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P Hoffman

Showing results (771-780 of 1,048) with videos related to

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The American Surgeon|November 1, 1993
A single institutional experience with preoperative chemoradiotherapy for stage I-III pancreatic adenocarcinomaJ P Hoffman, J L Weese, L J Solin, et al.
The American Surgeon|July 1, 1994
Morbidity after intraperitoneal insertion of saline-filled tissue expanders for small bowel exclusion from radiotherapy treatment fields: a prospective four year experience with 34 patientsJ P Hoffman, R Lanciano, N Z Carp, et al.
BMC Immunology|March 1, 2006
Sexual dimorphism in immune response genes as a function of pubertyRebecca Lamason, Po Zhao, Rashmi Rawat, et al.
Neurology|July 17, 1999
Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15F Martínez Murillo, H Kobayashi, E Pegoraro, et al.
International Journal of Gastrointestinal Cancer|September 14, 2004
Neoadjuvant chemoradiotherapy for adenocarcinoma of the pancreas: analysis of histopathology and outcomeAaron R Sasson, R Wesley Wetherington, John P Hoffman, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 8, 2012
Bodywide skipping of exons 45-55 in dystrophic mdx52 mice by systemic antisense deliveryYoshitsugu Aoki, Toshifumi Yokota, Tetsuya Nagata, et al.
Journal of Bioanalysis & Biomedicine|May 7, 2013
Accurate Quantitation of Dystrophin Protein in Human Skeletal Muscle Using Mass SpectrometryKristy J Brown, Ramya Marathi, Alyson A Fiorillo, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|May 17, 2012
Possible contamination of organ preservation fluid with Bacillus cereus: the United Kingdom responseC S Brown, M A Chand, P Hoffman, et al.
Neurology|December 13, 2000
A novel ryanodine receptor gene mutation causing both cores and rods in congenital myopathyP C Scacheri, E P Hoffman, J D Fratkin, et al.
Muscle & Nerve|April 16, 1999
Heart involvement in muscular dystrophies due to sarcoglycan gene mutationsP Melacini, M Fanin, D J Duggan, et al.
Pageof 105

Showing results (771-780 of 1,048) with videos related to

Sort By:
Pageof 105
The American Surgeon|November 1, 1993
A single institutional experience with preoperative chemoradiotherapy for stage I-III pancreatic adenocarcinomaJ P Hoffman, J L Weese, L J Solin, et al.
The American Surgeon|July 1, 1994
Morbidity after intraperitoneal insertion of saline-filled tissue expanders for small bowel exclusion from radiotherapy treatment fields: a prospective four year experience with 34 patientsJ P Hoffman, R Lanciano, N Z Carp, et al.
BMC Immunology|March 1, 2006
Sexual dimorphism in immune response genes as a function of pubertyRebecca Lamason, Po Zhao, Rashmi Rawat, et al.
Neurology|July 17, 1999
Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15F Martínez Murillo, H Kobayashi, E Pegoraro, et al.
International Journal of Gastrointestinal Cancer|September 14, 2004
Neoadjuvant chemoradiotherapy for adenocarcinoma of the pancreas: analysis of histopathology and outcomeAaron R Sasson, R Wesley Wetherington, John P Hoffman, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 8, 2012
Bodywide skipping of exons 45-55 in dystrophic mdx52 mice by systemic antisense deliveryYoshitsugu Aoki, Toshifumi Yokota, Tetsuya Nagata, et al.
Journal of Bioanalysis & Biomedicine|May 7, 2013
Accurate Quantitation of Dystrophin Protein in Human Skeletal Muscle Using Mass SpectrometryKristy J Brown, Ramya Marathi, Alyson A Fiorillo, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|May 17, 2012
Possible contamination of organ preservation fluid with Bacillus cereus: the United Kingdom responseC S Brown, M A Chand, P Hoffman, et al.
Neurology|December 13, 2000
A novel ryanodine receptor gene mutation causing both cores and rods in congenital myopathyP C Scacheri, E P Hoffman, J D Fratkin, et al.
Muscle & Nerve|April 16, 1999
Heart involvement in muscular dystrophies due to sarcoglycan gene mutationsP Melacini, M Fanin, D J Duggan, et al.
Pageof 105