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Hywel Williams

Showing results (51-60 of 86) with videos related to

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Trials|March 19, 2016
A behavioural change package to prevent hand dermatitis in nurses working in the national health service (the SCIN trial): study protocol for a cluster randomised controlled trialIra Madan, Vaughan Parsons, Barry Cookson, et al.
Biological Psychiatry|June 14, 2005
A family based study implicates solute carrier family 1-member 3 (SLC1A3) gene in attention-deficit/hyperactivity disorderDarko Turic, Kate Langley, Hywel Williams, et al.
Health Technology Assessment (Winchester, England)|October 23, 2019
A behaviour change package to prevent hand dermatitis in nurses working in health care: the SCIN cluster RCTIra Madan, Vaughan Parsons, Georgia Ntani, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 14, 2012
Genome-wide supported psychosis risk variant in ZNF804A gene and impact on cortico-limbic WM integrity in schizophreniaCarissa Nadia Kuswanto, Puay-San Woon, Xue Bin Zheng, et al.
The Journal of Allergy and Clinical Immunology|December 13, 2006
Poor sanitation and helminth infection protect against skin sensitization in Vietnamese children: A cross-sectional studyCarsten Flohr, Luc Nguyen Tuyen, Sarah Lewis, et al.
JIMD Reports|October 9, 2015
Seizures Due to a KCNQ2 Mutation: Treatment with Vitamin B6Emma S Reid, Hywel Williams, Polona Le Quesne Stabej, et al.
Trials|May 11, 2021
Developing the INCLUDE Ethnicity Framework-a tool to help trialists design trials that better reflect the communities they serveShaun Treweek, Katie Banister, Peter Bower, et al.
Archives of General Psychiatry|October 6, 2005
Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13Marian L Hamshere, Phil Bennett, Nigel Williams, et al.
The Journal of Clinical Psychiatry|November 8, 2011
ARVCF genetic influences on neurocognitive and neuroanatomical intermediate phenotypes in Chinese patients with schizophreniaKang Sim, Wai-Yen Chan, Puay-San Woon, et al.
Human Molecular Genetics|November 16, 2007
Strong evidence that GNB1L is associated with schizophreniaNigel M Williams, Beate Glaser, Nadine Norton, et al.
Pageof 9

Showing results (51-60 of 86) with videos related to

Sort By:
Pageof 9
Trials|March 19, 2016
A behavioural change package to prevent hand dermatitis in nurses working in the national health service (the SCIN trial): study protocol for a cluster randomised controlled trialIra Madan, Vaughan Parsons, Barry Cookson, et al.
Biological Psychiatry|June 14, 2005
A family based study implicates solute carrier family 1-member 3 (SLC1A3) gene in attention-deficit/hyperactivity disorderDarko Turic, Kate Langley, Hywel Williams, et al.
Health Technology Assessment (Winchester, England)|October 23, 2019
A behaviour change package to prevent hand dermatitis in nurses working in health care: the SCIN cluster RCTIra Madan, Vaughan Parsons, Georgia Ntani, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 14, 2012
Genome-wide supported psychosis risk variant in ZNF804A gene and impact on cortico-limbic WM integrity in schizophreniaCarissa Nadia Kuswanto, Puay-San Woon, Xue Bin Zheng, et al.
The Journal of Allergy and Clinical Immunology|December 13, 2006
Poor sanitation and helminth infection protect against skin sensitization in Vietnamese children: A cross-sectional studyCarsten Flohr, Luc Nguyen Tuyen, Sarah Lewis, et al.
JIMD Reports|October 9, 2015
Seizures Due to a KCNQ2 Mutation: Treatment with Vitamin B6Emma S Reid, Hywel Williams, Polona Le Quesne Stabej, et al.
Trials|May 11, 2021
Developing the INCLUDE Ethnicity Framework-a tool to help trialists design trials that better reflect the communities they serveShaun Treweek, Katie Banister, Peter Bower, et al.
Archives of General Psychiatry|October 6, 2005
Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13Marian L Hamshere, Phil Bennett, Nigel Williams, et al.
The Journal of Clinical Psychiatry|November 8, 2011
ARVCF genetic influences on neurocognitive and neuroanatomical intermediate phenotypes in Chinese patients with schizophreniaKang Sim, Wai-Yen Chan, Puay-San Woon, et al.
Human Molecular Genetics|November 16, 2007
Strong evidence that GNB1L is associated with schizophreniaNigel M Williams, Beate Glaser, Nadine Norton, et al.
Pageof 9