Search research articles
Contact Us
Filters
Showing results (411-420 of 565) with videos related to
Page
of 57
Sort By:
Plos One
|
June 21, 2013
Hypomethylation of serum blood clot DNA, but not plasma EDTA-blood cell pellet DNA, from vitamin B12-deficient subjects
Eoin P Quinlivan, Krista S Crider, Jiang-Hui Zhu, et al.
Journal of Neuromuscular Diseases
|
March 1, 2021
Improving Care and Empowering Adults Living with SMA: A Call to Action in the New Treatment Era
Maggie C Walter, Claudia Chiriboga, Tina Duong, et al.
Neuromuscular Disorders : NMD
|
February 10, 2018
GYG1 causing progressive limb girdle myopathy with onset during teenage years (polyglucosan body myopathy 2)
Mahalekshmi Desikan, Renata Siciliani Scalco, Andreea Manole, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 11, 2002
Folate synthesis in plants: the first step of the pterin branch is mediated by a unique bimodular GTP cyclohydrolase I
Gilles Basset, Eoin P Quinlivan, Michael J Ziemak, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
April 13, 2011
Evaluation of [¹²³I]-CLINDE as a potent SPECT radiotracer to assess the degree of astroglia activation in cuprizone-induced neuroinflammation
Filomena Mattner, David Linares Bandin, Maria Staykova, et al.
Neuromuscular Disorders : NMD
|
July 3, 2021
The phenotypic and genotypic features of a Scottish cohort with McArdle disease
Sacha E Gandhi, Cheryl Longman, Richard K H Petty, et al.
Bjpsych Open
|
September 8, 2025
Umbrella review of psychosocial and ward-based interventions to reduce self-harm and suicide risks in in-patient mental health settings
Leah Quinlivan, Jodie Westhead, Jane Graney, et al.
BMJ Open
|
October 22, 2024
Care gaps among people presenting to the hospital following self-harm: observational study of three emergency departments in England
Sarah Steeg, Harriet Bickley, Caroline Clements, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 24, 2010
McArdle disease: a clinical review
R Quinlivan, J Buckley, M James, et al.
Archives of Neurology
|
May 19, 2004
Extreme variability of phenotype in patients with an identical missense mutation in the lamin A/C gene: from congenital onset with severe phenotype to milder classic Emery-Dreifuss variant
Eugenio Mercuri, Maja Poppe, Ros Quinlivan, et al.
Page
of 57
Search research articles
Search
Showing results (411-420 of 565) with videos related to
Sort By:
Page
of 57
Plos One
|
June 21, 2013
Hypomethylation of serum blood clot DNA, but not plasma EDTA-blood cell pellet DNA, from vitamin B12-deficient subjects
Eoin P Quinlivan, Krista S Crider, Jiang-Hui Zhu, et al.
Journal of Neuromuscular Diseases
|
March 1, 2021
Improving Care and Empowering Adults Living with SMA: A Call to Action in the New Treatment Era
Maggie C Walter, Claudia Chiriboga, Tina Duong, et al.
Neuromuscular Disorders : NMD
|
February 10, 2018
GYG1 causing progressive limb girdle myopathy with onset during teenage years (polyglucosan body myopathy 2)
Mahalekshmi Desikan, Renata Siciliani Scalco, Andreea Manole, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 11, 2002
Folate synthesis in plants: the first step of the pterin branch is mediated by a unique bimodular GTP cyclohydrolase I
Gilles Basset, Eoin P Quinlivan, Michael J Ziemak, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
April 13, 2011
Evaluation of [¹²³I]-CLINDE as a potent SPECT radiotracer to assess the degree of astroglia activation in cuprizone-induced neuroinflammation
Filomena Mattner, David Linares Bandin, Maria Staykova, et al.
Neuromuscular Disorders : NMD
|
July 3, 2021
The phenotypic and genotypic features of a Scottish cohort with McArdle disease
Sacha E Gandhi, Cheryl Longman, Richard K H Petty, et al.
Bjpsych Open
|
September 8, 2025
Umbrella review of psychosocial and ward-based interventions to reduce self-harm and suicide risks in in-patient mental health settings
Leah Quinlivan, Jodie Westhead, Jane Graney, et al.
BMJ Open
|
October 22, 2024
Care gaps among people presenting to the hospital following self-harm: observational study of three emergency departments in England
Sarah Steeg, Harriet Bickley, Caroline Clements, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 24, 2010
McArdle disease: a clinical review
R Quinlivan, J Buckley, M James, et al.
Archives of Neurology
|
May 19, 2004
Extreme variability of phenotype in patients with an identical missense mutation in the lamin A/C gene: from congenital onset with severe phenotype to milder classic Emery-Dreifuss variant
Eugenio Mercuri, Maja Poppe, Ros Quinlivan, et al.
Page
of 57