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 42  for All Library Resources

Results 1 2 3 next page
Show only
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia
Material Type:
Article
Add to My Research

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia

Nature (London), 2011-09, Vol.477 (7363), p.211-215 [Peer Reviewed Journal]

2015 INIST-CNRS ;COPYRIGHT 2011 Nature Publishing Group ;COPYRIGHT 2011 Nature Publishing Group ;Copyright Nature Publishing Group Sep 8, 2011 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature10353 ;PMID: 21857683 ;CODEN: NATUAS

Full text available

2
Gastrostomy in patients with amyotrophic lateral sclerosis (ProGas): a prospective cohort study
Material Type:
Article
Add to My Research

Gastrostomy in patients with amyotrophic lateral sclerosis (ProGas): a prospective cohort study

Lancet neurology, 2015-07, Vol.14 (7), p.702-709 [Peer Reviewed Journal]

ProGas Study Group. Open Access article distributed under the terms of CC BY ;2015 ProGas Study Group. Open Access article distributed under the terms of CC BY ;Copyright © 2015 ProGas Study Group. Open Access article distributed under the terms of CC BY. Published by Elsevier Ltd.. All rights reserved. ;Copyright Elsevier Limited Jul 2015 ;2015 ProGas Study Group. Open Access article distributed under the terms of CC BY 2015 ;ISSN: 1474-4422 ;EISSN: 1474-4465 ;DOI: 10.1016/S1474-4422(15)00104-0 ;PMID: 26027943 ;CODEN: LANCAO

Full text available

3
Genotype–phenotype characterisation of long survivors with motor neuron disease in Scotland
Material Type:
Article
Add to My Research

Genotype–phenotype characterisation of long survivors with motor neuron disease in Scotland

Journal of neurology, 2023-03, Vol.270 (3), p.1702-1712 [Peer Reviewed Journal]

The Author(s) 2022 ;2022. The Author(s). ;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: 0340-5354 ;EISSN: 1432-1459 ;DOI: 10.1007/s00415-022-11505-0 ;PMID: 36515702

Full text available

4
Riluzole prescribing, uptake and treatment discontinuation in people with amyotrophic lateral sclerosis in Scotland
Material Type:
Article
Add to My Research

Riluzole prescribing, uptake and treatment discontinuation in people with amyotrophic lateral sclerosis in Scotland

Journal of neurology, 2020-08, Vol.267 (8), p.2459-2461 [Peer Reviewed Journal]

The Author(s) 2020 ;The Author(s) 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: 0340-5354 ;EISSN: 1432-1459 ;DOI: 10.1007/s00415-020-09919-9 ;PMID: 32447548

Full text available

5
Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance
Material Type:
Article
Add to My Research

Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance

Brain (London, England : 1878), 2014-05, Vol.137 (5), p.1323-1336 [Peer Reviewed Journal]

The Author (2014). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2014 ;2015 INIST-CNRS ;The Author (2014). Published by Oxford University Press on behalf of the Guarantors of Brain. 2014 ;ISSN: 0006-8950 ;EISSN: 1460-2156 ;DOI: 10.1093/brain/awu060 ;PMID: 24727571

Full text available

6
Dendritic spinopathy in transgenic mice expressing ALS/dementia-linked mutant UBQLN2
Material Type:
Article
Add to My Research

Dendritic spinopathy in transgenic mice expressing ALS/dementia-linked mutant UBQLN2

Proceedings of the National Academy of Sciences - PNAS, 2014-10, Vol.111 (40), p.14524-14529 [Peer Reviewed Journal]

copyright © 1993–2008 National Academy of Sciences of the United States of America ;Copyright National Academy of Sciences Oct 7, 2014 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1405741111 ;PMID: 25246588

Full text available

7
Efficacy of erenumab and factors predicting response after 3 months in treatment resistant chronic migraine: a clinical service evaluation
Material Type:
Article
Add to My Research

Efficacy of erenumab and factors predicting response after 3 months in treatment resistant chronic migraine: a clinical service evaluation

Journal of headache and pain, 2022-12, Vol.23 (1), p.86-86, Article 86 [Peer Reviewed Journal]

The Author(s) 2022 ;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: 1129-2369 ;EISSN: 1129-2377 ;DOI: 10.1186/s10194-022-01456-2 ;PMID: 35869443

Full text available

8
Conversion to the Amyotrophic Lateral Sclerosis Phenotype Is Associated with Intermolecular Linked Insoluble Aggregates of SOD1 in Mitochondria
Material Type:
Article
Add to My Research

Conversion to the Amyotrophic Lateral Sclerosis Phenotype Is Associated with Intermolecular Linked Insoluble Aggregates of SOD1 in Mitochondria

Proceedings of the National Academy of Sciences - PNAS, 2006-05, Vol.103 (18), p.7142-7147 [Peer Reviewed Journal]

Copyright 2006 National Academy of Sciences of the United States of America ;Copyright National Academy of Sciences May 2, 2006 ;2006 by The National Academy of Sciences of the USA 2006 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.0602046103 ;PMID: 16636275

Full text available

9
Diagnosing ALS: the Gold Coast criteria and the role of EMG
Material Type:
Article
Add to My Research

Diagnosing ALS: the Gold Coast criteria and the role of EMG

Practical neurology, 2022-06, Vol.22 (3), p.176-178 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ. ;2022 Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: 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. ;Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ. 2022 ;ISSN: 1474-7758 ;EISSN: 1474-7766 ;DOI: 10.1136/practneurol-2021-003256 ;PMID: 34992096

Full text available

10
Clinical trials in amyotrophic lateral sclerosis: a systematic review and perspective
Material Type:
Article
Add to My Research

Clinical trials in amyotrophic lateral sclerosis: a systematic review and perspective

Brain communications, 2021-10, Vol.3 (4), p.fcab242-fcab242 [Peer Reviewed Journal]

The Author(s) (2021). Published by Oxford University Press on behalf of the Guarantors of Brain. 2021 ;The Author(s) (2021). Published by Oxford University Press on behalf of the Guarantors of Brain. ;ISSN: 2632-1297 ;EISSN: 2632-1297 ;DOI: 10.1093/braincomms/fcab242 ;PMID: 34901853

Full text available

11
Distal axonopathy in an alsin-deficient mouse model
Material Type:
Article
Add to My Research

Distal axonopathy in an alsin-deficient mouse model

Human molecular genetics, 2007-12, Vol.16 (23), p.2911-2920 [Peer Reviewed Journal]

The Author 2007. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org 2007 ;2008 INIST-CNRS ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/ddm251 ;PMID: 17855450 ;CODEN: HNGEE5

Full text available

12
Modulation of GABAA receptors by tyrosine phosphorylation
Material Type:
Article
Add to My Research

Modulation of GABAA receptors by tyrosine phosphorylation

Nature (London), 1995-09, Vol.377 (6547), p.344-348 [Peer Reviewed Journal]

1995 INIST-CNRS ;Copyright Macmillan Journals Ltd. Sep 28, 1995 ;Copyright Nature Publishing Group Sep 28, 1995 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/377344a0 ;PMID: 7566089 ;CODEN: NATUAS

Full text available

13
206  Use of non-invasive vagal nerve stimulation in a tertiary headache service
Material Type:
Article
Add to My Research

206  Use of non-invasive vagal nerve stimulation in a tertiary headache service

Journal of neurology, neurosurgery and psychiatry, 2022-06, Vol.93 (6), p.A72-A72 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;2022 Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0022-3050 ;EISSN: 1468-330X ;DOI: 10.1136/jnnp-2022-ABN.235

Full text available

14
Cancer and motor neuron disease—causal or coincidental? Two contrasting cases
Material Type:
Article
Add to My Research

Cancer and motor neuron disease—causal or coincidental? Two contrasting cases

Neurological sciences, 2019-07, Vol.40 (7), p.1461-1463 [Peer Reviewed Journal]

Fondazione Società Italiana di Neurologia 2019 ;Neurological Sciences is a copyright of Springer, (2019). All Rights Reserved. ;ISSN: 1590-1874 ;EISSN: 1590-3478 ;DOI: 10.1007/s10072-019-03784-9 ;PMID: 30843116

Full text available

15
050  Evaluation of 3 month data for the use of erenumab for chronic migraine in Glasgow
Material Type:
Article
Add to My Research

050  Evaluation of 3 month data for the use of erenumab for chronic migraine in Glasgow

Journal of neurology, neurosurgery and psychiatry, 2022-06, Vol.93 (6), p.A116-A116 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;2022 Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0022-3050 ;EISSN: 1468-330X ;DOI: 10.1136/jnnp-2022-ABN.375

Full text available

16
Impaired Autoinhibition of Protein Kinase Cγ in Spinocerebellar Ataxia Type 14
Material Type:
Article
Add to My Research

Impaired Autoinhibition of Protein Kinase Cγ in Spinocerebellar Ataxia Type 14

The FASEB journal, 2020-04, Vol.34 (S1), p.1-1 [Peer Reviewed Journal]

ISSN: 0892-6638 ;EISSN: 1530-6860 ;DOI: 10.1096/fasebj.2020.34.s1.04177

Full text available

17
Impaired Autoinhibition of Protein Kinase Cγ in Spinocerebellar Ataxia Type 14
Material Type:
Article
Add to My Research

Impaired Autoinhibition of Protein Kinase Cγ in Spinocerebellar Ataxia Type 14

Biophysical journal, 2020-02, Vol.118 (3), p.535a-535a [Peer Reviewed Journal]

2020 ;ISSN: 0006-3495 ;EISSN: 1542-0086 ;DOI: 10.1016/j.bpj.2019.11.2936

Full text available

18
Changing epidemiology of motor neurone disease in Scotland
Material Type:
Article
Add to My Research

Changing epidemiology of motor neurone disease in Scotland

Journal of neurology, 2019-04, Vol.266 (4), p.817-825 [Peer Reviewed Journal]

Springer-Verlag GmbH Germany, part of Springer Nature 2019 ;Journal of Neurology is a copyright of Springer, (2019). All Rights Reserved. ;ISSN: 0340-5354 ;EISSN: 1432-1459 ;DOI: 10.1007/s00415-019-09190-7 ;PMID: 30805795

Full text available

19
15.33 Phenotype-genotype characterisation of ‘long survivors’ with motor neurone disease in Scotland
Material Type:
Article
Add to My Research

15.33 Phenotype-genotype characterisation of ‘long survivors’ with motor neurone disease in Scotland

Journal of neurology, neurosurgery and psychiatry, 2019-12, Vol.90 (12), p.e5-e5 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ. ;2019 Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0022-3050 ;EISSN: 1468-330X ;DOI: 10.1136/jnnp-2019-ABN-2.15

Full text available

20
032 Clinical audit research and evaluation for motor neurone disease (CARE-MND): alignment with clinical care standards
Material Type:
Article
Add to My Research

032 Clinical audit research and evaluation for motor neurone disease (CARE-MND): alignment with clinical care standards

Journal of neurology, neurosurgery and psychiatry, 2019-12, Vol.90 (12), p.A18-A18 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ. ;2019 Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0022-3050 ;EISSN: 1468-330X ;DOI: 10.1136/jnnp-2019-ABN-2.59

Full text available

Results 1 - 20 of 42  for All Library Resources

Results 1 2 3 next page

Personalize your results

  1. Edit

Refine Search Results

Expand My Results

  1.   

Show only

  1. Peer-reviewed Journals (38)

Refine My Results

Creation Date 

From To
  1. Before 1995  (3)
  2. 1995 To 1999  (12)
  3. 2000 To 2010  (4)
  4. 2011 To 2015  (8)
  5. After 2015  (16)
  6. More options open sub menu

Language 

  1. Japanese  (4)
  2. French  (1)
  3. More options open sub menu

Searching Remote Databases, Please Wait