044-021-00215-z ;PMID: 34637037

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5
Clinical and Biochemical Features in a Case of Familial Hypocalciuric Hypercalcemia Type 3 with AP2S1 Gene Mutation in Codon Arg15His
Clinical and Biochemical Features in a Case of Familial Hypocalciuric Hypercalcemia Type 3 with AP2S1 Gene Mutation in Codon Arg15His
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Clinical and Biochemical Features in a Case of Familial Hypocalciuric Hypercalcemia Type 3 with AP2S1 Gene Mutation in Codon Arg15His

Case reports in pediatrics, 2020-01, Vol.2020, p.7312894-3 [Peer Reviewed Journal]

Copyright © 2020 Mohamed Aashiq et al. ;Copyright © 2020 Mohamed Aashiq 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 © 2020 Mohamed Aashiq et al. 2020 ;ISSN: 2090-6803 ;EISSN: 2090-6811 ;DOI: 10.1155/2020/7312894 ;PMID: 32047691

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6
The natural history of epistaxis in hereditary hemorrhagic telangiectasia
The natural history of epistaxis in hereditary hemorrhagic telangiectasia
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Article 		Add to My Research

The natural history of epistaxis in hereditary hemorrhagic telangiectasia

The Laryngoscope, 1991-09, Vol.101 (9), p.977-980 [Peer Reviewed Journal]

Copyright © 1991 The Triological Society ;1992 INIST-CNRS ;ISSN: 0023-852X ;EISSN: 1531-4995 ;DOI: 10.1288/00005537-199109000-00008 ;PMID: 1886446 ;CODEN: LARYA8

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7
INHERITED EPIDERMOLYSIS BULLOSA
INHERITED EPIDERMOLYSIS BULLOSA
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INHERITED EPIDERMOLYSIS BULLOSA

International journal of dermatology, 1993-08, Vol.32 (8), p.561-568 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0011-9059 ;EISSN: 1365-4632 ;DOI: 10.1111/j.1365-4362.1993.tb05023.x ;PMID: 8407069 ;CODEN: IJDEBB

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8
Autosomal recessive epidermolysis bullosa simplex. A case report
Autosomal recessive epidermolysis bullosa simplex. A case report
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Article 		Add to My Research

Autosomal recessive epidermolysis bullosa simplex. A case report

British journal of dermatology (1951), 1994-01, Vol.130 (1), p.115-117 [Peer Reviewed Journal]

1994 INIST-CNRS ;ISSN: 0007-0963 ;EISSN: 1365-2133 ;DOI: 10.1111/j.1365-2133.1994.tb06895.x ;PMID: 8305300 ;CODEN: BJDEAZ

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9
Preoperative echocardiographic measures in interrupted aortic arch: Which ones best predict surgical approach and outcome?
Preoperative echocardiographic measures in interrupted aortic arch: Which ones best predict surgical approach and outcome?
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Article 		Add to My Research

Preoperative echocardiographic measures in interrupted aortic arch: Which ones best predict surgical approach and outcome?

Congenital heart disease, 2018-05, Vol.13 (3), p.476-482 [Peer Reviewed Journal]

2018 Wiley Periodicals, Inc. ;ISSN: 1747-079X ;EISSN: 1747-0803 ;DOI: 10.1111/chd.12599 ;PMID: 29520990

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10
SAFETY OF CONTRACEPTIVE USE AMONG WOMEN WITH CONGENITAL HEART DISEASE: A SYSTEMATIC REVIEW
SAFETY OF CONTRACEPTIVE USE AMONG WOMEN WITH CONGENITAL HEART DISEASE: A SYSTEMATIC REVIEW
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Article 		Add to My Research

SAFETY OF CONTRACEPTIVE USE AMONG WOMEN WITH CONGENITAL HEART DISEASE: A SYSTEMATIC REVIEW

Journal of the American College of Cardiology, 2016-04, Vol.67 (13), p.949-949 [Peer Reviewed Journal]

American College of Cardiology Foundation ;2016 American College of Cardiology Foundation ;Copyright Elsevier Limited Apr 5, 2016 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/S0735-1097(16)30950-0

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11
Safety of contraceptive use among women with congenital heart disease: A systematic review
Safety of contraceptive use among women with congenital heart disease: A systematic review
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Article 		Add to My Research

Safety of contraceptive use among women with congenital heart disease: A systematic review

Congenital heart disease, 2019-05, Vol.14 (3), p.331-340 [Peer Reviewed Journal]

2019 Wiley Periodicals, Inc. ;Copyright © 2019 Wiley Periodicals, Inc. ;ISSN: 1747-079X ;EISSN: 1747-0803 ;DOI: 10.1111/chd.12752 ;PMID: 30681774

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12
Intellectual developmental disorder with dysmorphic facies and ptosis caused by copy number variation including the BRPF1 gene in Peruvian patient
Intellectual developmental disorder with dysmorphic facies and ptosis caused by copy number variation including the BRPF1 gene in Peruvian patient
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Article 		Add to My Research

Intellectual developmental disorder with dysmorphic facies and ptosis caused by copy number variation including the BRPF1 gene in Peruvian patient

Egyptian Journal of Medical Human Genetics, 2022-12, Vol.23 (1), p.1-6 [Peer Reviewed Journal]

The Author(s) 2022 ;COPYRIGHT 2022 Springer ;The Author(s) 2022. 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: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-022-00356-z

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13
Cornelia de Lange Syndrome Caused by an Intragenic Heterozygous Deletion in RAD21 Detected through Very-High-Resolution Chromosomal Microarray Analysis
Cornelia de Lange Syndrome Caused by an Intragenic Heterozygous Deletion in RAD21 Detected through Very-High-Resolution Chromosomal Microarray Analysis
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Cornelia de Lange Syndrome Caused by an Intragenic Heterozygous Deletion in RAD21 Detected through Very-High-Resolution Chromosomal Microarray Analysis

Genes, 2023-12, Vol.14 (12), p.2212 [Peer Reviewed Journal]

2023 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: 2073-4425 ;EISSN: 2073-4425 ;DOI: 10.3390/genes14122212 ;PMID: 38137034

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14
Health-related quality of life in children with congenital heart disease aged 5 to 7 years: a multicentre controlled cross-sectional study
Health-related quality of life in children with congenital heart disease aged 5 to 7 years: a multicentre controlled cross-sectional study
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Article 		Add to My Research

Health-related quality of life in children with congenital heart disease aged 5 to 7 years: a multicentre controlled cross-sectional study

Health and quality of life outcomes, 2020-11, Vol.18 (1), p.366-366, Article 366 [Peer Reviewed Journal]

COPYRIGHT 2020 BioMed Central Ltd. ;2020. 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. ;Distributed under a Creative Commons Attribution 4.0 International License ;The Author(s) 2020 ;ISSN: 1477-7525 ;EISSN: 1477-7525 ;DOI: 10.1186/s12955-020-01615-6 ;PMID: 33183312

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15
Nonlethal CHRNA1-Related Congenital Myasthenic Syndrome with a Homozygous Null Mutation
Nonlethal CHRNA1-Related Congenital Myasthenic Syndrome with a Homozygous Null Mutation
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Article 		Add to My Research

Nonlethal CHRNA1-Related Congenital Myasthenic Syndrome with a Homozygous Null Mutation

Canadian journal of neurological sciences, 2017-01, Vol.44 (1), p.125-127 [Peer Reviewed Journal]

Copyright © The Canadian Journal of Neurological Sciences Inc. 2016 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0317-1671 ;EISSN: 2057-0155 ;DOI: 10.1017/cjn.2016.322 ;PMID: 27748205

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16
Integrative data mining highlights candidate genes for monogenic myopathies
Integrative data mining highlights candidate genes for monogenic myopathies
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Article 		Add to My Research

Integrative data mining highlights candidate genes for monogenic myopathies

PloS one, 2014-10, Vol.9 (10), p.e110888-e110888 [Peer Reviewed Journal]

2014 Neto 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. ;2014 Neto et al 2014 Neto et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0110888 ;PMID: 25353622

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17
Charcot–Marie‐Tooth type 2A in vivo models: Current updates
Charcot–Marie‐Tooth type 2A in vivo models: Current updates
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Charcot–Marie‐Tooth type 2A in vivo models: Current updates

Journal of cellular and molecular medicine, 2024-05, Vol.28 (9), p.e18293-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.18293 ;PMID: 38722298

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18
Neonatal Purpura Fulminans in a Patient With Arterial Thrombosis and Congenital Renal Agenesis
Neonatal Purpura Fulminans in a Patient With Arterial Thrombosis and Congenital Renal Agenesis
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Neonatal Purpura Fulminans in a Patient With Arterial Thrombosis and Congenital Renal Agenesis

Curēus (Palo Alto, CA), 2024-01, Vol.16 (1), p.e52503 [Peer Reviewed Journal]

Copyright © 2024, Abbaker et al. ;Copyright © 2024, Abbaker et al. This work is published under https://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: 2168-8184 ;EISSN: 2168-8184 ;DOI: 10.7759/cureus.52503 ;PMID: 38371013

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19
Cardiac CT Assessment of Left Atrial Accessory Appendages and Diverticula
Cardiac CT Assessment of Left Atrial Accessory Appendages and Diverticula
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Article 		Add to My Research

Cardiac CT Assessment of Left Atrial Accessory Appendages and Diverticula

American journal of roentgenology (1976), 2009-09, Vol.193 (3), p.807-812 [Peer Reviewed Journal]

2009 INIST-CNRS ;ISSN: 0361-803X ;EISSN: 1546-3141 ;DOI: 10.2214/AJR.08.2229 ;PMID: 19696296 ;CODEN: AAJRDX

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20
Consanguineous Marriages and Dental Anomalies: A Cross-Sectional Analytical Study
Consanguineous Marriages and Dental Anomalies: A Cross-Sectional Analytical Study
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Consanguineous Marriages and Dental Anomalies: A Cross-Sectional Analytical Study

International journal of dentistry, 2022, Vol.2022, p.9750460-5 [Peer Reviewed Journal]

Copyright © 2022 Beenish Abbas et al. ;Copyright © 2022 Beenish Abbas 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. https://creativecommons.org/licenses/by/4.0 ;Copyright © 2022 Beenish Abbas et al. 2022 ;ISSN: 1687-8728 ;EISSN: 1687-8736 ;DOI: 10.1155/2022/9750460 ;PMID: 35432541

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