skip to main content
Language:
Search Limited to: Search Limited to: Resource type Show Results with: Show Results with: Search type Index

Results 1 - 20 of 39  for All Library Resources

Results 1 2 next page
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Alcohol use disorders and the heart
Material Type:
Article
Add to My Research

Alcohol use disorders and the heart

Addiction (Abingdon, England), 2019-09, Vol.114 (9), p.1670-1678 [Peer Reviewed Journal]

2019 The Authors. published by John Wiley & Sons Ltd on behalf of Society for the Study of Addiction ;2019 The Authors. Addiction published by John Wiley & Sons Ltd on behalf of Society for the Study of Addiction. ;2019 Society for the Study of Addiction ;ISSN: 0965-2140 ;EISSN: 1360-0443 ;DOI: 10.1111/add.14703 ;PMID: 31309639

Digital Resources/Online E-Resources

2
A novel EMD mutation in a Chinese family with initial diagnosis of conduction cardiomyopathy
Material Type:
Article
Add to My Research

A novel EMD mutation in a Chinese family with initial diagnosis of conduction cardiomyopathy

Brain and behavior, 2019-01, Vol.9 (1), p.e01167-n/a [Peer Reviewed Journal]

2018 The Authors. published by Wiley Periodicals, Inc. ;2018 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. ;2019. 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: 2162-3279 ;EISSN: 2162-3279 ;DOI: 10.1002/brb3.1167 ;PMID: 30506906

Full text available

3
Harm reduction—a systematic review on effects of alcohol reduction on physical and mental symptoms
Material Type:
Article
Add to My Research

Harm reduction—a systematic review on effects of alcohol reduction on physical and mental symptoms

Addiction biology, 2017-09, Vol.22 (5), p.1119-1159 [Peer Reviewed Journal]

2016 Society for the Study of Addiction ;2016 Society for the Study of Addiction. ;2017 Society for the Study of Addiction ;ISSN: 1355-6215 ;EISSN: 1369-1600 ;DOI: 10.1111/adb.12414 ;PMID: 27353220

Digital Resources/Online E-Resources

4
Evaluating a communication aid for return of genetic results in families with hypertrophic cardiomyopathy: A randomized controlled trial
Material Type:
Article
Add to My Research

Evaluating a communication aid for return of genetic results in families with hypertrophic cardiomyopathy: A randomized controlled trial

Journal of genetic counseling, 2023-04, Vol.32 (2), p.425-434 [Peer Reviewed Journal]

2022 The Authors. published by Wiley Periodicals LLC on behalf of National Society of Genetic Counselors. ;2022 The Authors. Journal of Genetic Counseling published by Wiley Periodicals LLC on behalf of National Society of Genetic Counselors. ;2022. This article 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: 1059-7700 ;EISSN: 1573-3599 ;DOI: 10.1002/jgc4.1651 ;PMID: 36385718

Digital Resources/Online E-Resources

5
Natural history of Duchenne muscular dystrophy in the United Kingdom: A descriptive study using the Clinical Practice Research Datalink
Material Type:
Article
Add to My Research

Natural history of Duchenne muscular dystrophy in the United Kingdom: A descriptive study using the Clinical Practice Research Datalink

Brain and behavior, 2023-12, Vol.13 (12), p.e3331-n/a [Peer Reviewed Journal]

2023 The Authors. published by Wiley Periodicals LLC. ;2023 The Authors. Brain and Behavior published by Wiley Periodicals LLC. ;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: 2162-3279 ;EISSN: 2162-3279 ;DOI: 10.1002/brb3.3331 ;PMID: 37957895

Full text available

6
Cardiac monitoring and treatment for children and adolescents with neuromuscular disorders
Material Type:
Article
Add to My Research

Cardiac monitoring and treatment for children and adolescents with neuromuscular disorders

Developmental medicine and child neurology, 2006-03, Vol.48 (3), p.231-235 [Peer Reviewed Journal]

2006 Mac Keith Press ;Copyright Mac Keith Press Mar 2006 ;ISSN: 0012-1622 ;EISSN: 1469-8749 ;DOI: 10.1017/S0012162206000491 ;PMID: 16483403 ;CODEN: DMCNAW

Full text available

7
Progression of Friedreich ataxia: quantitative characterization over 5 years
Material Type:
Article
Add to My Research

Progression of Friedreich ataxia: quantitative characterization over 5 years

Annals of clinical and translational neurology, 2016-09, Vol.3 (9), p.684-694 [Peer Reviewed Journal]

2016 The Authors. published by Wiley Periodicals, Inc on behalf of American Neurological Association. ;2016. 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: 2328-9503 ;EISSN: 2328-9503 ;DOI: 10.1002/acn3.332 ;PMID: 27648458

Full text available

8
Advances in the treatment of hereditary transthyretin amyloidosis: A review
Material Type:
Article
Add to My Research

Advances in the treatment of hereditary transthyretin amyloidosis: A review

Brain and behavior, 2019-09, Vol.9 (9), p.e01371-n/a [Peer Reviewed Journal]

2019 The Authors. published by Wiley Periodicals, Inc. ;2019 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. ;2019. 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: 2162-3279 ;EISSN: 2162-3279 ;DOI: 10.1002/brb3.1371 ;PMID: 31368669

Full text available

9
Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features
Material Type:
Article
Add to My Research

Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features

Annals of clinical and translational neurology, 2023-04, Vol.10 (4), p.553-567 [Peer Reviewed Journal]

2023 The Authors. published by Wiley Periodicals LLC on behalf of American Neurological Association. ;2023 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. ;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: 2328-9503 ;EISSN: 2328-9503 ;DOI: 10.1002/acn3.51741 ;PMID: 36772971

Full text available

10
Adult‐onset dominant muscular dystrophy in Greek families caused by Annexin A11
Material Type:
Article
Add to My Research

Adult‐onset dominant muscular dystrophy in Greek families caused by Annexin A11

Annals of clinical and translational neurology, 2022-10, Vol.9 (10), p.1660-1667 [Peer Reviewed Journal]

2022 The Authors. published by Wiley Periodicals LLC on behalf of American Neurological Association. ;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: 2328-9503 ;EISSN: 2328-9503 ;DOI: 10.1002/acn3.51665

Full text available

11
Patterns of myelinated nerve fibers loss in transthyretin amyloid polyneuropathy and mimics
Material Type:
Article
Add to My Research

Patterns of myelinated nerve fibers loss in transthyretin amyloid polyneuropathy and mimics

Annals of clinical and translational neurology, 2022-07, Vol.9 (7), p.1059-1068 [Peer Reviewed Journal]

2022 The Authors. published by Wiley Periodicals LLC on behalf of American Neurological Association. ;2022 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. ;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: 2328-9503 ;EISSN: 2328-9503 ;DOI: 10.1002/acn3.51599 ;PMID: 35665499

Full text available

12
Hereditary transthyretin amyloidosis in mainland China: a unicentric retrospective study
Material Type:
Article
Add to My Research

Hereditary transthyretin amyloidosis in mainland China: a unicentric retrospective study

Annals of clinical and translational neurology, 2021-04, Vol.8 (4), p.831-841 [Peer Reviewed Journal]

2021 The Authors. published by Wiley Periodicals LLC on behalf of American Neurological Association ;2021 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. ;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: 2328-9503 ;EISSN: 2328-9503 ;DOI: 10.1002/acn3.51328 ;PMID: 33739616

Full text available

13
Amyloidogenicity assessment of transthyretin gene variants
Material Type:
Article
Add to My Research

Amyloidogenicity assessment of transthyretin gene variants

Annals of clinical and translational neurology, 2022-08, Vol.9 (8), p.1252-1263 [Peer Reviewed Journal]

2022 The Authors. published by Wiley Periodicals LLC on behalf of American Neurological Association. ;2022. 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: 2328-9503 ;EISSN: 2328-9503 ;DOI: 10.1002/acn3.51626 ;PMID: 35903975

Full text available

14
Shared genetic risk between anorexia nervosa and cardiovascular disease events: Evidence from genome‐wide association studies
Material Type:
Article
Add to My Research

Shared genetic risk between anorexia nervosa and cardiovascular disease events: Evidence from genome‐wide association studies

Brain and behavior, 2024-02, Vol.14 (2), p.e3294-n/a [Peer Reviewed Journal]

2024 The Authors. published by Wiley Periodicals LLC. ;2024 The Authors. Brain and Behavior published by Wiley Periodicals LLC. ;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: 2162-3279 ;EISSN: 2162-3279 ;DOI: 10.1002/brb3.3294 ;PMID: 38282367

Full text available

15
Cardiomyopathy correlates to nerve damage in p.A117S late‐onset transthyretin amyloid polyneuropathy
Material Type:
Article
Add to My Research

Cardiomyopathy correlates to nerve damage in p.A117S late‐onset transthyretin amyloid polyneuropathy

Annals of clinical and translational neurology, 2022-09, Vol.9 (9), p.1359-1369 [Peer Reviewed Journal]

2022 The Authors. published by Wiley Periodicals LLC on behalf of American Neurological Association. ;2022. 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: 2328-9503 ;EISSN: 2328-9503 ;DOI: 10.1002/acn3.51635 ;PMID: 35945697

Full text available

16
Phenotypic variation of FXN compound heterozygotes in a Friedreich ataxia cohort
Material Type:
Article
Add to My Research

Phenotypic variation of FXN compound heterozygotes in a Friedreich ataxia cohort

Annals of clinical and translational neurology, 2024-05, Vol.11 (5), p.1110-1121 [Peer Reviewed Journal]

2024 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. ;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. ;EISSN: 2328-9503 ;DOI: 10.1002/acn3.52027 ;PMID: 38396238

Full text available

17
Amyloid detection and typing yield of skin biopsy in systemic amyloidosis and polyneuropathy
Material Type:
Article
Add to My Research

Amyloid detection and typing yield of skin biopsy in systemic amyloidosis and polyneuropathy

Annals of clinical and translational neurology, 2023-12, Vol.10 (12), p.2347-2359 [Peer Reviewed Journal]

2023 The Authors. published by Wiley Periodicals LLC on behalf of American Neurological Association. ;2023 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. ;2023. 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: 2328-9503 ;EISSN: 2328-9503 ;DOI: 10.1002/acn3.51924 ;PMID: 37849451

Full text available

18
Clinical and genetic profiles of hereditary transthyretin amyloidosis in Taiwan
Material Type:
Article
Add to My Research

Clinical and genetic profiles of hereditary transthyretin amyloidosis in Taiwan

Annals of clinical and translational neurology, 2019-05, Vol.6 (5), p.913-922 [Peer Reviewed Journal]

2019 The Authors. published by Wiley Periodicals, Inc on behalf of American Neurological Association. ;2019. 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: 2328-9503 ;EISSN: 2328-9503 ;DOI: 10.1002/acn3.778 ;PMID: 31139689

Full text available

19
A comprehensive study of skeletal muscle imaging in FHL1‐related reducing body myopathy
Material Type:
Article
Add to My Research

A comprehensive study of skeletal muscle imaging in FHL1‐related reducing body myopathy

Annals of clinical and translational neurology, 2023-08, Vol.10 (8), p.1442-1455 [Peer Reviewed Journal]

2023 The Authors. published by Wiley Periodicals LLC on behalf of American Neurological Association. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA. ;2023 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA. ;2023. 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: 2328-9503 ;EISSN: 2328-9503 ;DOI: 10.1002/acn3.51834 ;PMID: 37483011

Full text available

20
Targeted gene panel use in 2249 neuromuscular patients: the Australasian referral center experience
Material Type:
Article
Add to My Research

Targeted gene panel use in 2249 neuromuscular patients: the Australasian referral center experience

Annals of clinical and translational neurology, 2020-03, Vol.7 (3), p.353-362 [Peer Reviewed Journal]

2020 The Authors. published by Wiley Periodicals, Inc on behalf of American Neurological Association. ;2020 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. ;2020. 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: 2328-9503 ;EISSN: 2328-9503 ;DOI: 10.1002/acn3.51002 ;PMID: 32153140

Full text available

Results 1 - 20 of 39  for All Library Resources

Results 1 2 next page

Personalize your results

  1. Edit

Refine Search Results

Expand My Results

  1.   

Searching Remote Databases, Please Wait