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Patrick J Morrison

Showing results (101-110 of 158) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|April 4, 2014
Two recurrent mutations are associated with GNE myopathy in the North of BritainAmina Chaouch, Kathryn M Brennan, Judith Hudson, et al.
Human Molecular Genetics|May 11, 2023
Epigenotype-genotype-phenotype correlations in SETD1A and SETD2 chromatin disordersSunwoo Lee, Lara Menzies, Eleanor Hay, et al.
Neurology. Genetics|March 27, 2020
<i>MYORG</i>-related disease is associated with central pontine calcifications and atypical parkinsonismViorica Chelban, Miryam Carecchio, Gillian Rea, et al.
Cancer Prevention Research (Philadelphia, Pa.)|July 25, 2022
Cancer Prevention with Resistant Starch in Lynch Syndrome Patients in the CAPP2-Randomized Placebo Controlled Trial: Planned 10-Year Follow-upJohn C Mathers, Faye Elliott, Finlay Macrae, et al.
Lancet (London, England)|June 15, 2020
Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trialJohn Burn, Harsh Sheth, Faye Elliott, et al.
Frontiers in Neurology|November 30, 2019
Tuberous Sclerosis Complex (TSC): Expert Recommendations for Provision of Coordinated CareNicholas M P Annear, Richard E Appleton, Zahabiyah Bassi, et al.
Brain : a Journal of Neurology|September 14, 2013
Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a modelAndrea H Németh, Alexandra C Kwasniewska, Stefano Lise, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 19, 2015
Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 StudyMohammad Movahedi, D Timothy Bishop, Finlay Macrae, et al.
The Journal of Clinical Endocrinology and Metabolism|March 30, 2013
SRGAP1 is a candidate gene for papillary thyroid carcinoma susceptibilityHuiling He, Agnieszka Bronisz, Sandya Liyanarachchi, et al.
Human Mutation|October 6, 2009
Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHDChristopher J Ricketts, Julia R Forman, Eleanor Rattenberry, et al.
Pageof 16

Showing results (101-110 of 158) with videos related to

Sort By:
Pageof 16
Journal of Neurology, Neurosurgery, and Psychiatry|April 4, 2014
Two recurrent mutations are associated with GNE myopathy in the North of BritainAmina Chaouch, Kathryn M Brennan, Judith Hudson, et al.
Human Molecular Genetics|May 11, 2023
Epigenotype-genotype-phenotype correlations in SETD1A and SETD2 chromatin disordersSunwoo Lee, Lara Menzies, Eleanor Hay, et al.
Neurology. Genetics|March 27, 2020
<i>MYORG</i>-related disease is associated with central pontine calcifications and atypical parkinsonismViorica Chelban, Miryam Carecchio, Gillian Rea, et al.
Cancer Prevention Research (Philadelphia, Pa.)|July 25, 2022
Cancer Prevention with Resistant Starch in Lynch Syndrome Patients in the CAPP2-Randomized Placebo Controlled Trial: Planned 10-Year Follow-upJohn C Mathers, Faye Elliott, Finlay Macrae, et al.
Lancet (London, England)|June 15, 2020
Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trialJohn Burn, Harsh Sheth, Faye Elliott, et al.
Frontiers in Neurology|November 30, 2019
Tuberous Sclerosis Complex (TSC): Expert Recommendations for Provision of Coordinated CareNicholas M P Annear, Richard E Appleton, Zahabiyah Bassi, et al.
Brain : a Journal of Neurology|September 14, 2013
Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a modelAndrea H Németh, Alexandra C Kwasniewska, Stefano Lise, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 19, 2015
Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 StudyMohammad Movahedi, D Timothy Bishop, Finlay Macrae, et al.
The Journal of Clinical Endocrinology and Metabolism|March 30, 2013
SRGAP1 is a candidate gene for papillary thyroid carcinoma susceptibilityHuiling He, Agnieszka Bronisz, Sandya Liyanarachchi, et al.
Human Mutation|October 6, 2009
Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHDChristopher J Ricketts, Julia R Forman, Eleanor Rattenberry, et al.
Pageof 16