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S Aggarwal

Showing results (311-320 of 344) with videos related to

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British Journal of Anaesthesia|February 25, 2012
Central venous thrombosis and perioperative vascular access in adult intestinal transplantationT Matsusaki, T Sakai, C D Boucek, et al.
Anesthesia and Analgesia|February 1, 1991
Pharmacokinetics and pharmacodynamics of doxacurium in normal patients and in those with hepatic or renal failureD R Cook, J A Freeman, A A Lai, et al.
Journal of Medical Virology|September 26, 2018
Mumps outbreak investigation in Jaisalmer, Rajasthan, India, June-September 2016Chandrakant S Moghe, Pramod Goel, Jalam Singh, et al.
South Asian Journal of Cancer|May 4, 2018
Practical consensus recommendations on management of HR + ve early breast cancer with specific reference to genomic profilingS Aggarwal, A Vaid, A Ramesh, et al.
South Asian Journal of Cancer|May 4, 2018
Practical consensus recommendations on duration of adjuvant hormonal therapy in breast cancerS Gupta, M Singh, Amish Vora, et al.
The National Medical Journal of India|April 20, 2005
The first successful simultaneous pancreas-kidney transplant in IndiaS Guleria, S Aggarwal, V K Bansal, et al.
British Journal of Cancer|March 25, 2010
Expansion of CD133(+) colon cancer cultures retaining stem cell properties to enable cancer stem cell target discoveryD D Fang, Y J Kim, C N Lee, et al.
BMC Neurology|August 13, 2015
Biomarkers to enhance accuracy and precision of prediction of short-term and long-term outcome after spontaneous intracerebral haemorrhage: a study protocol for a prospective cohort studyA Kumar, P Kumar, S Misra, et al.
American Journal of Medical Genetics. Part A|September 24, 2017
Loss-of-function variants in NFIA provide further support that NFIA is a critical gene in 1p32-p31 deletion syndrome: A four patient seriesAnya Revah-Politi, Mythily Ganapathi, Louise Bier, et al.
Journal of Human Genetics|September 19, 2020
Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophreniaAnna Alkelai, Shahar Shohat, Lior Greenbaum, et al.
Pageof 35

Showing results (311-320 of 344) with videos related to

Sort By:
Pageof 35
British Journal of Anaesthesia|February 25, 2012
Central venous thrombosis and perioperative vascular access in adult intestinal transplantationT Matsusaki, T Sakai, C D Boucek, et al.
Anesthesia and Analgesia|February 1, 1991
Pharmacokinetics and pharmacodynamics of doxacurium in normal patients and in those with hepatic or renal failureD R Cook, J A Freeman, A A Lai, et al.
Journal of Medical Virology|September 26, 2018
Mumps outbreak investigation in Jaisalmer, Rajasthan, India, June-September 2016Chandrakant S Moghe, Pramod Goel, Jalam Singh, et al.
South Asian Journal of Cancer|May 4, 2018
Practical consensus recommendations on management of HR + ve early breast cancer with specific reference to genomic profilingS Aggarwal, A Vaid, A Ramesh, et al.
South Asian Journal of Cancer|May 4, 2018
Practical consensus recommendations on duration of adjuvant hormonal therapy in breast cancerS Gupta, M Singh, Amish Vora, et al.
The National Medical Journal of India|April 20, 2005
The first successful simultaneous pancreas-kidney transplant in IndiaS Guleria, S Aggarwal, V K Bansal, et al.
British Journal of Cancer|March 25, 2010
Expansion of CD133(+) colon cancer cultures retaining stem cell properties to enable cancer stem cell target discoveryD D Fang, Y J Kim, C N Lee, et al.
BMC Neurology|August 13, 2015
Biomarkers to enhance accuracy and precision of prediction of short-term and long-term outcome after spontaneous intracerebral haemorrhage: a study protocol for a prospective cohort studyA Kumar, P Kumar, S Misra, et al.
American Journal of Medical Genetics. Part A|September 24, 2017
Loss-of-function variants in NFIA provide further support that NFIA is a critical gene in 1p32-p31 deletion syndrome: A four patient seriesAnya Revah-Politi, Mythily Ganapathi, Louise Bier, et al.
Journal of Human Genetics|September 19, 2020
Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophreniaAnna Alkelai, Shahar Shohat, Lior Greenbaum, et al.
Pageof 35