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E MacNamara

Showing results (51-60 of 61) with videos related to

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Diseases of the Colon and Rectum|April 6, 2001
Role of molecular diagnostic testing in familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer familiesR Rabelo, W Foulkes, P H Gordon, et al.
Anesthesia and Analgesia|December 1, 1985
Halothane effects on subendocardial oxygen supply-demand balance: estimation from intramyocardial tissue pressure and left ventricular pressureY D Kim, D Nematzadeh, D E Lees, et al.
Nephrologie|January 1, 1985
[Acute renal failure caused by acute oxalosis after massive ingestion of pyridoxilate]P Dequiedt, B Gosselin, O Benoit, et al.
Journal of Pediatric Psychology|February 21, 2018
A Pilot Study of Neural Correlates of Loss of Control Eating in Children With Overweight/Obesity: Probing Intermittent Access to Food as a Means of Eliciting Disinhibited EatingAndrea B Goldschmidt, Daniel P Dickstein, Annmarie E MacNamara, et al.
Clinical Genetics|July 16, 2004
Putative common origin of two MLH1 mutations in Italian-Quebec hereditary non-polyposis colorectal cancer familiesI Thiffault, W D Foulkes, V A Marcus, et al.
AJNR. American Journal of Neuroradiology|January 1, 1997
MR-based brain and cerebrospinal fluid measurement after traumatic brain injury: correlation with neuropsychological outcomeD D Blatter, E D Bigler, S D Gale, et al.
Brain Injury|March 1, 1996
Traumatic brain injury, alcohol and quantitative neuroimaging: preliminary findingsE D Bigler, D D Blatter, S C Johnson, et al.
Chronic Diseases in Canada|January 1, 1997
Using participatory action research to understand the meanings aboriginal Canadians attribute to the rising incidence of diabetesP Boston, S Jordan, E MacNamara, et al.
Journal of Medical Genetics|May 16, 2002
An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1P Hutter, J Wijnen, C Rey-Berthod, et al.
British Journal of Cancer|January 22, 2004
Germline truncating mutations in both MSH2 and BRCA2 in a single kindredI Thiffault, N Hamel, T Pal, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Diseases of the Colon and Rectum|April 6, 2001
Role of molecular diagnostic testing in familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer familiesR Rabelo, W Foulkes, P H Gordon, et al.
Anesthesia and Analgesia|December 1, 1985
Halothane effects on subendocardial oxygen supply-demand balance: estimation from intramyocardial tissue pressure and left ventricular pressureY D Kim, D Nematzadeh, D E Lees, et al.
Nephrologie|January 1, 1985
[Acute renal failure caused by acute oxalosis after massive ingestion of pyridoxilate]P Dequiedt, B Gosselin, O Benoit, et al.
Journal of Pediatric Psychology|February 21, 2018
A Pilot Study of Neural Correlates of Loss of Control Eating in Children With Overweight/Obesity: Probing Intermittent Access to Food as a Means of Eliciting Disinhibited EatingAndrea B Goldschmidt, Daniel P Dickstein, Annmarie E MacNamara, et al.
Clinical Genetics|July 16, 2004
Putative common origin of two MLH1 mutations in Italian-Quebec hereditary non-polyposis colorectal cancer familiesI Thiffault, W D Foulkes, V A Marcus, et al.
AJNR. American Journal of Neuroradiology|January 1, 1997
MR-based brain and cerebrospinal fluid measurement after traumatic brain injury: correlation with neuropsychological outcomeD D Blatter, E D Bigler, S D Gale, et al.
Brain Injury|March 1, 1996
Traumatic brain injury, alcohol and quantitative neuroimaging: preliminary findingsE D Bigler, D D Blatter, S C Johnson, et al.
Chronic Diseases in Canada|January 1, 1997
Using participatory action research to understand the meanings aboriginal Canadians attribute to the rising incidence of diabetesP Boston, S Jordan, E MacNamara, et al.
Journal of Medical Genetics|May 16, 2002
An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1P Hutter, J Wijnen, C Rey-Berthod, et al.
British Journal of Cancer|January 22, 2004
Germline truncating mutations in both MSH2 and BRCA2 in a single kindredI Thiffault, N Hamel, T Pal, et al.
Pageof 7