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Results 41 - 60 of 48,895  for All Library Resources

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41
Glomerular hyperfiltration
Glomerular hyperfiltration
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Glomerular hyperfiltration

Nature reviews. Nephrology, 2022-07, Vol.18 (7), p.435-451 [Peer Reviewed Journal]

2022. Springer Nature Limited. ;Springer Nature Limited 2022. ;ISSN: 1759-5061 ;EISSN: 1759-507X ;DOI: 10.1038/s41581-022-00559-y ;PMID: 35365815

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42
Acute Recurrent Pancreatitis in Association with Gallbladder Agenesis: 1335
Acute Recurrent Pancreatitis in Association with Gallbladder Agenesis: 1335
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Acute Recurrent Pancreatitis in Association with Gallbladder Agenesis: 1335

The American journal of gastroenterology, 2018-10, Vol.113 (Supplement), p.S764-S765 [Peer Reviewed Journal]

Copyright Wolters Kluwer Health Medical Research, Lippincott Williams & Wilkins Oct 2018 ;ISSN: 0002-9270 ;EISSN: 1572-0241 ;DOI: 10.14309/00000434-201810001-01335

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43
Cirrhosis a Long Term Consequence of Congenital Tricuspid Atresia After Fontan Procedure: 2327
Cirrhosis a Long Term Consequence of Congenital Tricuspid Atresia After Fontan Procedure: 2327
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Cirrhosis a Long Term Consequence of Congenital Tricuspid Atresia After Fontan Procedure: 2327

The American journal of gastroenterology, 2018-10, Vol.113 (Supplement), p.S1306-S1307 [Peer Reviewed Journal]

Copyright Wolters Kluwer Health Medical Research, Lippincott Williams & Wilkins Oct 2018 ;ISSN: 0002-9270 ;EISSN: 1572-0241 ;DOI: 10.14309/00000434-201810001-02326

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44
Detection and interpretation of shared genetic influences on 42 human traits
Detection and interpretation of shared genetic influences on 42 human traits
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Detection and interpretation of shared genetic influences on 42 human traits

Nature genetics, 2016-07, Vol.48 (7), p.709-717 [Peer Reviewed Journal]

COPYRIGHT 2016 Nature Publishing Group ;COPYRIGHT 2016 Nature Publishing Group ;Copyright Nature Publishing Group Jul 2016 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.3570 ;PMID: 27182965

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45
Underlying Medical Conditions Associated With Severe COVID-19 Illness Among Children
Underlying Medical Conditions Associated With Severe COVID-19 Illness Among Children
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Underlying Medical Conditions Associated With Severe COVID-19 Illness Among Children

JAMA Network Open, 2021-06, Vol.4 (6), p.e2111182-e2111182 [Peer Reviewed Journal]

2021. 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. ;Copyright 2021 Kompaniyets L et al. . ;ISSN: 2574-3805 ;EISSN: 2574-3805 ;DOI: 10.1001/jamanetworkopen.2021.11182 ;PMID: 34097050

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46
Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
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Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

The New England journal of medicine, 2020-09, Vol.383 (13), p.1248-1261 [Peer Reviewed Journal]

Copyright © 2020 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMra1909786

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47
Gene therapy comes of age
Gene therapy comes of age
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Gene therapy comes of age

Science (American Association for the Advancement of Science), 2018-01, Vol.359 (6372) [Peer Reviewed Journal]

Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. ;Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works ;ISSN: 0036-8075 ;EISSN: 1095-9203 ;DOI: 10.1126/science.aan4672 ;PMID: 29326244

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48
Myopathology of Isolated Congenital Ptosis
Myopathology of Isolated Congenital Ptosis
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Myopathology of Isolated Congenital Ptosis

Canadian journal of neurological sciences, 2017-02, Vol.44 (S1), p.S6-S7 [Peer Reviewed Journal]

Copyright © The Canadian Journal of Neurological Sciences Inc. 2017 ;ISSN: 0317-1671 ;EISSN: 2057-0155 ;DOI: 10.1017/cjn.2017.18

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49
Genetics and Genomics of Congenital Heart Disease
Genetics and Genomics of Congenital Heart Disease
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Genetics and Genomics of Congenital Heart Disease

Circulation research, 2017-03, Vol.120 (6), p.923-940 [Peer Reviewed Journal]

2017 American Heart Association, Inc. ;Copyright Lippincott Williams & Wilkins Ovid Technologies Mar 17, 2017 ;ISSN: 0009-7330 ;EISSN: 1524-4571 ;DOI: 10.1161/circresaha.116.309140 ;PMID: 28302740

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50
Molecular findings from 537 individuals with inherited retinal disease
Molecular findings from 537 individuals with inherited retinal disease
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Molecular findings from 537 individuals with inherited retinal disease

Journal of medical genetics, 2016-11, Vol.53 (11), p.761-767 [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/. ;Copyright: 2016 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/ 2016 ;ISSN: 0022-2593 ;EISSN: 1468-6244 ;DOI: 10.1136/jmedgenet-2016-103837 ;PMID: 27208204 ;CODEN: JMDGAE

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51
Integrative Genomics Implicates Genetic Disruption of Prenatal Neurogenesis in Congenital Hydrocephalus
Integrative Genomics Implicates Genetic Disruption of Prenatal Neurogenesis in Congenital Hydrocephalus
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Integrative Genomics Implicates Genetic Disruption of Prenatal Neurogenesis in Congenital Hydrocephalus

Neurosurgery, 2020-12, Vol.67 (Supplement_1) [Peer Reviewed Journal]

Copyright © 2020 by the Congress of Neurological Surgeons ;ISSN: 0148-396X ;EISSN: 1524-4040 ;DOI: 10.1093/neuros/nyaa447_572

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52
The mechanisms of Hedgehog signalling and its roles in development and disease
The mechanisms of Hedgehog signalling and its roles in development and disease
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The mechanisms of Hedgehog signalling and its roles in development and disease

Nature reviews. Molecular cell biology, 2013-07, Vol.14 (7), p.416-429 [Peer Reviewed Journal]

COPYRIGHT 2013 Nature Publishing Group ;COPYRIGHT 2013 Nature Publishing Group ;Copyright Nature Publishing Group Jul 2013 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1471-0072 ;EISSN: 1471-0080 ;DOI: 10.1038/nrm3598 ;PMID: 23719536

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53
Neurodevelopmental outcome at 5 years of age after general anaesthesia or awake-regional anaesthesia in infancy (GAS): an international, multicentre, randomised, controlled equivalence trial
Neurodevelopmental outcome at 5 years of age after general anaesthesia or awake-regional anaesthesia in infancy (GAS): an international, multicentre, randomised, controlled equivalence trial
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Neurodevelopmental outcome at 5 years of age after general anaesthesia or awake-regional anaesthesia in infancy (GAS): an international, multicentre, randomised, controlled equivalence trial

The Lancet (British edition), 2019-02, Vol.393 (10172), p.664-677 [Peer Reviewed Journal]

2019 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license ;Copyright © 2019 Elsevier Ltd. All rights reserved. ;2019. The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. ;ISSN: 0140-6736 ;EISSN: 1474-547X ;DOI: 10.1016/S0140-6736(18)32485-1 ;PMID: 30782342

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54
Pulmonary Arterial Hypertension
Pulmonary Arterial Hypertension
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Pulmonary Arterial Hypertension

The New England journal of medicine, 2021-12, Vol.385 (25), p.2361-2376 [Peer Reviewed Journal]

Copyright © 2021 Massachusetts Medical Society. All rights reserved. ;COPYRIGHT 2021 Massachusetts Medical Society ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMra2000348 ;PMID: 34910865

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55
The Major Causes of Death in Children and Adolescents in the United States
The Major Causes of Death in Children and Adolescents in the United States
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Article 		Add to My Research

The Major Causes of Death in Children and Adolescents in the United States

The New England journal of medicine, 2018-12, Vol.379 (25), p.2468-2475 [Peer Reviewed Journal]

Copyright © 2018 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMsr1804754 ;PMID: 30575483

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56
108. ADDITIONAL PATHOGENIC IRF6 MUTATIONS IN VAN DER WOUDE SYNDROME FROM SUB-SAHARAN AFRICAN POPULATIONS
108. ADDITIONAL PATHOGENIC IRF6 MUTATIONS IN VAN DER WOUDE SYNDROME FROM SUB-SAHARAN AFRICAN POPULATIONS
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108. ADDITIONAL PATHOGENIC IRF6 MUTATIONS IN VAN DER WOUDE SYNDROME FROM SUB-SAHARAN AFRICAN POPULATIONS

The Cleft palate-craniofacial journal, 2016-07, Vol.53 (4), p.E127 [Peer Reviewed Journal]

Copyright Allen Press Publishing Services Jul 2016 ;ISSN: 1055-6656 ;EISSN: 1545-1569 ;CODEN: CPJOEG

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57
FETAL ECHOCARDIOGRAPHY - THE FIRST OR SKIPPED STEP IN CARDIOLOGY
FETAL ECHOCARDIOGRAPHY - THE FIRST OR SKIPPED STEP IN CARDIOLOGY
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FETAL ECHOCARDIOGRAPHY - THE FIRST OR SKIPPED STEP IN CARDIOLOGY

Acta medica Saliniana, 2022-01, Vol.52, p.26-26 [Peer Reviewed Journal]

Copyright University Clinical Center Tuzla 2022 ;ISSN: 0350-364X ;EISSN: 1840-3956

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58
SPARK: A US Cohort of 50,000 Families to Accelerate Autism Research
SPARK: A US Cohort of 50,000 Families to Accelerate Autism Research
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SPARK: A US Cohort of 50,000 Families to Accelerate Autism Research

Neuron (Cambridge, Mass.), 2018-02, Vol.97 (3), p.488-493 [Peer Reviewed Journal]

2018 Elsevier Inc. ;Copyright © 2018 Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Feb 7, 2018 ;ISSN: 0896-6273 ;EISSN: 1097-4199 ;DOI: 10.1016/j.neuron.2018.01.015 ;PMID: 29420931

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59
Formation of new chromatin domains determines pathogenicity of genomic duplications
Formation of new chromatin domains determines pathogenicity of genomic duplications
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Formation of new chromatin domains determines pathogenicity of genomic duplications

Nature (London), 2016-10, Vol.538 (7624), p.265-269 [Peer Reviewed Journal]

COPYRIGHT 2016 Nature Publishing Group ;COPYRIGHT 2016 Nature Publishing Group ;Copyright Nature Publishing Group Oct 13, 2016 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature19800 ;PMID: 27706140 ;CODEN: NATUAS

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60
Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment
Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment
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Article 		Add to My Research

Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment

Nature reviews. Endocrinology, 2015-09, Vol.11 (9), p.547-564 [Peer Reviewed Journal]

Copyright Nature Publishing Group Sep 2015 ;ISSN: 1759-5029 ;EISSN: 1759-5037 ;DOI: 10.1038/nrendo.2015.112 ;PMID: 26194704

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