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H Farkas

Showing results (111-120 of 162) with videos related to

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Allergy|October 3, 2012
Short-term prophylaxis in hereditary angioedema due to deficiency of the C1-inhibitor--a long-term surveyH Farkas, Z Zotter, D Csuka, et al.
Molecular Vision|September 11, 2004
Comparative gene expression analysis of murine retina and brainAbigail S Hackam, Jiang Qian, Dongmei Liu, et al.
Orvosi Hetilap|June 5, 1998
[Simultaneous occurrence of hereditary angioneurotic edema and Crohn disease]H Farkas, L Gyeney, E Nemesánszky, et al.
Investigative Ophthalmology & Visual Science|June 30, 2004
Changes in retinal pigment epithelial gene expression induced by rod outer segment uptakeItay Chowers, Yoonhee Kim, Ronald H Farkas, et al.
Immunological Investigations|March 12, 1999
Coincidence of hereditary angioedema (HAE) with Crohn's diseaseH Farkas, L Gyeney, E Nemesánszky, et al.
The American Journal of Pathology|August 12, 2014
Mutations in pre-mRNA processing factors 3, 8, and 31 cause dysfunction of the retinal pigment epitheliumMichael H Farkas, Deborah S Lew, Maria E Sousa, et al.
Allergy|September 5, 2014
A novel assay to diagnose hereditary angioedema utilizing inhibition of bradykinin-forming enzymesK Joseph, S Bains, B G Tholanikunnel, et al.
BMC Infectious Diseases|June 20, 2003
Bioelectronic DNA detection of human papillomaviruses using eSensor: a model system for detection of multiple pathogensSuzanne D Vernon, Daniel H Farkas, Elizabeth R Unger, et al.
Cerebral Cortex (New York, N.Y. : 1991)|March 22, 2024
Auditory aversive generalization learning prompts threat-specific changes in alpha-band activityAndrew H Farkas, Richard T Ward, Faith E Gilbert, et al.
Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|February 15, 2001
Bioelectronic detection of point mutations using discrimination of the H63D polymorphism of the Hfe gene as a modelR M Umek, S S Lin, Y Chen Yp, et al.
Pageof 17

Showing results (111-120 of 162) with videos related to

Sort By:
Pageof 17
Allergy|October 3, 2012
Short-term prophylaxis in hereditary angioedema due to deficiency of the C1-inhibitor--a long-term surveyH Farkas, Z Zotter, D Csuka, et al.
Molecular Vision|September 11, 2004
Comparative gene expression analysis of murine retina and brainAbigail S Hackam, Jiang Qian, Dongmei Liu, et al.
Orvosi Hetilap|June 5, 1998
[Simultaneous occurrence of hereditary angioneurotic edema and Crohn disease]H Farkas, L Gyeney, E Nemesánszky, et al.
Investigative Ophthalmology & Visual Science|June 30, 2004
Changes in retinal pigment epithelial gene expression induced by rod outer segment uptakeItay Chowers, Yoonhee Kim, Ronald H Farkas, et al.
Immunological Investigations|March 12, 1999
Coincidence of hereditary angioedema (HAE) with Crohn's diseaseH Farkas, L Gyeney, E Nemesánszky, et al.
The American Journal of Pathology|August 12, 2014
Mutations in pre-mRNA processing factors 3, 8, and 31 cause dysfunction of the retinal pigment epitheliumMichael H Farkas, Deborah S Lew, Maria E Sousa, et al.
Allergy|September 5, 2014
A novel assay to diagnose hereditary angioedema utilizing inhibition of bradykinin-forming enzymesK Joseph, S Bains, B G Tholanikunnel, et al.
BMC Infectious Diseases|June 20, 2003
Bioelectronic DNA detection of human papillomaviruses using eSensor: a model system for detection of multiple pathogensSuzanne D Vernon, Daniel H Farkas, Elizabeth R Unger, et al.
Cerebral Cortex (New York, N.Y. : 1991)|March 22, 2024
Auditory aversive generalization learning prompts threat-specific changes in alpha-band activityAndrew H Farkas, Richard T Ward, Faith E Gilbert, et al.
Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|February 15, 2001
Bioelectronic detection of point mutations using discrimination of the H63D polymorphism of the Hfe gene as a modelR M Umek, S S Lin, Y Chen Yp, et al.
Pageof 17