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C Prasad

Showing results (451-460 of 494) with videos related to

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Journal of Inherited Metabolic Disease|June 9, 2009
Coenzyme Q(10) is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduriaD Haas, P Niklowitz, F Hörster, et al.
Molecular Genetics and Metabolism|January 1, 2008
Mutations of the E1beta subunit gene (PDHB) in four families with pyruvate dehydrogenase deficiencyK Okajima, L G Korotchkina, C Prasad, et al.
Indian Journal of Otolaryngology and Head and Neck Surgery : Official Publication of the Association of Otolaryngologists of India|March 5, 2024
Invasive Sinusitis Presenting with Orbital Complications in COVID Patients: Is Mucor the Only Cause?Kouser Mohammadi, S M Azeem Mohiyuddin, K C Prasad, et al.
British Journal of Clinical Pharmacology|January 30, 2004
Sildenafil does not improve nitric oxide-mediated endothelium-dependent vascular responses in smokersVictor Dishy, Paul A Harris, Rosanna Pierce, et al.
European Journal of Anaesthesiology|May 10, 2012
Airway difficulty in Mallampati 'class zero' patients: a prospective double-blind observational studyHarihar V Hegde, Kothegala C Prasad, Manjunath T Bhat, et al.
Current Opinion in Neurology|February 17, 2000
Multiple antioxidants in the prevention and treatment of neurodegenerative disease: analysis of biologic rationaleK N Prasad, W C Cole, A R Hovland, et al.
Clinical Genetics|January 8, 2003
Cryptic chromosome rearrangements detected by subtelomere assay in patients with mental retardation and dysmorphic featuresA J Dawson, S Putnam, J Schultz, et al.
Acta Neurologica Scandinavica|January 3, 2013
Tumefactive demyelination: clinical, imaging and follow-up observations in thirty-nine patientsM Nagappa, A B Taly, S Sinha, et al.
Journal of Neurodevelopmental Disorders|December 5, 2009
Modeling rare gene variation to gain insight into the oldest biomarker in autism: construction of the serotonin transporter Gly56Ala knock-in mouseJeremy Veenstra-Vanderweele, Tammy N Jessen, Brent J Thompson, et al.
American Journal of Human Genetics|July 5, 2005
Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviorsJames S Sutcliffe, Ryan J Delahanty, Harish C Prasad, et al.
Pageof 50

Showing results (451-460 of 494) with videos related to

Sort By:
Pageof 50
Journal of Inherited Metabolic Disease|June 9, 2009
Coenzyme Q(10) is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduriaD Haas, P Niklowitz, F Hörster, et al.
Molecular Genetics and Metabolism|January 1, 2008
Mutations of the E1beta subunit gene (PDHB) in four families with pyruvate dehydrogenase deficiencyK Okajima, L G Korotchkina, C Prasad, et al.
Indian Journal of Otolaryngology and Head and Neck Surgery : Official Publication of the Association of Otolaryngologists of India|March 5, 2024
Invasive Sinusitis Presenting with Orbital Complications in COVID Patients: Is Mucor the Only Cause?Kouser Mohammadi, S M Azeem Mohiyuddin, K C Prasad, et al.
British Journal of Clinical Pharmacology|January 30, 2004
Sildenafil does not improve nitric oxide-mediated endothelium-dependent vascular responses in smokersVictor Dishy, Paul A Harris, Rosanna Pierce, et al.
European Journal of Anaesthesiology|May 10, 2012
Airway difficulty in Mallampati 'class zero' patients: a prospective double-blind observational studyHarihar V Hegde, Kothegala C Prasad, Manjunath T Bhat, et al.
Current Opinion in Neurology|February 17, 2000
Multiple antioxidants in the prevention and treatment of neurodegenerative disease: analysis of biologic rationaleK N Prasad, W C Cole, A R Hovland, et al.
Clinical Genetics|January 8, 2003
Cryptic chromosome rearrangements detected by subtelomere assay in patients with mental retardation and dysmorphic featuresA J Dawson, S Putnam, J Schultz, et al.
Acta Neurologica Scandinavica|January 3, 2013
Tumefactive demyelination: clinical, imaging and follow-up observations in thirty-nine patientsM Nagappa, A B Taly, S Sinha, et al.
Journal of Neurodevelopmental Disorders|December 5, 2009
Modeling rare gene variation to gain insight into the oldest biomarker in autism: construction of the serotonin transporter Gly56Ala knock-in mouseJeremy Veenstra-Vanderweele, Tammy N Jessen, Brent J Thompson, et al.
American Journal of Human Genetics|July 5, 2005
Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviorsJames S Sutcliffe, Ryan J Delahanty, Harish C Prasad, et al.
Pageof 50