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Matthew Bower

Showing results (21-30 of 42) with videos related to

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American Journal of Surgery|December 15, 2010
The lower incidence of melanoma in women may be related to increased preventative behaviorsNathaniel P Reuter, Matthew Bower, Charles R Scoggins, et al.
BMC Medical Genetics|June 17, 2018
Mosaicism of the UDP-Galactose transporter SLC35A2 in a female causing a congenital disorder of glycosylation: a case reportKristen Westenfield, Kyriakie Sarafoglou, Laura C Speltz, et al.
Water Research|August 12, 2009
A comparison of disinfection by-products found in chlorinated and chloraminated drinking waters in ScotlandEmma H Goslan, Stuart W Krasner, Matthew Bower, et al.
HPB : the Official Journal of the International Hepato Pancreato Biliary Association|May 25, 2010
Surgical downstaging and neo-adjuvant therapy in metastatic colorectal carcinoma with irinotecan drug-eluting beads: a multi-institutional studyMatthew Bower, Tiffany Metzger, Ken Robbins, et al.
Frontiers in Neurology|January 7, 2021
Case Report: Early-Onset Behavioral Variant Frontotemporal Dementia in Patient With Retrotransposed Full-Length Transcript of <i>Matrin-3</i> Variant 5Madelyn Castro, Nisha Venkateswaran, Samuel T Peters, et al.
Neurocritical Care|April 8, 2020
Early Initiation of Oral Antihypertensives Reduces Intensive Care Unit Stay and Hospital Cost for Patients with Hypertensive Intracerebral HemorrhageZhu Zhu, Matthew Bower, Sara Stern-Nezer, et al.
Archives of Neurology|September 15, 2005
Clinical and pathologic evidence of corticobasal degeneration and progressive supranuclear palsy in familial tauopathyPaul J Tuite, H Brent Clark, Catherine Bergeron, et al.
JAAD Case Reports|July 18, 2019
A homozygous frameshift variant in the <i>KRT5</i> gene is compatible with life and results in severe recessive epidermolysis bullosa simplexRebecca K Tryon, Jakub Tolar, Sarah M Preusser, et al.
Journal of Human Genetics|June 24, 2011
Novel and recurrent EMD mutations in patients with Emery-Dreifuss muscular dystrophy, identify exon 2 as a mutation hot spotCharlotte A Brown, Juergen Scharner, Kevin Felice, et al.
Plos One|November 27, 2013
Expansion of the Spinocerebellar ataxia type 10 (SCA10) repeat in a patient with Sioux Native American ancestryKhalaf Bushara, Matthew Bower, Jilin Liu, et al.
Pageof 5

Showing results (21-30 of 42) with videos related to

Sort By:
Pageof 5
American Journal of Surgery|December 15, 2010
The lower incidence of melanoma in women may be related to increased preventative behaviorsNathaniel P Reuter, Matthew Bower, Charles R Scoggins, et al.
BMC Medical Genetics|June 17, 2018
Mosaicism of the UDP-Galactose transporter SLC35A2 in a female causing a congenital disorder of glycosylation: a case reportKristen Westenfield, Kyriakie Sarafoglou, Laura C Speltz, et al.
Water Research|August 12, 2009
A comparison of disinfection by-products found in chlorinated and chloraminated drinking waters in ScotlandEmma H Goslan, Stuart W Krasner, Matthew Bower, et al.
HPB : the Official Journal of the International Hepato Pancreato Biliary Association|May 25, 2010
Surgical downstaging and neo-adjuvant therapy in metastatic colorectal carcinoma with irinotecan drug-eluting beads: a multi-institutional studyMatthew Bower, Tiffany Metzger, Ken Robbins, et al.
Frontiers in Neurology|January 7, 2021
Case Report: Early-Onset Behavioral Variant Frontotemporal Dementia in Patient With Retrotransposed Full-Length Transcript of <i>Matrin-3</i> Variant 5Madelyn Castro, Nisha Venkateswaran, Samuel T Peters, et al.
Neurocritical Care|April 8, 2020
Early Initiation of Oral Antihypertensives Reduces Intensive Care Unit Stay and Hospital Cost for Patients with Hypertensive Intracerebral HemorrhageZhu Zhu, Matthew Bower, Sara Stern-Nezer, et al.
Archives of Neurology|September 15, 2005
Clinical and pathologic evidence of corticobasal degeneration and progressive supranuclear palsy in familial tauopathyPaul J Tuite, H Brent Clark, Catherine Bergeron, et al.
JAAD Case Reports|July 18, 2019
A homozygous frameshift variant in the <i>KRT5</i> gene is compatible with life and results in severe recessive epidermolysis bullosa simplexRebecca K Tryon, Jakub Tolar, Sarah M Preusser, et al.
Journal of Human Genetics|June 24, 2011
Novel and recurrent EMD mutations in patients with Emery-Dreifuss muscular dystrophy, identify exon 2 as a mutation hot spotCharlotte A Brown, Juergen Scharner, Kevin Felice, et al.
Plos One|November 27, 2013
Expansion of the Spinocerebellar ataxia type 10 (SCA10) repeat in a patient with Sioux Native American ancestryKhalaf Bushara, Matthew Bower, Jilin Liu, et al.
Pageof 5