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S Kedar

Showing results (41-50 of 88) with videos related to

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Annales De Radiologie|January 1, 1985
[NMR imaging of bladder tumors in man. Initial clinical experience]R Sigal, A Lanir, S Kedar, et al.
Advances in Experimental Medicine and Biology|January 1, 1980
Increased incidence of nephrolithiasis (N) in lifeguards (LG) in IsraelO S Better, M Shabtai, S Kedar, et al.
Annals of Hematology|March 1, 2020
Mechanosensitive Piezo1 ion channel protein (PIEZO1 gene): update and extended mutation analysis of hereditary xerocytosis in IndiaTejashree Anil More, Rashmi Dongerdiye, Rati Devendra, et al.
Journal of Community Genetics|June 23, 2026
Underutilisation of hydroxyurea in sickle cell disease: a global scoping review of multilevel barriers and facilitatorsRavi Gajbhiye, Prabhakar S Kedar, Priya Rani, et al.
Biochemistry|April 17, 1990
Mechanism of HIV reverse transcriptase: enzyme-primer interaction as revealed through studies of a dNTP analogue, 3'-azido-dTTPP S Kedar, J Abbotts, T Kovács, et al.
Harefuah|August 1, 1979
[Increased incidence of nephrolithiasis among lifeguards in Israel]M Shabtai, A Malamud, J Berenheim, et al.
European Urology|January 1, 1995
The influence of patient positioning on the hemodynamic changes in TURP patients with severe coronary diseaseS Kedar, L Gaitini, S Vaida, et al.
Journal of Clinical Pathology|October 20, 2018
Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p.Ala337Thr) novel mutation in GPI gene in two Indian patientsPrabhakar S Kedar, Vinod Gupta, Rashmi Dongerdiye, et al.
Journal of Clinical Pathology|December 28, 2020
Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the <i>HK1</i> gene causing severe haemolytic anaemia with developmental delay in an Indian familyRashmi Dongerdiye, Sujatha Jagadeesh, Beena Suresh, et al.
Journal of the Neurological Sciences|October 25, 2011
Objective home-based gait assessment in spinocerebellar ataxiaS H Subramony, S Kedar, E Murray, et al.
Pageof 9

Showing results (41-50 of 88) with videos related to

Sort By:
Pageof 9
Annales De Radiologie|January 1, 1985
[NMR imaging of bladder tumors in man. Initial clinical experience]R Sigal, A Lanir, S Kedar, et al.
Advances in Experimental Medicine and Biology|January 1, 1980
Increased incidence of nephrolithiasis (N) in lifeguards (LG) in IsraelO S Better, M Shabtai, S Kedar, et al.
Annals of Hematology|March 1, 2020
Mechanosensitive Piezo1 ion channel protein (PIEZO1 gene): update and extended mutation analysis of hereditary xerocytosis in IndiaTejashree Anil More, Rashmi Dongerdiye, Rati Devendra, et al.
Journal of Community Genetics|June 23, 2026
Underutilisation of hydroxyurea in sickle cell disease: a global scoping review of multilevel barriers and facilitatorsRavi Gajbhiye, Prabhakar S Kedar, Priya Rani, et al.
Biochemistry|April 17, 1990
Mechanism of HIV reverse transcriptase: enzyme-primer interaction as revealed through studies of a dNTP analogue, 3'-azido-dTTPP S Kedar, J Abbotts, T Kovács, et al.
Harefuah|August 1, 1979
[Increased incidence of nephrolithiasis among lifeguards in Israel]M Shabtai, A Malamud, J Berenheim, et al.
European Urology|January 1, 1995
The influence of patient positioning on the hemodynamic changes in TURP patients with severe coronary diseaseS Kedar, L Gaitini, S Vaida, et al.
Journal of Clinical Pathology|October 20, 2018
Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p.Ala337Thr) novel mutation in GPI gene in two Indian patientsPrabhakar S Kedar, Vinod Gupta, Rashmi Dongerdiye, et al.
Journal of Clinical Pathology|December 28, 2020
Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the <i>HK1</i> gene causing severe haemolytic anaemia with developmental delay in an Indian familyRashmi Dongerdiye, Sujatha Jagadeesh, Beena Suresh, et al.
Journal of the Neurological Sciences|October 25, 2011
Objective home-based gait assessment in spinocerebellar ataxiaS H Subramony, S Kedar, E Murray, et al.
Pageof 9